{"id":18216,"date":"2022-03-06T17:09:34","date_gmt":"2022-03-06T22:09:34","guid":{"rendered":"http:\/\/www.bumc.bu.edu\/ppb\/?post_type=profile&#038;p=18216"},"modified":"2025-10-07T13:34:02","modified_gmt":"2025-10-07T17:34:02","slug":"david-h-farb-ph-d","status":"publish","type":"profile","link":"https:\/\/www.bumc.bu.edu\/ppb\/profile\/david-h-farb-ph-d\/","title":{"rendered":"David H. Farb, Ph.D."},"content":{"rendered":"<h4>Principal\u00a0Investigator,\u00a0<a target=\"_blank\" href=\"https:\/\/www.bumc.bu.edu\/ppb\/training-program\/laboratories\/lmn\/\" rel=\"noopener noreferrer\"><span style=\"color: #3366ff;\">Laboratory of Molecular Neurobiology<\/span><\/a><\/h4>\n<p><span>David H. Farb, Ph.D., was appointed Professor and Chairman of the Department of Pharmacology &amp; Experimental Therapeutics at Boston University (BU) Medical Campus on July 1, 1990.\u00a0 After founding the NIGMS Training Program in BioMolecular Pharmacology at BU, and 26 years of continuous funding from NIGMS, Dr. Farb decided to return to research to pursue his interests in neural-circuitry-level drug discovery. He stepped down from the department chair position on December 15, 2022, and continues to work full-time in research and teaching. He has also served as a member of the Drug Development Work Group of Mass Insight, co-author of the Massachusetts Technology Road Map for Drug Discovery, and a consultant for a number of small to large pharmaceutical, biotechnology, and patent litigation companies. For the past 9 years he has represented the academic community of Massachusetts as an expert in clinical pharmacology on the Board of Pharmacy\u2019s Licensure Advisory Committee and the Sub Committee on Adverse Events in the Massachusetts Department of Public Health.<\/span><\/p>\n<p>As head of the Laboratory of Molecular Neurobiology, he focuses on the identification of pharmacological treatments for disorders of learning and memory function. His research integrates existing electrophysiological, behavioral, pharmacological, and molecular genetic technologies in a novel systems-level platform for assessing the impact of cognitive enhancers such as neuroactive steroids upon fundamental hippocampal systems for pattern separation (encoding), and pattern completion (retrieval), that are believed to be essential for cognition in all mammals, including man. Deficits in aspects of episodic memory dependent on hippocampal function are evident in a variety of mental disorders, including schizophrenia, autism, Alzheimer\u2019s Disease, and normal aging. Existing pharmacotherapies are limited and carry substantial risk of adverse effects.<\/p>\n<p>The Laboratory of Molecular Neurobiology has a strong history of using a multidisciplinary approach that includes electrophysiological techniques combined with classic behavioral and molecular biological methods to investigate the mechanisms and modalities of novel therapeutics and advance the treatment of disorders and diseases of the nervous system.<\/p>\n<p>In search of more effective approaches to drug discovery, high-density <em>in vivo<\/em> electrophysiological recordings in awake freely behaving rats are presently being used in the Farb Laboratory to identify changes in hippocampal function that underlie cognitive deficits due to aging and disease and, to assess for the functional neural network correlates associated with effective therapeutics. Dr. Farb and the Laboratory of Molecular Neurobiology are among the researchers and laboratories that comprise the <a href=\"http:\/\/www.bu.edu\/csn\/\" target=\"_blank\" rel=\"noopener noreferrer\">Boston University Center for Systems Neuroscience<\/a>.<\/p>\n<p>The use of nanoparticles encapsulating hydrophilic or hydrophobic molecules is being explored for delivery of drugs across the blood brain barrier. Nanoparticle composition is being engineered to facilitate better delivery of drugs to specific target sites. Neuroactive drugs and proteins, biomarkers for novel diagnostics, sensitive dyes for neural mapping, and many other applications of nanoparticles are envisioned. The major advantage of this technique is the noninvasive delivery of molecules to the CNS via a peripheral injection.<\/p>\n<div class=\"clearing\"> <\/div>\n<h3><span style=\"color: #3366ff;\"><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/training-program\/laboratories\/lmn\/\" style=\"color: #3366ff;\">Lab Page<\/a><\/span><\/h3>\n<h3><a href=\"https:\/\/profiles.bu.edu\/David.Farb\"><span style=\"color: #3366ff;\">Publications<\/span><\/a><\/h3>\n<div class=\"bu_collapsible_container \" aria-live=\"polite\" data-customize-animation=\"false\"><h3 class=\"bu_collapsible\" aria-expanded=\"false\"tabindex=\"0\" role=\"button\">Professional Background<\/h3><div class=\"bu_collapsible_section\" style=\"display: none;\"><\/p>\n<p>Prior to joining BU, Dr. Farb was a Fogarty Senior International Fellow (1989 \u2013 1990) with Sydney Brenner, PhD in the Molecular Genetics Unit at the Medical Research Council, Cambridge University, UK. Dr. Farb received his B.A. in Chemistry from Long Island University, where he was President of the American Chemical Society chapter and received honors including the American Institute of Chemists Award. He received the Ph.D. in Biochemistry (enzyme mechanisms\/bioorganic chemistry) with William P. Jencks, M.D. at Brandeis University. After completing postdoctoral fellowships at Harvard Medical School in Pharmacology with Gerald D. Fischbach, M.D. and in Physiology with Susan E. Leeman, Ph.D., he became Assistant Professor of Anatomy and Cell Biology at the SUNY Downstate Medical Center. Dr. Farb was promoted to full professor with tenure, Head of the Molecular Pharmacology Research Program, and elected Presiding Officer of the Graduate School at SUNY. While in New York, Dr. Farb was elected Chair of the Section of Biological Sciences at the New York Academy of Sciences, where he subsequently founded the Section of Neuroscience. Dr. Farb has served as a consultant to large and small pharmaceutical companies, intellectual property law and portfolio investment firms. Dr. Farb was a member of the founding Scientific Advisory Boards of CoCensys and DOV Pharmaceuticals. He holds 9 issued U.S. patents, one patent issued in Australia, and one issued in Japan. Dr. Farb pioneered development of technology for high throughput electrophysiology and was the Scientific Founder of Scion Pharmaceuticals (acquired by Wyeth), which commercialized his patents on high throughput electrophysiology and small molecule modulators of amino acid receptors. High throughput electrophysiology is currently in use throughout the pharmaceutical industry for ion channel and receptor directed drug discovery.<\/p>\n<p>As a postdoctoral fellow, Dr. Farb, in collaboration with Dr. Dennis W. Choi and Dr. Gerald D. Fischbach, co-discovered the cellular mechanisms of action of benzodiazepines\u2014the class of anxiolytics, sedative hypnotics, and anticonvulsants that includes trade-name drugs such as Xanax, Valium, and Versed. This research showed that benzodiazepines acted by positive allosteric modulation of the type-A GABA receptor (<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Chlordiazepoxide+selectively+augments+GABA+action+in+spinal+cord+cell+cultures.\" target=\"_blank\" rel=\"noopener noreferrer\">Nature (1977) 269: 342-344<\/a>). Dr. Farb\u2019s research program focused on the turnover and regulation of GABA receptor function (Science (1984) 226: 857) as a nexus for the control of nervous system function. Dr. Farb\u2019s current research is directed toward the discovery and development of neuromodulators as therapeutic agents and on the structure, function, and cellular dynamics of ion channels and receptors in the brain and spinal cord. Ongoing studies are directed toward understanding the mechanisms of action of abused substances and steroid modulators and their interactions with excitatory and inhibitory amino acid receptors in the central nervous system (PNAS (1997) 94: 10450; Science Signaling (2000) 60: PE1;\u00a0PNAS (2004) 101: 8198). Dr. Farb\u2019s laboratory demonstrated that pregnanolone hemisuccinate inhibits reinstatement of cocaine seeking behavior, and this compound has been selected by NIDA for preclinical development in its Medications Development Program. \u00a0 The laboratory has recently shown that picomolar concentrations of the neurosteroid pregnenolone sulfate modulate signal transduction pathways implicated in learning and memory function (<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/25057049\" target=\"_blank\" rel=\"noopener noreferrer\">Mol. Pharm.\u00a02014 Oct;86(4):390-8.<\/a>). \u00a0The laboratory is currently using <a href=\"https:\/\/www.bumc.bu.edu\/ppb\/training-program\/laboratories\/lmn\/\" target=\"_blank\" rel=\"noopener noreferrer\"><em>in vivo<\/em> electrophysiology<\/a> to investigate the how cognitive enhancers including modulate neural network activity in freely behaving rodent models of age related cognitive impairment\u00a0<span>(<\/span><a href=\"\/ppb\/files\/2020\/02\/Robitsek_et_al-2015-Hippocampus.pdf\" target=\"_blank\" rel=\"noopener noreferrer\"><span class=\"jrnl\" title=\"Hippocampus\">Hippocampus,<\/span>\u00a02015<\/a><span>) and Alzheimer\u2019s disease (<\/span><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/34568591\/\" target=\"_blank\" rel=\"noopener noreferrer\">Heliyon, 2021<\/a><span>).<\/span><\/p>\n<p><\/div>\n<\/div>\n\n<div class=\"bu_collapsible_container \" aria-live=\"polite\" data-customize-animation=\"false\"><h3 class=\"bu_collapsible\" aria-expanded=\"false\"tabindex=\"0\" role=\"button\">Recent News<\/h3><div class=\"bu_collapsible_section\" style=\"display: none;\"><\/p>\n<ul>\n<li><a href=\"https:\/\/www.bumc.bu.edu\/busm\/2018\/12\/12\/2019-wing-tat-lee-award-winners-announced\/\" target=\"_blank\" rel=\"noopener noreferrer\">We are pleased to share the news that Dr. David H. Farb Professor and Chair is a recipient of the\u00a02019 Wing Tat Lee Award<\/a><\/li>\n<li><a href=\"http:\/\/www.bu.edu\/articles\/2017\/zebrafish-breast-cancer-research\/\">Part I of Dr. Farb&#8217;s\u00a0<\/a><a href=\"http:\/\/www.bu.edu\/articles\/2017\/zebrafish-breast-cancer-research\/\">interview <\/a><a href=\"http:\/\/www.bu.edu\/articles\/2017\/zebrafish-breast-cancer-research\/\">about the need for new targets, so drugs can selectively target triple-negative breast cancer with fewer side effects<\/a>.<\/li>\n<li><a href=\"http:\/\/www.bu.edu\/articles\/2017\/dioxin-breast-cancer-treatment\/\">Part II of Dr. Farb&#8217;s of interview\u00a0about the need for new targets, so drugs can selectively target triple-negative breast cancer with fewer side effects.<\/a><\/li>\n<li><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/2016\/11\/08\/dr-david-farb-speaker-for-the-tuesday-april-26-700-pm-presentation-of-embrace-of-the-serpent-at-the-coolidge-corner-theatre\/\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. David Farb, Speaker for Tuesday, April 26, 2016 presentation for Embrace of the Serpent at the Coolidge Corner Theatre<\/a><\/li>\n<li><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/2015\/10\/09\/neurophysiology-charges-ahead-science-2015-david-farb-phd-pharmacology-experimental-therapeutics\/\" target=\"_blank\" rel=\"noopener noreferrer\">Neurophysiology Charges Ahead,\u00a0Science 2015,\u00a0<span class=\"A11\"><span>David Farb, PhD<\/span><\/span><\/a><\/li>\n<li><a href=\"http:\/\/health.usnews.com\/health-news\/patient-advice\/articles\/2014\/11\/05\/6-little-known-uses-for-antidepressants\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. Farb interviewed by Kristin Fawcett of US News &amp; World Report Health on antidepressants<\/a><\/li>\n<li>Dr. Farb interviewed by Allison Eck of WGBH for NOVA NEXT on treatment of schizophrenia<\/li>\n<li>Dr. Farb appointed to the Board of Pharmacy&#8217;s Advisory Committee.<\/li>\n<li><a href=\"http:\/\/youtu.be\/p_ubaEXk0SA\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. Farb interviewed by Boston Herald on new LSD-like drug: N-Bomb<\/a>\u00a0Full article <a href=\"http:\/\/bostonherald.com\/news_opinion\/local_coverage\/2014\/09\/officials_push_to_make_new_lsd_like_drug_n_bomb_illegal\" target=\"_blank\" rel=\"noopener noreferrer\">available here.<\/a><\/li>\n<li><a href=\"http:\/\/www.bumc.bu.edu\/busm\/2014\/07\/31\/busm-researchers-uncover-new-possible-approach-for-treating-schizophrenia\/\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. Farb and colleagues uncover new possible approach for treating Schizophrenia<\/a><\/li>\n<li><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/dr-david-farbs-postdoctoral-trainee-led-team-of-researchers-who-developed-tecfidera\/\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. Farb &#8216;s\u00a0Postdoctoral Trainee led team of researchers who developed Tecfidera\u00ae<\/a><\/li>\n<li><a href=\"http:\/\/www.bostonglobe.com\/magazine\/2014\/01\/26\/what-drug-molly-and-how-turned-lethal\/1x7T7p7lGlhxCaSUj3sUwI\/story.html?s_campaign=8315\" target=\"_blank\" rel=\"noopener noreferrer\">Dr. Farb interviewed by The Boston Globe &#8211; There&#8217;s something about Molly<\/a><\/li>\n<li><a target=\"_blank\" href=\"http:\/\/www.youtube.com\/watch?v=iM_EAAh4GkU\" rel=\"noopener noreferrer\">Dr. David Farb interviewed for BU COM news segment &#8211; Use of drug &#8216;Molly&#8217; increasing<\/a><\/li>\n<li><a target=\"_blank\" href=\"http:\/\/www.bu.edu\/today\/2013\/the-trouble-with-molly\/\" rel=\"noopener noreferrer\">Dr. David Farb interviewed by BU Today &#8211; The Trouble with Molly<\/a><\/li>\n<li><a target=\"_blank\" href=\"http:\/\/www.biomedcentral.com\/2050-6511\/14\/42\" rel=\"noopener noreferrer\">An interview with David H Farb, Section Editor for Basic Pharmacology<\/a><\/li>\n<li><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/people\/faculty\/faculty-profiles\/neurochemical-traffic-signals-may-open-new-avenues-for-the-treatment-of-schizophrenia\/\" target=\"_blank\" rel=\"noopener noreferrer\">Neurochemical Traffic Signals May Open New Avenues for the Treatment of Schizophrenia<\/a><\/li>\n<li><a href=\"http:\/\/www.bumc.bu.edu\/2013\/08\/01\/architecture-of-a-fruit-fly-new-clues-for-reducing-electrical-surges-in-the-human-brain\/\" target=\"_blank\" rel=\"noopener noreferrer\">Architecture of a Fruit Fly: New Clues for Reducing Electrical Surges in the Human Brain<\/a><\/li>\n<li>Dr. David H. Farb appointed to founding Scientific Advisory Board of Sage Therapeutics<\/li>\n<li><a href=\"http:\/\/www.bumc.bu.edu\/busm\/2011\/09\/30\/busm-dept-of-pharmacology-experimental-therapeutics-pilot-in-university-wide-effort-to-go-green\/\">BUSM Department of Pharmacology &amp; Experimental Therapeutics Pilot in University-wide Effort to Go Green<\/a><\/li>\n<li>Dr. David H. Farb helps a dyslexic mountaineer investigate his ancestor&#8217;s wartime exposure on BYUtv&#8217;s The Generations Project<\/li>\n<li>Dr. David Farb interviewed by WGBH &#8211; Abusing the ADD drug Adderall<\/li>\n<li><a href=\"https:\/\/www.bu.edu\/articles\/2009\/tis-the-season-to-be-anxious\/\" title=\"Dr. Farb featured in BU Today \u2013 \u2018Tis the Season To Be Anxious\">Dr. David Farb featured in BU Today \u2013 \u2018Tis the Season To Be Anxious<\/a><\/li>\n<li><a href=\"https:\/\/www.bu.edu\/articles\/2009\/adderall-for-an-a-plus\/\" title=\"a virtual chat on the issues that matter &quot;Adderall for an A-Plus?&quot;\">Dr. David Farb participates in BU Today&#8217;s <em>Op-Heads: a virtual chat on the issues that matter<\/em> &#8220;Adderall for an A-Plus?&#8221;<\/a><\/li>\n<li>Dr. David Farb interviewed by NPR about the Hughes Medical Institute&#8217;s funding of biomedical research.<\/li>\n<li>Dr. David Farb interviewed by NPR about biomedical funding<\/li>\n<li>Dr. David Farb interviewed by the BBC as a part of their &#8220;Visions of the Future&#8221; series<\/li>\n<li><a href=\"http:\/\/www.nature.com\/naturejobs\/2007\/070913\/full\/nj7159-256a.html\">Farb on Choi &#8211; Nature News<\/a><\/li>\n<li><a href=\"http:\/\/www.bu.edu\/news\/2006\/06\/09\/research-with-commercial-potential-honored-through-ignition-awards\/\">Dr. David Farb is a winner of the 2006 Boston University Ignition Award<\/a><\/li>\n<li>Dr. David Farb &#8211; Content Reviewer for NOVA Science Now &#8220;Mirror Neurons&#8221;<\/li>\n<li><a href=\"https:\/\/abcnews.go.com\/Health\/story?id=2925245&amp;page=1\" title=\"Dr. David Farb interviewed by ABC News 'A Perfect Storm' for Creating Drug Addicts\">Dr. David Farb interviewed by ABC News <em>&#8216;A Perfect Storm&#8217; for Creating Drug Addicts<\/em><\/a><\/li>\n<\/ul>\n<p><\/div>\n<\/div>\n\n<div class=\"bu_collapsible_container \" aria-live=\"polite\" data-customize-animation=\"false\"><h3 class=\"bu_collapsible\" aria-expanded=\"false\"tabindex=\"0\" role=\"button\">Patents<\/h3><div class=\"bu_collapsible_section\" style=\"display: none;\"><\/p>\n<h3>Modulation of receptor-mediated ion transport<\/h3>\n<p>May 18, 1993<br \/>\nPatent: 5,212,167<br \/>\nInventors: Farb, David H.<\/p>\n<h4>Abstract<\/h4>\n<p>The subject application discloses methods for modulating NMDA-mediated ion transport, and inhibiting non-NMDA glutamate-induced ion transport, in neuronal cells. The methods involve contacting a neuronal cell with an effective amount of the neurosteroid pregnenolone sulfate, or pharmacologically effective derivatives thereof.<\/p>\n<h3>Modulation of receptor-mediated ion transport<\/h3>\n<p>November 22, 1994<br \/>\nPatent: 5,366,968<br \/>\nInventors: Farb, David H.<\/p>\n<h4>Abstract<\/h4>\n<p>The subject application discloses methods for modulating NMDA-mediated ion transport, and inhibiting non-NMDA glutamate-induced ion transport, in neuronal cells. The methods involve contacting a neuronal cell with an effective amount of the neurosteroid pregnenolone sulfate, or pharmacologically effective derivatives thereof.<\/p>\n<h3>Inhibition of NMDA receptor activity and modulation of glutamate-mediated synaptic activity<\/h3>\n<p>March 30, 1999<br \/>\nPatent: 5,888,996<br \/>\nInventors: Farb, David H.<\/p>\n<h4>Abstract<\/h4>\n<p>The present invention relates to a method of inhibiting N-methyl-D-aspartate (NMDA) glutamate receptor-mediated ion channel activity (NMDA receptor activity), comprising contacting a neuronal cell (e.g., hippocampal neuron, spinal cord cell) with an effective amount (e.g., 1 to 500 mu.M) of a derivative of pregnenolone sulfate. Derivatives of pregnenolone sulfate that inhibit NMDA receptor activity include pregnenolone sulfate in which the A ring includes at least one double bond or is fully unsaturated, the double bond at the C5-C6 position is reduced, the moiety at the C3, C10, C11 or C13 position is modified, alone or in combination. It further relates to pregnenolone sulfate derivatives which have modifications at other positions (e.g., C5, C7, C10, C16, C17, C18, C19, C20, C21), alone or in combination, and are inhibitors of NMDA receptor activity. The pregnenolone sulfate derivatives differ from pregnenolone sulfate at least one position. The present invention also relates to a method of modulating or altering (e.g., potentiating; inhibiting) excitatory glutamate-mediated synaptic activity comprising contacting neurons with pregnenolone sulfate and derivatives of pregnenolone sulfate.<\/p>\n<h3>Cellular physiology workstations for automated data acquisition and perfusion control<\/h3>\n<p>April 11, 2000<br \/>\nPatent: 6,048,722<br \/>\nInventors: Farb, David H.; Yaghoubi; Nader; Gibbs; Terrell T.<\/p>\n<h4>Abstract<\/h4>\n<p>Cellular physiology workstations for automated data acquisition and perfusion control are described. The cellular physiology workstation may be used for physiological and electrophysiological experiments. Methods for employing such cellular physiology workstations in physiological and electrophysiological experiments are also disclosed. The cellular physiology workstations comprise one or more recording chambers each for holding one or more cells to be measured. One or more cells are place in each recording chamber. Perfusion device, such as an automatic perfusion system is connected to the recording chamber to perfuse the cells with a plurality of solutions containing different concentration of one or more agents to be tested. Biosensors, such as patch clamps, electrodes, or microscopes are positioned to detect a response from the cell. The cellular physiology workstation may optionally comprise injecting device for introducing an injection solution into the cell before and during analysis.<\/p>\n<h3>Neuron-specific transcriptional promoter<\/h3>\n<p>May 23, 2000<br \/>\nPatent: 6,066,726<br \/>\nInventors: Farb, David H. (Cambridge, MA); Russek; Shelley J.<\/p>\n<h4>Abstract<\/h4>\n<p>The 5&#8242;-flanking region and core regulatory domains that underlie neuronal specific expression of the human .gamma.-aminobutyric acid type A (GABA.sub.A) receptor .beta.1 subunit gene are identified herein. Sequence analysis, mapping of transcriptional initiation sites, and transfection of reporter gene constructs into primary cultures demonstrate that neuronal and region specific activity resides in a TATA-less minimal promoter of 186 bp, comprising an initiator, the major transcriptional start site, a presumptive TFIID binding site, and an enhancer. Enhancer sequence contained within a 26 bp region at the 5&#8242;-end of the minimal promoter is essential for activity but not for tissue specificity. Moreover, .beta.1 promoter activity is subject to autologous inhibition, indicating that GABA-induced receptor mRNA downregulation results from an inhibition of gene transcription. Regulation of neurotransmitter receptor gene expression plays an important role in nervous system development and function, and impaired gene regulation may underlie the etiology of certain neurological diseases.<\/p>\n<h3>Inhibition of NMDA receptor activity by pregnenolone sulfate derivatives<\/h3>\n<p>July 4, 2000<br \/>\nPatent: 6,083,941<br \/>\nInventors: Farb, David H.<\/p>\n<h4>Abstract<\/h4>\n<p>The present invention relates to a method of inhibiting N-methyl-D-aspartate (NMDA) glutamate receptor-mediated ion channel activity (NMDA receptor activity), comprising contacting a neuronal cell (e.g., hippocampal neuron, spinal cord cell) with an effective amount (e.g., 1 to 500 mu M) of a derivative of pregnenolone sulfate. Derivatives of pregnenolone sulfate that inhibit NMDA receptor activity include pregnenolone sulfate derivatives in which the A ring includes at least one double bond; PS in which the A ring is fully unsaturated; PS derivatives in which the double bond at the C5-C6 position is reduced; and PS in which the moiety at the C3, C5, C6, C7, C11, C17, C20 and\/or C21 position is modified. It further relates to PS derivatives which have modifications at other positions (e.g., C10, C10, C13, C18, C19), alone or in combination, and are inhibitors of NMDA receptor activity. The present invention also relates to a method of modulating or altering (e.g., potentiating; inhibiting) excitatory glutamate-mediated synaptic activity comprising contacting neurons with pregnenolone sulfate and derivatives of pregnenolone sulfate. The present invention also relates to a method of treating a disease associated with L-glutamate-induced NMDA receptor activation selected from the group consisting of: neuropathic pain, drug withdrawal\/dependency, epilepsy, glaucoma, chronic neurodegenerative diseases, amyotrophic lateral sclerosis, anxiety disorders, brain cell death, ischemia, stroke, trauma in a host comprising administering to the host an effective amount of a derivative of pregnenolone sulfate.<\/p>\n<h3>Cellular physiology workstations for automated data acquisition and perfusion control<\/h3>\n<p>July 31, 2001<br \/>\nPatent: 6,268,168<br \/>\nInventors: Farb, David H.; Yaghoubi; Nader; Gibbs; Terrell T.<\/p>\n<h4>Abstract<\/h4>\n<p>Cellular physiology workstations for automated data acquisition and perfusion control are described. The cellular physiology workstation may be used for physiological and electrophysiological experiments. Methods for employing such cellular physiology workstations in physiological and electrophysiological experiments are also disclosed. The cellular physiology workstations comprise one or more recording chambers each for holding one or more cells to be measured. One or more cells are place in each recording chamber. Perfusions means, such as an automatic perfusion system is connected to the recording chamber to perfuse the cells with a plurality of solutions containing different concentration of one or more agents to be tested. Biosensors, such as patch clamps, electrodes, or microscopes are positioned to detect a response from the cell. The cellular physiology workstation may optionally comprise injecting means for introducing an injection solution into the cell before and during analysis.<\/p>\n<h3>Methods for identifying a subunit specific modulator of N-methyl-D-asparate receptor<\/h3>\n<p>September 23, 2003<br \/>\nPatent: 6,623,933<br \/>\nInventors: Farb, David H.; Yaghoubi, Nader; Russek, Shelley; Jang, Ming-Kuei; Gibbs, Terrell T.<\/p>\n<h4>Abstract<\/h4>\n<p>Disclosed is a method for identifying a subunit specific modulator of the N-methyl-D-aspartate (NMDA) receptor. The method involves providing a plurality of NMDA receptors which differ in their subunit identity. The receptors are contacted with a neurotransmitter recognition site ligand in the presence and absence of a candidate modulator. Receptor activity is then assayed, with an increase or decrease in activity in at least one, but not all members of the plurality of NMDA receptors, in the presence but not the absence of a candidate modulator, being an indication that the candidate modulator is a subunit specific modulator. The subunit identity of the subset of the NMDA receptors to determine the subunit specificity of the candidate modulator. Various combinations of NMDA receptor subunits are provided.<\/p>\n<h3>Cellular physiology workstations for automated data acquisition and perfusion control<\/h3>\n<p>July 13, 2004<br \/>\nPatent: 6,762,036<br \/>\nInventors: Farb, David H.; Yaghoubi; Nader; Gibbs; Terrell T.<\/p>\n<h4>Abstract<\/h4>\n<p>Cellular physiology workstations for automated data acquisition and perfusion control are described. The cellular physiology workstation may<br \/>\nbe used for physiological and electrophysiological experiments. Methods for employing such cellular physiology workstations in physiological and electrophysiological experiments are also disclosed. The cellular physiology workstations comprise one or more recording chambers each for holding one or more cells to be measured. One or more cells are place in each recording chamber. Perfusions means, such as an automatic perfusion syslatem is connected to the recording chamber to perfuse the cells with a plurality of solutions containing different concentration of one or more agents to be tested. Biosensors, such as patch clamps, electrodes, or microscopes are positioned to detect a response from the cell. The cellular physiology workstation may optionally comprise injecting means for introducing an injection solution into the cell before and during analysis.<\/p>\n<h3>Effect of steroids on NMDA receptors depends on subunit composition<\/h3>\n<p>July 7, 2005<br \/>\nPatent: AU 200070981<br \/>\nInventors: Farb, David H.; Russek, Shelley J.; Jang, Ming-Kuei; Gibbs,<br \/>\nTerrell T.; Yaghoubi, Nader.<\/p>\n<h3>Effect of Steroids on NMDA Receptors Depends on Subunit Composition<\/h3>\n<p>March 11, 2009<br \/>\nPatent: EP 1 212 618 B1<br \/>\nInventors: Farb, David H.; Russek, Shelley J.; Jang, Ming-Kuei; Gibbs,<br \/>\nTerrell; Yaghoubi, Nader.<\/p>\n<h3>Inhibition of NMDA Receptor Activity by Pregnenolone Sulfate Derivatives<\/h3>\n<p>May 22, 2009<br \/>\nPatent: Japan No. 4313435<br \/>\nInventors: Farb, David H.<\/p>\n<h2>United States Patent Applications<\/h2>\n<p><em>(published since March 15, 2001)<\/em><\/p>\n<h3>Effect of steroids on NMDA receptors depends on subunit composition<\/h3>\n<p>October 14, 2004<br \/>\n20040204490 Kind Code A1<br \/>\nInventors: Farb, David H.; Russek, Shelley;; Jang, Ming-Kuei; Gibbs, Terrell T.; Yaghoubi, Nader<\/p>\n<h4>Abstract<\/h4>\n<p>Disclosed is a method for identifying a subunit specific modulator of the N-methyl-D-aspartate (NMDA) receptor. The method involves providing a plurality of NMDA receptors which differ in their subunit identity. The receptors are contacted with a neurotransmitter recognition site ligand in the presence and absence of a candidate modulator. Receptor activity is then assayed, with an increase or decrease in activity in at least one, but not all members of the plurality of NMDA receptors, in the presence but not the absence of a candidate modulator, being an indication that the candidate modulator is a subunit specific modulator. The subunit identity of the subset of the NMDA receptors to determine the subunit specificity of the candidate modulator. Various combinations of NMDA receptor subunits are provided.<\/p>\n<h3>Neuroactive steroid derivatives and method of use<\/h3>\n<p>April 29, 2004<br \/>\n20040082554 Kind Code A1<br \/>\nInventors: Farb, David H.; (Brookline, MA) ; Sadri-Vakili, Ghazaleh; (Boston, MA) ; Pierce, Robert Christopher; (Boston, MA) ; Johnson, David W; (Kennebunk, ME); Gibbs, Terrell T<\/p>\n<h4>Abstract<\/h4>\n<p>The invention relates to neuroactive steroid compounds that are useful in modulating CNS effects, diseases or disease symptoms. The invention also relates to use of the compounds in methods of treating or preventing disease or disease symptoms, and methods of modulating or mediating CNS effects or processes<\/p>\n<h3>Cellular physiology workstations for automated data acquisition and perfusion control<\/h3>\n<p>June 20, 2002<br \/>\n20020076689 Kind Code A1<br \/>\nInventors: Farb, David H.; Yaghoubi, Nader; Gibbs, Terrell T<\/p>\n<h4>Abstract<\/h4>\n<p>Cellular physiology workstations for automated data acquisition and perfusion control are described. The cellular physiology workstation may be used for physiological and electrophysiological experiments. Methods for employing such cellular physiology workstations in physiological and electrophysiological experiments are also disclosed. The cellular physiology workstations comprise one or more recording chambers each for holding one or more cells to be measured. One or more cells are place in each recording chamber. Perfusions means, such as an automatic perfusion system is connected to the recording chamber to perfuse the cells with a plurality of solutions containing different concentration of one or more agents to be tested. Biosensors, such as patch clamps, electrodes, or microscopes are positioned to detect a response from the cell. The cellular physiology workstation may optionally comprise injecting means for introducing an injection solution into the cell before and during analysis.<\/p>\n<h3>Cellular physiology workstations for automated data acquisition and perfusion control<\/h3>\n<p>September 30, 2004<br \/>\n20040191853 Kind Code A1<br \/>\nInventors: Farb, David H.; Gibbs, Terrell T.; Yaghoubi, Nader<\/p>\n<h4>Abstract<\/h4>\n<p>Cellular physiology workstations for automated data acquisition and perfusion control are described. The cellular physiology workstation may be used for physiological and electrophysiological experiments. Methods for employing such cellular physiology workstations in physiological and electrophysiological experiments are also disclosed. The cellular physiology workstations comprise one or more recording chambers each for holding one or more cells to be measured. One or more cells are place in each recording chamber. Perfusions means, such as an automatic perfusion system is connected to the recording chamber to perfuse the cells with a plurality of solutions containing different concentration of one or more agents to be tested. Biosensors, such as patch clamps, electrodes, or microscopes are positioned to detect a response from the cell. The cellular physiology workstation may optionally comprise injecting means for introducing an injection solution into the cell before and during analysis.<\/p>\n<h2>Patents Pending (excluding international phase of above issued patents)<\/h2>\n<h3>A Neural Specific Cytosolic Sulfotransferase for Drug Screening (BU 00-29)<\/h3>\n<p>60\/229,929<br \/>\nInventors: Farb, David H.; Martin, Stella C.<\/p>\n<h3>Seizure -induced upregulation of the GABRA4 promoter identifies a condition-specific vector for the treatment of epilepsy.<\/h3>\n<p>BU04-03<br \/>\nInventors: Russek, Shelley J; Brooks-Kayal, A; Farb, David H.<\/p>\n<p><\/div>\n<\/div>\n\n<div class=\"bu_collapsible_container \" aria-live=\"polite\" data-customize-animation=\"false\"><h3 class=\"bu_collapsible\" aria-expanded=\"false\"tabindex=\"0\" role=\"button\">Current Laboratory Members<\/h3><div class=\"bu_collapsible_section\" style=\"display: none;\"><\/p>\n<h3><strong>Senior Laboratory Members<\/strong><\/h3>\n<p><strong><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/marcia-h-ratner-phd-dabt\/\" target=\"_blank\" rel=\"noopener noreferrer\">Marcia H. Ratner, PhD, DABT<\/a>,<\/strong>\u00a0Assistant Professor and Laboratory Manager<\/p>\n<p><strong><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/vidhya-kumaresan-ph-d\/\" target=\"_blank\" rel=\"noopener noreferrer\">Vidhya Kumaresan, PhD,\u00a0<\/a><\/strong>Research Assistant Professor<\/p>\n<h3><strong>Faculty Collaborators\u00a0<\/strong><\/h3>\n<p><b><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/shelley-j-russek-ph-d\/\" target=\"_blank\" rel=\"noopener noreferrer\">Shelley J. Russek, MA, PhD,\u00a0<\/a><\/b>Professor or\u00a0Pharmacology<\/p>\n<p><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/richard-d-wainford-ph-d\/\"><strong>Richard Wainford, PhD,<\/strong> <\/a><span>Associate Professor of Pharmacology<\/span><\/p>\n<p><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/weiming-xia-ph-d\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Weiming Xia, PhD,<\/strong> <\/a>Professor of Pharmacology<\/p>\n<p><\/div>\n<\/div>\n\n<div class=\"bu_collapsible_container \" aria-live=\"polite\" data-customize-animation=\"false\"><h3 class=\"bu_collapsible\" aria-expanded=\"false\"tabindex=\"0\" role=\"button\">Laboratory Alumni: Where They Are Now<\/h3><div class=\"bu_collapsible_section\" style=\"display: none;\"><\/p>\n<h3><strong>Visiting Scholars<\/strong><\/h3>\n<p><b><a href=\"https:\/\/www.researchgate.net\/profile\/Yunlong_Bai2\">Yunlong Bai, Ph.D.<\/a>\u2013 2019<br \/>\nWing Tat Lee Visiting Scholar<br \/>\nPosition:\u00a0<\/b>Professor and Chair of Pharmacology, and Deputy Dean of the College of Pharmacy, Harbin Medical University,\u00a0Harbin, China.<\/p>\n<p><b><strong>Nariara Karim, Ph.D.<\/strong><strong>\u2013 2018<\/strong><br \/>\n<strong>Fulbright Postdoctoral Visiting Scholar<br \/>\nPosition:\u00a0<\/strong><\/b>Assistant Professor, Department of Pharmacy, University of Malakand, Pakistan.<\/p>\n<h3>Pre-Doctoral Students<\/h3>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/kavithasugunan\/\" target=\"_blank\" rel=\"noopener noreferrer\"><strong>Kavitha Sugunan<\/strong>, Ph.D.<\/a> \u2013 2015<\/b><br \/>\n<b>Thesis:\u00a0<\/b>Pregnenolone Sulfate as a Modulator of Synaptic Plasticity<br \/>\n<b>Position: <\/b>Clinical Operations Lead Manager, Biogen<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/taramehan\/\" target=\"_blank\" rel=\"noopener noreferrer\">Tara Stewart, Ph.D<\/a>. \u2013 2014<\/b><br \/>\n<b>Thesis:\u00a0<\/b>A Systems Pharmacology Approach to Modulating Spatial Memory<br \/>\n<b>Position:\u00a0<\/b>Associate Director, Pipeline Management, Plasma-Derived Therapies R&amp;D at Takeda<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/conorsmith001\/\" target=\"_blank\" rel=\"noopener noreferrer\">Conor Smith, Ph.D.<\/a> \u2013 2014<\/b><br \/>\n<b>Thesis:\u00a0<\/b>Non-Canonical Cell Signaling Actions of Pregnenolone Sulfate, A Neurosteroid that Increases Intracellular Calcium, Activates CREB Phosphorylation and Stimulates Trafficking of NMDA Receptors to the Surface of Neurons<br \/>\n<b>Position:\u00a0<\/b>Technical Writer for Astellas Pharma US on behalf of PSC Biotech Corporation<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/sophiedesbiens\/\" target=\"_blank\" rel=\"noopener noreferrer\">Sophie Desbiens, Ph.D.<\/a> \u2013 2009 (BME)<\/b><br \/>\n<b>Thesis: <\/b>Therapeutic Agents for Cocaine Addiction: A Systems Pharmacology Approach.<br \/>\n<b>Position: <\/b>Director, New Product Commercialization,\u00a0Alnylam Pharmaceuticals<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/matthew-whittaker-ph-d-478b09b\/\" target=\"_blank\" rel=\"noopener noreferrer\">Matthew Whitaker, Ph.D<\/a>. \u2013 2009<\/b><br \/>\n<b>Thesis: <\/b>Pregnenolone Sulfate Modulates Neurotransmitter Release from Isolated Neuron Terminals of the Rat Striatum<br \/>\n<b>Position: <\/b>Director, Toxicology at Alnylam Pharmaceuticals<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/ekostakis21\/\" target=\"_blank\" rel=\"noopener noreferrer\">Emmanuel Kostakis, M.A., Ph.D.<\/a> &#8211; 2007<\/b><br \/>\n<b>MA Thesis: <\/b>Effect of Neurosteroids on NMDA Receptors Comprising Different Isoforms of the NMDA R1 Subunit<br \/>\n<b>PhD Thesis: <\/b> Dual Regulation of N-Methyl-D-Aspartate Receptor Function by Neuroactive Steroids<br \/>\n<b>Position: <\/b>Senior Project Manager &#8211; Global Value, Access &amp; Policy &#8211; Strategic Planning &amp; Operations at Amgen Z\u00fcrich, Switzerland<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/felicia-tsai-2552b96\/\" target=\"_blank\" rel=\"noopener noreferrer\">Felicia Tsai, M.A.<\/a> &#8211; 2004<\/b><br \/>\n<b>Thesis: <\/b> Examined the modulatory effects of neurosteroid (Pregnenolone sulfate) on neurotransmitter receptors (NMDA Receptors)<br \/>\n<b>Position:<\/b>Manager of Clinical Trials at AbbVie<\/p>\n<p><b>Ming-Kuei Jang, Ph.D. &#8211; 2003<\/b><br \/>\n<b>Thesis: <\/b> Molecular Mechanisms for Pregnenolone Sulfate Modulation of the N-Methyl-D-Aspartate Receptor<br \/>\n<b>Position: <\/b>Cofounder and CEO of Aprinoia Therapeutics.<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/ghazaleh-sadri-vakili-a831b76\/\" target=\"_blank\" rel=\"noopener noreferrer\">Ghazaleh Sadri-Vakili, Ph.D.<\/a> &#8211; 2003<\/b><br \/>\n<b>Thesis: <\/b> Neurosteroids Modulate Ionotrophic Glutamate Receptor-Induced Dopamine Release and Locomotor Activity in Rats<br \/>\n<b>Position: <\/b>Associaate Professor of Neurology, Harvard Medical School, Massachusetts General Hospital<\/p>\n<p><b>Janine L. Steiger, Ph.D. &#8211; 2003 (Co-Advisor)<\/b><br \/>\n<b>Thesis: <\/b>Regulation of GABA Receptor Gene Experssion in the CNS:\u00a0 A Role for CREB\/ATF Transcription Factors and Effects of Prenatal Protein Malnutrition<br \/>\n<b>Position:\u00a0<\/b>Scientific Consultant<\/p>\n<p><b>Mio Kato, M.A. &#8211; 2001<\/b><br \/>\n<b>Position: <\/b>Assistant Professor,\u00a0Graduate School of Public Health,\u00a0Teikyo University<\/p>\n<p><b>Garrick Lau, M.D.\/Ph.D. &#8211; 1999 (Co-Advisor)<\/b><br \/>\n<b>Thesis:<\/b>Transcriptional Regulation of the NMDA Receptor Subunit 1 Gene in Rat Neocortical Neurons by the Map Kinase and Cyclic AMP-Dependent Signaling Pathway<br \/>\n<b>Position: <\/b>Anesthesiologist, Walnut Creek Medical Center, Department of Anesthesia<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/leachm\/\" target=\"_blank\" rel=\"noopener noreferrer\">Martin D. Leach, Ph.D<\/a>. &#8211; 1998<\/b><br \/>\n<b>Thesis: <\/b> Isolation and Characterization of a Promotor for the Human GABA-A Receptor Alpha-1 Subunit Gene<br \/>\n<b>Position:<\/b>Vice President R&amp;D IT, Global Quality IT and Human Experience IT\u00a0at Alexion Pharmaceuticals, Inc.<\/p>\n<p><b>Helen Lyons, Ph.D. &#8211; 1998<\/b><br \/>\n<b>Thesis: <\/b> Agonist-Induced GABA A Receptor Down-Regulation and Uncoupling in Neuronal Culture: Multiple Signal Transduction Pathways and a Role for Intracellular Calcium<br \/>\n<b>Position: <\/b>Research Scientist II, IDEXX<\/p>\n<p><b>Pamela J. McLean, Ph.D. &#8211; 1998<\/b><br \/>\n<b>Thesis: <\/b> Regulation and Chromosomal Localization of GABA-A Receptor Alpha-Subunit Genes, GABRA6 and GABRA 4<br \/>\n<b>Position: <\/b>Associate Professor of Neuroscience and Senior Associate Consultant and PI , Mayo Clinic, Jacksonville, FL<\/p>\n<p><b>Charles E. Weaver Jr., M.D.\/Ph.D. &#8211; 1998<\/b><br \/>\n<b>Thesis: <\/b> Steroid Modulation of NMDA-Inducwed Death of Rat Hippocampal Neurons in Primary Cell Culture<br \/>\n<b>Position: <\/b>Neurosurgeon at Spectrum Neurosurgical Specialists, P.C.<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/nader-yaghoubi-m-d-ph-d-0bb4849\/\" target=\"_blank\" rel=\"noopener noreferrer\">Nader Yaghoubi, M.D.\/Ph.D.<\/a> &#8211; 1998<\/b><br \/>\n<b>Thesis: <\/b> Modulation of Recombinant Glutamate Receptors of Neuroactive Steroids Studied Using an Automated Workstation for Oocyte Electrophysiology<br \/>\n<b>Position:\u00a0<\/b>Co-Founder and Chief Executive Officer, Pathmaker Neurosystems, Inc.<\/p>\n<p><b>Mijeong Chung, Ph.D. &#8211; 1997<\/b><br \/>\n<b>Thesis: <\/b>Steroids as Functional Modulators of Amino Acids Receptors<br \/>\n<b>Position: <\/b>Senior Scientist, Institute of Bioscience and Biotechnology, Taejon, Korea<\/p>\n<p><b>Yan Tony Lee, M.A. &#8211; 1997<\/b><br \/>\n<b>Thesis: <\/b>Partial GABA A Agonists and the Testing of a Two-State Model of GABA A Receptor Modulatio<br \/>\n<b>Position: <\/b><\/p>\n<p><b>Diana Shpektor, M.A. &#8211; 1997<\/b><br \/>\n<b>Thesis: <\/b> Ethanol Modulation of GABA A Receptor Functoin Regulates Subunit-Specific Gene Expression<br \/>\n<b>Position: <\/b>Research\u00a0Scientist III, at Novartis Institutes for BioMedical Research<\/p>\n<p><b><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/shelley-j-russek-ph-d\/\" target=\"_blank\" rel=\"noopener noreferrer\">Shelley J. Russek, M.A., Ph.D.<\/a> &#8211; 1994<\/b><br \/>\n<b>Thesis: <\/b> Molecular Genetics of the GABA A Receptor: Structural Analysis and Autologus Regulation of the Beta Subunit Genes<br \/>\n<b>Position: <\/b>Professor of Pharmacology, BUSM, and Director, BU Graduate Program for Neuroscience<\/p>\n<p><b>Dominic Roca, M.D.\/Ph.D. &#8211; 1990<\/b><br \/>\n<b>Position: <\/b>Pulmonologist<\/p>\n<p><b>James Celentano, M.D.\/Ph.D. &#8211; 1987<\/b><br \/>\n<b>Position: <\/b>Emergency Medicine, Columbia University Medical Center<\/p>\n<p><b>Daniel Mierlak, M.D.\/Ph.D. &#8211; 1987<\/b><br \/>\n<b>Position: <\/b>Psychiatrist<\/p>\n<p><b><a href=\"https:\/\/neuro.wisc.edu\/staff\/czajkowski-cynthia\/\">Cynthia Czajkowski, Ph.D<\/a>. &#8211; 1987<\/b><br \/>\n<b>Position: <\/b>Vilas Distinguished Professor, Department of Neuroscience, University of Wisconsin &#8211; Madison<\/p>\n<p><b>Laurence A. Borden, Ph.D. &#8211; 1985<\/b><br \/>\n<b>Position: <\/b>Scientific Advisor, Kaye, Scholer, FIerman, Hayes &amp; Handler, LLP, New York, New York<\/p>\n<h3>Post-Doctoral Fellows<\/h3>\n<p><a href=\"https:\/\/www.hsph.harvard.edu\/kristopher-sarosiek\/rumani-singh-phd\/\"><strong>Rumani Singh<\/strong><\/a><strong>,<\/strong><strong>\u00a0Ph.D. <b>\u2013 2015<br \/>\nPosition:<\/b><\/strong>Research and Development Scientist,\u00a0BOA Biomedical<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/loren-martin-00a6b257\/\" target=\"_blank\" rel=\"noopener noreferrer\">Loren J. Martin, Ph.D<\/a>. \u2013 2009-2010<\/b><br \/>\n<b>Position:\u00a0<\/b>Associate Professor, Department of Psychology, University of Toronto,\u00a0Mississauga<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/r-jonathan-robitsek-phd-811a1333\/\" target=\"_blank\" rel=\"noopener noreferrer\">Jonathan Robitsek, Ph.D.<\/a> \u2013 2008-2013<\/b><br \/>\n<b>Position: <\/b>Research Director, Department of Surgery at Jamaica Hospital, New York City<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/scott-downing-504bba5\/\" target=\"_blank\" rel=\"noopener noreferrer\">Scott Downing, Ph.D.<\/a> \u2013 2005-<\/b><br \/>\n<b>Position: <\/b>Bioinformatics Research\u00a0Scientist,\u00a0Department of Pharmacology &amp; Experimental Therapeutics, Boston University School of Medicine<\/p>\n<p><b><a href=\"https:\/\/www.bumc.bu.edu\/ppb\/profile\/marcia-h-ratner-phd-dabt\/\" target=\"_blank\" rel=\"noopener noreferrer\">Marcia H. Ratner, Ph.D., DABT\u00a0<\/a>\u2013 2004-2007<\/b><br \/>\n<b>Position: <\/b>Assistant Professor, Department of Pharmacology &amp; Experimental Therapeutics, Boston University School of Medicine<\/p>\n<p><b>Stella Martin, Ph.D. \u2013 1997-2014<\/b><br \/>\n<b>Position:\u00a0<\/b><\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/sophiedesbiens\/\" target=\"_blank\" rel=\"noopener noreferrer\">Sophie Desbiens, Ph.D<\/a>. \u2013 2009-2010<\/b><br \/>\n<b>Position:\u00a0<\/b>Director, New Product Commercialization,\u00a0Alnylam Pharmaceuticals<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/dmytro-berezhnoy-6a66a02\/\" target=\"_blank\" rel=\"noopener noreferrer\">Dmytro Berezhnoy, Ph.D<\/a>. &#8211; 2005-2009<\/b><br \/>\n<b>Position:\u00a0<\/b>Chief Science Officer at Ogenx Therapeutics<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/dariodieguezjr\/\" target=\"_blank\" rel=\"noopener noreferrer\">Dario Dieguez, Ph.D<\/a>. &#8211; 2006-2008<\/b><br \/>\n<b>Position:\u00a0<\/b>Health Scientist Administrator, National Institutes of Health<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/ekostakis21\/?originalSubdomain=ch\">Emmanuel Kostakis, M.A., Ph.D.<\/a> &#8211; 2005-2008<\/b><br \/>\n<b>Position: <\/b>Global Project Manager \u2013 Operational Project Management, Merck Serono Geneva, Switzerland<\/p>\n<p><b>Janine L. Steiger, Ph.D. &#8211; 2003-2006<\/b><br \/>\n<b>Position: <\/b>Director, Discovery Operations at Zalicus Incorporated<\/p>\n<p><b>Hui Zhong, M.D.\/Ph.D. &#8211; 2001-2003<\/b><br \/>\n<b>Position: <\/b>Associate Professor of Microbiology, Immunology and Cancer Biology, University of Virginia<\/p>\n<p><b>Weimin Dai, M.D.\/Ph.D. &#8211; 1998<\/b><br \/>\n<b>Position: <\/b>General Manager, UT (Shanghai) Pharma<\/p>\n<p><b>Shamol Saha, Ph.D. &#8211; 2000-2005<\/b><br \/>\n<b>Position: Retired<\/b><\/p>\n<p><b>Helen Lyons, Ph.D. &#8211; 1998-2001<\/b><br \/>\n<b>Position: <\/b>Research Scientist II, IDEXX<\/p>\n<p><b>Valerie Itier, Ph.D. &#8211; 1997-1999<\/b><br \/>\n<b>Position: <\/b>Neurophysiologist, Universit\u00e9 Paris-Est Cr\u00e9teil,\u00a0CRRET<\/p>\n<p><b>Andrew Malayev, Ph.D. &#8211; 1996-1999<br \/>\nPosition: <\/b><\/p>\n<p><b>Qiang Wang, Ph.D. &#8211; 1989-1992<br \/>\nPosition: <\/b>Associate Professor, Department of Chemical and Biological Engineering, Colorado State University<\/p>\n<p><b>Lois Rabow, Ph.D. &#8211; 1989-1992<br \/>\nPosition: <\/b><\/p>\n<p><b>Fong-Sen Wu, Ph.D. &#8211; 1988-1992<br \/>\nPosition: <\/b>Associate Professor, National Cheng Kung University, Taiwan<\/p>\n<p><b><a href=\"https:\/\/www.researchgate.net\/profile\/Linda_Friedman\">Linda K. Friedman, Ph.D.<\/a> &#8211; 1988-1990<br \/>\nPosition: <\/b>Associate Professor, New Jersey Neuroscience Institute<b><br \/>\n<\/b><\/p>\n<p><b>Mark Farrant, Ph.D. &#8211; 1987-1989<br \/>\nPosition: <\/b>Professor of Neuroscience, University College London<\/p>\n<p><b>Sue Yin, Ph.D. &#8211; 1986-1987<br \/>\nPosition: <\/b>Associate Professor, National Taiwan University, Taiwan<\/p>\n<p><b><a href=\"https:\/\/www.linkedin.com\/in\/ken-rhodes-7673754\/\">Kenneth J. Rhodes, Ph.D<\/a>. &#8211; 1986-1991<br \/>\nPosition:\u00a0<\/b>Vice President, Rare Neurology &amp; Discovery Biology, Pfizer<\/p>\n<p><b>Laurence A. Borden, Ph.D. &#8211; 1985-1987<br \/>\nPosition:<\/b><\/p>\n<p><b>Thomas R. Tobin, Ph.D. &#8211; 1985-1986<br \/>\nPosition:<\/b><\/p>\n<p><b>Grant D. Schiller, Ph.D. &#8211; 1982-1986<br \/>\nPosition: <\/b><\/p>\n<p><b>Terrell T. Gibbs, Ph.D. &#8211; 1980-1982<br \/>\nPosition: <\/b>Associate Professor, Department of Pharmacology, Boston University School of Medicine<\/p>\n<p><b><a href=\"https:\/\/www.researchgate.net\/profile\/Christopher_Chan16\">Christopher Y. Chan, Ph.D.<\/a> &#8211; 1980-1982<\/b><br \/>\n<b>Position: <\/b>Assistant Medical Professor,\u00a0Physiology and Pharmacology,\u00a0School of Biomedical Education, The City College of New York<\/p>\n<p><\/div>\n<\/div>\n\n","protected":false},"author":15890,"template":"","_links":{"self":[{"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/profile\/18216"}],"collection":[{"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/profile"}],"about":[{"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/types\/profile"}],"author":[{"embeddable":true,"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/users\/15890"}],"version-history":[{"count":36,"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/profile\/18216\/revisions"}],"predecessor-version":[{"id":23977,"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/profile\/18216\/revisions\/23977"}],"wp:attachment":[{"href":"https:\/\/www.bumc.bu.edu\/ppb\/wp-json\/wp\/v2\/media?parent=18216"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}