Elyse Kozlowski presents platform talk at Keystone Conference
GPGG graduate student Elyse Kozlowski (third year, Jones Lab) recently attended the...
Full details about the integrated curriculum can be found online here and here.
This course will serve as a foundation for understanding the heritable basis of numerous biological traits, the relationships among genes, and the regulation of their expression. We will focus on the ability to use genetic systems to probe these problems, and therefore will heavily explore the experimental aspects of these investigations. In addition, we will discuss the impact of the genome sequences on the practice of modern science. Moreover, we will use a case study approach to investigate the rich variety of scientific insights gained through genetic studies.
This course will explore the process by which insights from basic science research ultimately lead to new strategies for patient care with a focus on examples from genetics and more recent genome-wide experimental approaches. The course will cover examples of translational research using genetic, epigenomic, transcriptomic, proteomic, approaches in human and/or model systems. Research that leads to new approaches for establishing disease diagnosis, prognosis, therapy, and personalized medicine will be discussed. The ethical and societal implications of these developments will also be considered.
GMS GE 703 and 704, 2 credits each
Fall and Spring Semesters, Second Year
The Genetics and Genomics Colloquium will be a highly participatory journal club where the students will be asked to give presentations on cutting edge research with the focus on communication skills rather than scientific content. This approach will allow students to become more comfortable with public speaking while developing the skills necessary for effective communication of scientific ideas.
GMS MM 703, 2 credits
The course will begin with an historical perspective; review the major mechanistic pathways relating to oncogenes, antioncogenes, cell cycle control, genome instability, repair, and apoptosis; discuss standard and experimental genomic principles of cancer treatment and diagnosis; and conclude with a discussion of cancer epidemiology and health policy issues that affect all basic translational cancer research.
Additional electives offered by various Departments at BUSM are also approved including:

Human Genetics, GMS MS 781, 4 credits
Cellular Aspects of Development and Differentiation, GRS BI 610, 4 credits
Computational Biology: Genomes, Networks, Evolution, ENG BE 562, 4 credits
Genetics and Epidemiology of Disease, GMS MM 701, 2 credits
Comprehensive Immunology, GMS MI 713, 4 credits
Cancer Biology and Genetics, GMS MM 703, 2 credits
Pharmacogenomics, GMS PM 832, 2 credits
Protein Structure and Function, GMS BI 783, 2 credits
Molecular Mechanisms of Growth and Development, GMS BI 787, 2 credits
Receptors and Signal Transduction, GMS BI 790, 2 credits
DNA and Protein Sequence Analysis, ENG BE 561, 4 credits
Gene Regulation and Pharmacology, GMS PM 880, 2 credits
Molecular Basis of Neurological Disease, GMS MS 783, 2 credits
Systems Neuroscience, GMS AN 810, 4 credits
Gene Targeting in Transgenic Mice, GMS BI 776, 2 credits
Biochemical Mechanisms of Aging, GMS BI 786, 2 credits
Mass Spectrometry and Functional Genomics, GMS BI 793, 2 credits
Elementary Biostatistics, GMS MS 700, 2 credits
Genetics of Microorganisms, GMS MI 714, 4 credits
Growth Control and Cell Transformation, GMS MI 717, 4 credits
Teaching Methods in the Biomedical Sciences, GMS AN 804, 2 credits
Technology Commercialization: From Lab to Market, MET AD 893, 4 credits
Mechanisms and Models of Cellular Regulation, ENG BE 700, 4 credits
Genetics, Ethics, and the Law, GMS BT 440, 4 credits
Technology Commercialization: From Lab to Market, MET AD 893, 4 credits
Neuroanatomical Basis of Neurological Disorders, GMS AN 808 ,2 credits
Cognitive Neuroscience, GMS AN 811, 4 credits
Medical Genetics (for MD students)
The pace of genetic advances during the last century has been unparalleled scientifically, and these discoveries have already made and are poised to make an incredible impact on the practice of medicine. Currently, OMIM (Online Mendelian Inheritance in Man) lists over 2000 identified disease genes, and GeneTests lists over 1000 diseases for which there are molecular tests. Moreover, OMIM lists over 19,000 loci that are associated with particular phenotypes. In this course we will explore the precise molecular determinants of medical conditions and of human phenotypic variation that are being elucidated on a daily basis. Clearly, a detailed understanding of the genetic basis of human disease will lead to more precise molecular assays and diagnostics, better-targeted treatments, and more efficient treatment plans overall. Moreover, these developments will certainly affect all clinical specialties of the medical field since genetic components have a clear influence on a wide variety of human traits and conditions, from height and developmental birth defects to cancer susceptibility and neurological degeneration.