The Integrated Program in Cellular, Molecular and Biomedical Studies (CMBS) at Columbia University Medical Center is a Ph.D. granting program that combines faculty from all the basic science departments. The CMBS Program is an umbrella program that presents students with a unique opportunity to obtain individualized training in basic cell and molecular biology, microbiology, structural biology, biophysics, genetics, immunology, neurobiology, computational biology, as well as translational biomedical disease-related research. Our hope is to train the next leaders in the field of biomedical research and also to provide training for future leaders in other areas where a biomedical research background will be of great benefit. The CMBS program is an accredited degree-granting program that was first established in 1986 and has been supported by this Training Grant since 1987. The program has a distinguished, well- funded faculty of 135 trainers, whose research expertise represents nearly all the areas of modern cellular and molecular biology, neurobiology and computational biology. There are currently 69 students in this program. Seventy two students have graduated from the CMBS Program in the past five years and have gone on to postdoctoral positions in outstanding laboratories, careers in the pharmaceutical of biotechnology industry, or careers where they use their biomedical training to provide other societal benefits. Students take core courses in molecular genetics, molecular and cell biology as well as statistics during their first year and complete three laboratory rotations. In the secod year, students take their qualifying examination and a course in the Responsible Conduct of Research. The CMBS Program hosts a student research seminar series and a biennial student-faculty retreat. Most students graduated in 5-6 years. The CMBS Program remains the premier cellular and molecular biology graduate program at Columbia University Medical Center and support from this Training Grant is crucial for the continued success of this program.
The goal of this program is to provide students with a unique opportunity to obtain individualized training in basic cell and molecular biology, microbiology, structural biology, biophysics, genetics, immunology, neurobiology, computational biology, as well as translational biomedical disease-related research.
| Twomey, Edward C; Yelshanskaya, Maria V; Vassilevski, Alexander A et al. (2018) Mechanisms of Channel Block in Calcium-Permeable AMPA Receptors. Neuron 99:956-968.e4 |
| Hill, Vanessa M; O'Connor, Reed M; Sissoko, Gunter B et al. (2018) A bidirectional relationship between sleep and oxidative stress in Drosophila. PLoS Biol 16:e2005206 |
| Dieck, Chelsea L; Tzoneva, Gannie; Forouhar, Farhad et al. (2018) Structure and Mechanisms of NT5C2 Mutations Driving Thiopurine Resistance in Relapsed Lymphoblastic Leukemia. Cancer Cell 34:136-147.e6 |
| Singh, Appu K; Saotome, Kei; McGoldrick, Luke L et al. (2018) Structural bases of TRP channel TRPV6 allosteric modulation by 2-APB. Nat Commun 9:2465 |
| Levitin, Hanna Mendes; Yuan, Jinzhou; Sims, Peter A (2018) Single-Cell Transcriptomic Analysis of Tumor Heterogeneity. Trends Cancer 4:264-268 |
| Rao, Satyanarayan; Chiu, Tsu-Pei; Kribelbauer, Judith F et al. (2018) Systematic prediction of DNA shape changes due to CpG methylation explains epigenetic effects on protein-DNA binding. Epigenetics Chromatin 11:6 |
| McGoldrick, Luke L; Singh, Appu K; Saotome, Kei et al. (2018) Opening of the human epithelial calcium channel TRPV6. Nature 553:233-237 |
| Singh, Appu K; McGoldrick, Luke L; Sobolevsky, Alexander I (2018) Structure and gating mechanism of the transient receptor potential channel TRPV3. Nat Struct Mol Biol 25:805-813 |
| Van Alstyne, Meaghan; Simon, Christian M; Sardi, S Pablo et al. (2018) Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophy. Genes Dev 32:1045-1059 |
| Zhang, Liyang; Martini, Gabriella D; Rube, H Tomas et al. (2018) SelexGLM differentiates androgen and glucocorticoid receptor DNA-binding preference over an extended binding site. Genome Res 28:111-121 |
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