Resultados de búsqueda - Mukherjee, Souhrid

Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network por Mukherjee, Souhrid, Cogan, Joy D., Newman, John H., Phillips, John A., Hamid, Rizwan, Meiler, Jens, Capra, John A.

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Molecular mechanisms and structural features of cardiomyopathy-causing troponin T mutants in the tropomyosin overlap region por Gangadharan, Binnu, Sunitha, Margaret S., Mukherjee, Souhrid, Chowdhury, Ritu Roy, Haque, Farah, Sekar, Narendrakumar, Sowdhamini, Ramanathan, Spudich, James A., Mercer, John A.

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Mechanistic Heterogeneity in Contractile Properties of α-Tropomyosin (TPM1) Mutants Associated with Inherited Cardiomyopathies por Gupte, Tejas M., Haque, Farah, Gangadharan, Binnu, Sunitha, Margaret S., Mukherjee, Souhrid, Anandhan, Swetha, Rani, Deepa Selvi, Mukundan, Namita, Jambekar, Amruta, Thangaraj, Kumarasamy, Sowdhamini, Ramanathan, Sommese, Ruth F., Nag, Suman, Spudich, James A., Mercer, John A.

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Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer-Rokitansky-Küster-Hauser Syndrome por Mikhael, Sasha, Dugar, Sonal, Morton, Madison, Chorich, Lynn P., Tam, Kerlene Berwick, Lossie, Amy C., Kim, Hyung-Goo, Knight, James, Taylor, Hugh S., Mukherjee, Souhrid, Capra, John A., Phillips, John A., Friez, Michael, Layman, Lawrence C.

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