Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Namrata D. Udeshi"'
Autor:
Jon M. Madison, Karen Duong, Ellen F. Vieux, Namrata D. Udeshi, Sumaiya Iqbal, Elise Requadt, Shaunt Fereshetian, Michael C. Lewis, Antonio S. Gomes, Kerry A. Pierce, Randall J. Platt, Feng Zhang, Arthur J. Campbell, Dennis Lal, Florence F. Wagner, Clary B. Clish, Steven A. Carr, Morgan Sheng, Edward M. Scolnick, Jeffrey R. Cottrell
Publikováno v:
iScience, Vol 24, Iss 1, Pp 101935- (2021)
Summary: Genetic variation of the 16p11.2 deletion locus containing the KCTD13 gene and of CUL3 is linked with autism. This genetic connection suggested that substrates of a CUL3-KCTD13 ubiquitin ligase may be involved in disease pathogenesis. Compar
Externí odkaz:
https://doaj.org/article/02815da01a7f40da86fd1e72b7901ade
Autor:
Clary B. Clish, Sumaiya Iqbal, Dennis Lal, Karen Duong, Namrata D. Udeshi, Arthur J. Campbell, Edward M. Scolnick, Kerry A. Pierce, Feng Zhang, Michael C. Lewis, Jon M. Madison, Antonio S. Gomes, Florence F. Wagner, Randall Jeffrey Platt, Jeffrey R. Cottrell, Morgan Sheng, Ellen F. Vieux, Shaunt Fereshetian, Steven A. Carr, Elise Requadt
Publikováno v:
iScience
iScience, Vol 24, Iss 1, Pp 101935-(2021)
iScience, Vol 24, Iss 1, Pp 101935-(2021)
Summary Genetic variation of the 16p11.2 deletion locus containing the KCTD13 gene and of CUL3 is linked with autism. This genetic connection suggested that substrates of a CUL3-KCTD13 ubiquitin ligase may be involved in disease pathogenesis. Compari