Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Wilcox Edward R"'
Autor:
Shotland Lawrence I, Ploplis Barbara, MacLaren Linda, Dhillon Kiran, Luscombe Sandra, Ahmad Zahoor, Ramzan Khushnooda, Young Terry-Lynn, Riazuddin Saima, Powell Shontell D, Cindy Li Xiaoyan, Ahmed Zubair M, Ives Elizabeth, Riazuddin Sheikh, Friedman Thomas B, Morell Robert J, Wilcox Edward R
Publikováno v:
BMC Medical Genetics, Vol 5, Iss 1, p 24 (2004)
Abstract Background Mutant alleles of TMPRSS3 are associated with nonsyndromic recessive deafness (DFNB8/B10). TMPRSS3 encodes a predicted secreted serine protease, although the deduced amino acid sequence has no signal peptide. In this study, we sea
Externí odkaz:
https://doaj.org/article/05a0676230e64840b0aedb1c786310a4
Autor:
Hotaling, Scott1 (AUTHOR) scott.hotaling1@gmail.com, Wilcox, Edward R.2 (AUTHOR), Heckenhauer, Jacqueline3,4 (AUTHOR), Stewart, Russell J.5 (AUTHOR), Frandsen, Paul B.3,6,7 (AUTHOR) paul_frandsen@byu.edu
Publikováno v:
BMC Genomics. 3/16/2023, Vol. 24 Issue 1, p1-9. 9p.
Autor:
Wang, Aihui, Liang, Yong, Fridell, Robert A., Probst, Frank J., Wilcox, Edward R., Touchman, Jeffrey W., Morton, Cynthia C., Morell, Robert J., Noben-Trauth, Konrad, Camper, Sally A., Friedman, Thomas B.
Publikováno v:
Science, 1998 May . 280(5368), 1447-1451.
Externí odkaz:
https://www.jstor.org/stable/2895920
Autor:
Schultz, Julie M., Khan, Shaheen N., Ahmed, Zubair M., Riazuddin, Saima, Waryah, Ali M., Chhatre, Dhananjay, Starost, Matthew F., Ploplis, Barbara, Buckley, Stephanie, Velásquez, David, Kabra, Madhulika, Lee, Kwanghyuk, Hassan, Muhammad J., Ali, Ghazanfar, Ansar, Muhammad, Ghosh, Manju, Wilcox, Edward R., Ahmad, Wasim, Merlino, Glenn, Leal, Suzanne M., Riazuddin, Sheikh, Friedman, Thomas B., Morell, Robert J.
Publikováno v:
In The American Journal of Human Genetics 2009 85(1):25-39
Autor:
Wilcox, Edward R *, Burton, Quianna L, Naz, Sadaf, Riazuddin, Saima, Smith, Tenesha N, Ploplis, Barbara, Belyantseva, Inna, Ben-Yosef, Tamar, Liburd, Nikki A, Morell, Robert J, Kachar, Bechara, Wu, Doris K, Griffith, Andrew J, Riazuddin, Sheikh, Friedman, Thomas B
Publikováno v:
In Cell 2001 104(1):165-172
Autor:
Bork, Julie M., Peters, Linda M., Riazuddin, Saima, Bernstein, Steve L., Ahmed, Zubair M., Ness, Seth L., Polomeno, Robert, Ramesh, Arabandi, Schloss, Melvin, Srisailpathy, C. R. Srikumari, Wayne, Sigrid, Bellman, Susan, Desmukh, Dilip, Ahmed, Zahoor, Khan, Shaheen N., Kaloustian, Vazken M. Der, Li, X. Cindy, Lalwani, Anil, Riazuddin, Sheikh, Bitner-Glindzicz, Maria, Nance, Walter E., Liu, Xue-Zhong, Wistow, Graeme, Smith, Richard J.H., Griffith, Andrew J., Wilcox, Edward R., Friedman, Thomas B., Morell, Robert J.
Publikováno v:
In The American Journal of Human Genetics 2001 68(1):26-37
Autor:
Ahmed, Zubair M., Riazuddin, Saima, Bernstein, Steve L., Ahmed, Zahoor, Khan, Shaheen, Griffith, Andrew J., Morell, Robert J., Friedman, Thomas B., Riazuddin, Sheikh, Wilcox, Edward R.
Publikováno v:
In The American Journal of Human Genetics 2001 69(1):25-34
Autor:
Yasunaga, Shin'ichiro, Grati, M'hamed, Chardenoux, Sébastien, Smith, Tenesha N., Friedman, Thomas B., Lalwani, Anil K., Wilcox, Edward R., Petit, Christine
Publikováno v:
In The American Journal of Human Genetics 2000 67(3):591-600
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Li, Xiaoyan C., Everett, Lorraine A., Lalwani, Anil K., Desmukh, Dilip, Friedman, Thomas B., Green, Eric D., Wilcox, Edward R.
A mutation in PDS causes non-syndromic recessive deafness
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::bbb0bcf948ee083b0b3e3116d1401f2c
https://zenodo.org/record/1233379
https://zenodo.org/record/1233379
