Zobrazeno 1 - 6
of 6
pro vyhledávání: '"MaKenna R. Browne"'
Autor:
Marie Bargiela, Janina Kueper, Arman T. Serebrakian, MaKenna R. Browne, Susan Brogna, Zachary S. Peacock, Branko Bojovic, Natalie D. Shaw, Eric C. Liao
Publikováno v:
Journal of Craniofacial Surgery. 34:849-854
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00127ea19b8eace4096a3e7a1a2d2409
https://doi.org/10.1097/scs.0000000000009261
https://doi.org/10.1097/scs.0000000000009261
Autor:
Kaoru Inoue, Hamed Bostan, MaKenna R. Browne, Owen F. Bevis, Carl D. Bortner, Steven A. Moore, Aaron A. Stence, Negin P. Martin, Shih-Heng Chen, Adam B. Burkholder, Jian-Liang Li, Natalie D. Shaw
Publikováno v:
Science Advances. 9
SMCHD1 mutations cause congenital arhinia (absent nose) and a muscular dystrophy called FSHD2. In FSHD2, loss of SMCHD1 repressive activity causes expression of double homeobox 4 (DUX4) in muscle tissue, where it is toxic. Studies of arhinia patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bcf824f139670e435aa0d08790cf6e4c
https://doi.org/10.1126/sciadv.abq7744
https://doi.org/10.1126/sciadv.abq7744
Autor:
Bargiela, Marie, Kueper, Janina, Serebrakian, Arman T., Browne, MaKenna R., Brogna, Susan, Peacock, Zachary S., Bojovic, Branko, Shaw, Natalie D., Liao, Eric C.
Publikováno v:
Journal of Craniofacial Surgery; May2023, Vol. 34 Issue 3, p849-854, 6p
Publikováno v:
Clinical Oncology Week; 4/16/2024, p1022-1022, 1p
Publikováno v:
Stem Cell Week; 8/25/2023, p1332-1332, 1p
Publikováno v:
Health & Medicine Week; 3/10/2023, p1840-1840, 1p