Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Michaela Zaik"'
Autor:
Pauliina Kronqvist, Finn Cilius Nielsen, Kay E. Davies, Michaela Zaik, Henrik Daa Schrøder, Eva Engvall, Rehannah Borup, Ulla M. Wewer, Thomas Voit, Nobuko Kawaguchi, Behzad Moghadaszadeh, Ling T. Guo, Reidar Albrechtsen
Publikováno v:
Moghadaszadeh, B, Albrechtsen, R, Guo, L T, Zaik, M, Kawaguchi, N, Borup, R H, Kronqvist, P, Schrøder, H D, Davies, K E, Voit, T, Nielsen, F C, Engvall, E & Wewer, U M 2003, ' Compensation for dystrophin-deficiency : ADAM12 overexpression in skeletal muscle results in increased α7 integrin, utrophin and associated glycoproteins ', Human Molecular Genetics, vol. 12, no. 19, pp. 2467-79 . https://doi.org/10.1093/hmg/ddg264
Udgivelsesdato: 2003-Oct-1 Mouse models for genetic diseases are among the most powerful tools available for developing and testing new treatment strategies. ADAM12 is a disintegrin and metalloprotease, previously demonstrated to significantly allevi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d6dada31c7846ef493374e37eb53a8
https://ora.ox.ac.uk/objects/uuid:19d87fd3-c7d3-420c-97c5-f384b8ac7d7a
https://ora.ox.ac.uk/objects/uuid:19d87fd3-c7d3-420c-97c5-f384b8ac7d7a
Autor:
Mayana Zatz, Danielle Frappier, Klaus Wrogemann, Michaela Zaik, Nicole M. Roslin, Kate Bushby, Cheryl Hirst, Kenneth Morgan, Edward Nylen, Ryan E. Lamont, Cheryl R. Greenberg, T. Mary Fujiwara, Flavia de Paula, Patrick Frosk, Alysa A.P. Tennese, Volker Straub
Publikováno v:
Human Mutation. 25:38-44
Limb girdle muscular dystrophy (LGMD) is common in the Hutterite population of North America. We previously identified a mutation in the TRIM32 gene in chromosome region 9q32, causing LGMD2H in approximately two-thirds of the 60 Hutterite LGMD patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b218166ea4b4dd1a901118b3956ee8be
https://doi.org/10.1002/humu.20110
https://doi.org/10.1002/humu.20110
