The sequence of human chromosome 21 and implications for research into Down syndrome

por Gardiner, Katheleen, Davisson, Muriel
Publicado 2000

Biology and Diseases of Mice

por Jacoby, Robert O., Fox, James G., Davisson, Muriel
Publicado 2002

A mouse collagen4α4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers

por Korstanje, Ron, Caputo, Christina, Doty, Rosalinda, Cook, Susan, Bronson, Roderick, Davisson, Muriel, Miner, Jeffrey H.
Publicado 2014

A Spontaneous Mutation in Contactin 1 in the Mouse

por Davisson, Muriel T., Bronson, Roderick T., Tadenev, Abigail L. D., Motley, William W., Krishnaswamy, Arjun, Seburn, Kevin L., Burgess, Robert W.
Publicado 2011

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

por Anderson, Michael G, Smith, Richard S, Savinova, Olga V, Hawes, Norman L, Chang, Bo, Zabaleta, Adriana, Wilpan, Robert, Heckenlively, John R, Davisson, Muriel, John, Simon WM
Publicado 2001

VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P(2) in yeast and mouse

por Jin, Natsuko, Chow, Clement Y, Liu, Li, Zolov, Sergey N, Bronson, Roderick, Davisson, Muriel, Petersen, Jason L, Zhang, Yanling, Park, Sujin, Duex, Jason E, Goldowitz, Daniel, Meisler, Miriam H, Weisman, Lois S
Publicado 2008

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure

por Chang, Bo, Smith, Richard S, Peters, Maureen, Savinova, Olga V, Hawes, Norman L, Zabaleta, Adriana, Nusinowitz, Steven, Martin, Janice E, Davisson, Muriel L, Cepko, Constance L, Hogan, Brigid LM, John, Simon WM
Publicado 2001