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

Por Gardiner, Katheleen, Davisson, Muriel
Publicado em 2000

Cytogenetic Analysis of Pseudolinkage of Ldh Loci in the Teleost Genus Salvelinus

Por Davisson, Muriel Trask, Wright, James E., Atherton, Louisa M.
Publicado em 1973

Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pdeb(rd1)

Por Costa, Alberto C. S., Stasko, Melissa R., Schmidt, Cecilia, Davisson, Muriel T.
Publicado em 2009

Discovery Genetics – The History and Future of Spontaneous Mutation Research

Por Davisson, Muriel T., Bergstrom, David E., Reinholdt, Laura G., Donahue, Leah Rae
Publicado em 2012

Editing of the Serotonin 2C Receptor Pre-mRNA: Effects of the Morris Water Maze

Por Du, Yunzhi, Stasko, Melissa, Costa, Alberto C., Davisson, Muriel T., Gardiner, Katheleen J.
Publicado em 2007

The Mouse Genome Database (MGD): expanding genetic and genomic resources for the laboratory mouse

Por Blake, Judith A., Eppig, Janan T., Richardson, Joel E., Davisson, Muriel T., the Mouse Genome Database Group
Publicado em 2000

The Bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization

Por Smith, Richard S., John, Simon W. M., Zabeleta, Adriana, Davisson, Muriel T., Hawes, Norman L., Chang, Bo
Publicado em 2000

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 em 2014

Otitis media in a mouse model for Down syndrome

Por Han, Fengchan, Yu, Heping, Zhang, Jiangping, Tian, Cong, Schmidt, Cecilia, Nava, Casey, Davisson, Muriel T, Zheng, Qing Y
Publicado em 2009

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

Por Zheng, Qing Yin, Harris, Belinda S, Ward-Bailey, Patricia F, Yu, Heping, Bronson, Roderick T, Davisson, Muriel T, Johnson, Kenneth R
Publicado em 2004

Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

Por Newton, J. M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Publicado em 2001

A Mouse Model for Meckel Syndrome Type 3

Por Cook, Susan A., Collin, Gayle B., Bronson, Roderick T., Naggert, Jürgen K., Liu, Dong P., Akeson, Ellen C., Davisson, Muriel T.
Publicado em 2009

The Mouse Model of Down Syndrome Ts65Dn Presents Visual Deficits as Assessed by Pattern Visual Evoked Potentials

Por Scott-McKean, Jonah Jacob, Chang, Bo, Hurd, Ronald E., Nusinowitz, Steven, Schmidt, Cecilia, Davisson, Muriel T., Costa, Alberto C. S.
Publicado em 2010

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 em 2011

Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease

Por Potter, Gregory B., Santos, Marta, Davisson, Muriel T., Rowitch, David H., Marks, Dan L., Bongarzone, Ernesto R., Petryniak, Magdalena A.
Publicado em 2013

Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosi...

Por Davisson, Muriel T., Cook, Susan A., Akeson, Ellen C., Liu, Don, Heffner, Caleb, Gudis, Polyxeni, Fairfield, Heather, Murray, Stephen A.
Publicado no Am J Physiol Renal Physiol (2015)

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 em 2001

Molecular Characterization of the Translocation Breakpoints in the Down Syndrome Mouse Model, Ts65Dn

Por Reinholdt, Laura G., Ding, Yueming, Gilbert, Griffith J., Czechanski, Anne, Solzak, Jeffrey P., Roper, Randall J., Johnson, Mark T., Donahue, Leah Rae, Lutz, Cathleen, Davisson, Muriel T.
Publicado em 2011

The Mouse Brain Transcriptome by SAGE: Differences in Gene Expression between P30 Brains of the Partial Trisomy 16 Mouse Model of Down Syndrome (Ts65Dn) and Normals

Por Chrast, Roman, Scott, Hamish S., Papasavvas, Marie Pierre, Rossier, Colette, Antonarakis, Emmanuel S., Barras, Christine, Davisson, Muriel T., Schmidt, Cecilia, Estivill, Xavier, Dierssen, Mara, Pritchard, Melanie, Antonarakis, Stylianos E.
Publicado em 2000

ZFP191 is required by oligodendrocytes for CNS myelination

Por Howng, Shen Yi B., Avila, Robin L., Emery, Ben, Traka, Maria, Lin, Wensheng, Watkins, Trent, Cook, Susan, Bronson, Roderick, Davisson, Muriel, Barres, Ben A., Popko, Brian
Publicado em 2010