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

Yazar: Gardiner, Katheleen, Davisson, Muriel
Baskı/Yayın Bilgisi 2000

Biology and Diseases of Mice

Yazar: Jacoby, Robert O., Fox, James G., Davisson, Muriel
Yayımlandı Laboratory Animal Medicine (2002)

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

Yazar: Davisson, Muriel Trask, Wright, James E., Atherton, Louisa M.
Baskı/Yayın Bilgisi 1973

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

Yazar: Costa, Alberto C. S., Stasko, Melissa R., Schmidt, Cecilia, Davisson, Muriel T.
Baskı/Yayın Bilgisi 2009

Discovery Genetics – The History and Future of Spontaneous Mutation Research

Yazar: Davisson, Muriel T., Bergstrom, David E., Reinholdt, Laura G., Donahue, Leah Rae
Baskı/Yayın Bilgisi 2012

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

Yazar: Du, Yunzhi, Stasko, Melissa, Costa, Alberto C., Davisson, Muriel T., Gardiner, Katheleen J.
Baskı/Yayın Bilgisi 2007

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

Yazar: Blake, Judith A., Eppig, Janan T., Richardson, Joel E., Davisson, Muriel T., the Mouse Genome Database Group
Baskı/Yayın Bilgisi 2000

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

Yazar: Smith, Richard S., John, Simon W. M., Zabeleta, Adriana, Davisson, Muriel T., Hawes, Norman L., Chang, Bo
Baskı/Yayın Bilgisi 2000

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

Yazar: Korstanje, Ron, Caputo, Christina, Doty, Rosalinda, Cook, Susan, Bronson, Roderick, Davisson, Muriel, Miner, Jeffrey H.
Baskı/Yayın Bilgisi 2014

Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

Yazar: González, Jorge L., Russo, Christopher J., Goldowitz, Dan, Sweet, Hope O., Davisson, Muriel T., Walsh, Christopher A.
Yayımlandı J Neurosci (1997)

Otitis media in a mouse model for Down syndrome

Yazar: Han, Fengchan, Yu, Heping, Zhang, Jiangping, Tian, Cong, Schmidt, Cecilia, Nava, Casey, Davisson, Muriel T, Zheng, Qing Y
Baskı/Yayın Bilgisi 2009

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

Yazar: Zheng, Qing Yin, Harris, Belinda S, Ward-Bailey, Patricia F, Yu, Heping, Bronson, Roderick T, Davisson, Muriel T, Johnson, Kenneth R
Baskı/Yayın Bilgisi 2004

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

Yazar: Newton, J. M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Baskı/Yayın Bilgisi 2001

A Mouse Model for Meckel Syndrome Type 3

Yazar: Cook, Susan A., Collin, Gayle B., Bronson, Roderick T., Naggert, Jürgen K., Liu, Dong P., Akeson, Ellen C., Davisson, Muriel T.
Baskı/Yayın Bilgisi 2009

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

Yazar: Scott-McKean, Jonah Jacob, Chang, Bo, Hurd, Ronald E., Nusinowitz, Steven, Schmidt, Cecilia, Davisson, Muriel T., Costa, Alberto C. S.
Baskı/Yayın Bilgisi 2010

A Spontaneous Mutation in Contactin 1 in the Mouse

Yazar: Davisson, Muriel T., Bronson, Roderick T., Tadenev, Abigail L. D., Motley, William W., Krishnaswamy, Arjun, Seburn, Kevin L., Burgess, Robert W.
Baskı/Yayın Bilgisi 2011

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

Yazar: Potter, Gregory B., Santos, Marta, Davisson, Muriel T., Rowitch, David H., Marks, Dan L., Bongarzone, Ernesto R., Petryniak, Magdalena A.
Baskı/Yayın Bilgisi 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...

Yazar: Davisson, Muriel T., Cook, Susan A., Akeson, Ellen C., Liu, Don, Heffner, Caleb, Gudis, Polyxeni, Fairfield, Heather, Murray, Stephen A.
Yayımlandı Am J Physiol Renal Physiol (2015)

Cerebellar Disorganization Characteristic of Reeler in Scrambler Mutant Mice Despite Presence of Reelin

Yazar: Goldowitz, Dan, Cushing, Richard C., Laywell, Eric, D’Arcangelo, Gabriella, Sheldon, Michael, Sweet, Hope O., Davisson, Muriel, Steindler, Dennis, Curran, Tom
Yayımlandı J Neurosci (1997)

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

Yazar: 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
Baskı/Yayın Bilgisi 2001