Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration
Longo-Guess, Chantal M, Sundberg, John P, Davisson, Muriel T, Schimmel, Paul, Ackerman, Susan L, Lee, Jeong Woong, Beebe, Kirk, Jang, Jaeseon, Nangle, Leslie A, Cook, Susan A
Published in Nature (07.09.2006)
Published in Nature (07.09.2006)
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Journal Article
Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
Reinholdt, Laura G, Ding, Yueming, Gilbert, Griffith T, Czechanski, Anne, Solzak, Jeffrey P, Roper, Randall J, Johnson, Mark T, Donahue, Leah Rae, Lutz, Cathleen, Davisson, Muriel T
Published in Mammalian genome (01.12.2011)
Published in Mammalian genome (01.12.2011)
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Journal Article
Age Exacerbates Abnormal Protein Expression in a Mouse Model of Down Syndrome
Ahmed, Mahiuddin, Md, Block, Aaron, Tong, Suhong, Davisson, Muriel T, Gardiner, Katheleen J
Published in Neurobiology of aging (01.09.2017)
Published in Neurobiology of aging (01.09.2017)
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Journal Article
A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers
Korstanje, Ron, Caputo, Christina R., Doty, Rosalinda A., Cook, Susan A., Bronson, Roderick T., Davisson, Muriel T., Miner, Jeffrey H.
Published in Kidney international (01.06.2014)
Published in Kidney international (01.06.2014)
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Journal Article
Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome
Voronov, Sergey V, Frere, Samuel G, Giovedi, Silvia, Pollina, Elizabeth A, Borel, Christelle, Zhang, Hong, Schmidt, Cecilia, Akeson, Ellen C, Wenk, Markus R, Cimasoni, Laurent, Arancio, Ottavio, Davisson, Muriel T, Antonarakis, Stylianos E, Gardiner, Katheleen, De Camilli, Pietro, Di Paolo, Gilbert
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.2008)
Published in Proceedings of the National Academy of Sciences - PNAS (08.07.2008)
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Journal Article
Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease
Potter, Gregory B, Santos, Marta, Davisson, Muriel T, Rowitch, David H, Marks, Dan L, Bongarzone, Ernesto R, Petryniak, Magdalena A
Published in Human molecular genetics (01.09.2013)
Published in Human molecular genetics (01.09.2013)
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Journal Article
Behavioral validation of the Ts65Dn mouse model for Down syndrome of a genetic background free of the retinal degeneration mutation Pde6b(rd1)
Costa, Alberto C S, Stasko, Melissa R, Schmidt, Cecilia, Davisson, Muriel T
Published in Behavioural brain research (05.01.2010)
Published in Behavioural brain research (05.01.2010)
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Journal Article
ZFP191 is required by oligodendrocytes for CNS myelination
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
Published in Genes & development (01.02.2010)
Published in Genes & development (01.02.2010)
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Journal Article
Mutations in the Human Orthologue of the Mouse underwhite Gene ( uw) Underlie a New Form of Oculocutaneous Albinism, OCA4
Newton, J.M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Published in American journal of human genetics (01.11.2001)
Published in American journal of human genetics (01.11.2001)
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Journal Article
A spontaneous mutation in contactin 1 in the mouse
Davisson, Muriel T, Bronson, Roderick T, Tadenev, Abigail L D, Motley, William W, Krishnaswamy, Arjun, Seburn, Kevin L, Burgess, Robert W
Published in PloS one (29.12.2011)
Published in PloS one (29.12.2011)
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Journal Article
Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse
Lindfors, Charlotte, Nilsson, Ida A. K, Garcia-Roves, Pablo M, Zuberi, Aamir R, Karimi, Mohsen, Donahue, Leah Rae, Roopenian, Derry C, Mulder, Jan, Uhlén, Mathias, Ekström, Tomas J, Davisson, Muriel T, Hökfelt, Tomas G. M, Schalling, Martin, Johansen, Jeanette E
Published in Proceedings of the National Academy of Sciences - PNAS (01.11.2011)
Published in Proceedings of the National Academy of Sciences - PNAS (01.11.2011)
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Journal Article
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 hydronephrosis
Davisson, Muriel T, Cook, Susan A, Akeson, Ellen C, Liu, Don, Heffner, Caleb, Gudis, Polyxeni, Fairfield, Heather, Murray, Stephen A
Published in American journal of physiology. Renal physiology (15.06.2015)
Published in American journal of physiology. Renal physiology (15.06.2015)
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Journal Article
Differential effects of environmental enrichment on behavior and learning of male and female Ts65Dn mice, a model for Down syndrome
Martı́nez-Cué, Carmen, Baamonde, Carmela, Lumbreras, Marian, Paz, Jesús, Davisson, Muriel T, Schmidt, Cecilia, Dierssen, Mara, Flórez, Jesús
Published in Behavioural brain research (21.08.2002)
Published in Behavioural brain research (21.08.2002)
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Journal Article
Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse
Simon-Chazottes, Dominique, Tutois, Sylvie, Kuehn, Michael, Evans, Martin, Bourgade, Franck, Cook, Sue, Davisson, Muriel T., Guénet, Jean-Louis
Published in Genomics (San Diego, Calif.) (01.05.2006)
Published in Genomics (San Diego, Calif.) (01.05.2006)
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Journal Article
Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA)
Pang, Ji-Jing, Chang, Bo, Hawes, Norman L, Hurd, Ronald E, Davisson, Muriel T, Li, Jie, Noorwez, Syed M, Malhotra, Ritu, McDowell, J Hugh, Kaushal, Shalesh, Hauswirth, William W, Nusinowitz, Steven, Thompson, Debra A, Heckenlively, John R
Published in Molecular vision (28.02.2005)
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Published in Molecular vision (28.02.2005)
Journal Article
VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse
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
Published in The EMBO journal (17.12.2008)
Published in The EMBO journal (17.12.2008)
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