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Muriel T. Davisson

Jackson Laboratory

62H指数
274论文数
1.6W被引数
收录论文 37
发表时间
Age exacerbates abnormal protein expression in a mouse model of Down syndrome
err2017-09-01
err14
PREAI
errAhmed, Md. Mahiuddin; Block, Aaron; Tong, Suhong; Davisson, Muriel T.; Gardiner, Katheleen J.
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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
err2015-06-15
err2
errOAAI
errDavisson, Muriel T.; Cook, Susan A.; Akeson, Ellen C.; Liu, Don; Heffner, Caleb; Gudis, Polyxeni; Fairfield, Heather; Murray, Stephen A.
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A mouse Col4a4 mutation causing Alport glomerulosclerosis with abnormal collagen α3α4α5(IV) trimers小鼠Col4a4突变引起异常胶原 α3α4α5(IV) 三聚体的Alport肾小球硬化
err2014-06-01
err40
errOAAI
errKorstanje, Ron; Caputo, Christina R.; Doty, Rosalinda A.; Cook, Susan A.; Bronson, Roderick T.; Davisson, Muriel T.; Miner, Jeffrey H.
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Missense mutation in mouse GALC mimics human gene defect and offers new insights into Krabbe disease
err2013-04-24
err51
errOAAI
errPotter, Gregory B.; Santos, Marta; Davisson, Muriel T.; Rowitch, David H.; Marks, Dan L.; Bongarzone, Ernesto R.; Petryniak, Magdalena A.
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Mouse models of cancer at The Jackson Laboratory Repository
err2012-04-01
err0
PREAI
errBoswell, Deborah M.; Rockwood, Stephen F.; Sasner, Michael; Lutz, Cathleen M.; Davisson, Muriel T.; Donahue, Leah Rae
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A Spontaneous Mutation in Contactin 1 in the Mouse
err2011-12-29
err16
errOAAI
errDavisson, Muriel T.; Bronson, Roderick T.; Tadenev, Abigail L. D.; Motley, William W.; Krishnaswamy, Arjun; Seburn, Kevin L.; Burgess, Robert W.
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Hypothalamic mitochondrial dysfunction associated with anorexia in the anx/anx mouse
err2011-10-24
err34
errOAAI
errLindfors, Charlotte; Nilsson, Ida A. K.; Garcia-Roves, Pablo M.; Zuberi, Aamir R.; Karimi, Mohsen; Donahue, Leah Rae; Roopenian, Derry C.; Mulder, Jan; Uhlen, Mathias; Ekstrom, Tomas J.; Davisson, Muriel T.; Hokfelt, Tomas G. M.; Schalling, Martin; Johansen, Jeanette E.
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The Mouse Model of Down Syndrome Ts65Dn Presents Visual Deficits as Assessed by Pattern Visual Evoked Potentials
err2010-06-01
err25
errOAAI
errScott-McKean, Jonah Jacob; Chang, Bo; Hurd, Ronald E.; Nusinowitz, Steven; Schmidt, Cecilia; Davisson, Muriel T.; Costa, Alberto C. S.
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Missense mutation in the mouse Col2al gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis
err2009-12-02
err64
errOAAI
errDonahue, LR; Chang, B; Mohan, S; Miyakoshi, N; Wergedal, JE; Baylink, DJ; Hawes, NL; Rosen, CJ; Ward-Bailey, P; Zheng, QY; Bronson, RT; Johnson, KR; Davisson, MT
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A Mouse Model for Meckel Syndrome Type 3
err2009-04-01
err44
errOAAI
errCook, Susan A.; Collin, Gayle B.; Bronson, Roderick T.; Naggert, Juergen K.; Liu, Dong P.; Akeson, Ellen C.; Davisson, Muriel T.
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VAC14 nucleates a protein complex essential for the acute interconversion of PI3P and PI(3,5)P2 in yeast and mouse
err2008-11-27
err218
errOAAI
errJin, 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.
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Synaptojanin 1-linked phosphoinositide dyshomeostasis and cognitive deficits in mouse models of Down's syndrome
err2008-07-08
err151
errOAAI
errVoronov, 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
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Know thy mouse
err2006-12-01
err152
PREAI
errTaft, Robert A.; Davisson, Muriel; Wiles, Michael V.
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Impact of trisomy on fertility and meiosis in male mice
err2006-10-17
err11
errOAAI
errDavisson, M.; Akeson, E.; Schmidt, C.; Harris, B.; Farley, J.; Handel, M. A.
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Mutations in the gene encoding the low-density lipoprotein receptor LRP4 cause abnormal limb development in the mouse
err2006-05-01
err74
PREAI
errSimon-Chazottes, Dominique; Tutois, Sylvie; Kuehn, Michael; Evans, Martin; Bourgade, Franck; Cook, Sue; Davisson, Muriel T.; Guenet, Jean-Louis
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Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice (vol 38, pg 245, 2006)
err2006-03-01
err0
errOAAI
errGilbert, SL; Zhang, L; Forster, ML; Anderson, JR; Iwase, T; Soliven, B; Donahue, LR; Sweet, HO; Bronson, RT; Davisson, MT; Wollmann, RL; T Lahn, B
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Chromosomal inversion discovered in C3H/HeJ mice在C3H/HeJ小鼠中发现染色体倒位
err2006-02-01
err15
PREAI
errAkeson, EC; Donahue, LR; Beamer, WG; Shultz, KL; Ackert-Bicknell, C; Rosen, CJ; Corrigan, J; Davisson, MT
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Mouse models of Alzheimer's disease in the induced mutant resource
err2004-07-01
err0
PREAI
errSasner, M; Linder, CC; Rockwood, SF; Davisson, MT
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Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
err2003-01-01
err24
PREAI
errJohnson, KR; Lane, PW; Cook, SA; Harris, BS; Ward-Bailey, PF; Bronson, RT; Lyons, BL; Shultz, LD; Davisson, MT
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Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4
err2001-11-01
err298
errOAAI
errNewton, JM; Cohen-Barak, O; Hagiwara, N; Gardner, JM; Davisson, MT; King, RA; Brilliant, MH
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