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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 Davisson, Muriel T.; Cook, Susan A.; Akeson, Ellen C.; Liu, Don; Heffner, Caleb; Gudis, Polyxeni; Fairfield, Heather; Murray, Stephen A. 分享 收藏
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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; Uhlen, Mathias; Ekstrom, Tomas J.; Davisson, Muriel T.; Hokfelt, Tomas G. M.; Schalling, Martin; Johansen, Jeanette E. 分享 收藏
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Missense mutation in the mouse Col2al gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis Donahue, 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 分享 收藏
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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 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. 分享 收藏
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 分享 收藏
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Trak1 mutation disrupts GABAA receptor homeostasis in hypertonic mice (vol 38, pg 245, 2006) Gilbert, SL; Zhang, L; Forster, ML; Anderson, JR; Iwase, T; Soliven, B; Donahue, LR; Sweet, HO; Bronson, RT; Davisson, MT; Wollmann, RL; T Lahn, B 分享 收藏
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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 Johnson, KR; Lane, PW; Cook, SA; Harris, BS; Ward-Bailey, PF; Bronson, RT; Lyons, BL; Shultz, LD; Davisson, MT 分享 收藏
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