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Functional analysis of Gscl in the pathogenesis of the DiGeorge and Velocardiofacial syndromes 1-gen-1998 Wakamiya, M; Illingworth, ELISABETH ANNE; RIVERA PEREZ, Ja; Baldini, A; Behringer, R.
ES2, a gene deleted in DiGeorge syndrome, encodes a nuclear protein and is expressed during early mouse development, where it shares an expression domain with a Goosecoid-like gene 1-gen-1998 Illingworth, ELISABETH ANNE; Harvey, El; Scambler, Pj; Baldini, A.
Congenital heart defects and 22q11 deletions: Which genes count? 1-gen-1998 Illingworth, ELISABETH ANNE; Baldini, A.
Congenital heart disease in mice deficient for the DiGeorge syndrome region 1-gen-1999 Illingworth, ELISABETH ANNE; Jurecic, V; CARATTINI RIVERA, S; Cheah, Y. C.; Rosenblatt, Hm; Bradley, A; Baldini,
Genetic factors are major determinants of phenotypic variability in a mouse model of DiGeorge syndrome 1-gen-2001 Taddei, I; Morishima, M; Huynh, T; Illingworth, ELISABETH ANNE
Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. 1-gen-2001 Illingworth, ELISABETH ANNE; Vitelli, F; Su, H; Morishima, M; Huynh, T; Pramparo, T; Jurecic, V; Ogunrinu, G; Sutherland, Hf; Scambler, Pj; Bradley, A; Baldini, A.
Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments. 1-gen-2001 Paylor, R; Mcilwain, Kl; Mcaninch, R; Nellis, A; YUVA PAYLOR, La; Baldini, A; Illingworth, ELISABETH ANNE
Recovey from arterial growth delay reduces penetrance of cardiovascular defects in mice deleted for the DiGeorge syndrome region 1-gen-2001 Illingworth, ELISABETH ANNE
Chromosomal microdeletions: dissecting del22q11 syndrome. 1-gen-2001 Illingworth, ELISABETH ANNE
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways. 1-gen-2002 Vitelli, F; Morishima, M; Taddei, I; Illingworth, ELISABETH ANNE; Baldini, A.
A genetic link between Tbx1 and fibroblast growth factor signaling. 1-gen-2002 Vitelli, F; Taddei, I; Morishima, M; Meyers, En; Illingworth, ELISABETH ANNE; Baldini, A.
TBX1 is required for inner ear morphogenesis. 1-gen-2003 Vitelli, F; Viola, A; Morishima, M; Pramparo, T; Baldini, A; Illingworth, ELISABETH ANNE
Tbx1 has a dual role in the morphogenesis of the cardiac outflow tract. 1-gen-2004 Xu, H; Morishima, M; Wylie, Jn; Schwartz, Rj; Bruneau, Bg; Illingworth, ELISABETH ANNE; Baldini, A.
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development. 1-gen-2005 Zhang, Z; Cerrato, F; Xu, H; Vitelli, F; Morishima, M; Vincentz, J; Furuta, Y; Ma, L; Martin, Jf; Baldini, A; Illingworth, ELISABETH ANNE
Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1. 1-gen-2005 Ivins, S; LAMMERTS VAN BEUREN, K; Roberts, C; James, C; Illingworth, ELISABETH ANNE; Baldini, A; Ataliotis, P; Scambler, Pj
Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome. 1-gen-2005 Prescott, K; Ivins, S; Hubank, M; Illingworth, ELISABETH ANNE; Baldini, A; Scambler, P.
Mouse models of 22q11 deletion syndrome. 1-gen-2006 Paylor, R; Illingworth, ELISABETH ANNE
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome. 1-gen-2006 Paylor, R; Glaser, B; Mupo, A; Ataliotis, P; Spencer, C; Sobotka, A; Sparks, C; Choi, Ch; Oghalai, J; Curran, S; Murphy, Kc; Monks, S; Williams, N; O'Donovan, Mc; Owen, Mj; Scambler, Pj; Illingworth, ELISABETH ANNE
Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity 1-gen-2006 Eichers, Er; ABD EL BARR, Mm; Paylor, R; Lewis, Ra; Bi, W; Lin, X; Meehan, Tp; Stockton, Dw; Wu, Sm; Illingworth, ELISABETH ANNE
Altered expression of hippocampal dentate granule neuron genes in a mouse model of human 22q11 deletion syndrome. 1-gen-2006 Jurata, Lw; Gallagher, P; Lemire, Al; Charles, V; Brockman, Ja; Illingworth, ELISABETH ANNE; Altar, Ca
Mostrati risultati da 1 a 20 di 51
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