Cranial neural crest ablation of Jagged1 recapitulates the craniofacial phenotype of Alagille syndrome patients

By Humphreys Ryan   Zheng Wei   Prince Lawrence S   Qu Xianghu   Brown Christopher   Loomes Kathleen   Huppert Stacey S.   Baldwin Scott   Goudy Steven  

Human Molecular Genetics, Vol. 21, Iss. 6, 2012-03 ,pp. : 1374-1383

Oxford University Press

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Disruption of scribble ( Scrb1 ) causes severe neural tube defects in the circletail mouse

By Murdoch Jennifer N.  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-01 ,pp. : 87-98

Oxford University Press

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Col4a1 mutation in mice causes defects in vascular function and low blood pressure associated with reduced red blood cell volume

By Van Agtmael Tom   Bailey Matthew A.   Schltzer-Schrehardt Ursula   Craigie Eilidh   Jackson Ian J.   Brownstein David G.   Megson Ian L.   Mullins John J.  

Human Molecular Genetics, Vol. 19, Iss. 6, 2010-03 ,pp. : 1119-1128

Oxford University Press

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Recessive mutation in desmoplakin disrupts desmoplakin–intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

By Norgett Elizabeth E.   Hatsell SarahJ.   Carvajal-Huerta Luis  

Human Molecular Genetics, Vol. 9, Iss. 18, 2000-11 ,pp. : 2761-2766

Oxford University Press

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Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1 , a novel gene involved in floor plate specification

By Doudney K.   Stanier P.   Murdoch J.N.   Paternotte C.   Copp A.J.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2593-2601

Oxford University Press

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