Nance–Horan syndrome protein, NHS, associates with epithelial cell junctions

By Sharma Shiwani   Ang Sharyn L.   Shaw Marie   Mackey David A.   Gécz Jozef   McAvoy John W.   Craig Jamie E.  

Human Molecular Genetics, Vol. 15, Iss. 12, 2006-06 ,pp. : 1972-1983

Oxford University Press

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X-linked cataract and Nance-Horan syndrome are allelic disorders

By Coccia Margherita   Brooks Simon P.   Webb Tom R.   Christodoulou Katja   Wozniak Izabella O.   Murday Victoria   Balicki Martha   Yee Harris A.   Wangensteen Teresia   Riise Ruth   Saggar Anand K.   Park Soo-Mi   Kanuga Naheed   Francis Peter J.   Maher Eamonn R.   Moore Anthony T.   Russell-Eggitt Isabelle M.   Hardcastle Alison J.  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2643-2655

Oxford University Press

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Xcat, a novel mouse model for Nance–Horan syndrome inhibits expression of the cytoplasmic-targeted Nhs1 isoform

By Huang Kristen M.   Wu Junhua   Duncan Melinda K.   Moy Chris   Dutra Amalia   Favor Jack   Da Tong   Stambolian Dwight  

Human Molecular Genetics, Vol. 15, Iss. 2, 2006-01 ,pp. : 319-327

Oxford University Press

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Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome

By Jobard Florence  

Human Molecular Genetics, Vol. 12, Iss. 8, 2003-04 ,pp. : 925-935

Oxford University Press

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The human-specific Yp11.2/Xq21.3 homology block encodes a potentially functional testis-specific TGIF-like retroposon

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Mammalian Genome, Vol. 13, Iss. 8, 2002-08 ,pp. : 463-468

Springer Publishing Company

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