Mutation in the A3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse

By Graw J.   Jung M.   Loster J.   Klopp N.   Soewarto D.   Fella C.   Fuchs H.   Reis A.   Wolf E.   Balling R.   Hrabe de Angelis M.  

Genomics, Vol. 62, Iss. 1, 1999-11 ,pp. : 67-73

Elsevier

Access to resources Recommend Favorite

A New Mouse Model for Autosomal Recessive Polycystic Kidney Disease

By Chittenden L.   Lu X.   Cacheiro N.L.A.   Cain K.T.   Generoso W.   Bryda E.C.   Stubbs L.  

Genomics, Vol. 79, Iss. 4, 2002-04 ,pp. : 499-504

Academic Press

Access to resources Recommend Favorite

Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld s ) mouse

By Fernando F.S.   Conforti L.   Tosi S.   Smith A.D.   Coleman M.P.  

Gene, Vol. 284, Iss. 1, 2002-02 ,pp. : 23-29

Elsevier

Access to resources Recommend Favorite

Mutations in the PDE6B Gene in Autosomal Recessive Retinitis Pigmentosa

By D Anciger M.I.   B Laney J.O.   G Ao Y.Q.   Z Hao D.Y.   H Eckenlively J.O.R.   J Acobson S.A.G.   F Arber D.E.B.  

Genomics, Vol. 30, Iss. 1, 1995-11 ,pp. : 1-7

Academic Press

Access to resources Recommend Favorite

Transcriptional regulation of the mouse A-crystallin gene: binding of USF to the -7/+5 region

By Sax C.M.   Cvekl A.   Piatigorsky J.  

Gene, Vol. 185, Iss. 2, 1997-02 ,pp. : 209-216

Elsevier

Access to resources Recommend Favorite