PuSH - HMGU Publikationen https://push-zb.helmholtz-munich.de PuSH - Publikationen-Server des Helmholtz Zentrums München de-de <![CDATA[Ullah, A.* et al. Sequence variants in four genes underlying Bardet-Biedl syndrome in consanguineous families. Mol. Vis. 23, 482-494 (2017)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51631&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=51631&la=de Fri, 08 Sep 2017 00:00:00 +0000 <![CDATA[Puk, O. et al. Novel small-eye allele in paired box gene 6 (Pax6) is caused by a point mutation in intron 7 and creates a new exon. Mol. Vis. 19, 877-884 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24018&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24018&la=de Mon, 22 Apr 2013 00:00:00 +0000 <![CDATA[Veiga-Crespo, P.* et al. Phenotypic map of porcine retinal ganglion cells. Mol. Vis. 19, 904-916 (2013)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24689&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=24689&la=de Fri, 31 May 2013 00:00:00 +0000 <![CDATA[Roshan, M.* et al. Analysis of mitochondrial DNA variations in Indian patients with congenital cataract. Mol. Vis. 18, 181-193 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7304&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=7304&la=de Fri, 20 Apr 2012 00:00:00 +0000 <![CDATA[Steinhart, M.R.* et al. Mice with an induced mutation in collagen 8A2 develop larger eyes and are resistant to retinal ganglion cell damage in an experimental glaucoma model. Mol. Vis. 18, 1093-1106 (2012)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8398&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=8398&la=de Thu, 23 Aug 2012 00:00:00 +0000 <![CDATA[Puk, O. ; Ahmad, N. ; Wagner, S. ; Hrabě de Angelis, M. & Graw, J. Microphakia and congenital cataract formation in a novel Lim2C51R mutant mouse. Mol. Vis. 17, 1164-1171 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6333&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6333&la=de Tue, 21 Jun 2011 00:00:00 +0000 <![CDATA[Siemiatkowska, A.M.* et al. Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping. Mol. Vis. 17, 3013-3024 (2011)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6817&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=6817&la=de Fri, 23 Dec 2011 00:00:00 +0000 <![CDATA[Azam, M.* et al. Novel CNGA3 and CNGB3 mutations in two Pakistani families with achromatopsia. Mol. Vis. 16, 774-781 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=528&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=528&la=de Mon, 18 Oct 2010 00:00:00 +0000 <![CDATA[Roshan, M.* et al. A novel human CRYGD mutation in a juvenile autosomal dominant cataract. Mol. Vis. 16, 887-896 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5365&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5365&la=de Mon, 15 Nov 2010 00:00:00 +0000 <![CDATA[Santhiya, S.T.* et al. Molecular analysis of cataract families in India: New mutations in the CRYBB2 and GJA3 genes and rare polymorphisms. Mol. Vis. 16, 1837-1847 (2010)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5993&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5993&la=de Fri, 03 Dec 2010 00:00:00 +0000 <![CDATA[Graw, J. et al. The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutation. Mol. Vis. 15, 1881-1885 (2009)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=271&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=271&la=de Mon, 23 Nov 2009 00:00:00 +0000 <![CDATA[Schmidt, W.* ; Klopp, N. ; Illig, T. & Graw, J. A novel GJA8 mutation causing a recessive triangular cataract. Mol. Vis. 14, 851-856 (2008)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5896&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5896&la=de Thu, 29 May 2008 00:00:00 +0000 <![CDATA[Pauli, S.* et al. Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene. Mol. Vis. 13, 962-967 (2007)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5887&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=5887&la=de Tue, 19 Jun 2007 00:00:00 +0000 <![CDATA[Santhiya, S.T.* et al. Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. Mol. Vis. 12, 768-773 (2006)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4536&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4536&la=de Mon, 24 Jul 2006 00:00:00 +0000 <![CDATA[Jablonski, M.M.* et al. An ENU-induced mutation in Rs1h causes disruption of retinal structure and function. Mol. Vis. 11, 569-581 (2005)]]> https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4295&la=de https://push-zb.helmholtz-munich.de/frontdoor.php?source_opus=4295&la=de Mon, 08 Aug 2005 00:00:00 +0000