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International Journal of Molecular Sciences|December 19, 2020
Application of WES Towards Molecular Investigation of Congenital Cataracts: Identification of Novel Alleles and Genes in a Hospital-Based Cohort of South IndiaDinesh Kumar Kandaswamy, Makarla Venkata Sathya Prakash, Jochen Graw, et al.
Molecular Neurobiology|October 7, 2018
Crybb2 Mutations Consistently Affect Schizophrenia Endophenotypes in MiceTamara Heermann, Lillian Garrett, Wolfgang Wurst, et al.
Molecular Vision|May 29, 2010
A novel human CRYGD mutation in a juvenile autosomal dominant cataractMascarenhas Roshan, Pai H Vijaya, G Rao Lavanya, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 13, 2006
Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humansNatalia S Pellegata, Leticia Quintanilla-Martinez, Heide Siggelkow, et al.
BMC Developmental Biology|December 24, 2008
Pleiotropic effects in Eya3 knockout miceTorben Söker, Claudia Dalke, Oliver Puk, et al.
Investigative Ophthalmology & Visual Science|September 29, 2004
Mutation analysis of congenital cataracts in Indian families: identification of SNPS and a new causative allele in CRYBB2 geneSathiyavedu T Santhiya, Shyam Manohar Manisastry, Deepika Rawlley, et al.
Cancer Research|May 31, 2002
Recessive transmission of a multiple endocrine neoplasia syndrome in the ratAndreas Fritz, Axel Walch, Kamilla Piotrowska, et al.
Radiation and Environmental Biophysics|January 13, 2018
Lifetime study in mice after acute low-dose ionizing radiation: a multifactorial study with special focus on cataract riskClaudia Dalke, Frauke Neff, Savneet Kaur Bains, et al.
Radiation Research|November 17, 2021
Introduction to the Special LDLensRad Focus IssueElizabeth A Ainsbury, Claudia Dalke, Mariateresa Mancuso, et al.
Molecular Vision|September 17, 2009
The GJA8 allele encoding CX50I247M is a rare polymorphism, not a cataract-causing mutationJochen Graw, Werner Schmidt, Peter J Minogue, et al.
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