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Jochen Graw

Showing results (61-70 of 127) with videos related to

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Endocrinology|September 24, 2005
Betacellulin overexpression in transgenic mice causes disproportionate growth, pulmonary hemorrhage syndrome, and complex eye pathologyMarlon R Schneider, Maik Dahlhoff, Nadja Herbach, et al.
Radiation Research|July 8, 2021
Complex Long-term Effects of Radiation on Adult Mouse BehaviorLillian Garrett, Marie-Claire Ung, Jan Einicke, et al.
Plos One|August 23, 2011
The pathologic effect of a novel neomorphic Fgf9(Y162C) allele is restricted to decreased vision and retarded lens growthOliver Puk, Gabriele Möller, Arie Geerlof, et al.
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.
Investigative Ophthalmology & Visual Science|April 4, 2008
Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotypeOliver Puk, Jana Löster, Claudia Dalke, 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.
Pageof 13

Showing results (61-70 of 127) with videos related to

Sort By:
Pageof 13
Endocrinology|September 24, 2005
Betacellulin overexpression in transgenic mice causes disproportionate growth, pulmonary hemorrhage syndrome, and complex eye pathologyMarlon R Schneider, Maik Dahlhoff, Nadja Herbach, et al.
Radiation Research|July 8, 2021
Complex Long-term Effects of Radiation on Adult Mouse BehaviorLillian Garrett, Marie-Claire Ung, Jan Einicke, et al.
Plos One|August 23, 2011
The pathologic effect of a novel neomorphic Fgf9(Y162C) allele is restricted to decreased vision and retarded lens growthOliver Puk, Gabriele Möller, Arie Geerlof, et al.
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.
Investigative Ophthalmology & Visual Science|April 4, 2008
Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotypeOliver Puk, Jana Löster, Claudia Dalke, 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.
Pageof 13