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Development (Cambridge, England)|February 20, 2004
Early developmental failure of substantia nigra dopamine neurons in mice lacking the homeodomain gene Pitx3Marten P Smidt, Simone M Smits, Hans Bouwmeester, et al.
Investigative Ophthalmology & Visual Science|November 24, 2005
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promotersJochen Graw, Jana Löster, Oliver Puk, et al.
Blood|December 13, 2005
Lack of F8 mRNA: a novel mechanism leading to hemophilia AOsman El-Maarri, Heike Singer, Claudia Klein, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 8, 2013
Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal functionMinxuan Sun, Sabine M Hölter, Jens Stepan, et al.
The EMBO Journal|November 12, 2002
Altered aggregation properties of mutant gamma-crystallins cause inherited cataractAileen Sandilands, Aileen M Hutcheson, Heather A Long, et al.
Cell Death Discovery|September 17, 2022
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal modelSurabhi Kandaswamy, Lena Zobel, Bina John, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 25, 2009
Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) miceMichael Rosemann, Alesia Ivashkevich, Jack Favor, et al.
Investigative Ophthalmology & Visual Science|August 30, 2011
The KORA Eye Study: a population-based study on eye diseases in Southern Germany (KORA F4)Jochen Graw, Gerhard Welzl, Nafees Ahmad, et al.
Translational Psychiatry|April 23, 2020
Polymorphisms in CRYBB2 encoding βB2-crystallin are associated with antisaccade performance and memory functionIna Giegling, Annette M Hartmann, Just Genius, et al.
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