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J Graw

Showing results (71-80 of 78) with videos related to

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Genomics|December 10, 1999
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouseJ Graw, M Jung, J Löster, et al.
Genomics|October 23, 1998
Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genesN Klopp, J Favor, J Löster, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2NE Berber, I D Fidanci, C Un, et al.
Journal of Thrombosis and Haemostasis : JTH|January 27, 2005
Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII geneO El-Maarri, U Herbiniaux, J Graw, et al.
The Anatomical Record|December 22, 1999
Up-regulation of novel intermediate filament proteins in primary fiber cells: an indicator of all vertebrate lens fiber differentiation?M E Ireland, P Wallace, A Sandilands, et al.
Radiation Research|May 13, 2021
Radiation-Induced Lens Opacity and Cataractogenesis: A Lifetime Study Using Mice of Varying Genetic BackgroundsR A McCarron, S G R Barnard, G Babini, et al.
Journal of the Neurological Sciences|September 5, 2025
The expanding clinical utility of blood neurofilament light chain (bNfL): a multi-disciplinary diagnostic toolPeter Körtvelyessy, Burak Arslan, Jonah Nietiet, et al.
Current Pharmaceutical Biotechnology|February 10, 2009
The German Mouse Clinic: a platform for systemic phenotype analysis of mouse modelsH Fuchs, V Gailus-Durner, T Adler, et al.
Pageof 8

Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Genomics|December 10, 1999
Mutation in the betaA3/A1-crystallin encoding gene Cryba1 causes a dominant cataract in the mouseJ Graw, M Jung, J Löster, et al.
Genomics|October 23, 1998
Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genesN Klopp, J Favor, J Löster, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|July 13, 2006
Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2NE Berber, I D Fidanci, C Un, et al.
Journal of Thrombosis and Haemostasis : JTH|January 27, 2005
Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII geneO El-Maarri, U Herbiniaux, J Graw, et al.
The Anatomical Record|December 22, 1999
Up-regulation of novel intermediate filament proteins in primary fiber cells: an indicator of all vertebrate lens fiber differentiation?M E Ireland, P Wallace, A Sandilands, et al.
Radiation Research|May 13, 2021
Radiation-Induced Lens Opacity and Cataractogenesis: A Lifetime Study Using Mice of Varying Genetic BackgroundsR A McCarron, S G R Barnard, G Babini, et al.
Journal of the Neurological Sciences|September 5, 2025
The expanding clinical utility of blood neurofilament light chain (bNfL): a multi-disciplinary diagnostic toolPeter Körtvelyessy, Burak Arslan, Jonah Nietiet, et al.
Current Pharmaceutical Biotechnology|February 10, 2009
The German Mouse Clinic: a platform for systemic phenotype analysis of mouse modelsH Fuchs, V Gailus-Durner, T Adler, et al.
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