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M Grompe

Showing results (41-50 of 78) with videos related to

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Blood|May 15, 1996
Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activityT Yamashita, N Wu, G Kupfer, et al.
Somatic Cell and Molecular Genetics|January 1, 1997
Complementation group assignments in Fanconi anemia fibroblast cell lines from North AmericaP M Jakobs, E Fiddler-Odell, C Reifsteck, et al.
The New England Journal of Medicine|August 11, 1994
A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type IM Grompe, M St-Louis, S I Demers, et al.
The Journal of Biological Chemistry|August 25, 1990
Ectopic correction of ornithine transcarbamylase deficiency in sparse fur miceS N Jones, M Grompe, M I Munir, et al.
The Journal of Biological Chemistry|January 13, 2001
Mechanistic inferences from the crystal structure of fumarylacetoacetate hydrolase with a bound phosphorus-based inhibitorR L Bateman, P Bhanumoorthy, J F Witte, et al.
Nature Genetics|June 1, 1993
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi JewsM A Whitney, H Saito, P M Jakobs, et al.
Nature Genetics|March 1, 1996
Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type IK Overturf, M Al-Dhalimy, R Tanguay, et al.
Genes & Development|December 1, 1993
Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino miceM Grompe, M al-Dhalimy, M Finegold, et al.
Molecular Genetics and Metabolism|December 26, 2001
The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phaseY M Akkari, R L Bateman, C A Reifsteck, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1991
Fidelity of targeted recombination in human fibroblasts and murine embryonic stem cellsH Zheng, P Hasty, M A Brenneman, et al.
Pageof 8

Showing results (41-50 of 78) with videos related to

Sort By:
Pageof 8
Blood|May 15, 1996
Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activityT Yamashita, N Wu, G Kupfer, et al.
Somatic Cell and Molecular Genetics|January 1, 1997
Complementation group assignments in Fanconi anemia fibroblast cell lines from North AmericaP M Jakobs, E Fiddler-Odell, C Reifsteck, et al.
The New England Journal of Medicine|August 11, 1994
A single mutation of the fumarylacetoacetate hydrolase gene in French Canadians with hereditary tyrosinemia type IM Grompe, M St-Louis, S I Demers, et al.
The Journal of Biological Chemistry|August 25, 1990
Ectopic correction of ornithine transcarbamylase deficiency in sparse fur miceS N Jones, M Grompe, M I Munir, et al.
The Journal of Biological Chemistry|January 13, 2001
Mechanistic inferences from the crystal structure of fumarylacetoacetate hydrolase with a bound phosphorus-based inhibitorR L Bateman, P Bhanumoorthy, J F Witte, et al.
Nature Genetics|June 1, 1993
A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi JewsM A Whitney, H Saito, P M Jakobs, et al.
Nature Genetics|March 1, 1996
Hepatocytes corrected by gene therapy are selected in vivo in a murine model of hereditary tyrosinaemia type IK Overturf, M Al-Dhalimy, R Tanguay, et al.
Genes & Development|December 1, 1993
Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino miceM Grompe, M al-Dhalimy, M Finegold, et al.
Molecular Genetics and Metabolism|December 26, 2001
The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phaseY M Akkari, R L Bateman, C A Reifsteck, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 15, 1991
Fidelity of targeted recombination in human fibroblasts and murine embryonic stem cellsH Zheng, P Hasty, M A Brenneman, et al.
Pageof 8