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

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Osteoarthritis and Cartilage|May 1, 2012
Ochronosis in a murine model of alkaptonuria is synonymous to that in the human conditionA M Taylor, A J Preston, N K Paulk, et al.
Journal of Neurochemistry|June 18, 2002
Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenaseK M Gibson, D S M Schor, M Gupta, et al.
Blood|July 1, 1996
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C geneM A Whitney, G Royle, M J Low, et al.
Cytogenetic and Genome Research|September 10, 2009
Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agentsA W Hemphill, Y Akkari, A H Newell, et al.
Blood|August 1, 1997
Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cellsR K Rathbun, G R Faulkner, M H Ostroski, et al.
Blood|February 7, 1998
DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint functionM C Heinrich, M E Hoatlin, A J Zigler, et al.
Clinical Genetics|February 6, 2004
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutationsG Turner, K M Lower, S M White, et al.
American Journal of Human Genetics|April 14, 2000
Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3J A Hejna, C D Timmers, C Reifsteck, 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.
Osteoarthritis and Cartilage|May 1, 2012
Ochronosis in a murine model of alkaptonuria is synonymous to that in the human conditionA M Taylor, A J Preston, N K Paulk, et al.
Journal of Neurochemistry|June 18, 2002
Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenaseK M Gibson, D S M Schor, M Gupta, et al.
Blood|July 1, 1996
Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C geneM A Whitney, G Royle, M J Low, et al.
Cytogenetic and Genome Research|September 10, 2009
Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agentsA W Hemphill, Y Akkari, A H Newell, et al.
Blood|August 1, 1997
Inactivation of the Fanconi anemia group C gene augments interferon-gamma-induced apoptotic responses in hematopoietic cellsR K Rathbun, G R Faulkner, M H Ostroski, et al.
Blood|February 7, 1998
DNA cross-linker-induced G2/M arrest in group C Fanconi anemia lymphoblasts reflects normal checkpoint functionM C Heinrich, M E Hoatlin, A J Zigler, et al.
Clinical Genetics|February 6, 2004
The clinical picture of the Börjeson-Forssman-Lehmann syndrome in males and heterozygous females with PHF6 mutationsG Turner, K M Lower, S M White, et al.
American Journal of Human Genetics|April 14, 2000
Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3J A Hejna, C D Timmers, C Reifsteck, et al.
Pageof 8