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C A Weber

Showing results (41-50 of 54) with videos related to

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Genomics|November 1, 1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19L H Thompson, L L Bachinski, R L Stallings, et al.
Mutation Research|December 31, 1997
Molecular analysis of ERCC2 mutations in the repair deficient hamster mutants UVL-1 and V-H1S Kadkhodayan, E P Salazar, M J Ramsey, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
American Journal of Human Genetics|February 1, 1996
Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophyK Takayama, E P Salazar, B C Broughton, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19H W Mohrenweiser, A V Carrano, A Fertitta, et al.
Journal of Human Hypertension|June 25, 2010
Indication-specific 6-h systolic blood pressure thresholds can approximate 24-h determination of blood pressure controlM E Ernst, G S Sezate, W Lin, et al.
Journal of Cell Science. Supplement|January 1, 1987
Recent progress with the DNA repair mutants of Chinese hamster ovary cellsL H Thompson, E P Salazar, K W Brookman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994
Molecular cloning of the human nucleotide-excision-repair gene ERCC4L H Thompson, K W Brookman, C A Weber, et al.
Cancer Research|July 15, 1994
The human DNA repair gene, ERCC2 (XPD), corrects ultraviolet hypersensitivity and ultraviolet hypermutability of a shuttle vector replicated in xeroderma pigmentosum group D cellsE M Gözükara, C N Parris, C A Weber, et al.
The Journal of Investigative Dermatology|November 1, 1994
Trichothiodystrophy: clinical spectrum, central nervous system imaging, and biochemical characterization of two siblingsE Chen, J E Cleaver, C A Weber, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Genomics|November 1, 1989
Complementation of repair gene mutations on the hemizygous chromosome 9 in CHO: a third repair gene on human chromosome 19L H Thompson, L L Bachinski, R L Stallings, et al.
Mutation Research|December 31, 1997
Molecular analysis of ERCC2 mutations in the repair deficient hamster mutants UVL-1 and V-H1S Kadkhodayan, E P Salazar, M J Ramsey, et al.
Mutation Research|March 1, 1994
Molecular analysis of the XP-D gene in Italian families with patients affected by trichothiodystrophy and xeroderma pigmentosum group DC Mondello, T Nardo, S Giliani, et al.
American Journal of Human Genetics|February 1, 1996
Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophyK Takayama, E P Salazar, B C Broughton, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19H W Mohrenweiser, A V Carrano, A Fertitta, et al.
Journal of Human Hypertension|June 25, 2010
Indication-specific 6-h systolic blood pressure thresholds can approximate 24-h determination of blood pressure controlM E Ernst, G S Sezate, W Lin, et al.
Journal of Cell Science. Supplement|January 1, 1987
Recent progress with the DNA repair mutants of Chinese hamster ovary cellsL H Thompson, E P Salazar, K W Brookman, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 19, 1994
Molecular cloning of the human nucleotide-excision-repair gene ERCC4L H Thompson, K W Brookman, C A Weber, et al.
Cancer Research|July 15, 1994
The human DNA repair gene, ERCC2 (XPD), corrects ultraviolet hypersensitivity and ultraviolet hypermutability of a shuttle vector replicated in xeroderma pigmentosum group D cellsE M Gözükara, C N Parris, C A Weber, et al.
The Journal of Investigative Dermatology|November 1, 1994
Trichothiodystrophy: clinical spectrum, central nervous system imaging, and biochemical characterization of two siblingsE Chen, J E Cleaver, C A Weber, et al.
Pageof 6