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T W Glover

Showing results (31-40 of 97) with videos related to

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Oncogene|May 30, 2006
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1979
Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblastsT W Glover, C C Chang, J E Trosko, et al.
Human Genetics|September 1, 1995
Two highly polymorphic CA repeats in the Menkes gene (ATP7A)C R Begy, H A Dierick, J W Innis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1987
Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblastsR A Schultz, P J Saxon, T W Glover, et al.
Arizona Medicine|November 1, 1980
The fragile X chromosome mental retardation and large testesF Hecht, B Kaiser-McCaw, B C Moore, et al.
American Journal of Medical Genetics|March 1, 1989
Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)J L Gorski, B A Cox, M Kyine, et al.
Human Molecular Genetics|March 1, 1997
Immunocytochemical localization of the Menkes copper transport protein (ATP7A) to the trans-Golgi networkH A Dierick, A N Adam, J F Escara-Wilke, et al.
Genomics|August 10, 1995
Molecular structure of the Menkes disease gene (ATP7A)H A Dierick, L Ambrosini, J Spencer, et al.
Gene|September 7, 2000
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutantJ Lee, J R Prohaska, S L Dagenais, et al.
Genomics|May 1, 1995
Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10D Kapfhamer, D E Miller, S Lambert, et al.
Pageof 10

Showing results (31-40 of 97) with videos related to

Sort By:
Pageof 10
Oncogene|May 30, 2006
Depletion of CHK1, but not CHK2, induces chromosomal instability and breaks at common fragile sitesS G Durkin, M F Arlt, N G Howlett, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 1979
Ultraviolet light induction of diphtheria toxin-resistant mutants of normal and xeroderma pigmentosum human fibroblastsT W Glover, C C Chang, J E Trosko, et al.
Human Genetics|September 1, 1995
Two highly polymorphic CA repeats in the Menkes gene (ATP7A)C R Begy, H A Dierick, J W Innis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1987
Microcell-mediated transfer of a single human chromosome complements xeroderma pigmentosum group A fibroblastsR A Schultz, P J Saxon, T W Glover, et al.
Arizona Medicine|November 1, 1980
The fragile X chromosome mental retardation and large testesF Hecht, B Kaiser-McCaw, B C Moore, et al.
American Journal of Medical Genetics|March 1, 1989
Terminal deletion of the long arm of chromosome 2 in a mildly dysmorphic hypotonic infant with karyotype 46,XY,del(2)(q37)J L Gorski, B A Cox, M Kyine, et al.
Human Molecular Genetics|March 1, 1997
Immunocytochemical localization of the Menkes copper transport protein (ATP7A) to the trans-Golgi networkH A Dierick, A N Adam, J F Escara-Wilke, et al.
Genomics|August 10, 1995
Molecular structure of the Menkes disease gene (ATP7A)H A Dierick, L Ambrosini, J Spencer, et al.
Gene|September 7, 2000
Isolation of a murine copper transporter gene, tissue specific expression and functional complementation of a yeast copper transport mutantJ Lee, J R Prohaska, S L Dagenais, et al.
Genomics|May 1, 1995
Chromosomal localization of the ankyrinG gene (ANK3/Ank3) to human 10q21 and mouse 10D Kapfhamer, D E Miller, S Lambert, et al.
Pageof 10