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E M Taylor

Showing results (91-100 of 101) with videos related to

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Cancer Research|February 10, 2000
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defectM Berneburg, P H Clingen, S A Harcourt, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.
Nature Genetics|August 24, 2004
Abnormal TNF activity in Timp3-/- mice leads to chronic hepatic inflammation and failure of liver regenerationFazilat F Mohammed, David S Smookler, Suzanne E M Taylor, et al.
Current Biology : CB|February 21, 1998
Atm-dependent interactions of a mammalian chk1 homolog with meiotic chromosomesG Flaggs, A W Plug, K M Dunks, et al.
Genes and Immunity|October 30, 2009
Multiple sclerosis susceptibility alleles in African AmericansB A Johnson, J Wang, E M Taylor, et al.
Genes & Development|October 1, 1996
The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomesK S Keegan, D A Holtzman, A W Plug, et al.
Human Molecular Genetics|November 16, 2001
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD geneB C Broughton, M Berneburg, H Fawcett, et al.
International Health|May 30, 2024
Tropical Data: supporting health ministries worldwide to conduct high-quality trachoma surveysE M Harding-Esch, A Bakhtiari, S Boyd, et al.
Translational Psychiatry|March 8, 2017
Effects of naltrexone are influenced by childhood adversity during negative emotional processing in addiction recoveryG Savulich, R Riccelli, L Passamonti, et al.
American Journal of Human Genetics|March 10, 2005
Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosisDavid P Kelsell, Elizabeth E Norgett, Harriet Unsworth, et al.
Pageof 11

Showing results (91-100 of 101) with videos related to

Sort By:
Pageof 11
Cancer Research|February 10, 2000
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defectM Berneburg, P H Clingen, S A Harcourt, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.
Nature Genetics|August 24, 2004
Abnormal TNF activity in Timp3-/- mice leads to chronic hepatic inflammation and failure of liver regenerationFazilat F Mohammed, David S Smookler, Suzanne E M Taylor, et al.
Current Biology : CB|February 21, 1998
Atm-dependent interactions of a mammalian chk1 homolog with meiotic chromosomesG Flaggs, A W Plug, K M Dunks, et al.
Genes and Immunity|October 30, 2009
Multiple sclerosis susceptibility alleles in African AmericansB A Johnson, J Wang, E M Taylor, et al.
Genes & Development|October 1, 1996
The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomesK S Keegan, D A Holtzman, A W Plug, et al.
Human Molecular Genetics|November 16, 2001
Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD geneB C Broughton, M Berneburg, H Fawcett, et al.
International Health|May 30, 2024
Tropical Data: supporting health ministries worldwide to conduct high-quality trachoma surveysE M Harding-Esch, A Bakhtiari, S Boyd, et al.
Translational Psychiatry|March 8, 2017
Effects of naltrexone are influenced by childhood adversity during negative emotional processing in addiction recoveryG Savulich, R Riccelli, L Passamonti, et al.
American Journal of Human Genetics|March 10, 2005
Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosisDavid P Kelsell, Elizabeth E Norgett, Harriet Unsworth, et al.
Pageof 11