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Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|March 23, 2011

Making new out of old: recycling and modification of an ancient protein translocation system during eukaryotic evolution. Mechanistic comparison and phylogenetic analysis of ERAD, SELMA and the peroxisomal importomerKathrin Bolte, Nicole Gruenheit, Gregor Felsner, et al.

Human Mutation|July 29, 1999

Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypesJ Feng, C H Buzin, S H Tang, et al.

British Heart Journal|June 1, 1975

His bundle recordings in bradycardia-dependent AV block induced by premature beatsA Castellanos, S A Khuddus, L S Sommer, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996

Mutation detection by highly sensitive methods indicates that p53 gene mutations in breast cancer can have important prognostic valueJ S Kovach, A Hartmann, H Blaszyk, et al.

Cytogenetic and Genome Research|May 27, 2004

Cytogenetic damage in lymphocytes for the purpose of dose reconstruction: a review of three recent radiation accidentsA Wojcik, E Gregoire, I Hayata, et al.

Human Genetics|July 1, 1991

T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.

Mutation Research|October 23, 1997

Spontaneous mutation frequencies and spectra in p53 (+/+) and p53 (-/-) mice: a test of the 'guardian of the genome' hypothesis in the Big Blue transgenic mouse mutation detection systemV L Buettner, H Nishino, J Haavik, et al.

Clinical and Experimental Dermatology|June 26, 2003

Prediction of outcome in the treatment of onychomycosisS Sommer, R A Sheehan-Dare, M J D Goodfield, et al.

Oncogene|April 1, 2008

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acidsZ Chen, J Feng, J-S Saldivar, et al.

Journal of the American College of Cardiology|October 2, 2002

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathyJinong Feng, Jin Yan Yan, Carolyn H Buzin, et al.

Pageof 48

Showing results (271-280 of 471) with videos related to

Sort By:

Pageof 48

Bioessays : News and Reviews in Molecular, Cellular and Developmental Biology|March 23, 2011

Making new out of old: recycling and modification of an ancient protein translocation system during eukaryotic evolution. Mechanistic comparison and phylogenetic analysis of ERAD, SELMA and the peroxisomal importomerKathrin Bolte, Nicole Gruenheit, Gregor Felsner, et al.

Human Mutation|July 29, 1999

Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypesJ Feng, C H Buzin, S H Tang, et al.

British Heart Journal|June 1, 1975

His bundle recordings in bradycardia-dependent AV block induced by premature beatsA Castellanos, S A Khuddus, L S Sommer, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 6, 1996

Mutation detection by highly sensitive methods indicates that p53 gene mutations in breast cancer can have important prognostic valueJ S Kovach, A Hartmann, H Blaszyk, et al.

Cytogenetic and Genome Research|May 27, 2004

Cytogenetic damage in lymphocytes for the purpose of dose reconstruction: a review of three recent radiation accidentsA Wojcik, E Gregoire, I Hayata, et al.

Human Genetics|July 1, 1991

T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detectionR P Ketterling, C D Bottema, D D Koeberl, et al.

Mutation Research|October 23, 1997

Spontaneous mutation frequencies and spectra in p53 (+/+) and p53 (-/-) mice: a test of the 'guardian of the genome' hypothesis in the Big Blue transgenic mouse mutation detection systemV L Buettner, H Nishino, J Haavik, et al.

Clinical and Experimental Dermatology|June 26, 2003

Prediction of outcome in the treatment of onychomycosisS Sommer, R A Sheehan-Dare, M J D Goodfield, et al.

Oncogene|April 1, 2008

EGFR somatic doublets in lung cancer are frequent and generally arise from a pair of driver mutations uncommonly seen as singlet mutations: one-third of doublets occur at five pairs of amino acidsZ Chen, J Feng, J-S Saldivar, et al.

Journal of the American College of Cardiology|October 2, 2002

Comprehensive mutation scanning of the dystrophin gene in patients with nonsyndromic X-linked dilated cardiomyopathyJinong Feng, Jin Yan Yan, Carolyn H Buzin, et al.

Pageof 48