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Showing results (301-310 of 321) with videos related to

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Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 17, 1998
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer riskT S Frank, S A Manley, O I Olopade, et al.
Journal of Community Genetics|December 16, 2025
Barriers and facilitators of cancer genetic risk screening at community-based organizations serving LatinasBella Ortega, Maisha R Huq, Dariana Sedeño-Delgado, et al.
Nature Communications|March 31, 2018
Author Correction: Attenuation of RNA polymerase II pausing mitigates BRCA1-associated R-loop accumulation and tumorigenesisXiaowen Zhang, Huai-Chin Chiang, Yao Wang, et al.
Nature Communications|June 27, 2017
Attenuation of RNA polymerase II pausing mitigates BRCA1-associated R-loop accumulation and tumorigenesisXiaowen Zhang, Huai-Chin Chiang, Yao Wang, et al.
Cell Metabolism|July 5, 2008
Resveratrol delays age-related deterioration and mimics transcriptional aspects of dietary restriction without extending life spanKevin J Pearson, Joseph A Baur, Kaitlyn N Lewis, et al.
Annals of Internal Medicine|October 3, 2007
Validity of models for predicting BRCA1 and BRCA2 mutationsGiovanni Parmigiani, Sining Chen, Edwin S Iversen, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Nature|October 14, 2011
Genome sequencing reveals insights into physiology and longevity of the naked mole ratEun Bae Kim, Xiaodong Fang, Alexey A Fushan, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2012
A public resource facilitating clinical use of genomesMadeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Pageof 33

Showing results (301-310 of 321) with videos related to

Sort By:
Pageof 33
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|July 17, 1998
Sequence analysis of BRCA1 and BRCA2: correlation of mutations with family history and ovarian cancer riskT S Frank, S A Manley, O I Olopade, et al.
Journal of Community Genetics|December 16, 2025
Barriers and facilitators of cancer genetic risk screening at community-based organizations serving LatinasBella Ortega, Maisha R Huq, Dariana Sedeño-Delgado, et al.
Nature Communications|March 31, 2018
Author Correction: Attenuation of RNA polymerase II pausing mitigates BRCA1-associated R-loop accumulation and tumorigenesisXiaowen Zhang, Huai-Chin Chiang, Yao Wang, et al.
Nature Communications|June 27, 2017
Attenuation of RNA polymerase II pausing mitigates BRCA1-associated R-loop accumulation and tumorigenesisXiaowen Zhang, Huai-Chin Chiang, Yao Wang, et al.
Cell Metabolism|July 5, 2008
Resveratrol delays age-related deterioration and mimics transcriptional aspects of dietary restriction without extending life spanKevin J Pearson, Joseph A Baur, Kaitlyn N Lewis, et al.
Annals of Internal Medicine|October 3, 2007
Validity of models for predicting BRCA1 and BRCA2 mutationsGiovanni Parmigiani, Sining Chen, Edwin S Iversen, et al.
European Journal of Human Genetics : EJHG|February 2, 2017
Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Nature|October 14, 2011
Genome sequencing reveals insights into physiology and longevity of the naked mole ratEun Bae Kim, Xiaodong Fang, Alexey A Fushan, et al.
European Journal of Human Genetics : EJHG|August 24, 2018
Correction: Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLogan C Walker, Louise Marquart, John F Pearson, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 17, 2012
A public resource facilitating clinical use of genomesMadeleine P Ball, Joseph V Thakuria, Alexander Wait Zaranek, et al.
Pageof 33