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Nancy Hamel

Showing results (41-50 of 70) with videos related to

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NPJ Breast Cancer|August 26, 2021
Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer familiesThibaut S Matis, Nadia Zayed, Bouchra Labraki, et al.
Cancer Discovery|December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancerSusan M Domchek, Jiangbo Tang, Jill Stopfer, et al.
The Journal of Pathology|June 19, 2013
Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back againLeora Witkowski, Emilie Lalonde, Jian Zhang, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approachMarc Tischkowitz, Nancy Hamel, Marcelo A Carvalho, et al.
Cancer Research|April 3, 2008
Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international studyShiyu Zhang, Catherine M Phelan, Phil Zhang, et al.
Human Mutation|September 2, 2011
Extending the phenotypes associated with DICER1 mutationsWilliam D Foulkes, Amin Bahubeshi, Nancy Hamel, et al.
Cell Death & Disease|September 7, 2021
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicingKajal Biswas, Martin Couillard, Luca Cavallone, et al.
Scientific Reports|January 29, 2021
Investigating the causal role of MRE11A p.E506* in breast and ovarian cancerIslam E Elkholi, Massimo Di Iorio, Somayyeh Fahiminiya, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2007
Analysis of PALB2/FANCN-associated breast cancer familiesMarc Tischkowitz, Bing Xia, Nelly Sabbaghian, et al.
JAMA Network Open|September 3, 2024
Universal Genetic Testing for Newly Diagnosed Invasive Breast CancerZoulikha Rezoug, Stephanie P Totten, David Szlachtycz, et al.
Pageof 7

Showing results (41-50 of 70) with videos related to

Sort By:
Pageof 7
NPJ Breast Cancer|August 26, 2021
Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer familiesThibaut S Matis, Nadia Zayed, Bouchra Labraki, et al.
Cancer Discovery|December 28, 2012
Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancerSusan M Domchek, Jiangbo Tang, Jill Stopfer, et al.
The Journal of Pathology|June 19, 2013
Familial rhabdoid tumour 'avant la lettre'--from pathology review to exome sequencing and back againLeora Witkowski, Emilie Lalonde, Jian Zhang, et al.
European Journal of Human Genetics : EJHG|February 21, 2008
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approachMarc Tischkowitz, Nancy Hamel, Marcelo A Carvalho, et al.
Cancer Research|April 3, 2008
Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international studyShiyu Zhang, Catherine M Phelan, Phil Zhang, et al.
Human Mutation|September 2, 2011
Extending the phenotypes associated with DICER1 mutationsWilliam D Foulkes, Amin Bahubeshi, Nancy Hamel, et al.
Cell Death & Disease|September 7, 2021
A novel mouse model of PMS2 founder mutation that causes mismatch repair defect due to aberrant splicingKajal Biswas, Martin Couillard, Luca Cavallone, et al.
Scientific Reports|January 29, 2021
Investigating the causal role of MRE11A p.E506* in breast and ovarian cancerIslam E Elkholi, Massimo Di Iorio, Somayyeh Fahiminiya, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2007
Analysis of PALB2/FANCN-associated breast cancer familiesMarc Tischkowitz, Bing Xia, Nelly Sabbaghian, et al.
JAMA Network Open|September 3, 2024
Universal Genetic Testing for Newly Diagnosed Invasive Breast CancerZoulikha Rezoug, Stephanie P Totten, David Szlachtycz, et al.
Pageof 7