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Showing results (251-260 of 266) with videos related to

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Endocrine-Related Cancer|September 3, 2015
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancerTracy A O'Mara, Dylan M Glubb, Jodie N Painter, et al.
Cancer Medicine|April 3, 2018
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analysesJodie N Painter, Tracy A O'Mara, Andrew P Morris, et al.
Endocrine-Related Cancer|November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancerDeborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
European Journal of Cancer (Oxford, England : 1990)|March 20, 2021
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportToni T Seppälä, Mev Dominguez-Valentin, Emma J Crosbie, et al.
Nature Genetics|May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysisTimothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportMev Dominguez-Valentin, Emma J Crosbie, Christoph Engel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2019
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Journal of Clinical Medicine|July 2, 2021
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database StudyMev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, et al.
Pageof 27

Showing results (251-260 of 266) with videos related to

Sort By:
Pageof 27
Endocrine-Related Cancer|September 3, 2015
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancerTracy A O'Mara, Dylan M Glubb, Jodie N Painter, et al.
Cancer Medicine|April 3, 2018
Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analysesJodie N Painter, Tracy A O'Mara, Andrew P Morris, et al.
Endocrine-Related Cancer|November 18, 2015
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancerDeborah J Thompson, Tracy A O'Mara, Dylan M Glubb, et al.
European Journal of Cancer (Oxford, England : 1990)|March 20, 2021
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportToni T Seppälä, Mev Dominguez-Valentin, Emma J Crosbie, et al.
Nature Genetics|May 3, 2016
Five endometrial cancer risk loci identified through genome-wide association analysisTimothy Ht Cheng, Deborah J Thompson, Tracy A O'Mara, et al.
Human Genetics|December 10, 2014
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer riskLuis G Carvajal-Carmona, Tracy A O'Mara, Jodie N Painter, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 1, 2020
Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportMev Dominguez-Valentin, Emma J Crosbie, Christoph Engel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2020
Correction: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 25, 2019
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseMev Dominguez-Valentin, Julian R Sampson, Toni T Seppälä, et al.
Journal of Clinical Medicine|July 2, 2021
No Difference in Penetrance between Truncating and Missense/Aberrant Splicing Pathogenic Variants in <i>MLH1</i> and <i>MSH2</i>: A Prospective Lynch Syndrome Database StudyMev Dominguez-Valentin, John-Paul Plazzer, Julian R Sampson, et al.
Pageof 27