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Finlay Macrae

Showing results (141-150 of 151) with videos related to

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Nature Genetics|December 24, 2013
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific databaseBryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, et al.
Gut|July 18, 2023
An efficient strategy for evaluating new non-invasive screening tests for colorectal cancer: the guiding principlesRobert S Bresalier, Carlo Senore, Graeme P Young, et al.
Hereditary Cancer in Clinical Practice|March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportToni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.
Ebiomedicine|May 15, 2024
Genome-wide interaction study of dietary intake of fibre, fruits, and vegetables with risk of colorectal cancerNikos Papadimitriou, Andre Kim, Eric S Kawaguchi, 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.
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.
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.
Eclinicalmedicine|May 14, 2023
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome databaseMev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, et al.
Pageof 16

Showing results (141-150 of 151) with videos related to

Sort By:
Pageof 16
Nature Genetics|December 24, 2013
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific databaseBryony A Thompson, Amanda B Spurdle, John-Paul Plazzer, et al.
Gut|July 18, 2023
An efficient strategy for evaluating new non-invasive screening tests for colorectal cancer: the guiding principlesRobert S Bresalier, Carlo Senore, Graeme P Young, et al.
Hereditary Cancer in Clinical Practice|March 13, 2019
Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database reportToni T Seppälä, Aysel Ahadova, Mev Dominguez-Valentin, et al.
Ebiomedicine|May 15, 2024
Genome-wide interaction study of dietary intake of fibre, fruits, and vegetables with risk of colorectal cancerNikos Papadimitriou, Andre Kim, Eric S Kawaguchi, 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.
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.
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.
Eclinicalmedicine|May 14, 2023
Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome databaseMev Dominguez-Valentin, Saskia Haupt, Toni T Seppälä, et al.
Pageof 16