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Daniel D Buchanan

Showing results (11-20 of 298) with videos related to

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The Australasian Journal of Dermatology|December 4, 2018
Clinico-pathological predictors of mismatch repair deficiency in sebaceous neoplasia: A large case series from a single Australian private pathology serviceMichael D Walsh, Harindra Jayasekara, Alvin Huang, et al.
Histopathology|June 5, 2014
Do serrated neoplasms of the small intestine represent a distinct entity? Pathological findings and molecular alterations in a series of 13 casesChristophe Rosty, Catherine Campbell, Mark Clendenning, et al.
Journal of Medical Genetics|February 28, 2012
Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classificationMichael T Parsons, Daniel D Buchanan, Bryony Thompson, et al.
Gastroenterology|January 9, 2025
DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient CancersRomy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Journal of Cancer Research and Clinical Oncology|October 17, 2022
Risk of cancer in individuals with Lynch-like syndrome and their families: a systematic reviewPandu P Nugroho, Siti Alyaa S Ghozali, Daniel D Buchanan, et al.
Hereditary Cancer in Clinical Practice|October 17, 2021
"Left in limbo": Exploring how patients with colorectal cancer interpret and respond to a suspected Lynch syndrome diagnosisNicole den Elzen, Sharelle L Joseland, Sibel Saya, et al.
Human Pathology|February 7, 2012
KRAS mutations in ovarian low-grade endometrioid adenocarcinoma: association with concurrent endometriosisColin J R Stewart, Yee Leung, Michael D Walsh, et al.
Gastroenterology|August 30, 2020
Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal CancerFadwa A Elsayed, Judith E Grolleman, Abiram Ragunathan, et al.
Hereditary Cancer in Clinical Practice|July 15, 2022
Heterogeneity in the psychosocial and behavioral responses associated with a diagnosis of suspected Lynch syndrome in women with endometrial cancerSowmya Jonnagadla, Sharelle L Joseland, Sibel Saya, et al.
Oncotarget|December 8, 2017
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry CohortLeon Raskin, Yan Guo, Liping Du, et al.
Pageof 30

Showing results (11-20 of 298) with videos related to

Sort By:
Pageof 30
The Australasian Journal of Dermatology|December 4, 2018
Clinico-pathological predictors of mismatch repair deficiency in sebaceous neoplasia: A large case series from a single Australian private pathology serviceMichael D Walsh, Harindra Jayasekara, Alvin Huang, et al.
Histopathology|June 5, 2014
Do serrated neoplasms of the small intestine represent a distinct entity? Pathological findings and molecular alterations in a series of 13 casesChristophe Rosty, Catherine Campbell, Mark Clendenning, et al.
Journal of Medical Genetics|February 28, 2012
Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classificationMichael T Parsons, Daniel D Buchanan, Bryony Thompson, et al.
Gastroenterology|January 9, 2025
DNA Mismatch Repair Gene Mosaicism Is Rare in People With Mismatch Repair-Deficient CancersRomy Walker, Jihoon E Joo, Khalid Mahmood, et al.
Journal of Cancer Research and Clinical Oncology|October 17, 2022
Risk of cancer in individuals with Lynch-like syndrome and their families: a systematic reviewPandu P Nugroho, Siti Alyaa S Ghozali, Daniel D Buchanan, et al.
Hereditary Cancer in Clinical Practice|October 17, 2021
"Left in limbo": Exploring how patients with colorectal cancer interpret and respond to a suspected Lynch syndrome diagnosisNicole den Elzen, Sharelle L Joseland, Sibel Saya, et al.
Human Pathology|February 7, 2012
KRAS mutations in ovarian low-grade endometrioid adenocarcinoma: association with concurrent endometriosisColin J R Stewart, Yee Leung, Michael D Walsh, et al.
Gastroenterology|August 30, 2020
Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal CancerFadwa A Elsayed, Judith E Grolleman, Abiram Ragunathan, et al.
Hereditary Cancer in Clinical Practice|July 15, 2022
Heterogeneity in the psychosocial and behavioral responses associated with a diagnosis of suspected Lynch syndrome in women with endometrial cancerSowmya Jonnagadla, Sharelle L Joseland, Sibel Saya, et al.
Oncotarget|December 8, 2017
Targeted sequencing of established and candidate colorectal cancer genes in the Colon Cancer Family Registry CohortLeon Raskin, Yan Guo, Liping Du, et al.
Pageof 30