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Peter Devilee

Showing results (61-70 of 282) with videos related to

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Cell Death & Disease|January 11, 2022
RNF12 is regulated by AKT phosphorylation and promotes TGF-β driven breast cancer metastasisYongsheng Huang, Sijia Liu, Mengjie Shan, et al.
Plos One|May 5, 2012
MDM2 promoter SNP344T>A (rs1196333) status does not affect cancer riskStian Knappskog, Liv B Gansmo, Pål Romundstad, et al.
Nature Communications|November 24, 2019
Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2Rick A C M Boonen, Amélie Rodrigue, Chantal Stoepker, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2020
Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-ParagangliomaAlexandre Buffet, Juan Zhang, Heggert Rebel, et al.
Journal of Medical Genetics|September 8, 2019
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paragangliomaJean Pierre Bayley, Birke Bausch, Johannes Adriaan Rijken, et al.
Genes, Chromosomes & Cancer|March 12, 2010
Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancerAnneke Middeldorp, Shantie C Jagmohan-Changur, Heleen M van der Klift, et al.
Science (New York, N.Y.)|July 25, 2009
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paragangliomaHuai-Xiang Hao, Oleh Khalimonchuk, Margit Schraders, et al.
European Journal of Human Genetics : EJHG|December 10, 2015
Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancersAnne Ml Jansen, Tom van Wezel, Brendy Ewm van den Akker, et al.
Breast Cancer Research and Treatment|March 2, 2010
Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancerMarijke Wasielewski, Astrid A Out, Joyce Vermeulen, et al.
BMC Medical Genetics|January 13, 2006
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytomaJean-Pierre Bayley, Ivonne van Minderhout, Marjan M Weiss, et al.
Pageof 29

Showing results (61-70 of 282) with videos related to

Sort By:
Pageof 29
Cell Death & Disease|January 11, 2022
RNF12 is regulated by AKT phosphorylation and promotes TGF-β driven breast cancer metastasisYongsheng Huang, Sijia Liu, Mengjie Shan, et al.
Plos One|May 5, 2012
MDM2 promoter SNP344T>A (rs1196333) status does not affect cancer riskStian Knappskog, Liv B Gansmo, Pål Romundstad, et al.
Nature Communications|November 24, 2019
Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2Rick A C M Boonen, Amélie Rodrigue, Chantal Stoepker, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2020
Germline DLST Variants Promote Epigenetic Modifications in Pheochromocytoma-ParagangliomaAlexandre Buffet, Juan Zhang, Heggert Rebel, et al.
Journal of Medical Genetics|September 8, 2019
Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma-paragangliomaJean Pierre Bayley, Birke Bausch, Johannes Adriaan Rijken, et al.
Genes, Chromosomes & Cancer|March 12, 2010
Comprehensive genetic analysis of seven large families with mismatch repair proficient colorectal cancerAnneke Middeldorp, Shantie C Jagmohan-Changur, Heleen M van der Klift, et al.
Science (New York, N.Y.)|July 25, 2009
SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paragangliomaHuai-Xiang Hao, Oleh Khalimonchuk, Margit Schraders, et al.
European Journal of Human Genetics : EJHG|December 10, 2015
Combined mismatch repair and POLE/POLD1 defects explain unresolved suspected Lynch syndrome cancersAnne Ml Jansen, Tom van Wezel, Brendy Ewm van den Akker, et al.
Breast Cancer Research and Treatment|March 2, 2010
Increased MUTYH mutation frequency among Dutch families with breast cancer and colorectal cancerMarijke Wasielewski, Astrid A Out, Joyce Vermeulen, et al.
BMC Medical Genetics|January 13, 2006
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytomaJean-Pierre Bayley, Ivonne van Minderhout, Marjan M Weiss, et al.
Pageof 29