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Rodney J Scott

Showing results (131-140 of 461) with videos related to

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International Journal of Cancer|July 16, 2008
IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancerStuart G Reeves, Dominique Rich, Cliff J Meldrum, et al.
Hereditary Cancer in Clinical Practice|June 24, 2014
Expanding the genetic basis of copy number variation in familial breast cancerAmy L Masson, Bente A Talseth-Palmer, Tiffany-Jane Evans, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Germline Missense Changes in the APC Gene and Their Relationship to DiseaseRodney J Scott, Renee Crooks, Lindy Rose, et al.
Breast Cancer Research and Treatment|September 28, 2006
The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutationAnna Jakubowska, Jacek Gronwald, Bohdan Górski, et al.
Genes|January 21, 2022
Capturing SNP Association across the NK Receptor and HLA Gene Regions in Multiple Sclerosis by Targeted Penalised Regression ModelsSean M Burnard, Rodney A Lea, Miles Benton, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 15, 2006
Buccal DNA collection: comparison of buccal swabs with FTA cardsElizabeth Milne, Frank M van Bockxmeer, Laila Robertson, et al.
Plos One|May 5, 2012
Transcriptome sequencing revealed significant alteration of cortical promoter usage and splicing in schizophreniaJing Qin Wu, Xi Wang, Natalie J Beveridge, et al.
Journal of Psychiatric Research|November 21, 2013
Catechol-O-methyltransferase (COMT) genotype moderates the effects of childhood trauma on cognition and symptoms in schizophreniaMelissa J Green, T-Yunn Chia, Murray J Cairns, et al.
Biopreservation and Biobanking|June 3, 2015
Biobank classification in an Australian settingAmanda Rush, Jeffrey H Christiansen, Jake P Farrell, et al.
Frontiers in Reproductive Health|April 28, 2023
Prevalence and clinical significance of co-existing mutations in <i>MED12</i> and <i>FH</i> in uterine fibroids of Australian womenM Fairuz B Jamaluddin, Prathima B Nagendra, Yi-An Ko, et al.
Pageof 47

Showing results (131-140 of 461) with videos related to

Sort By:
Pageof 47
International Journal of Cancer|July 16, 2008
IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancerStuart G Reeves, Dominique Rich, Cliff J Meldrum, et al.
Hereditary Cancer in Clinical Practice|June 24, 2014
Expanding the genetic basis of copy number variation in familial breast cancerAmy L Masson, Bente A Talseth-Palmer, Tiffany-Jane Evans, et al.
Hereditary Cancer in Clinical Practice|March 18, 2010
Germline Missense Changes in the APC Gene and Their Relationship to DiseaseRodney J Scott, Renee Crooks, Lindy Rose, et al.
Breast Cancer Research and Treatment|September 28, 2006
The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutationAnna Jakubowska, Jacek Gronwald, Bohdan Górski, et al.
Genes|January 21, 2022
Capturing SNP Association across the NK Receptor and HLA Gene Regions in Multiple Sclerosis by Targeted Penalised Regression ModelsSean M Burnard, Rodney A Lea, Miles Benton, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 15, 2006
Buccal DNA collection: comparison of buccal swabs with FTA cardsElizabeth Milne, Frank M van Bockxmeer, Laila Robertson, et al.
Plos One|May 5, 2012
Transcriptome sequencing revealed significant alteration of cortical promoter usage and splicing in schizophreniaJing Qin Wu, Xi Wang, Natalie J Beveridge, et al.
Journal of Psychiatric Research|November 21, 2013
Catechol-O-methyltransferase (COMT) genotype moderates the effects of childhood trauma on cognition and symptoms in schizophreniaMelissa J Green, T-Yunn Chia, Murray J Cairns, et al.
Biopreservation and Biobanking|June 3, 2015
Biobank classification in an Australian settingAmanda Rush, Jeffrey H Christiansen, Jake P Farrell, et al.
Frontiers in Reproductive Health|April 28, 2023
Prevalence and clinical significance of co-existing mutations in <i>MED12</i> and <i>FH</i> in uterine fibroids of Australian womenM Fairuz B Jamaluddin, Prathima B Nagendra, Yi-An Ko, et al.
Pageof 47