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M R Stratton

Showing results (61-70 of 97) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1S Bevan, T Pal, C R Greenberg, et al.
British Journal of Cancer|August 1, 1989
Structural alterations of the RB1 gene in human soft tissue tumoursM R Stratton, S Williams, C Fisher, et al.
Oncogene|May 1, 1993
Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findingsR A Eeles, W Warren, G Knee, et al.
Cancer Letters|May 23, 2001
Contribution of germline MLH1 and MSH2 mutations to lobular carcinoma in situ of the breastJ G Stone, G Coleman, B Gusterson, et al.
British Journal of Cancer|January 24, 2009
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibitionC L Mahoney, B Choudhury, H Davies, et al.
British Journal of Cancer|October 9, 1998
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patientsM Shayeghi, S Seal, J Regan, et al.
Journal of the National Cancer Institute|April 20, 2000
Penetrance of mutations in the familial Wilms tumor gene FWT1N Rahman, L Arbour, R Houlston, et al.
British Journal of Cancer|November 1, 2007
Testicular microlithiasis as a familial risk factor for testicular germ cell tumourJ Coffey, R A Huddart, F Elliott, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 17, 2001
Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinicA M Martin, M A Blackwood, D Antin-Ozerkis, et al.
Pageof 10

Showing results (61-70 of 97) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Endocrinology and Metabolism|August 15, 2001
A comprehensive analysis of MNG1, TCO1, fPTC, PTEN, TSHR, and TRKA in familial nonmedullary thyroid cancer: confirmation of linkage to TCO1S Bevan, T Pal, C R Greenberg, et al.
British Journal of Cancer|August 1, 1989
Structural alterations of the RB1 gene in human soft tissue tumoursM R Stratton, S Williams, C Fisher, et al.
Oncogene|May 1, 1993
Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findingsR A Eeles, W Warren, G Knee, et al.
Cancer Letters|May 23, 2001
Contribution of germline MLH1 and MSH2 mutations to lobular carcinoma in situ of the breastJ G Stone, G Coleman, B Gusterson, et al.
British Journal of Cancer|January 24, 2009
LKB1/KRAS mutant lung cancers constitute a genetic subset of NSCLC with increased sensitivity to MAPK and mTOR signalling inhibitionC L Mahoney, B Choudhury, H Davies, et al.
British Journal of Cancer|October 9, 1998
Heterozygosity for mutations in the ataxia telangiectasia gene is not a major cause of radiotherapy complications in breast cancer patientsM Shayeghi, S Seal, J Regan, et al.
Journal of the National Cancer Institute|April 20, 2000
Penetrance of mutations in the familial Wilms tumor gene FWT1N Rahman, L Arbour, R Houlston, et al.
British Journal of Cancer|November 1, 2007
Testicular microlithiasis as a familial risk factor for testicular germ cell tumourJ Coffey, R A Huddart, F Elliott, et al.
Clinical Genetics|November 15, 2006
Mutations in the RSK2(RPS6KA3) gene cause Coffin-Lowry syndrome and nonsyndromic X-linked mental retardationM Field, P Tarpey, J Boyle, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|April 17, 2001
Germline mutations in BRCA1 and BRCA2 in breast-ovarian families from a breast cancer risk evaluation clinicA M Martin, M A Blackwood, D Antin-Ozerkis, et al.
Pageof 10