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Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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P J Goodfellow

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Gynecologic Oncology|June 25, 2002

Microsatellite instability, MLH1 promoter methylation, and loss of mismatch repair in endometrial cancer and concomitant atypical hyperplasiaN Horowitz, K Pinto, D G Mutch, et al.

Molecular Carcinogenesis|March 17, 1999

A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancersK K Herfarth, T P Brent, R P Danam, et al.

Cancer Genetics and Cytogenetics|August 1, 1987

Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against syntenyL A Farrer, P J Goodfellow, B N White, et al.

Genes, Chromosomes & Cancer|January 1, 1997

Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instabilityK K Herfarth, I J Kodner, A J Whelan, et al.

Oncogene|June 26, 1997

Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTCY Kitamura, P J Goodfellow, K Shimizu, et al.

Human Genetics|January 1, 1993

A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locusJ B Lichter, J Wu, A R Brooks-Wilson, et al.

Gynecologic Oncology|March 31, 2000

Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genesD E Cohn, S Babb, A J Whelan, et al.

Nature Genetics|September 18, 2001

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.

Human Mutation|March 25, 1999

Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defectsM G Mutch, W G Dilley, F Sanjurjo, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994

Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2BK M Carlson, S Dou, D Chi, et al.

Pageof 11

Search research articles

Showing results (81-90 of 106) with videos related to

Sort By:

Pageof 11

Gynecologic Oncology|June 25, 2002

Microsatellite instability, MLH1 promoter methylation, and loss of mismatch repair in endometrial cancer and concomitant atypical hyperplasiaN Horowitz, K Pinto, D G Mutch, et al.

Molecular Carcinogenesis|March 17, 1999

A specific CpG methylation pattern of the MGMT promoter region associated with reduced MGMT expression in primary colorectal cancersK K Herfarth, T P Brent, R P Danam, et al.

Cancer Genetics and Cytogenetics|August 1, 1987

Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: evidence against syntenyL A Farrer, P J Goodfellow, B N White, et al.

Genes, Chromosomes & Cancer|January 1, 1997

Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instabilityK K Herfarth, I J Kodner, A J Whelan, et al.

Oncogene|June 26, 1997

Novel germline RET proto-oncogene mutations associated with medullary thyroid carcinoma (MTC): mutation analysis in Japanese patients with MTCY Kitamura, P J Goodfellow, K Shimizu, et al.

Human Genetics|January 1, 1993

A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locusJ B Lichter, J Wu, A R Brooks-Wilson, et al.

Gynecologic Oncology|March 31, 2000

Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genesD E Cohn, S Babb, A J Whelan, et al.

Nature Genetics|September 18, 2001

The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossiaC Braybrook, K Doudney, A C Marçano, et al.

Human Mutation|March 25, 1999

Germline mutations in the multiple endocrine neoplasia type 1 gene: evidence for frequent splicing defectsM G Mutch, W G Dilley, F Sanjurjo, et al.

Proceedings of the National Academy of Sciences of the United States of America|February 15, 1994

Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2BK M Carlson, S Dou, D Chi, et al.

Pageof 11