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M Peacocke

Showing results (41-50 of 56) with videos related to

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Experimental Dermatology|April 20, 2000
Germline PTEN mutations in three families with Cowden syndromeJ T Celebi, X L Ping, H Zhang, et al.
Human Molecular Genetics|July 1, 1995
Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locusR Kolluri, A Shehabeldin, M Peacocke, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 2, 1999
Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancerK A Cooney, H C Tsou, E M Petty, et al.
Urology|June 28, 2000
Expression of senescence-associated beta-galactosidase in enlarged prostates from men with benign prostatic hyperplasiaJ Choi, I Shendrik, M Peacocke, et al.
The Journal of Investigative Dermatology|February 1, 1993
Clonal origin of dermatofibrosarcoma protuberansA E Allan, H C Tsou, A Harrington, et al.
Human Genetics|October 1, 1989
Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic predictionW L Greer, M M Mahtani, P C Kwong, et al.
Journal of Medical Genetics|June 3, 1999
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTENJ T Celebi, H C Tsou, F F Chen, et al.
The Journal of Investigative Dermatology|April 5, 2001
PTCH mutations in squamous cell carcinoma of the skinX L Ping, D Ratner, H Zhang, et al.
Human Genetics|January 1, 1997
Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase geneH Lam, L Dragan, H C Tsou, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|September 1, 1989
Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylationW L Greer, E Higgins, D R Sutherland, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Experimental Dermatology|April 20, 2000
Germline PTEN mutations in three families with Cowden syndromeJ T Celebi, X L Ping, H Zhang, et al.
Human Molecular Genetics|July 1, 1995
Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locusR Kolluri, A Shehabeldin, M Peacocke, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 2, 1999
Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancerK A Cooney, H C Tsou, E M Petty, et al.
Urology|June 28, 2000
Expression of senescence-associated beta-galactosidase in enlarged prostates from men with benign prostatic hyperplasiaJ Choi, I Shendrik, M Peacocke, et al.
The Journal of Investigative Dermatology|February 1, 1993
Clonal origin of dermatofibrosarcoma protuberansA E Allan, H C Tsou, A Harrington, et al.
Human Genetics|October 1, 1989
Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic predictionW L Greer, M M Mahtani, P C Kwong, et al.
Journal of Medical Genetics|June 3, 1999
Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTENJ T Celebi, H C Tsou, F F Chen, et al.
The Journal of Investigative Dermatology|April 5, 2001
PTCH mutations in squamous cell carcinoma of the skinX L Ping, D Ratner, H Zhang, et al.
Human Genetics|January 1, 1997
Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase geneH Lam, L Dragan, H C Tsou, et al.
Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|September 1, 1989
Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylationW L Greer, E Higgins, D R Sutherland, et al.
Pageof 6