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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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A Y Lin

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Cell|June 16, 1995

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndromeG H Fisher, F J Rosenberg, S E Straus, et al.

Blood|October 15, 1996

Epstein-Barr virus and familial Hodgkin's diseaseA Y Lin, D W Kingma, E T Lennette, et al.

Journal of Immunological Methods|September 15, 1993

Characterization of monoclonal antibodies specific for the V beta 3 family of the human T cell receptor generated using soluble TCR beta-chainS D Calaman, G R Carson, L D Henry, et al.

American Journal of Medical Genetics|March 21, 1998

Familial eosinophilia: clinical and laboratory results on a U.S. kindredA Y Lin, T B Nutman, D Kaslow, et al.

American Journal of Human Genetics|October 3, 1998

Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33J D Rioux, V A Stone, M J Daly, et al.

The American Journal of Pathology|November 12, 1998

Pathological findings in human autoimmune lymphoproliferative syndromeM S Lim, S E Straus, J K Dale, et al.

Genes, Chromosomes & Cancer|January 27, 1998

Allelic imbalance, including deletion of PTEN/MMACI, at the Cowden disease locus on 10q22-23, in hamartomas from patients with Cowden syndrome and germline PTEN mutationD J Marsh, P L Dahia, V Coulon, et al.

Blood|June 22, 2001

The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosisS E Straus, E S Jaffe, J M Puck, et al.

Nature Genetics|May 1, 1996

Localization of the gene for Cowden disease to chromosome 10q22-23M R Nelen, G W Padberg, E A Peeters, et al.

Human Molecular Genetics|April 18, 1998

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutationD J Marsh, V Coulon, K L Lunetta, et al.

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Search research articles

Showing results (51-60 of 60) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 60 results.

Cell|June 16, 1995

Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndromeG H Fisher, F J Rosenberg, S E Straus, et al.

Blood|October 15, 1996

Epstein-Barr virus and familial Hodgkin's diseaseA Y Lin, D W Kingma, E T Lennette, et al.

Journal of Immunological Methods|September 15, 1993

Characterization of monoclonal antibodies specific for the V beta 3 family of the human T cell receptor generated using soluble TCR beta-chainS D Calaman, G R Carson, L D Henry, et al.

American Journal of Medical Genetics|March 21, 1998

Familial eosinophilia: clinical and laboratory results on a U.S. kindredA Y Lin, T B Nutman, D Kaslow, et al.

American Journal of Human Genetics|October 3, 1998

Familial eosinophilia maps to the cytokine gene cluster on human chromosomal region 5q31-q33J D Rioux, V A Stone, M J Daly, et al.

The American Journal of Pathology|November 12, 1998

Pathological findings in human autoimmune lymphoproliferative syndromeM S Lim, S E Straus, J K Dale, et al.

Genes, Chromosomes & Cancer|January 27, 1998

Blood|June 22, 2001

The development of lymphomas in families with autoimmune lymphoproliferative syndrome with germline Fas mutations and defective lymphocyte apoptosisS E Straus, E S Jaffe, J M Puck, et al.

Nature Genetics|May 1, 1996

Localization of the gene for Cowden disease to chromosome 10q22-23M R Nelen, G W Padberg, E A Peeters, et al.

Human Molecular Genetics|April 18, 1998

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutationD J Marsh, V Coulon, K L Lunetta, et al.

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