J M Rommens - JoVE Visualize

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Nature Genetics|January 1, 1997

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeT Matsuura, J S Sutcliffe, P Fang, et al.

Genomics|August 10, 1995

Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21J M Rommens, F Durocher, J McArthur, et al.

Human Molecular Genetics|June 1, 1993

Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 regionS W Scherer, J M Rommens, S Soder, et al.

Human Molecular Genetics|October 1, 1993

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionB Lin, J M Rommens, R K Graham, et al.

American Journal of Human Genetics|November 1, 1988

Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis geneJ M Rommens, S Zengerling, J Burns, et al.

The Journal of General Physiology|October 6, 1997

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anionsP Linsdell, J A Tabcharani, J M Rommens, et al.

Science (New York, N.Y.)|September 8, 1989

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNAJ R Riordan, J M Rommens, B Kerem, et al.

Genomics|February 1, 1996

Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 13, 1994

Phosphatase inhibitors activate normal and defective CFTR chloride channelsF Becq, T J Jensen, X B Chang, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis geneB S Kerem, J Zielenski, D Markiewicz, et al.

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Showing results (31-40 of 66) with videos related to

Sort By:

Pageof 7

Nature Genetics|January 1, 1997

De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeT Matsuura, J S Sutcliffe, P Fang, et al.

Genomics|August 10, 1995

Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21J M Rommens, F Durocher, J McArthur, et al.

Human Molecular Genetics|June 1, 1993

Refined localization and yeast artificial chromosome (YAC) contig--mapping of genes and DNA segments in the 7q21-q32 regionS W Scherer, J M Rommens, S Soder, et al.

Human Molecular Genetics|October 1, 1993

Differential 3' polyadenylation of the Huntington disease gene results in two mRNA species with variable tissue expressionB Lin, J M Rommens, R K Graham, et al.

American Journal of Human Genetics|November 1, 1988

Identification and regional localization of DNA markers on chromosome 7 for the cloning of the cystic fibrosis geneJ M Rommens, S Zengerling, J Burns, et al.

The Journal of General Physiology|October 6, 1997

Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anionsP Linsdell, J A Tabcharani, J M Rommens, et al.

Science (New York, N.Y.)|September 8, 1989

Identification of the cystic fibrosis gene: cloning and characterization of complementary DNAJ R Riordan, J M Rommens, B Kerem, et al.

Genomics|February 1, 1996

Hereditary hemochromatosis: generation of a transcription map within a refined and extended map of the HLA class I regionA Totaro, J M Rommens, A Grifa, et al.

Proceedings of the National Academy of Sciences of the United States of America|September 13, 1994

Phosphatase inhibitors activate normal and defective CFTR chloride channelsF Becq, T J Jensen, X B Chang, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis geneB S Kerem, J Zielenski, D Markiewicz, et al.

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