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J F LeBlanc

Showing results (11-20 of 17) with videos related to

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Biochemistry|May 23, 1998
Recognition properties of a sequence-specific DNA binding antibodyJ F LeBlanc, K E McLane, P W Parren, et al.
Journal of Virology|June 1, 1989
Induction of human interferon gene expression is associated with a nuclear factor that interacts with the NF-kappa B site of the human immunodeficiency virus enhancerJ Hiscott, D Alper, L Cohen, et al.
Nature Genetics|December 1, 1994
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesJ Simard, P Tonin, F Durocher, 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|February 1, 1994
Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani originJ Simard, E Rhéaume, J F Leblanc, et al.
Genomics|August 15, 1996
Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13F J Couch, J M Rommens, S L Neuhausen, et al.
Nature Genetics|March 1, 1996
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsS V Tavtigian, J Simard, J Rommens, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Biochemistry|May 23, 1998
Recognition properties of a sequence-specific DNA binding antibodyJ F LeBlanc, K E McLane, P W Parren, et al.
Journal of Virology|June 1, 1989
Induction of human interferon gene expression is associated with a nuclear factor that interacts with the NF-kappa B site of the human immunodeficiency virus enhancerJ Hiscott, D Alper, L Cohen, et al.
Nature Genetics|December 1, 1994
Common origins of BRCA1 mutations in Canadian breast and ovarian cancer familiesJ Simard, P Tonin, F Durocher, 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|February 1, 1994
Congenital adrenal hyperplasia caused by a novel homozygous frameshift mutation 273 delta AA in type II 3 beta-hydroxysteroid dehydrogenase gene (HSD3B2) in three male patients of Afghan/Pakistani originJ Simard, E Rhéaume, J F Leblanc, et al.
Genomics|August 15, 1996
Generation of an integrated transcription map of the BRCA2 region on chromosome 13q12-q13F J Couch, J M Rommens, S L Neuhausen, et al.
Nature Genetics|March 1, 1996
The complete BRCA2 gene and mutations in chromosome 13q-linked kindredsS V Tavtigian, J Simard, J Rommens, et al.
Pageof 2