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S Weremowicz

Showing results (51-60 of 64) with videos related to

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The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Diabetes|February 1, 1995
Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16qA Doria, J S Caldwell, L Ji, et al.
Genomics|January 27, 1998
Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.
Genomics|June 30, 2000
A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
Genomics|January 7, 1998
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomasM Schoenberg Fejzo, H R Ashar, K S Krauter, et al.
Genomics|September 7, 2001
STK25 is a candidate gene for pseudopseudohypoparathyroidismM S Davids, E Crawford, S Weremowicz, et al.
Molecular and Cellular Biology|September 1, 1993
Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partnerP A Ney, N C Andrews, S M Jane, et al.
Genomics|March 20, 1995
Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomataM S Fejzo, S J Yoon, K T Montgomery, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
The Journal of Clinical Investigation|September 7, 2000
Mutations in the protein kinase A R1alpha regulatory subunit cause familial cardiac myxomas and Carney complexM Casey, C J Vaughan, J He, et al.
Diabetes|February 1, 1995
Trinucleotide repeats at the rad locus. Allele distributions in NIDDM and mapping to a 3-cM region on chromosome 16qA Doria, J S Caldwell, L Ji, et al.
Genomics|January 27, 1998
Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9N G Robertson, A B Skvorak, Y Yin, et al.
Genomics|June 30, 2000
A novel conserved cochlear gene, OTOR: identification, expression analysis, and chromosomal mappingN G Robertson, S Heller, J S Lin, et al.
The Journal of Biological Chemistry|September 25, 1998
Identification of PKDL, a novel polycystic kidney disease 2-like gene whose murine homologue is deleted in mice with kidney and retinal defectsH Nomura, A E Turco, Y Pei, et al.
Genomics|January 7, 1998
An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1)A B Skvorak, N G Robertson, Y Yin, et al.
Genes, Chromosomes & Cancer|September 1, 1996
Translocation breakpoints upstream of the HMGIC gene in uterine leiomyomata suggest dysregulation of this gene by a mechanism different from that in lipomasM Schoenberg Fejzo, H R Ashar, K S Krauter, et al.
Genomics|September 7, 2001
STK25 is a candidate gene for pseudopseudohypoparathyroidismM S Davids, E Crawford, S Weremowicz, et al.
Molecular and Cellular Biology|September 1, 1993
Purification of the human NF-E2 complex: cDNA cloning of the hematopoietic cell-specific subunit and evidence for an associated partnerP A Ney, N C Andrews, S M Jane, et al.
Genomics|March 20, 1995
Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomataM S Fejzo, S J Yoon, K T Montgomery, et al.
Pageof 7