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S W Scherer

Showing results (81-90 of 164) with videos related to

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DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|June 30, 1996
A panel of radiation hybrids defining the 7q31-q32 region of human chromosome 7K Nakabayashi, T Ogata, M Fujii, et al.
Oncogene|November 7, 1996
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of METJ C Lin, S W Scherer, L Tougas, et al.
American Journal of Human Genetics|March 20, 2001
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeE Petek, C Windpassinger, J B Vincent, et al.
Somatic Cell and Molecular Genetics|July 1, 1997
Maintenance of hypomethylation status and preferential expression of exogenous human MDR1/PGY1 gene in mouse L cells by YAC mediated transferH Kusaba, M Nakayama, T Harada, et al.
Gene|August 26, 1998
Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequenceH Mochizuki, S W Scherer, T Xi, et al.
Genomics|March 2, 1999
Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and humanM A Crackower, D S Sinasac, J Xia, et al.
Gene|February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndromeD M Jadayel, L R Osborne, L J Coignet, et al.
Human Molecular Genetics|August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyS W Scherer, P Poorkaj, H Massa, et al.
Clinical Genetics|June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiencyM J Nowaczyk, M J Huggins, D J Tomkins, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal CanadiansR A Hegele, S B Harris, B Zinman, et al.
Pageof 17

Showing results (81-90 of 164) with videos related to

Sort By:
Pageof 17
DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|June 30, 1996
A panel of radiation hybrids defining the 7q31-q32 region of human chromosome 7K Nakabayashi, T Ogata, M Fujii, et al.
Oncogene|November 7, 1996
Detailed deletion mapping with a refined physical map of 7q31 localizes a putative tumor suppressor gene for breast cancer in the region of METJ C Lin, S W Scherer, L Tougas, et al.
American Journal of Human Genetics|March 20, 2001
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeE Petek, C Windpassinger, J B Vincent, et al.
Somatic Cell and Molecular Genetics|July 1, 1997
Maintenance of hypomethylation status and preferential expression of exogenous human MDR1/PGY1 gene in mouse L cells by YAC mediated transferH Kusaba, M Nakayama, T Harada, et al.
Gene|August 26, 1998
Human PON2 gene at 7q21.3: cloning, multiple mRNA forms, and missense polymorphisms in the coding sequenceH Mochizuki, S W Scherer, T Xi, et al.
Genomics|March 2, 1999
Cloning and characterization of two cytoplasmic dynein intermediate chain genes in mouse and humanM A Crackower, D S Sinasac, J Xia, et al.
Gene|February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndromeD M Jadayel, L R Osborne, L J Coignet, et al.
Human Molecular Genetics|August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyS W Scherer, P Poorkaj, H Massa, et al.
Clinical Genetics|June 14, 2000
Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiencyM J Nowaczyk, M J Huggins, D J Tomkins, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1998
Variation in the AU(AT)-rich element within the 3'-untranslated region of PPP1R3 is associated with variation in plasma glucose in aboriginal CanadiansR A Hegele, S B Harris, B Zinman, et al.
Pageof 17