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Human Mutation
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September 1, 2005
Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genes
Leonarda Ianzano, Junjun Zhang, Elayne M Chan, et al.
Oncogene
|
May 15, 1997
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas
W R Zeng, S W Scherer, M Koutsilieris, et al.
American Journal of Human Genetics
|
August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome
L R Osborne, S Soder, X M Shi, et al.
Genomics
|
June 1, 2005
Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay
Dorota A Kwasnicka-Crawford, Andrew R Carson, Wendy Roberts, et al.
Gene
|
November 24, 1999
Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene
D Leclerc, M Odièvre, Q Wu, et al.
Brain Research
|
September 28, 2010
Gene and miRNA expression profiles in autism spectrum disorders
Mohammad M Ghahramani Seno, Pingzhao Hu, Fuad G Gwadry, et al.
Genomics
|
November 1, 2005
Murine segmental duplications are hot spots for chromosome and gene evolution
Lluís Armengol, Tomàs Marquès-Bonet, Joseph Cheung, et al.
The Cochrane Database of Systematic Reviews
|
August 17, 2012
Exercise interventions on health-related quality of life for cancer survivors
Shiraz I Mishra, Roberta W Scherer, Paula M Geigle, et al.
Cancer Genetics and Cytogenetics
|
April 13, 1999
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype
M G de Silva, P Kantharidis, S W Scherer, et al.
The Journal of Biological Chemistry
|
September 15, 1995
Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families
E A Barron-Casella, M A Torres, S W Scherer, et al.
Page
of 92
Search research articles
Search
Showing results (371-380 of 915) with videos related to
Sort By:
Page
of 92
Human Mutation
|
September 1, 2005
Lafora progressive Myoclonus Epilepsy mutation database-EPM2A and NHLRC1 (EPM2B) genes
Leonarda Ianzano, Junjun Zhang, Elayne M Chan, et al.
Oncogene
|
May 15, 1997
Loss of heterozygosity and reduced expression of the CUTL1 gene in uterine leiomyomas
W R Zeng, S W Scherer, M Koutsilieris, et al.
American Journal of Human Genetics
|
August 1, 1997
Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome
L R Osborne, S Soder, X M Shi, et al.
Genomics
|
June 1, 2005
Characterization of a novel cation transporter ATPase gene (ATP13A4) interrupted by 3q25-q29 inversion in an individual with language delay
Dorota A Kwasnicka-Crawford, Andrew R Carson, Wendy Roberts, et al.
Gene
|
November 24, 1999
Molecular cloning, expression and physical mapping of the human methionine synthase reductase gene
D Leclerc, M Odièvre, Q Wu, et al.
Brain Research
|
September 28, 2010
Gene and miRNA expression profiles in autism spectrum disorders
Mohammad M Ghahramani Seno, Pingzhao Hu, Fuad G Gwadry, et al.
Genomics
|
November 1, 2005
Murine segmental duplications are hot spots for chromosome and gene evolution
Lluís Armengol, Tomàs Marquès-Bonet, Joseph Cheung, et al.
The Cochrane Database of Systematic Reviews
|
August 17, 2012
Exercise interventions on health-related quality of life for cancer survivors
Shiraz I Mishra, Roberta W Scherer, Paula M Geigle, et al.
Cancer Genetics and Cytogenetics
|
April 13, 1999
Physical mapping of a tandem duplication on the long arm of chromosome 7 associated with a multidrug resistant phenotype
M G de Silva, P Kantharidis, S W Scherer, et al.
The Journal of Biological Chemistry
|
September 15, 1995
Sequence analysis and chromosomal localization of human Cap Z. Conserved residues within the actin-binding domain may link Cap Z to gelsolin/severin and profilin protein families
E A Barron-Casella, M A Torres, S W Scherer, et al.
Page
of 92