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J W Touchman

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

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Gene|April 20, 2001
The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggsP J Blackshear, W S Lai, J M Thorn, et al.
Genomics|November 24, 1999
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.
Genome Research|July 1, 1997
A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kbG G Bouffard, J R Idol, V V Braden, et al.
Pharmacogenetics|October 23, 2001
The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variantsJ Zhang, P Kuehl, E D Green, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genesR E Ellsworth, D C Jamison, J W Touchman, et al.
Nature|August 15, 2003
Comparative analyses of multi-species sequences from targeted genomic regionsJ W Thomas, J W Touchman, R W Blakesley, 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.
Gene|April 20, 2001
The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggsP J Blackshear, W S Lai, J M Thorn, et al.
Genomics|November 24, 1999
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2Y Liang, A Wang, I A Belyantseva, et al.
Genome Research|July 1, 1997
A physical map of human chromosome 7: an integrated YAC contig map with average STS spacing of 79 kbG G Bouffard, J R Idol, V V Braden, et al.
Pharmacogenetics|October 23, 2001
The human pregnane X receptor: genomic structure and identification and functional characterization of natural allelic variantsJ Zhang, P Kuehl, E D Green, et al.
Human Molecular Genetics|November 5, 1999
Mutations in the gene encoding KRIT1, a Krev-1/rap1a binding protein, cause cerebral cavernous malformations (CCM1)T Sahoo, E W Johnson, J W Thomas, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2000
Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genesR E Ellsworth, D C Jamison, J W Touchman, et al.
Nature|August 15, 2003
Comparative analyses of multi-species sequences from targeted genomic regionsJ W Thomas, J W Touchman, R W Blakesley, et al.
Pageof 2