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Gene
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April 20, 2001
The NIEHS Xenopus maternal EST project: interim analysis of the first 13,879 ESTs from unfertilized eggs
P 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 2
Y 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 kb
G 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 variants
J 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 genes
R E Ellsworth, D C Jamison, J W Touchman, et al.
Nature
|
August 15, 2003
Comparative analyses of multi-species sequences from targeted genomic regions
J W Thomas, J W Touchman, R W Blakesley, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 eggs
P 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 2
Y 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 kb
G 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 variants
J 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 genes
R E Ellsworth, D C Jamison, J W Touchman, et al.
Nature
|
August 15, 2003
Comparative analyses of multi-species sequences from targeted genomic regions
J W Thomas, J W Touchman, R W Blakesley, et al.
Page
of 2