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N Hastie

Showing results (11-20 of 19) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 2, 1998
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasiaV M Wunderle, R Critcher, N Hastie, et al.
Human Molecular Genetics|March 1, 1995
DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutationsM Little, G Holmes, W Bickmore, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13C Miles, G Elgar, E Coles, et al.
Oncogene|August 23, 2006
hnRNP-U directly interacts with WT1 and modulates WT1 transcriptional activationL Spraggon, T Dudnakova, J Slight, et al.
Genes, Chromosomes & Cancer|June 1, 1993
Frequent loss of 11p13 and 11p15 loci in male germ cell tumoursR A Lothe, N Hastie, K Heimdal, et al.
Reproductive Toxicology (Elmsford, N.Y.)|March 1, 1997
NIEHS/EPA Workshops. Genomic imprintingC L Stewart, R Pedersen, P Rotwein, et al.
Nature Genetics|August 1, 1992
The human PAX6 gene is mutated in two patients with aniridiaT Jordan, I Hanson, D Zaletayev, et al.
Human Genetics|June 1, 1987
Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal XqJ A Buchanan, K E Buckton, C M Gosden, et al.
Cancer Research|April 10, 1999
Multiple roles for the Wilms' tumor suppressor, WT1R Davies, A Moore, A Schedl, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Proceedings of the National Academy of Sciences of the United States of America|September 2, 1998
Deletion of long-range regulatory elements upstream of SOX9 causes campomelic dysplasiaV M Wunderle, R Critcher, N Hastie, et al.
Human Molecular Genetics|March 1, 1995
DNA binding capacity of the WT1 protein is abolished by Denys-Drash syndrome WT1 point mutationsM Little, G Holmes, W Bickmore, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13C Miles, G Elgar, E Coles, et al.
Oncogene|August 23, 2006
hnRNP-U directly interacts with WT1 and modulates WT1 transcriptional activationL Spraggon, T Dudnakova, J Slight, et al.
Genes, Chromosomes & Cancer|June 1, 1993
Frequent loss of 11p13 and 11p15 loci in male germ cell tumoursR A Lothe, N Hastie, K Heimdal, et al.
Reproductive Toxicology (Elmsford, N.Y.)|March 1, 1997
NIEHS/EPA Workshops. Genomic imprintingC L Stewart, R Pedersen, P Rotwein, et al.
Nature Genetics|August 1, 1992
The human PAX6 gene is mutated in two patients with aniridiaT Jordan, I Hanson, D Zaletayev, et al.
Human Genetics|June 1, 1987
Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal XqJ A Buchanan, K E Buckton, C M Gosden, et al.
Cancer Research|April 10, 1999
Multiple roles for the Wilms' tumor suppressor, WT1R Davies, A Moore, A Schedl, et al.
Pageof 2