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D I Smith

Showing results (151-160 of 166) with videos related to

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Circulation Research|March 1, 1993
Identification of a specific radioligand for the cardiac rapidly activating delayed rectifier K+ channelC C Chadwick, A M Ezrin, B O'Connor, et al.
The Journal of Clinical Investigation|June 15, 1997
Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implications for neuroendocrine cell survivalC G Willett, D I Smith, V Shridhar, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.
Prenatal Diagnosis|May 1, 1997
Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramniosW F Hansen, L E Bernard, S Langlois, et al.
Nucleic Acids Research|November 25, 1991
A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apartS L Secore, A P Walker, M H Herbstreith, et al.
Journal of Medical Genetics|June 1, 1993
Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26M A Pericak-Vance, K J Nunes, E Whisenant, et al.
Genome Research|March 1, 1996
Construction of a consistent YAC contig for human chromosome region 3p14.1W Bardenheuer, S Michaelis, A Lux, et al.
Nature|October 18, 2000
Role for the p53 homologue p73 in E2F-1-induced apoptosisM Irwin, M C Marin, A C Phillips, et al.
Genes, Chromosomes & Cancer|August 1, 1997
Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B regionA van den Berg, T G Draaijers, K Kok, et al.
Nature Genetics|October 4, 2000
Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signallingW Liu, X Dong, M Mai, et al.
Pageof 17

Showing results (151-160 of 166) with videos related to

Sort By:
Pageof 17
Circulation Research|March 1, 1993
Identification of a specific radioligand for the cardiac rapidly activating delayed rectifier K+ channelC C Chadwick, A M Ezrin, B O'Connor, et al.
The Journal of Clinical Investigation|June 15, 1997
Differential screening of a human chromosome 3 library identifies hepatocyte growth factor-like/macrophage-stimulating protein and its receptor in injured lung. Possible implications for neuroendocrine cell survivalC G Willett, D I Smith, V Shridhar, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.
Prenatal Diagnosis|May 1, 1997
Maternal uniparental disomy of chromosome 2 and confined placental mosaicism for trisomy 2 in a fetus with intrauterine growth restriction, hypospadias, and oligohydramniosW F Hansen, L E Bernard, S Langlois, et al.
Nucleic Acids Research|November 25, 1991
A StuI polymorphism on chromosome 3p14.1-14.2 (D3S622) defined by two polymorphic StuI sites 2.4 kb apartS L Secore, A P Walker, M H Herbstreith, et al.
Journal of Medical Genetics|June 1, 1993
Genetic mapping of dinucleotide repeat polymorphisms and von Hippel-Lindau disease on chromosome 3p25-26M A Pericak-Vance, K J Nunes, E Whisenant, et al.
Genome Research|March 1, 1996
Construction of a consistent YAC contig for human chromosome region 3p14.1W Bardenheuer, S Michaelis, A Lux, et al.
Nature|October 18, 2000
Role for the p53 homologue p73 in E2F-1-induced apoptosisM Irwin, M C Marin, A C Phillips, et al.
Genes, Chromosomes & Cancer|August 1, 1997
Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B regionA van den Berg, T G Draaijers, K Kok, et al.
Nature Genetics|October 4, 2000
Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating beta-catenin/TCF signallingW Liu, X Dong, M Mai, et al.
Pageof 17