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F Latif

Showing results (141-150 of 173) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinomaJ G Herman, F Latif, Y Weng, et al.
Human Genetics|April 1, 1991
Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genesM I Lerman, F Latif, G M Glenn, et al.
Human Molecular Genetics|July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresisF M Richards, M E Phipps, F Latif, et al.
Oncogene|July 22, 1998
Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor geneY Sekido, M Ahmadian, I I Wistuba, et al.
Genes, Chromosomes & Cancer|September 1, 1992
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: a strategy for cloning the putative tumor suppressor geneF Latif, K Tory, W S Modi, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Human Genetics|September 1, 1992
Molecular and genetic characterization and physical mapping of 11 new markers detecting multiallele restriction fragment length polymorphisms on the short arm of human chromosome 3F Latif, W S Modi, F M Duh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 1996
Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patternsY Sekido, S Bader, F Latif, et al.
Epigenetics|January 27, 2015
Genome-wide DNA methylation profiling of recurrent and non-recurrent chordomasA Alholle, A T Brini, J Bauer, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Pageof 18

Showing results (141-150 of 173) with videos related to

Sort By:
Pageof 18
Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
Silencing of the VHL tumor-suppressor gene by DNA methylation in renal carcinomaJ G Herman, F Latif, Y Weng, et al.
Human Genetics|April 1, 1991
Isolation and regional localization of a large collection (2,000) of single-copy DNA fragments on human chromosome 3 for mapping and cloning tumor suppressor genesM I Lerman, F Latif, G M Glenn, et al.
Human Molecular Genetics|July 1, 1993
Mapping the Von Hippel-Lindau disease tumour suppressor gene: identification of germline deletions by pulsed field gel electrophoresisF M Richards, M E Phipps, F Latif, et al.
Oncogene|July 22, 1998
Cloning of a breast cancer homozygous deletion junction narrows the region of search for a 3p21.3 tumor suppressor geneY Sekido, M Ahmadian, I I Wistuba, et al.
Genes, Chromosomes & Cancer|September 1, 1992
Molecular characterization of a large homozygous deletion in the small cell lung cancer cell line U2020: a strategy for cloning the putative tumor suppressor geneF Latif, K Tory, W S Modi, et al.
Human Molecular Genetics|March 1, 1993
Genetic linkage between von Hippel-Lindau disease and three microsatellite polymorphisms refines the localisation of the VHL locusP A Crossey, E R Maher, M H Jones, et al.
Human Genetics|September 1, 1992
Molecular and genetic characterization and physical mapping of 11 new markers detecting multiallele restriction fragment length polymorphisms on the short arm of human chromosome 3F Latif, W S Modi, F M Duh, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 30, 1996
Human semaphorins A(V) and IV reside in the 3p21.3 small cell lung cancer deletion region and demonstrate distinct expression patternsY Sekido, S Bader, F Latif, et al.
Epigenetics|January 27, 2015
Genome-wide DNA methylation profiling of recurrent and non-recurrent chordomasA Alholle, A T Brini, J Bauer, et al.
Human Molecular Genetics|August 1, 1994
Identification of intragenic mutations in the von Hippel-Lindau disease tumour suppressor gene and correlation with disease phenotypeP A Crossey, F M Richards, K Foster, et al.
Pageof 18