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Genomics

Showing results (271-280 of 10,746) with videos related to

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Genomics|January 16, 1999
Mapping and characterization of the X-linked dyskeratosis congenita (DKC) geneS Hassock, D Vetrie, F Giannelli
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Genomics|January 16, 1999
Genomic cloning, structure, expression pattern, and chromosomal location of the human SIX3 geneB Granadino, M E Gallardo, J López-Ríos, et al.
Genomics|January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome geneP Paavola, N Horelli-Kuitunen, A Palotie, et al.
Genomics|January 16, 1999
Localization of human transcription factor TEF-4 and TEF-5 (TEAD2, TEAD3) genes to chromosomes 19q13.3 and 6p21.2 using fluorescence in situ hybridization and radiation hybrid analysisP Jacquemin, D Depetris, M G Mattei, et al.
Genomics|January 8, 1999
Bisulfite genomic sequencing-derived methylation profile of the xist gene throughout early mouse developmentL E McDonald, C A Paterson, G F Kay
Genomics|January 8, 1999
Rescue of the HNF4 --> HNF1alpha pathway in hepatoma variant cells containing human chromosome 12G A Bulla, J R Batanian, H M Young, et al.
Genomics|January 8, 1999
Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutationM Wan, B F Cravatt, H Z Ring, et al.
Genomics|January 8, 1999
Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotesS Kitao, I Ohsugi, K Ichikawa, et al.
Genomics|January 8, 1999
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder geneJ Björkman, G Stetten, C S Moore, et al.
Pageof 1,075

Showing results (271-280 of 10,746) with videos related to

Sort By:
Pageof 1,075
Genomics|January 16, 1999
Mapping and characterization of the X-linked dyskeratosis congenita (DKC) geneS Hassock, D Vetrie, F Giannelli
Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.
Genomics|January 16, 1999
Genomic cloning, structure, expression pattern, and chromosomal location of the human SIX3 geneB Granadino, M E Gallardo, J López-Ríos, et al.
Genomics|January 16, 1999
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome geneP Paavola, N Horelli-Kuitunen, A Palotie, et al.
Genomics|January 16, 1999
Localization of human transcription factor TEF-4 and TEF-5 (TEAD2, TEAD3) genes to chromosomes 19q13.3 and 6p21.2 using fluorescence in situ hybridization and radiation hybrid analysisP Jacquemin, D Depetris, M G Mattei, et al.
Genomics|January 8, 1999
Bisulfite genomic sequencing-derived methylation profile of the xist gene throughout early mouse developmentL E McDonald, C A Paterson, G F Kay
Genomics|January 8, 1999
Rescue of the HNF4 --> HNF1alpha pathway in hepatoma variant cells containing human chromosome 12G A Bulla, J R Batanian, H M Young, et al.
Genomics|January 8, 1999
Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutationM Wan, B F Cravatt, H Z Ring, et al.
Genomics|January 8, 1999
Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotesS Kitao, I Ohsugi, K Ichikawa, et al.
Genomics|January 8, 1999
Genomic structure of PEX13, a candidate peroxisome biogenesis disorder geneJ Björkman, G Stetten, C S Moore, et al.
Pageof 1,075