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M Rocchi

Showing results (71-80 of 309) with videos related to

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Progress in Clinical and Biological Research|January 1, 1985
A two step model for mammalian X-chromosome inactivationS M Gartler, K A Dyer, J A Graves, et al.
Genomics|November 5, 1997
Cloning, structural organization analysis, and chromosomal assignment of the human gene for the neurosecretory protein VGFN Canu, R Possenti, A S Ricco, et al.
Genome Research|October 19, 1999
Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21A W Lo, G C Liao, M Rocchi, et al.
Human Genetics|August 21, 2001
AcroM fluorescent in situ hybridization analyses of marker chromosomesS Langer, C Fauth, M Rocchi, et al.
American Journal of Medical Genetics|August 1, 1984
A prenatally detected inv dup(15)V Pecile, N Archidiacono, M A Rustico, et al.
Human Genetics|October 28, 1997
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2H Kehrer-Sawatzki, T Schwickardt, G Assum, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12B Bardoni, S Giglio, A Schenck, et al.
Journal of Cell Science|March 1, 1985
The transcriptional activity of individual ribosomal DNA gene clusters is modulated by serum concentrationA de Capoa, P Marlekaj, A Baldini, et al.
Human Genetics|January 7, 1998
Analysis of the transcriptional activity of amplified genes in tumour cells by fluorescence in situ hybridizationC Jolly, S Michelland, M Rocchi, et al.
Somatic Cell and Molecular Genetics|March 1, 1993
Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10A K Kamat, M Rocchi, D I Smith, et al.
Pageof 31

Showing results (71-80 of 309) with videos related to

Sort By:
Pageof 31
Progress in Clinical and Biological Research|January 1, 1985
A two step model for mammalian X-chromosome inactivationS M Gartler, K A Dyer, J A Graves, et al.
Genomics|November 5, 1997
Cloning, structural organization analysis, and chromosomal assignment of the human gene for the neurosecretory protein VGFN Canu, R Possenti, A S Ricco, et al.
Genome Research|October 19, 1999
Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21A W Lo, G C Liao, M Rocchi, et al.
Human Genetics|August 21, 2001
AcroM fluorescent in situ hybridization analyses of marker chromosomesS Langer, C Fauth, M Rocchi, et al.
American Journal of Medical Genetics|August 1, 1984
A prenatally detected inv dup(15)V Pecile, N Archidiacono, M A Rustico, et al.
Human Genetics|October 28, 1997
A third neurofibromatosis type 1 (NF1) pseudogene at chromosome 15q11.2H Kehrer-Sawatzki, T Schwickardt, G Assum, et al.
Cytogenetics and Cell Genetics|July 15, 2000
Assignment of NUFIP1 (nuclear FMRP interacting protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12B Bardoni, S Giglio, A Schenck, et al.
Journal of Cell Science|March 1, 1985
The transcriptional activity of individual ribosomal DNA gene clusters is modulated by serum concentrationA de Capoa, P Marlekaj, A Baldini, et al.
Human Genetics|January 7, 1998
Analysis of the transcriptional activity of amplified genes in tumour cells by fluorescence in situ hybridizationC Jolly, S Michelland, M Rocchi, et al.
Somatic Cell and Molecular Genetics|March 1, 1993
Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10A K Kamat, M Rocchi, D I Smith, et al.
Pageof 31