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Cytogenetics and Cell Genetics
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January 1, 1997
Evolution of the black muntjac (Muntiacus crinifrons) karyotype revealed by comparative chromosome painting
F Yang, P C O'Brien, J Wienberg, et al.
Cell
|
February 23, 2019
Genomic Imprinting and Physiological Processes in Mammals
Valter Tucci, Anthony R Isles, Gavin Kelsey, et al.
Nature Genetics
|
May 3, 2005
Epigenetic status of human embryonic stem cells
Peter J Rugg-Gunn, Anne C Ferguson-Smith, Roger A Pedersen
Genomics
|
December 21, 2004
Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution
Ying Yue, Bärbel Grossmann, Malcolm Ferguson-Smith, et al.
Cell Cycle (Georgetown, Tex.)
|
October 6, 2005
Human embryonic stem cells as a model for studying epigenetic regulation during early development
Peter J Rugg-Gunn, Anne C Ferguson-Smith, Roger A Pedersen
The American Journal of Pathology
|
May 18, 2013
Syncytial knots (Tenney-Parker changes) in the human placenta: evidence of loss of transcriptional activity and oxidative damage
Norah M E Fogarty, Anne C Ferguson-Smith, Graham J Burton
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
April 29, 1999
Conservation of human gamma-X centromeric satellite DNA among primates with an autosomal localization in certain Old World monkeys
C Lee, R Stanyon, C C Lin, et al.
Development (Cambridge, England)
|
October 12, 2000
Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12
P Georgiades, M Watkins, M A Surani, et al.
Molecular Cytogenetics
|
October 7, 2022
Observations on chromosome-specific sequencing for the construction of cross-species chromosome homology maps and its resolution of human:alpaca homology
Malcolm A Ferguson-Smith, Jorge C Pereira, Ana Borges, et al.
Human Genetics
|
January 1, 1989
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome
J Galt, E Boyd, J M Connor, et al.
Page
of 77
Search research articles
Search
Showing results (211-220 of 766) with videos related to
Sort By:
Page
of 77
Cytogenetics and Cell Genetics
|
January 1, 1997
Evolution of the black muntjac (Muntiacus crinifrons) karyotype revealed by comparative chromosome painting
F Yang, P C O'Brien, J Wienberg, et al.
Cell
|
February 23, 2019
Genomic Imprinting and Physiological Processes in Mammals
Valter Tucci, Anthony R Isles, Gavin Kelsey, et al.
Nature Genetics
|
May 3, 2005
Epigenetic status of human embryonic stem cells
Peter J Rugg-Gunn, Anne C Ferguson-Smith, Roger A Pedersen
Genomics
|
December 21, 2004
Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution
Ying Yue, Bärbel Grossmann, Malcolm Ferguson-Smith, et al.
Cell Cycle (Georgetown, Tex.)
|
October 6, 2005
Human embryonic stem cells as a model for studying epigenetic regulation during early development
Peter J Rugg-Gunn, Anne C Ferguson-Smith, Roger A Pedersen
The American Journal of Pathology
|
May 18, 2013
Syncytial knots (Tenney-Parker changes) in the human placenta: evidence of loss of transcriptional activity and oxidative damage
Norah M E Fogarty, Anne C Ferguson-Smith, Graham J Burton
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
April 29, 1999
Conservation of human gamma-X centromeric satellite DNA among primates with an autosomal localization in certain Old World monkeys
C Lee, R Stanyon, C C Lin, et al.
Development (Cambridge, England)
|
October 12, 2000
Parental origin-specific developmental defects in mice with uniparental disomy for chromosome 12
P Georgiades, M Watkins, M A Surani, et al.
Molecular Cytogenetics
|
October 7, 2022
Observations on chromosome-specific sequencing for the construction of cross-species chromosome homology maps and its resolution of human:alpaca homology
Malcolm A Ferguson-Smith, Jorge C Pereira, Ana Borges, et al.
Human Genetics
|
January 1, 1989
Isolation of chromosome-21-specific DNA probes and their use in the analysis of nondisjunction in Down syndrome
J Galt, E Boyd, J M Connor, et al.
Page
of 77