Search research articles
Contact Us
Filters
Showing results (31-40 of 45) with videos related to
Page
of 5
Sort By:
Genomics
|
November 1, 1988
Molecular and genetic mapping of the mouse mdx locus
J S Cavanna, G Coulton, J E Morgan, et al.
The EMBO Journal
|
May 18, 1999
A developmental switch in H4 acetylation upstream of Xist plays a role in X chromosome inactivation
L P O'Neill, A M Keohane, J S Lavender, et al.
Nature
|
July 9, 1987
The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome
N Brockdorff, G S Cross, J S Cavanna, et al.
Human Molecular Genetics
|
February 5, 1999
Xist RNA exhibits a banded localization on the inactive X chromosome and is excluded from autosomal material in cis
S M Duthie, T B Nesterova, E J Formstone, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
January 1, 1999
Repetitive DNA sequences in the common vole: cloning, characterization and chromosome localization of two novel complex repeats MS3 and MS4 from the genome of the East European vole Microtus rossiaemeridionalis
E A Elisaphenko, T B Nesterova, S M Duthie, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 24, 1998
Comparative mapping of X chromosomes in vole species of the genus Microtus
T B Nesterova, S M Duthie, N A Mazurok, et al.
Cell
|
October 30, 1992
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
N Brockdorff, A Ashworth, G F Kay, et al.
Cell
|
September 30, 1998
Developmentally regulated Xist promoter switch mediates initiation of X inactivation
C M Johnston, T B Nesterova, E J Formstone, et al.
American Journal of Human Genetics
|
January 1, 1993
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment
J Zonana, J Gault, K J Davies, et al.
American Journal of Human Genetics
|
November 1, 1992
High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus
J Zonana, M Jones, D Browne, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
Genomics
|
November 1, 1988
Molecular and genetic mapping of the mouse mdx locus
J S Cavanna, G Coulton, J E Morgan, et al.
The EMBO Journal
|
May 18, 1999
A developmental switch in H4 acetylation upstream of Xist plays a role in X chromosome inactivation
L P O'Neill, A M Keohane, J S Lavender, et al.
Nature
|
July 9, 1987
The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome
N Brockdorff, G S Cross, J S Cavanna, et al.
Human Molecular Genetics
|
February 5, 1999
Xist RNA exhibits a banded localization on the inactive X chromosome and is excluded from autosomal material in cis
S M Duthie, T B Nesterova, E J Formstone, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
January 1, 1999
Repetitive DNA sequences in the common vole: cloning, characterization and chromosome localization of two novel complex repeats MS3 and MS4 from the genome of the East European vole Microtus rossiaemeridionalis
E A Elisaphenko, T B Nesterova, S M Duthie, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology
|
March 24, 1998
Comparative mapping of X chromosomes in vole species of the genus Microtus
T B Nesterova, S M Duthie, N A Mazurok, et al.
Cell
|
October 30, 1992
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus
N Brockdorff, A Ashworth, G F Kay, et al.
Cell
|
September 30, 1998
Developmentally regulated Xist promoter switch mediates initiation of X inactivation
C M Johnston, T B Nesterova, E J Formstone, et al.
American Journal of Human Genetics
|
January 1, 1993
Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment
J Zonana, J Gault, K J Davies, et al.
American Journal of Human Genetics
|
November 1, 1992
High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus
J Zonana, M Jones, D Browne, et al.
Page
of 5