Search research articles
Contact Us
Filters
Showing results (61-70 of 133) with videos related to
Page
of 14
Sort By:
Experimental Hematology
|
May 1, 1996
Expression of two alternatively spliced forms of the 5' untranslated region of the GM-CSF receptor alpha chain mRNA
R Chopra, G Kendall, R E Gale, et al.
The Journal of Biological Chemistry
|
September 3, 1998
p130, p107, and pRb are differentially regulated in proliferating cells and during cell cycle arrest by alpha-interferon
N S Thomas, A R Pizzey, S Tiwari, et al.
Clinical Genetics
|
June 1, 1990
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA
M Upadhyaya, R A Smith, N S Thomas, et al.
The Journal of Biological Chemistry
|
November 5, 1991
Interferon-alpha treatment of Daudi cells down-regulates the octamer binding transcription/DNA replication factors Oct-1 and Oct-2
C L Dent, K A Lillycrop, A Bybee, et al.
American Journal of Human Genetics
|
October 16, 2003
Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity
S E Roberts, F Maggouta, N S Thomas, et al.
Blood
|
July 1, 1992
Down-regulation of human protein kinase C alpha is associated with terminal neutrophil differentiation
V Devalia, N S Thomas, P J Roberts, et al.
Genomics
|
November 4, 1998
Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores
J Wilkinson, S Grimley, A Collins, et al.
Journal of Medical Genetics
|
August 1, 1983
Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome
H M Kingston, N S Thomas, P L Pearson, et al.
Journal of Medical Genetics
|
March 21, 1998
Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications
B M Ferguson, N S Thomas, F Munoz, et al.
The Journal of Pediatrics
|
March 1, 1989
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis
J Zonana, M Sarfarazi, N S Thomas, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 133) with videos related to
Sort By:
Page
of 14
Experimental Hematology
|
May 1, 1996
Expression of two alternatively spliced forms of the 5' untranslated region of the GM-CSF receptor alpha chain mRNA
R Chopra, G Kendall, R E Gale, et al.
The Journal of Biological Chemistry
|
September 3, 1998
p130, p107, and pRb are differentially regulated in proliferating cells and during cell cycle arrest by alpha-interferon
N S Thomas, A R Pizzey, S Tiwari, et al.
Clinical Genetics
|
June 1, 1990
Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA
M Upadhyaya, R A Smith, N S Thomas, et al.
The Journal of Biological Chemistry
|
November 5, 1991
Interferon-alpha treatment of Daudi cells down-regulates the octamer binding transcription/DNA replication factors Oct-1 and Oct-2
C L Dent, K A Lillycrop, A Bybee, et al.
American Journal of Human Genetics
|
October 16, 2003
Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity
S E Roberts, F Maggouta, N S Thomas, et al.
Blood
|
July 1, 1992
Down-regulation of human protein kinase C alpha is associated with terminal neutrophil differentiation
V Devalia, N S Thomas, P J Roberts, et al.
Genomics
|
November 4, 1998
Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores
J Wilkinson, S Grimley, A Collins, et al.
Journal of Medical Genetics
|
August 1, 1983
Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome
H M Kingston, N S Thomas, P L Pearson, et al.
Journal of Medical Genetics
|
March 21, 1998
Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications
B M Ferguson, N S Thomas, F Munoz, et al.
The Journal of Pediatrics
|
March 1, 1989
Improved definition of carrier status in X-linked hypohidrotic ectodermal dysplasia by use of restriction fragment length polymorphism-based linkage analysis
J Zonana, M Sarfarazi, N S Thomas, et al.
Page
of 14