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Genomics
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February 15, 1996
Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 gene
P E Bennett-Baker, S Kiousis, S C Chandrasekharappa, et al.
Human Molecular Genetics
|
March 11, 1999
Characterization of dystrophin and utrophin diversity in the mouse
C N Lumeng, S F Phelps, J A Rafael, et al.
Biophysical Journal
|
February 18, 2010
Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle
O Friedrich, M Both, C Weber, et al.
Human Molecular Genetics
|
May 23, 1998
mdx muscle pathology is independent of nNOS perturbation
R H Crosbie, V Straub, H Y Yun, et al.
Journal of the National Cancer Institute. Monographs
|
January 1, 1995
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations
F J Couch, J Garber, S Kiousis, et al.
Current Biology : CB
|
August 30, 2001
Activation of JNK1 contributes to dystrophic muscle pathogenesis
S M Kolodziejczyk, G S Walsh, K Balazsi, et al.
American Journal of Human Genetics
|
April 1, 1993
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis
J S Chamberlain, M Boehnke, T S Frank, et al.
The Journal of Experimental Medicine
|
August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy
D S Chao, J R Gorospe, J E Brenman, et al.
American Journal of Human Genetics
|
October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene
E F Gillard, J S Chamberlain, E G Murphy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 19, 2000
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors
M A Hauser, A Robinson, D Hartigan-O'Connor, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 93) with videos related to
Sort By:
Page
of 10
Genomics
|
February 15, 1996
Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 gene
P E Bennett-Baker, S Kiousis, S C Chandrasekharappa, et al.
Human Molecular Genetics
|
March 11, 1999
Characterization of dystrophin and utrophin diversity in the mouse
C N Lumeng, S F Phelps, J A Rafael, et al.
Biophysical Journal
|
February 18, 2010
Microarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle
O Friedrich, M Both, C Weber, et al.
Human Molecular Genetics
|
May 23, 1998
mdx muscle pathology is independent of nNOS perturbation
R H Crosbie, V Straub, H Y Yun, et al.
Journal of the National Cancer Institute. Monographs
|
January 1, 1995
Genetic analysis of eight breast-ovarian cancer families with suspected BRCA1 mutations
F J Couch, J Garber, S Kiousis, et al.
Current Biology : CB
|
August 30, 2001
Activation of JNK1 contributes to dystrophic muscle pathogenesis
S M Kolodziejczyk, G S Walsh, K Balazsi, et al.
American Journal of Human Genetics
|
April 1, 1993
BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis
J S Chamberlain, M Boehnke, T S Frank, et al.
The Journal of Experimental Medicine
|
August 1, 1996
Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy
D S Chao, J R Gorospe, J E Brenman, et al.
American Journal of Human Genetics
|
October 1, 1989
Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene
E F Gillard, J S Chamberlain, E G Murphy, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 19, 2000
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors
M A Hauser, A Robinson, D Hartigan-O'Connor, et al.
Page
of 10