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The Journal of Biological Chemistry
|
January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA
David M Hudson, MaryAnn Weis, Jyoti Rai, et al.
Cancer Letters
|
April 24, 2012
Breast cancer, side population cells and ABCG2 expression
K M Britton, R Eyre, I J Harvey, et al.
The Journal of Bone and Joint Surgery. British Volume
|
September 28, 2004
The association of lumbar spondylolisthesis with collagen IX tryptophan alleles
Y Matsui, S K Mirza, J J Wu, et al.
European Journal of Biochemistry
|
July 15, 1988
Susceptibility of cartilage collagens type II, IX, X, and XI to human synovial collagenase and neutrophil elastase
S J Gadher, D R Eyre, V C Duance, et al.
Archives of Biochemistry and Biophysics
|
July 24, 1998
Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasia
R J Fernandes, D J Wilkin, M A Weis, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
September 20, 2011
Murine tendon function is adversely affected by aggrecan accumulation due to the knockout of ADAMTS5
Vincent M Wang, Rebecca M Bell, Ruchir Thakore, et al.
American Journal of Human Genetics
|
February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita
G E Tiller, M A Weis, P A Polumbo, et al.
Human Molecular Genetics
|
February 1, 1995
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimer
G R Mortier, D J Wilkin, W R Wilcox, et al.
European Journal of Medical Genetics
|
June 13, 2020
New insights on the clinical variability of FKBP10 mutations
Osama H Essawi, Piyanoot Tapaneeyaphan, Sofie Symoens, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
August 6, 2008
The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype
Robert E Seegmiller, Brandon D Bomsta, Laura C Bridgewater, et al.
Page
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Search research articles
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Showing results (171-180 of 234) with videos related to
Sort By:
Page
of 24
The Journal of Biological Chemistry
|
January 25, 2017
P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA
David M Hudson, MaryAnn Weis, Jyoti Rai, et al.
Cancer Letters
|
April 24, 2012
Breast cancer, side population cells and ABCG2 expression
K M Britton, R Eyre, I J Harvey, et al.
The Journal of Bone and Joint Surgery. British Volume
|
September 28, 2004
The association of lumbar spondylolisthesis with collagen IX tryptophan alleles
Y Matsui, S K Mirza, J J Wu, et al.
European Journal of Biochemistry
|
July 15, 1988
Susceptibility of cartilage collagens type II, IX, X, and XI to human synovial collagenase and neutrophil elastase
S J Gadher, D R Eyre, V C Duance, et al.
Archives of Biochemistry and Biophysics
|
July 24, 1998
Incorporation of structurally defective type II collagen into cartilage matrix in kniest chondrodysplasia
R J Fernandes, D J Wilkin, M A Weis, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
September 20, 2011
Murine tendon function is adversely affected by aggrecan accumulation due to the knockout of ADAMTS5
Vincent M Wang, Rebecca M Bell, Ruchir Thakore, et al.
American Journal of Human Genetics
|
February 1, 1995
An RNA-splicing mutation (G+5IVS20) in the type II collagen gene (COL2A1) in a family with spondyloepiphyseal dysplasia congenita
G E Tiller, M A Weis, P A Polumbo, et al.
Human Molecular Genetics
|
February 1, 1995
A radiographic, morphologic, biochemical and molecular analysis of a case of achondrogenesis type II resulting from substitution for a glycine residue (Gly691-->Arg) in the type II collagen trimer
G R Mortier, D J Wilkin, W R Wilcox, et al.
European Journal of Medical Genetics
|
June 13, 2020
New insights on the clinical variability of FKBP10 mutations
Osama H Essawi, Piyanoot Tapaneeyaphan, Sofie Symoens, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
August 6, 2008
The heterozygous disproportionate micromelia (dmm) mouse: morphological changes in fetal cartilage precede postnatal dwarfism and compared with lethal homozygotes can explain the mild phenotype
Robert E Seegmiller, Brandon D Bomsta, Laura C Bridgewater, et al.
Page
of 24