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The Journal of Biological Chemistry
|
February 21, 2021
A repeated triple lysine motif anchors complexes containing bone sialoprotein and the type XI collagen A1 chain involved in bone mineralization
Jeff P Gorski, Nichole T Franz, Daniel Pernoud, et al.
Anticancer Research
|
January 30, 2003
Differential expression of aggrecan mRNA isoforms by chondrosarcoma cells
Yoshito Matsui, Nobuhito Araki, Hideki Tsuboi, et al.
The Journal of Biological Chemistry
|
May 23, 2014
Increased C-telopeptide cross-linking of tendon type I collagen in fibromodulin-deficient mice
Sebastian Kalamajski, Cuiping Liu, Viveka Tillgren, et al.
The Journal of Biological Chemistry
|
February 4, 2015
Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations
David M Hudson, Kyu Sang Joeng, Rachel Werther, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
October 12, 2013
Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform
Audrey McAlinden, Geoffrey Traeger, Uwe Hansen, et al.
JBMR Plus
|
March 29, 2021
Abnormal Bone Collagen Cross-Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous <i>PLOD2</i> Mutations
Charlotte Gistelinck, MaryAnn Weis, Jyoti Rai, et al.
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.
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.
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.
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Search research articles
Search
Showing results (31-40 of 76) with videos related to
Sort By:
Page
of 8
The Journal of Biological Chemistry
|
February 21, 2021
A repeated triple lysine motif anchors complexes containing bone sialoprotein and the type XI collagen A1 chain involved in bone mineralization
Jeff P Gorski, Nichole T Franz, Daniel Pernoud, et al.
Anticancer Research
|
January 30, 2003
Differential expression of aggrecan mRNA isoforms by chondrosarcoma cells
Yoshito Matsui, Nobuhito Araki, Hideki Tsuboi, et al.
The Journal of Biological Chemistry
|
May 23, 2014
Increased C-telopeptide cross-linking of tendon type I collagen in fibromodulin-deficient mice
Sebastian Kalamajski, Cuiping Liu, Viveka Tillgren, et al.
The Journal of Biological Chemistry
|
February 4, 2015
Post-translationally abnormal collagens of prolyl 3-hydroxylase-2 null mice offer a pathobiological mechanism for the high myopia linked to human LEPREL1 mutations
David M Hudson, Kyu Sang Joeng, Rachel Werther, et al.
Matrix Biology : Journal of the International Society for Matrix Biology
|
October 12, 2013
Molecular properties and fibril ultrastructure of types II and XI collagens in cartilage of mice expressing exclusively the α1(IIA) collagen isoform
Audrey McAlinden, Geoffrey Traeger, Uwe Hansen, et al.
JBMR Plus
|
March 29, 2021
Abnormal Bone Collagen Cross-Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous <i>PLOD2</i> Mutations
Charlotte Gistelinck, MaryAnn Weis, Jyoti Rai, et al.
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.
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.
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 8