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Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
July 9, 2005
Role for the alpha7beta1 integrin in vascular development and integrity
Nichole L Flintoff-Dye, Jennifer Welser, Jachinta Rooney, et al.
Scientific Reports
|
August 15, 2020
Collagen VIα2 chain deficiency causes trabecular bone loss by potentially promoting osteoclast differentiation through enhanced TNFα signaling
Hai T Pham, Vardit Kram, Qurratul-Ain Dar, et al.
The Journal of Clinical Investigation
|
May 1, 2025
Collagen type VI regulates TGF-β bioavailability in skeletal muscle in mice
Payam Mohassel, Hailey Hearn, Jachinta Rooney, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
Collagen type VI regulates TGFβ bioavailability in skeletal muscle
Payam Mohassel, Jachinta Rooney, Yaqun Zou, et al.
JAMA Neurology
|
May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family
Kristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
July 9, 2005
Role for the alpha7beta1 integrin in vascular development and integrity
Nichole L Flintoff-Dye, Jennifer Welser, Jachinta Rooney, et al.
Scientific Reports
|
August 15, 2020
Collagen VIα2 chain deficiency causes trabecular bone loss by potentially promoting osteoclast differentiation through enhanced TNFα signaling
Hai T Pham, Vardit Kram, Qurratul-Ain Dar, et al.
The Journal of Clinical Investigation
|
May 1, 2025
Collagen type VI regulates TGF-β bioavailability in skeletal muscle in mice
Payam Mohassel, Hailey Hearn, Jachinta Rooney, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
Collagen type VI regulates TGFβ bioavailability in skeletal muscle
Payam Mohassel, Jachinta Rooney, Yaqun Zou, et al.
JAMA Neurology
|
May 5, 2015
Association of a Novel ACTA1 Mutation With a Dominant Progressive Scapuloperoneal Myopathy in an Extended Family
Kristen Zukosky, Katherine Meilleur, Bryan J Traynor, et al.
Annals of Neurology
|
May 14, 2020
GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome
A Reghan Foley, Yaqun Zou, James E Dunford, et al.
Page
of 1