Analysis of Mouse Growth Plate Development-Reference-Cited by-同舟云学术

Analysis of Mouse Growth Plate Development

Published:2016-03 Issue:1 Volume:6 Page:67-130
ISSN:2161-2617
Container-title:Current Protocols in Mouse Biology
language:en
Short-container-title:Current Protocols in Mouse Biology

Author:

Mangiavini Laura¹,Merceron Christophe¹²³,Schipani Ernestina¹

Affiliation:

1. Department of Orthopaedic Surgery, Department of Medicine, Division of Endocrinology and Department of Cell and Developmental Biology, University of Michigan Medical School Ann Arbor Michigan

2. Inserm, UMRS 791‐LIOAD, Centre for Osteoarticular and Dental Tissue Engineering, Group STEP ‘Skeletal Tissue Engineering and Physiopathology’ Nantes France

3. Faculty of Dental Surgery, LUNAM, Nantes University Nantes France

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/9780470942390.mo150094

Reference61 articles.

1. Collagens—major component of the physiological cartilage matrix, major target of cartilage degeneration, major tool in cartilage repair

2. HIF1α regulation of Sox9 is necessary to maintain differentiation of hypoxic prechondrogenic cells during early skeletogenesis

3. Site‐specific recombination mediated by an adenovirus vector expressing the Cre recombinase protein: a molecular switch for control of gene expression;Anton M.;J. Virol.,1995

4. Hypoxia-inducible Factor-1 (HIF-1) but Not HIF-2 Is Essential for Hypoxic Induction of Collagen Prolyl 4-Hydroxylases in Primary Newborn Mouse Epiphyseal Growth Plate Chondrocytes

5. Molecular mechanisms of antigen retrieval: antigen retrieval reverses steric interference caused by formalin-induced cross-links

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