Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2
出版年份 2016 全文链接
标题
Disentangling mechanisms involved in collagen pyridinoline cross-linking: The immunophilin FKBP65 is critical for dimerization of lysyl hydroxylase 2
作者
关键词
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出版物
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volume 113, Issue 26, Pages 7142-7147
出版商
Proceedings of the National Academy of Sciences
发表日期
2016-06-14
DOI
10.1073/pnas.1600074113
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Zespół Brucka — rzadki zespół charakteryzujący się kruchością kości, przykurczami stawowymi i nowoodkrytą homozygotyczną mutacją FKBP10
- (2015) Hossein Moravej et al. Endokrynologia Polska
- Procollagen Lysyl Hydroxylase 2 Expression Is Regulated by an Alternative Downstream Transforming Growth Factor β-1 Activation Mechanism
- (2015) Rutger A. F. Gjaltema et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Lysyl hydroxylase 2 induces a collagen cross-link switch in tumor stroma
- (2015) Yulong Chen et al. JOURNAL OF CLINICAL INVESTIGATION
- Lysine post-translational modifications of collagen
- (2014) Mitsuo Yamauchi et al. Essays in Biochemistry
- Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients
- (2014) Peiran Zhou et al. PLoS One
- Kuskokwim Syndrome, a Recessive Congenital Contracture Disorder, Extends the Phenotype ofFKBP10 Mutations
- (2013) Aileen M. Barnes et al. HUMAN MUTATION
- Ehlers–Danlos syndrome: A showcase of conditions that lead to understanding matrix biology
- (2013) Peter H. Byers et al. MATRIX BIOLOGY
- Hypoxia-Dependent Modification of Collagen Networks Promotes Sarcoma Metastasis
- (2013) T. S. K. Eisinger-Mathason et al. Cancer Discovery
- Gene Expression Analysis of Murine and Human Osteoarthritis Synovium Reveals Elevation of Transforming Growth Factor β-Responsive Genes in Osteoarthritis-Related Fibrosis
- (2013) D. F. G. Remst et al. Arthritis & Rheumatology
- Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen
- (2012) U. Schwarze et al. HUMAN MOLECULAR GENETICS
- Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum
- (2012) Maria Trinidad Puig-Hervás et al. HUMAN MUTATION
- Absence ofFKBP10in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrix
- (2012) Aileen M. Barnes et al. HUMAN MUTATION
- The myofibroblast matrix: implications for tissue repair and fibrosis
- (2012) Franco Klingberg et al. JOURNAL OF PATHOLOGY
- Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans
- (2011) Ranad Shaheen et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
- (2011) Ortrud K Steinlein et al. BMC Medical Genetics
- A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect
- (2011) Giacomo Venturi et al. BONE
- A novel homozygous 5bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient
- (2011) E.D. Setijowati et al. European Journal of Medical Genetics
- New perspectives on osteogenesis imperfecta
- (2011) Antonella Forlino et al. Nature Reviews Endocrinology
- Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta
- (2010) Yasemin Alanay et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mutations in FKBP10 cause recessive osteogenesis imperfecta and bruck syndrome
- (2010) Brian P Kelley et al. JOURNAL OF BONE AND MINERAL RESEARCH
- Dimerization of human lysyl hydroxylase 3 (LH3) is mediated by the amino acids 541–547
- (2010) Jari Heikkinen et al. MATRIX BIOLOGY
- Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling
- (2009) Kandice R. Levental et al. CELL
- Missense Mutations That Cause Bruck Syndrome Affect Enzymatic Activity, Folding, and Oligomerization of Lysyl Hydroxylase 2
- (2009) Marjo Hyry et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- The Rough Endoplasmic Reticulum-resident FK506-binding Protein FKBP65 Is a Molecular Chaperone That Interacts with Collagens
- (2008) Yoshihiro Ishikawa et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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