Ehlers-Danlos Syndrome Type VI: Collagen Type Specificity of Defective Lysyl Hydroxylation in Various Tissues-Reference-Cited by-同舟云学术

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Ehlers-Danlos Syndrome Type VI: Collagen Type Specificity of Defective Lysyl Hydroxylation in Various Tissues

Published:1984-09 Issue:3 Volume:83 Page:161-165
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Ihme Annegret,Krieg Thomas,Nerlich Andreas,Feldmann Ursula,Rauterberg Jürgen,Glanville Robert W.,Edel Georg,Müller Peter K.

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference17 articles.

1. Molecular defects of collagen metabolism in the Ehlers-Danlos Syndrome;Krieg;Int J Dermatol,1981

2. Genetic disorders of collagen metabolism;Hollister;Hum Genet,1982

3. A heritable disorder of connective tissue. Hydroxylysine deficient collagen disease;Pinnell;N Engl J Med,1972

4. Lysyl-protocollagen hydroxylase deficiency in fibroblasts from siblings with hydroxylysine-deficient collagen;Krane;Proc Natl Acad Sci USA,1972

Cited by 42 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Lysyl hydroxylase 3–mediated post-translational modifications are required for proper biosynthesis of collagen α1α1α2(IV);Journal of Biological Chemistry;2022-12

2. Type I and type V procollagen triple helix uses different subsets of the molecular ensemble for lysine posttranslational modifications in the rER;Journal of Biological Chemistry;2021-01

3. Collagens in the Physiopathology of the Ehlers–Danlos Syndromes;The Collagen Superfamily and Collagenopathies;2021

4. Osteogenesis imperfecta and other defects of bone development as occasional causes of adult osteoporosis;Marcus and Feldman's Osteoporosis;2021

5. Full‐Length Human Collagen Lysyl Hydroxylases;Encyclopedia of Inorganic and Bioinorganic Chemistry;2020-06-19

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