Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q33587611)
Watch
English
Inheritance of Ehlers-Danlos type IV syndrome
scientific article
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
title
Inheritance of Ehlers-Danlos type IV syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
main subject
Ehlers-Danlos syndrome
0 references
author name string
Pope FM
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
Martin GR
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
McKusick VA
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
language of work or name
English
0 references
publication date
1 June 1977
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
published in
Journal of Medical Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
volume
14
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
issue
3
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
page(s)
200-204
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
cites work
Heterogeneity of the Ehlers-Danlos syndrome: description of three clinical types and a hypothesis to explain the basic defect(s)
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Variants of the Ehlers-Danlos syndrome. Clinical, biochemical, haematological, and chromosomal features of 100 patients
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
The nature of the collagen synthesized by cultured human fibroblasts
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Collagen polymorphism: characterization of molecules with the chain composition (alpha 1 (3)03 in human tissues.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Defect in Conversion of Procollagen to Collagen in a Form of Ehlers-Danlos Syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
(Alpha1(3))3 human skin collagen. Release by pepsin digestion and preponderance in fetal life.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Production of Procollagen by Human Fibroblasts in Culture
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Characterization of collagen peptides by sodium dodecylsulfate-polyacrylamide electrophoresis.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Patients with Ehlers-Danlos syndrome type IV lack type III collagen
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
Lysyl Oxidase Deficiency in Ehlers–Danlos Syndrome Type V
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
21 June 2018
A Heritable Disorder of Connective Tissue
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
31 October 2018
Human aorta collagens: Evidence for three distinct species
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013557
retrieved
31 October 2018
Identification of two distinct species of procollagen synthesized by a clonal line of calf dermatosparactic cells
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/881711
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identification of the collagenous proteins synthesized by cultured cells from human skin
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/881711
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Immunohistochemical evidence for the presence of collagen type III in human arterial walls, arterial thrombi, and in leukocytes, incubated with collagen in vitro
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/881711
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identification of three genetically distinct collagens by cyanogen bromide cleavage of insoluble human skin and cartilage collagen
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/881711
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
PMCID
1013557
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
PubMed ID
881711
1 reference
stated in
Europe PubMed Central
PubMed ID
881711
retrieved
28 July 2017
Â
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit
