(Q36991255)

English

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta

scientific article published on October 1, 1983

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Restriction fragment length polymorphism associated with the pro alpha 2(I) gene of human type I procollagen. Application to a family with an autosomal dominant form of osteogenesis imperfecta (English)

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

osteogenesis imperfecta

0 references

genetic polymorphism

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

author name string

P. Tsipouras

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

J. C. Myers

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

F. Ramirez

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

D. J. Prockop

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

language of work or name

0 references

publication date

1 October 1983

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

full work available at URL

http://www.jci.org/articles/view/111082/files/pdf

Portable Document Format

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

https://europepmc.org/articles/PMC370410

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

https://europepmc.org/articles/PMC370410?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6313757

25 September 2023

http://www.jci.org/articles/view/111082/files/pdf

1 reference

10.1172/JCI111082

https://api.crossref.org/works/10.1172/JCI111082

25 September 2023

Journal of Clinical Investigation

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

72

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

1262-1267

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Isolation and characterization of genomic DNA coding for alpha 2 type I collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Marfan syndrome: abnormal alpha 2 chain in type I collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Genetic disorders of collagen metabolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

DNA Sequence Analysis of a Mouse Proα1(I) Procollagen Gene: Evidence for a Mouse B1 Element Within the Gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Human type I procollagen genes are located on different chromosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Polymorphism in the 5′ Flanking Region of the Human Insulin Gene: A Genetic Marker for Non-Insulin-Dependent Diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Genetic analysis of familial isolated growth hormone deficiency type I

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Assignment of the human pro alpha 2(I) collagen structural gene (COLIA2) to chromosome 7 by molecular hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Isolation and characterization of a human collagen α 1(I)-like gene from a cosmid library

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Molecular basis for familial isolated growth hormone deficiency

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Cloning a cDNA for the pro-alpha 2 chain of human type I collagen

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Construction of a genetic linkage map in man using restriction fragment length polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Cloning and characterization of five overlapping cDNAs specific for the human proα 1(I) collagen chain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

The isolation and characterization of linked delta- and beta-globin genes from a cloned library of human DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Physical Mapping of Temperature-sensitive Mutations of Adenoviruses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

The biosynthesis of collagen and its disorders (second of two parts).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

29 September 2017

Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VII.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

Structure of the pro alpha 2 (I) collagen gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

Organization of human delta--and beta-globin genes in cellular DNA and the presence of intragenic inserts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

The complete sequence of a chromosomal mouse α-globin gene reveals elements conserved throughout vertebrate evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

The biosynthesis of collagen and its disorders (first of two parts).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

27 June 2018

Structure of a cDNA for the pro alpha 2 chain of human type I procollagen. Comparison with chick cDNA for pro alpha 2(I) identifies structurally conserved features of the protein and the gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=370410

4 September 2018

Maternal inheritance of mammalian mitochondrial DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Sensitive New Prenatal Test for Sickle-Cell Anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copy number of a human type I alpha 2 collagen gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Hind III restriction site polymorphism in the human collagen ?1(I)-like gene on chromosome No. 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/6313757

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI111082

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36991255&oldid=1981244512"