(Q68563814)

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Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen

scientific article published on 01 July 1990

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Europe PubMed Central

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25 September 2019

Moderately severe osteogenesis imperfecta: biochemical studies showing variable defect localization in the triple-helical domain of type I collagen (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

osteogenesis imperfecta

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author name string

Valli M

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

Tenni R

2

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

Cetta G

3

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Europe PubMed Central

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25 September 2019

publication date

1 July 1990

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25 September 2019

1 reference

Europe PubMed Central

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25 September 2019

10

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25 September 2019

3

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Europe PubMed Central

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25 September 2019

200-205

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

Homozygous osteogenesis imperfecta unlinked to collagen I genes

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Peptide mapping of collagen chains using CNBr cleavage of proteins within polyacrylamide gels

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Two-dimensional CNBr peptide patterns of collagen types I, II and III

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Subtle structural alterations in the chains of type I procollagen produce osteogenesis imperfecta type II

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

A Film Detection Method for Tritium-Labelled Proteins and Nucleic Acids in Polyacrylamide Gels

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteolytic enzymes as probes for the triple-helical conformation of procollagen

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal alpha 2-chain in type I collagen from a patient with a form of osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Biochemical Investigations of Different Forms of Osteogenesis Imperfecta. Evaluation of 44 Cases

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Collagen genes and inherited connective tissue disease

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Heritable diseases of collagen

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Diminished type I collagen synthesis and reduced alpha 1(I) collagen messenger RNA in cultured fibroblasts from patients with dominantly inherited (type I) osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic heterogeneity in osteogenesis imperfecta

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Osteogenesis imperfecta nosology and genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Osteogenesis imperfecta. The position of substitution for glycine by cysteine in the triple helical domain of the pro alpha 1(I) chains of type I collagen determines the clinical phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Osteogenesis imperfecta is linked to both type I collagen structural genes

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0934-8832%2811%2980169-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0934-8832(11)80169-1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2215359%20AND%20SRC:MED&resulttype=core&format=json

25 September 2019

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