(Q46890356)

English

Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix

scientific article published on 5 January 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Ehlers-Danlos syndrome

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osteogenesis imperfecta

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4

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

author name string

Elena Makareeva

1

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Wayne A Cabral

2

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Joan C Marini

3

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

language of work or name

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publication date

5 January 2006

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

281

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

10

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

6463-6470

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

Collagens: molecular biology, diseases, and potentials for therapy

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Stability and mobility of the collagen structure

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Recombinant procollagen II: Deletion of D period segments identifies sequences that are required for helix stabilization and generates a temperature-sensitive N-proteinase cleavage site.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Type I collagen triplet duplication mutation in lethal osteogenesis imperfecta shifts register of alpha chains throughout the helix and disrupts incorporation of mutant helices into fibrils and extracellular matrix

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Type I collagen is thermally unstable at body temperature

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Amino acid propensities for the collagen triple-helix

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Electrostatic interactions involving lysine make major contributions to collagen triple-helix stability

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Prediction of collagen stability from amino acid sequence

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Changes in thermal stability and microunfolding pattern of collagen helix resulting from the loss of alpha2(I) chain in osteogenesis imperfecta murine

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: exon skipping caused by an 11-bp deletion from an intron in one COL1A2 allele

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Mutations that alter the primary structure of type I procollagen have long-range effects on its cleavage by procollagen N-proteinase

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Partial COL1A2 gene duplication produces features of osteogenesis imperfecta and Ehlers-Danlos syndrome type VII

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Mapping the ligand-binding sites and disease-associated mutations on the most abundant protein in the human, type I collagen

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M511830200

21 January 2018

Identifiers

10.1074/JBC.M511830200

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 December 2017

http://europepmc.org/abstract/MED/16407265

ResearchGate publication ID

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