(Q24291329)

supramolecular fiber organization

GOA release 2020-03-11

1 reference

Ehlers-Danlos syndrome, dermatosparaxis type

GOA release 2020-03-11

1 reference

R J Fernandes

1

0 references

S Hirohata

2

0 references

J M Engle

3

0 references

A Colige

4

0 references

D H Cohn

5

0 references

D R Eyre

6

0 references

S S Apte

Journal of Biological Chemistry

7

0 references

language of work or name

English

0 references

publication date

24 August 2001

0 references

published in

0 references

volume

276

0 references

issue

34

0 references

page(s)

31502-9

0 references

cites work

Nonfibrillar collagens

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

The C-proteinase that processes procollagens to fibrillar collagens is identical to the protein previously identified as bone morphogenic protein-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Procollagen peptidase: an enzyme excising the coordination peptides of procollagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

cDNA cloning and expression of bovine procollagen I N-proteinase: a new member of the superfamily of zinc-metalloproteinases with binding sites for cells and other matrix components.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Molecular cloning of a gene encoding a new type of metalloproteinase-disintegrin family protein with thrombospondin motifs as an inflammation associated gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

ADAM-TS5, ADAM-TS6, and ADAM-TS7, novel members of a new family of zinc metalloproteases. General features and genomic distribution of the ADAM-TS family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Clinical, morphological, and biochemical phenotype of a new case of Ehlers-Danlos syndrome type VIIC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Initial observations of human dermatosparaxis: Ehlers-Danlos syndrome type VIIC.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Incomplete processing of type II procollagen by a rat chondrosarcoma cell line

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

The scanning model for translation: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Expression of lacunin, a large multidomain extracellular matrix protein, accompanies morphogenesis of epithelial monolayers in Manduca sexta

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Chondrodysplasia in transgenic mice harboring a 15-amino acid deletion in the triple helical domain of pro alpha 1(II) collagen chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

ADAMTS-1 protein anchors at the extracellular matrix through the thrombospondin type I motifs and its spacing region

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

The thrombospondin motif of aggrecanase-1 (ADAMTS-4) is critical for aggrecan substrate recognition and cleavage

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Assembly in vitro of thin and thick fibrils of collagen II from recombinant procollagen II. The monomers in the tips of thick fibrils have the opposite orientation from monomers in the growing tips of collagen I fibrils

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Assessment of procollagen processing defects by fibroblasts cultured in the presence of dextran sulphate

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Structure of cDNA clones coding for human type II procollagen. The alpha 1(II) chain is more similar to the alpha 1(I) chain than two other alpha chains of fibrillar collagens

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Sequence differences between glycosylated and non-glycosylated Asn-X-Thr/Ser acceptor sites: implications for protein engineering

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

Ehlers-Danlos type VII-C, or human dermatosparaxis. The offspring of a union between basic and clinical research

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

7 January 2021

Cleavage of type I procollagen by C- and N-proteinases is more rapid if the substrate is aggregated with dextran sulfate or polyethylene glycol

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

7 January 2021

Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

7 January 2021

Inheritance of dermatosparaxis in the calf. A genetic defect of connective tissues

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

7 January 2021

Collagen Made of Extended alpha-Chains, Procollagen, in Genetically-Defective Dermatosparaxic Calves

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M103466200

7 January 2021