(Q28608951)

Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3

1 reference

Procollagen-lysine,2-oxoglutarate 5-dioxygenase 1

1 reference

peptidyl-lysine hydroxylation

1 reference

author name string

M. Valtavaara

1

1 reference

3 February 2017

C. Szpirer

2

1 reference

3 February 2017

J. Szpirer

3

1 reference

3 February 2017

R. Myllylä

Journal of Biological Chemistry

4

1 reference

3 February 2017

language of work or name

English

0 references

publication date

22 May 1998

1 reference

3 February 2017

1 reference

3 February 2017

273

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3 February 2017

21

1 reference

3 February 2017

12881–12886

1 reference

3 February 2017

Collagens and their abnormalities in a wide spectrum of diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Collagens: molecular biology, diseases, and potentials for therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

The discoidin domain receptor tyrosine kinases are activated by collagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

An orphan receptor tyrosine kinase family whose members serve as nonintegrin collagen receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Cloning and characterization of a novel human lysyl hydroxylase isoform highly expressed in pancreas and muscle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Cloning of human lysyl hydroxylase: complete cDNA-derived amino acid sequence and assignment of the gene (PLOD) to chromosome 1p36.3----p36.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

High-resolution fluorescence mapping of 46 DNA markers to the short arm of human chromosome 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Localization of the gene encoding a novel isoform of lysyl hydroxylase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Chromosomal assignment of three rat and human H-rev genes, putative tumor suppressors, down-regulated in malignantly HRAS-transformed cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Genetic mapping of 21 genes on mouse chromosome 11 reveals disruptions in linkage conservation with human chromosome 5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Structure and expression of the human lysyl hydroxylase gene (PLOD): introns 9 and 16 contain Alu sequences at the sites of recombination in Ehlers-Danlos syndrome type VI patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Modification of vertebrate and algal prolyl 4-hydroxylases and vertebrate lysyl hydroxylase by diethyl pyrocarbonate. Evidence for histidine residues in the catalytic site of 2-oxoglutarate-coupled dioxygenases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Crystal structure of isopenicillin N synthase is the first from a new structural family of enzymes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Site-directed mutagenesis of human lysyl hydroxylase expressed in insect cells. Identification of histidine residues and an aspartic acid residue critical for catalytic activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

Polyclonal and monoclonal antibodies to human lysyl hydroxylase and studies on the molecular heterogeneity of the enzyme

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

A patient with Ehlers-Danlos syndrome type VI is a compound heterozygote for mutations in the lysyl hydroxylase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881

A Heritable Disorder of Connective Tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.273.21.12881