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PLOD1 gene

Known as: PLOD1, LYSYL HYDROXYLASE 1, procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Genes
Procollagen-Lysine, 2-Oxoglutarate 5-Dioxygenase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
Hypoglicemic effect of Leandra lacunosa in normal and alloxan-induced diabetic rats.
2005
2005
An Ehlers-Danlos syndrome type VIA patient with cystic malformations of the meninges.
We have characterized a patient with the phenotype of Ehlers-Danlos syndrome type VIA (EDS VIA: kyphoscoliotic form), accompanied… 
2000
2000
Deletion of cysteine 369 in lysyl hydroxylase 1 eliminates enzyme activity and causes Ehlers-Danlos syndrome type VI.
2000
2000
Mutational analysis of the lysyl hydroxylase 1 gene (PLOD) in six unrelated patients with Ehlers-Danlos syndrome type VI: prenatal exclusion of this disorder in one family.
Screening of full length cDNAs for lysyl hydroxylase 1 (LH1; also PLOD) amplified from dermal fibroblasts from six unrelated… 
2000
2000
Exchanging cofactors in the core antennae from purple bacteria: structure and properties of Zn-bacteriopheophytin-containing LH1.
The core light-harvesting LH1 complex of Rhodospirillum rubrum consists of an assembly of membrane-spanning alpha and beta… 
Highly Cited
1999
Highly Cited
1999
Characterization of cDNAs for mouse lysyl hydroxylase 1, 2 and 3, their phylogenetic analysis and tissue-specific expression in the mouse.
1999
1999
A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene.
In the present study, we have characterized a patient with Ehlers-Danlos syndrome type VI (EDS VI) as homozygous for a… 
1998
1998
A compound heterozygote patient with Ehlers‐Danlos syndrome type VI has a deletion in one allele and a splicing defect in the other allele of the lysyl hydroxylase gene
We report the first deletion mutation and the first splicing defect in the lysyl hydroxylase gene in a compound heterozygote… 
1995
1995
Rat lysyl hydroxylase: molecular cloning, mRNA distribution and expression in a baculovirus system.
1994
1994
Sequence analysis of a cDNA for lysyl hydroxylase isolated from human skin fibroblasts from a normal donor: differences from human placental lysyl hydroxylase cDNA.
Using polymerase chain reaction, we have isolated and sequenced a 3-kb cDNA for lysyl hydroxylase (LH) from human skin… 
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