Complete exon-intron organization of the gene for human lysyl hydroxylase 3 (LH3). (Q33891121)

29 July 2017

Complete exon-intron organization of the gene for human lysyl hydroxylase 3 (LH3). (English)

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29 July 2017

Rautavuoma K

1

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29 July 2017

Passoja K

series ordinal

2

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29 July 2017

Helaakoski T

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3

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29 July 2017

Kivirikko KI

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4

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29 July 2017

1 February 2000

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29 July 2017

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29 July 2017

19

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29 July 2017

1

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29 July 2017

73-79

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Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C)

29 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

A large duplication in the gene for lysyl hydroxylase accounts for the type VI variant of Ehlers-Danlos syndrome in two siblings

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

A homozygous stop codon in the lysyl hydroxylase gene in two siblings with Ehlers-Danlos syndrome type VI

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

DNA sequence requirements for transcriptional initiator activity in mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

The serotonin 1a receptor gene contains a TATA-less promoter that responds to MAZ and Sp1

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Cloning and characterization of a third human lysyl hydroxylase isoform

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Characterization of a pro-alpha 2(I) collagen gene mutation by nuclease S1 mapping

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Characterization of cDNAs for mouse lysyl hydroxylase 1, 2 and 3, their phylogenetic analysis and tissue-specific expression in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi.

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

The partial tandem duplication of ALL1 (MLL) is consistently generated by Alu-mediated homologous recombination in acute myeloid leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Primary structure, tissue distribution, and chromosomal localization of a novel isoform of lysyl hydroxylase (lysyl hydroxylase 3)

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

A patient with Ehlers-Danlos syndrome type VI is homozygous for a premature termination codon in exon 14 of the lysyl hydroxylase 1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Tissue specificity of a new splice form of the human lysyl hydroxylase 2 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

Characterization of a partial cDNA for lysyl hydroxylase from human skin fibroblasts; lysyl hydroxylase mRNAs are regulated differently by minoxidil derivatives and hydralazine

1 reference

https://api.crossref.org/works/10.1016%2FS0945-053X%2899%2900058-X

7 January 2021

10.1016/S0945-053X(99)00058-X

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DOI

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29 July 2017

1 reference