Genomic characterization of human DSPG3. - Wikidata - awgldk - TriplyDB

Genomic characterization of human DSPG3.

Genomic characterization of human DSPG3.

http://www.wikidata.org/entity/Q40413664

about

Posterior amorphous corneal dystrophy is associated with a deletion of small leucine-rich proteoglycans on chromosome 12 An evaluation of OPTC and EPYC as candidate genes for high myopia.

P2860

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P2860

Genomic characterization of human DSPG3.

http://www.wikidata.org/entity/Q40413664

description

1999 nî lūn-bûn

@nan

1999年の論文

@ja

1999年論文

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1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

1999年论文

@zh

1999年论文

@zh-cn

name

Genomic characterization of human DSPG3.

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type

label

Genomic characterization of human DSPG3.

@en

prefLabel

Genomic characterization of human DSPG3.

@en

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Genome Research

P1476

Genomic characterization of human DSPG3

@en

P2093

A de la Chapelle

http://www.w3.org/2001/XMLSchema#string

D Hewett-Emmett

http://www.w3.org/2001/XMLSchema#string

J L Dieguez

http://www.w3.org/2001/XMLSchema#string

J T Hecht

http://www.w3.org/2001/XMLSchema#string

M Deere

http://www.w3.org/2001/XMLSchema#string

S J Yoon

http://www.w3.org/2001/XMLSchema#string

P2860

Characterization of human DSPG3, a small dermatan sulfate proteoglycan

Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization

Sex reversal by loss of the C-terminal transactivation domain of human SOX9

The primary structure of a basic leucine-rich repeat protein, PRELP, found in connective tissues

The murine decorin. Complete cDNA cloning, genomic organization, chromosomal assignment, and expression during organogenesis and tissue differentiation

The human lumican gene. Organization, chromosomal location, and expression in articular cartilage

Primary structure of an extracellular matrix proteoglycan core protein deduced from cloned cDNA

The neighbor-joining method: a new method for reconstructing phylogenetic trees

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9

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449-456

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5

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1999-05-01T00:00:00Z

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310783

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