Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

about

Research progress on human genes involved in the pathogenesis of glaucoma (Review).

P2860

Q54977773-AA239D40-0879-4031-B3D1-32A6F422D8A2

P2860

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

Item

http://www.wikidata.org/entity/Q38723042

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

@en

type

Item

label

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

@en

prefLabel

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

@en

P1476

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

@en

P2093

Asha L Mettla

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

Goutham Pyatla

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

Inderjeet Kaur

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

Konegari Shekhar

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

Meha Kabra

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

Muralidhar Ramappa

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

Rohit C Khanna

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

Seema Banerjee

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

Sirisha Senthil

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

Sonika Rathi

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

P2860

Specificity determinants of CYP1B1 estradiol hydroxylation

A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

Digenic inheritance of early-onset glaucoma: CYP1B1, a potential modifier gene

Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma

Analysis of protein-coding genetic variation in 60,706 humans

Haploview: analysis and visualization of LD and haplotype maps

A lymphatic defect causes ocular hypertension and glaucoma in mice

Molecular genetics of primary congenital glaucoma.

Schlemm's canal: more than meets the eye, lymphatics in disguise

P2888

s00439-017-1823-6

P304

941-949

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

P31

scholarly article

P356

10.1007/S00439-017-1823-6

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

P433

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

P478

136

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

P50

Anil Kumar Mandal

Hemant Khanna

P577

2017-06-15T00:00:00Z

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

P6179

1086043233

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

P698

28620713

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

P932

5953556

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

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

about

P2860

P2860

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P6179

P698

P932