Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

about

Emerging Putative Associations between Non-Coding RNAs and Protein-Coding Genes in Neuropathic Pain: Added Value from Reusing Microarray Data Comparative proteome analysis for identification of differentially abundant proteins in SIDS.

P2860

Q31140441-62A0C12F-20D6-49B6-8294-A950066042CD Q48110984-3EFC662E-1288-40D7-A676-7DDDCB3170EB

P2860

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

Item

http://www.wikidata.org/entity/Q50861155

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年学术文章

@wuu

2013年学术文章

@zh-cn

2013年学术文章

@zh-hans

2013年学术文章

@zh-my

2013年学术文章

@zh-sg

2013年學術文章

@yue

2013年學術文章

@zh

2013年學術文章

@zh-hant

name

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@en

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@nl

type

Item

label

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@en

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@nl

prefLabel

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@en

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@nl

P1476

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

@en

P2860

Human heat shock protein gene polymorphisms and sudden infant death syndrome

Body temperature changes before minor illness in infants.

Epidemiology of babies dying at different ages from the sudden infant death syndrome.

Factors affecting rectal temperature in infancy.

Sudden infant death syndrome: overview and update.

Combined effect of infection and heavy wrapping on the risk of sudden unexpected infant death.

The brainstem and serotonin in the sudden infant death syndrome.

Mitochondrial hsp60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.

Brainstem mechanisms underlying the sudden infant death syndrome: evidence from human pathologic studies.

Gene variants predisposing to SIDS: current knowledge.

P2888

pr.2013.112

P304

380-383

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

P31

scholarly article

P356

10.1038/PR.2013.112

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

P407

English

P433

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

P478

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

P50

Cornelius Courts

Burkhard Madea

Melanie Grabmüller

P577

2013-07-03T00:00:00Z

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

P5875

245027592

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

P698

23823174

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

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

about

P2860

P2860

Functional single-nucleotide variant of HSPD1 in sudden infant death syndrome.

description

name

type

label

prefLabel

P1433

P1476

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P356

P1433

P1476

P2860

P2888

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698