No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

about

Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.A follow-up study of chromosome 19q13 in multiple sclerosis susceptibility TREM2 in Neurodegenerative Diseases.

P2860

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P2860

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

Item

http://www.wikidata.org/entity/Q37192694

description

2008 nî lūn-bûn

@nan

2008年の論文

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2008年学术文章

@wuu

2008年学术文章

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2008年学术文章

@zh-hans

2008年学术文章

@zh-my

2008年学术文章

@zh-sg

2008年學術文章

@yue

2008年學術文章

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2008年學術文章

@zh-hant

name

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

@en

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.

@nl

type

Item

label

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

@en

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.

@nl

prefLabel

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

@en

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL.

@nl

P1476

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

@en

P2093

Anna-Maija Sulonen

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

Irina Elovaara

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

Janna Saarela

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

Keijo Koivisto

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

Mauri Reunanen

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

Minna Suvela

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

Pekka Ellonen

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

Pentti J Tienari

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

Suvi P Kallio

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

Tuula Pirttilä

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

P2860

Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype

Haploview: analysis and visualization of LD and haplotype maps

Osteopetrosis and thalamic hypomyelinosis with synaptic degeneration in DAP12-deficient mice

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

Risk alleles for multiple sclerosis identified by a genomewide study

Easy calculations of lod scores and genetic risks on small computers

Faster sequential genetic linkage computations

TREM2-transduced myeloid precursors mediate nervous tissue debris clearance and facilitate recovery in an animal model of multiple sclerosis.

Loss-of-function mutations in TYROBP (DAP12) result in a presenile dementia with bone cysts.

Brain and bone damage in KARAP/DAP12 loss-of-function mice correlate with alterations in microglia and osteoclast lineages.

P304

86-90

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scholarly article

P356

10.1016/J.JNEUROIM.2008.10.005

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P433

1-2

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P478

206

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P50

Leena Peltonen-Palotie

Aarno Palotie

P577

2008-11-18T00:00:00Z

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P5875

23483540

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19019460

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P932

2682253

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No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

about

P2860

P2860

No evidence for shared etiology in two demyelinative disorders, MS and PLOSL

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P932