Human MHC architecture and evolution: implications for disease association studies (Q37132341): Difference between revisions

From Wikidata
Jump to navigation Jump to search
Charles Matthews (talk | contribs)
Added reference to claim: main subject (P921): major histocompatibility complex (Q423163), #quickstatements; #temporary_batch_1596524772106
Emijrpbot (talk | contribs)
Changed label, description and/or aliases in fr, pt, da: BOT - Fixing descriptions (3 languages): da, fr, pt
 
(13 intermediate revisions by 5 users not shown)
label / enlabel / en
Human MHC architecture and evolution: implications for disease association studies.
Human MHC architecture and evolution: implications for disease association studies
label / nllabel / nl
Human MHC architecture and evolution: implications for disease association studies.
Human MHC architecture and evolution: implications for disease association studies
label / astlabel / ast
 
Human MHC architecture and evolution: implications for disease association studies
description / frdescription / fr
article scientifique
article scientifique publié en 2008
description / ptdescription / pt
artigo científico
artigo científico (publicado na 2008)
description / dadescription / da
videnskabelig artikel
videnskabelig artikel (udgivet 2008)
description / astdescription / ast
 
artículu científicu espublizáu en 2008
description / bgdescription / bg
 
научна статия
description / bndescription / bn
 
২০০৮-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ
description / eldescription / el
 
επιστημονικό άρθρο
description / eodescription / eo
 
scienca artikolo
description / esdescription / es
 
artículo científico publicado en 2008
description / etdescription / et
 
teaduslik artikkel
description / fadescription / fa
 
مقالهٔ علمی
description / fidescription / fi
 
tieteellinen artikkeli
description / gldescription / gl
 
artigo científico
description / hedescription / he
 
מאמר מדעי
description / hudescription / hu
 
tudományos cikk
description / hydescription / hy
 
գիտական հոդված
description / jadescription / ja
 
2008年の論文
description / kadescription / ka
 
სამეცნიერო სტატია
description / kodescription / ko
 
2008년 논문
description / ltdescription / lt
 
mokslinis straipsnis
description / nandescription / nan
 
2008 nî lūn-bûn
description / nbdescription / nb
 
vitenskapelig artikkel
description / nndescription / nn
 
vitskapeleg artikkel
description / ocdescription / oc
 
article scientific
description / pldescription / pl
 
artykuł naukowy
description / pt-brdescription / pt-br
 
artigo científico (publicado na 2008)
description / rodescription / ro
 
articol științific
description / rudescription / ru
 
научная статья
description / sqdescription / sq
 
artikull shkencor
description / sr-ecdescription / sr-ec
 
научни чланак
description / sr-eldescription / sr-el
 
naučni članak
description / tgdescription / tg
 
мақолаи илмӣ
description / tg-cyrldescription / tg-cyrl
 
мақолаи илмӣ
description / thdescription / th
 
บทความทางวิทยาศาสตร์
description / tldescription / tl
 
artikulong pang-agham
description / urdescription / ur
 
سائنسی مضمون
description / videscription / vi
 
bài báo khoa học
description / wuudescription / wuu
 
2008年学术文章
description / yuedescription / yue
 
2008年學術文章
description / zhdescription / zh
 
2008年學術文章
description / zh-cndescription / zh-cn
 
2008年学术文章
description / zh-hansdescription / zh-hans
 
2008年学术文章
description / zh-hantdescription / zh-hant
 
2008年學術文章
description / zh-hkdescription / zh-hk
 
2008年學術文章
description / zh-modescription / zh-mo
 
2008年學術文章
description / zh-mydescription / zh-my
 
2008年学术文章
description / zh-sgdescription / zh-sg
 
2008年学术文章
description / zh-twdescription / zh-tw
 
2008年學術文章
Property / titleProperty / title
Human MHC architecture and evolution: implications for disease association studies. (English)
Human MHC architecture and evolution: implications for disease association studies (English)
Property / instance of: review article / reference
 
stated in: PubMed
retrieved: 10 September 2020
Timestamp+2020-09-10T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / cites work: The nature of selection on the major histocompatibility complex / reference
 
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1111%2FJ.1744-313X.2008.00765.X
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / cites work
 
Property / cites work: The nature of selection on the major histocompatibility complex / rank
Normal rank
 
Property / cites work: The nature of selection on the major histocompatibility complex / reference
stated in: Crossref
reference URL: https://api.crossref.org/works/10.1111%2FJ.1744-313X.2008.00765.X
retrieved: 21 January 2018
Timestamp+2018-01-21T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
 
Property / main subject: genetic predisposition to disease / reference
 
stated in: PubMed
retrieved: 10 September 2020
Timestamp+2020-09-10T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / cites work
 
Property / cites work: Transferability of tag SNPs in genetic association studies in multiple populations / rank
 
Normal rank
Property / cites work: Transferability of tag SNPs in genetic association studies in multiple populations / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Transcriptional regulation of MICA and MICB: A novel polymorphism in MICB promoter alters transcriptional regulation by Sp1 / rank
 
Normal rank
Property / cites work: Transcriptional regulation of MICA and MICB: A novel polymorphism in MICB promoter alters transcriptional regulation by Sp1 / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Functional characterization of NF- B inhibitor-like protein 1 (NF BIL1), a candidate susceptibility gene for rheumatoid arthritis / rank
 
Normal rank
Property / cites work: Functional characterization of NF- B inhibitor-like protein 1 (NF BIL1), a candidate susceptibility gene for rheumatoid arthritis / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: An integrated epigenetic and genetic approach to common human disease / rank
 
Normal rank
Property / cites work: An integrated epigenetic and genetic approach to common human disease / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Effect of base pair mismatches on recombination via the RecBCD pathway / rank
 
Normal rank
Property / cites work: Effect of base pair mismatches on recombination via the RecBCD pathway / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: WHO warns of microbial threat / rank
 
Normal rank
Property / cites work: WHO warns of microbial threat / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: The origin and spread of the HFE-C282Y haemochromatosis mutation / rank
 
Normal rank
Property / cites work: The origin and spread of the HFE-C282Y haemochromatosis mutation / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Branch site haplotypes that control alternative splicing / rank
 
Normal rank
Property / cites work: Branch site haplotypes that control alternative splicing / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: Characterization of in vivo recombination activities in the mouse embryo / rank
 
Normal rank
Property / cites work: Characterization of in vivo recombination activities in the mouse embryo / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: A high-resolution survey of deletion polymorphism in the human genome / rank
 
Normal rank
Property / cites work: A high-resolution survey of deletion polymorphism in the human genome / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup
Property / cites work
 
Property / cites work: CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions / rank
 
Normal rank
Property / cites work: CYP21A2 mutations in Portuguese patients with congenital adrenal hyperplasia: Identification of two novel mutations and characterization of four different partial gene conversions / reference
 
stated in: PubMed
reference URL: https://pubmed.ncbi.nlm.nih.gov/18397301
retrieved: 12 December 2020
Timestamp+2020-12-12T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0

based on heuristic: inferred from PubMed ID database lookup

Latest revision as of 22:05, 27 March 2024

scientific article published on 08 April 2008
Language Label Description Also known as
English
Human MHC architecture and evolution: implications for disease association studies
scientific article published on 08 April 2008

    Statements

    Human MHC architecture and evolution: implications for disease association studies (English)
    8 April 2008
    1 June 2008
    2 references

    Identifiers