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The SPINK gene family and celiac disease susceptibility
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title
The SPINK gene family and celiac disease susceptibility
(English)
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author
Cisca Wijmenga
series ordinal
9
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Jos Poell
object named as
Jos Poell
series ordinal
3
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author name string
Martin C Wapenaar
series ordinal
1
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Alienke J Monsuur
series ordinal
2
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Ruben van 't Slot
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4
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Jos W R Meijer
series ordinal
5
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Gerrit A Meijer
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6
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Chris J Mulder
series ordinal
7
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Maria Luisa Mearin
series ordinal
8
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language of work or name
English
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publication date
May 2007
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published in
Immunogenetics
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volume
59
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issue
5
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page(s)
349-57
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exact match
https://scigraph.springernature.com/pub.10.1007/s00251-007-0199-5
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cites work
LEKTI, a novel 15-domain type of human serine proteinase inhibitor
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
Haploview: analysis and visualization of LD and haplotype maps
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
Myosin IXB variant increases the risk of celiac disease and points toward a primary intestinal barrier defect
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
A major non-HLA locus in celiac disease maps to chromosome 19
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
SPINK1 mutations are associated with multiple phenotypes
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
Netherton syndrome: disease expression and spectrum of SPINK5 mutations in 21 families
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
7 April 2017
Pathomechanisms in celiac disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Genetics in coeliac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Genetics of Crohn disease, an archetypal inflammatory barrier disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Gliadin as a stimulator of innate responses in celiac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
The role of genetics in the development of asthma and atopy
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
The interface between innate and adaptive immunity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Commensal bacteria (normal microflora), mucosal immunity and chronic inflammatory and autoimmune diseases.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Gene expression patterns associated with infertility in humans and rodent models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Meta and pooled analysis of European coeliac disease data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Coeliac disease: dissecting a complex inflammatory disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
The evolution and genetics of innate immunity
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Genome search in celiac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Isolation and characterization of a 60-residue intestinal peptide structurally related to the pancreatic secretory type of trypsin inhibitor: influence on insulin secretion
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 September 2017
Molecular cloning of PEC-60 and expression of its mRNA and peptide in the gastrointestinal tract and immune system
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
30 May 2018
Gut microflora associated characteristics in children with celiac disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Polymorphisms in SPINK5 are not associated with asthma in a Dutch population
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Chromosome 5q candidate genes in coeliac disease: genetic variation at IL4, IL5, IL9, IL13, IL17B and NR3C1.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Lethal, neonatal ichthyosis with increased proteolytic processing of filaggrin in a mouse model of Netherton syndrome
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
A direct role for NKG2D/MICA interaction in villous atrophy during celiac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Coordinated induction by IL15 of a TCR-independent NKG2D signaling pathway converts CTL into lymphokine-activated killer cells in celiac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
The interferon gamma gene in celiac disease: augmented expression correlates with tissue damage but no evidence for genetic susceptibility.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Presence of bacteria and innate immunity of intestinal epithelium in childhood celiac disease.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Identification of the bioactive peptide PEC-60 in brain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1914236
retrieved
28 November 2018
Coeliac disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17333166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Saturation of the 5q31-q33 Candidate Region for Coeliac Disease
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/17333166
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
A major non-HLA locus in celiac disease maps to chromosome 191 1This study is dedicated to the memory of Lodewijk Sandkuijl (1953–2002), who died shortly after its completion. He was an inspiration to us and was a world expert on biostatistics
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1007%2FS00251-007-0199-5
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1007%2FS00251-007-0199-5
retrieved
7 January 2021
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Identifiers
DOI
10.1007/S00251-007-0199-5
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2458705
Dimensions Publication ID
1029447549
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OpenCitations bibliographic resource ID
2458705
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2458705
PMCID
1914236
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2458705
PubMed ID
17333166
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
2458705
ResearchGate publication ID
27706401
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