(Q41263488)

English

Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1.

scientific article published on 6 May 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

28 September 2017

Hereditary mixed polyposis syndrome is caused by a 40-kb upstream duplication that leads to increased and ectopic expression of the BMP antagonist GREM1. (English)

1 reference

Europe PubMed Central

PMC publication ID

28 September 2017

hereditary mixed polyposis syndrome

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

Annabelle Lewis

object named as

Annabelle Lewis

3

0 references

15

object named as

Ian Tomlinson

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Europe PubMed Central

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28 September 2017

author name string

Emma Jaeger

1

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28 September 2017

Simon Leedham

2

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Europe PubMed Central

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28 September 2017

Stefania Segditsas

4

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Europe PubMed Central

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28 September 2017

Martin Becker

5

1 reference

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28 September 2017

Pedro Rodenas Cuadrado

6

1 reference

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28 September 2017

Hayley Davis

7

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28 September 2017

Kulvinder Kaur

8

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28 September 2017

Karl Heinimann

9

1 reference

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28 September 2017

Kimberley Howarth

10

1 reference

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28 September 2017

HMPS Collaboration

11

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28 September 2017

James East

12

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28 September 2017

Jenny Taylor

13

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28 September 2017

Huw Thomas

14

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28 September 2017

language of work or name

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publication date

6 May 2012

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28 September 2017

Nature Genetics

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28 September 2017

44

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28 September 2017

6

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28 September 2017

699-703

1 reference

Europe PubMed Central

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28 September 2017

https://scigraph.springernature.com/pub.10.1038/ng.2263

0 references

Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Identification of candidate predisposing copy number variants in familial and early-onset colorectal cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

PTEN hamartoma tumor syndrome: an overview

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Putative direct and indirect Wnt targets identified through consistent gene expression changes in APC-mutant intestinal adenomas from humans and mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Sporadic and syndromic hyperplastic polyps and serrated adenomas of the colon: classification, molecular genetics, natural history, and clinical management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Common genetic variants at the CRAC1 (HMPS) locus on chromosome 15q13.3 influence colorectal cancer risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Gene expression patterns of human colon tops and basal crypts and BMP antagonists as intestinal stem cell niche factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Mouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Allelic variation in gene expression is common in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

An ancestral Ashkenazi haplotype at the HMPS/CRAC1 locus on 15q13-q14 is associated with hereditary mixed polyposis syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

1 October 2017

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

14 June 2018

Germline bone morphogenesis protein receptor 1A mutation causes colorectal tumorigenesis in hereditary mixed polyposis syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

19 August 2018

Deciphering the genetics of hereditary non-syndromic colorectal cancer.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

19 August 2018

Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4594751

19 August 2018

Clinical and molecular features of the hereditary mixed polyposis syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG.2263

21 January 2018

15000 unique zebrafish EST clusters and their future use in microarray for profiling gene expression patterns during embryogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG.2263

21 January 2018

Inherited susceptibility to colorectal adenomas and carcinomas: Evidence for a new predisposition gene on 15q14-q22

1 reference

https://api.crossref.org/works/10.1038%2FNG.2263

21 January 2018

Mapping chromatin interactions by chromosome conformation capture

1 reference

https://pubmed.ncbi.nlm.nih.gov/22561515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A robust method for isotopic riboprobe in situ hybridisation to localise mRNAs in routine pathology specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/22561515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bridging the BMP and Wnt pathways by PI3 kinase/Akt and 14-3-3zeta

1 reference

https://pubmed.ncbi.nlm.nih.gov/22561515

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NG.2263

1 reference

Europe PubMed Central

PMC publication ID

28 September 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

28 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

28 September 2017

ResearchGate publication ID

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