Hamartomatous polyposis syndromes. (Q34582357)

3 August 2017

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title

Hamartomatous polyposis syndromes. (English)

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3 August 2017

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2

Charis Eng

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3 August 2017

Kevin M Zbuk

1

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3 August 2017

language of work or name

English

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publication date

1 September 2007

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Nature Reviews Gastroenterology & Hepatology

3 August 2017

published in

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3 August 2017

volume

4

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3 August 2017

issue

9

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3 August 2017

page(s)

492-502

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Highly penetrant hereditary cancer syndromes.

3 August 2017

cites work

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Allelic imbalance at the LKB1 (STK11) locus in tumours from patients with Peutz-Jeghers' syndrome provides evidence for a hamartoma-(adenoma)-carcinoma sequence.

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7 January 2021

Incidence of Peutz-Jeghers syndrome

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7 January 2021

Peutz-Jeghers syndrome: clinicopathology and molecular alterations

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7 January 2021

Peutz-Jeghers syndrome and management recommendations

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7 January 2021

Increased risk of cancer in the Peutz-Jeghers syndrome

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7 January 2021

Very high risk of cancer in familial Peutz-Jeghers syndrome

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Relative frequency and morphology of cancers in STK11 mutation carriers

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Disseminated cervical adenoma malignum and bilateral ovarian sex cord tumors with annular tubules associated with Peutz-Jeghers syndrome

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Sex cord tumor with annular tubules a distinctive ovarian tumor of the Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Double-balloon endoscopy and Peutz-Jeghers syndrome: a new look at an old disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis

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7 January 2021

LKB1-dependent signaling pathways

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Regulation of the TSC pathway by LKB1: evidence of a molecular link between tuberous sclerosis complex and Peutz-Jeghers syndrome

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7 January 2021

Genotype-phenotype correlations in Peutz-Jeghers syndrome

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7 January 2021

Cancer phenomics: RET and PTEN as illustrative models

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7 January 2021

Germline mutations in the PTEN/MMAC1 gene in patients with Cowden disease.

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7 January 2021

Bannayan-Riley-Ruvalcaba syndrome

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7 January 2021

The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

The Cowden syndrome: a clinical and genetic study in 21 patients

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7 January 2021

Cowden's disease with extensive gastrointestinal polyposis

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7 January 2021

GI polyposis and glycogenic acanthosis of the esophagus associated with PTEN mutation positive Cowden syndrome in the absence of cutaneous manifestations

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7 January 2021

Will the real Cowden syndrome please stand up: revised diagnostic criteria

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7 January 2021

Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutation

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7 January 2021

Localization of the Bannayan-Riley-Ruvalcaba syndrome gene to chromosome 10q23.

1 reference

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7 January 2021

Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

High cancer susceptibility and embryonic lethality associated with mutation of the PTEN tumor suppressor gene in mice

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Protean PTEN: form and function

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

PTEN function in normal and neoplastic growth

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Pten is essential for embryonic development and tumour suppression

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Juvenile polyps of the rectum and colon

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Inherited polyposis syndromes: molecular mechanisms, clinicopathology, and genetic testing

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Colorectal neoplasia in juvenile polyposis or juvenile polyps

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

The risk of gastrointestinal carcinoma in familial juvenile polyposis

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7 January 2021

Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Juvenile polyposis: massive gastric polyposis is more common in MADH4 mutation carriers than in BMPR1A mutation carriers

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Malignant potential in intestinal juvenile polyposis syndromes

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

The hamartomatous polyposis syndromes: a clinical and molecular review

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Risk of colorectal cancer in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide high-density single nucleotide polymorphism (SNP) scan and identification of BMPR1A loss of function

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4).

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

From developmental disorder to heritable cancer: it's all in the BMP/TGF-beta family

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Demonstration That Mutation of the Type II Transforming Growth Factor β Receptor Inactivates Its Tumor Suppressor Activity in Replication Error-positive Colon Carcinoma Cells

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Genetic and epigenetic alterations in colon cancer

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

ENG mutations in MADH4/BMPR1A mutation negative patients with juvenile polyposis.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Contiguous gene deletion within chromosome arm 10q is associated with juvenile polyposis of infancy, reflecting cooperation between the BMPR1A and PTEN tumor-suppressor genes

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Del(10)(q22.3q24.1) associated with juvenile polyposis.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Molecular classification of the inherited hamartoma polyposis syndromes: clearing the muddied waters

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

1 reference

7 January 2021

Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

A murine model of hereditary hemorrhagic telangiectasia

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Clinical and molecular features of the hereditary mixed polyposis syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Rapamycin causes regression of astrocytomas in tuberous sclerosis complex

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Targeting mTOR for cancer treatment

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Suppression of Peutz-Jeghers polyposis by inhibition of cyclooxygenase-2.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Characteristics of familial juvenile polyps expressing cyclooxygenase-2.

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

The hamartoma-adenoma-carcinoma sequence

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Adenomatous and carcinomatous changes in hamartomatous polyps of the small intestine (Peutz-Jeghers syndrome): report of a case and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Unusual adenomatous polyps in juvenile polyposis coli

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Mucosal prolapse in the pathogenesis of Peutz-Jeghers polyposis.

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Stem cells, asymmetric division and cancer

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Gastrointestinal Inherited Polyposis Syndromes

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https://api.crossref.org/works/10.1038%2FNCPGASTHEP0902

7 January 2021

Identifiers

DOI

10.1038/NCPGASTHEP0902

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Dimensions Publication ID

3 August 2017

1037702323

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1 reference