PTEN hamartoma tumor syndrome: an overview (Q34996547)

5 August 2017

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title

PTEN hamartoma tumor syndrome: an overview (English)

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5 August 2017

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2

Charis Eng

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5 August 2017

Judith A Hobert

1

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PubMed ID

19668082

5 August 2017

language of work or name

English

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publication date

1 October 2009

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5 August 2017

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5 August 2017

11

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5 August 2017

687-694

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5 August 2017

10

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https://scigraph.springernature.com/pub.10.1097/gim.0b013e3181ac9aea

5 August 2017

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cites work

Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Cancer phenomics: RET and PTEN as illustrative models

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

PTEN hamartoma tumour syndrome: variability of an entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Hamartomatous polyposis syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Cowden's disease. A possible new symptom complex with multiple system involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Male breast cancer in Cowden syndrome patients with germline PTEN mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Protean PTEN: form and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Germline Inactivation of PTEN and Dysregulation of the Phosphoinositol-3-Kinase/Akt Pathway Cause Human Lhermitte-Duclos Disease in Adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

PTEN: one gene, many syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

PTEN mutation in a family with Cowden syndrome and autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Peutz-Jeghers syndrome: clinicopathology and molecular alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Cowden syndrome-diagnostic skin signs

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Efficacy of Bilateral Prophylactic Mastectomy in Women with a Family History of Breast Cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Altered PTEN expression as a diagnostic marker for the earliest endometrial precancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Mutations of the human PTEN gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Nuclear-cytoplasmic partitioning of phosphatase and tensin homologue deleted on chromosome 10 (PTEN) differentially regulates the cell cycle and apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

Molecular Classification of Patients With Unexplained Hamartomatous and Hyperplastic Polyposis

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2FGIM.0B013E3181AC9AEA

10.1097/GIM.0B013E3181AC9AEA

21 January 2018

Identifiers

DOI

1 reference

PubMed ID

19668082

Dimensions Publication ID

5 August 2017

0 references

1 reference

PubMed ID

19668082