(Q28203387)

https://api.crossref.org/works/10.1002%2FHUMU.10257

Frequent loss of PTEN expression is linked to elevated phosphorylated Akt levels, but not associated with p27 and cyclin D1 expression, in primary epithelial ovarian carcinomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

Immunohistochemical evidence of loss of PTEN expression in primary ductal adenocarcinomas of the breast

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

Mutation and expression analyses reveal differential subcellular compartmentalization of PTEN in endocrine pancreatic tumors compared to normal islet cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

Mutation analysis of the PTEN / MMAC1 gene in Japanese patients with Cowden disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

Epigenetic PTEN silencing in malignant melanomas without PTEN mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

PTEN mutational spectra, expression levels, and subcellular localization in microsatellite stable and unstable colorectal cancers

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

Balanced translocation of 10q and13q, including the PTEN gene, in a boy with a human chorionic gonadotropin-secreting tumor and the Bannayan-Riley-Ruvalcaba syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN mutations are uncommon in Proteus syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Mutations of the human PTEN gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Allelic loss of chromosome 10q23 is associated with tumor progression in breast carcinomas.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN expression is reduced in a subset of sporadic thyroid carcinomas: evidence that PTEN-growth suppressing activity in thyroid cancer cells mediated by p27kip1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Absence of germline mutations in MINPP1, a phosphatase encoding gene centromeric of PTEN, in patients with Cowden and Bannayan-Riley-Ruvalcaba syndrome without germline PTEN mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Novel germline mutations in the PTEN tumour suppressor gene found in women with multiple cancers

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Pten is essential for embryonic development and tumour suppression

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Impaired Fas response and autoimmunity in Pten+/- mice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN mutations in gliomas and glioneuronal tumors.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

RET proto-oncogene in the development of human cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.10257

1 reference

7 January 2021

Interpreting epidemiological research: blinded comparison of methods used to estimate the prevalence of inherited mutations in BRCA1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Male breast cancer in Cowden syndrome patients with germline PTEN mutations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Analysis of the 10q23 chromosomal region and the PTEN gene in human sporadic breast carcinoma.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Growth suppression of glioma cells by PTEN requires a functional phosphatase catalytic domain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

The tumor-suppressor activity of PTEN is regulated by its carboxyl-terminal region

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Bannayan-Riley-Ruvalcaba syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Tumor suppressor PTEN inhibits integrin- and growth factor-mediated mitogen-activated protein (MAP) kinase signaling pathways

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Protein kinase B (PKB/Akt) activity is elevated in glioblastoma cells due to mutation of the tumor suppressor PTEN/MMAC.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Somatic mutations of the PTEN tumor suppressor gene in sporadic follicular thyroid tumors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

https://api.crossref.org/works/10.1002%2FHUMU.10257

1 reference

7 January 2021

Novel germline mutation of the PTEN gene in a Japanese family with Cowden disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

A gene for familial juvenile polyposis maps to chromosome 18q21.1.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Mutations in the SMAD4/DPC4 gene in juvenile polyposis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN1 is frequently mutated in primary endometrial carcinomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

A novel PTEN mutation in a Japanese patient with Cowden disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Variant manifestation of Cowden disease in Japan: hamartomatous polyposis of the digestive tract with mutation of the PTEN gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Genetic model of multi-step breast carcinogenesis involving the epithelium and stroma: clues to tumour-microenvironment interactions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomas

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Crystal structure of the PTEN tumor suppressor: implications for its phosphoinositide phosphatase activity and membrane association

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN/MMAC1/TEP1 suppresses the tumorigenicity and induces G1 cell cycle arrest in human glioblastoma cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Inherited mutations in PTEN that are associated with breast cancer, cowden disease, and juvenile polyposis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

The tumor suppressor, PTEN/MMAC1, dephosphorylates the lipid second messenger, phosphatidylinositol 3,4,5-trisphosphate

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Cowden syndrome (multiple hamartoma syndrome).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline mutations in PTEN are present in Bannayan-Zonana syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline PTEN mutations in Cowden syndrome-like families.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN: sometimes taking it off can be better than putting it on.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

The lipid phosphatase activity of PTEN is critical for its tumor supressor function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Localization of the gene for Cowden disease to chromosome 10q22–23

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Enhanced sensitivity of PTEN-deficient tumors to inhibition of FRAP/mTOR.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN germ-line mutations in juvenile polyposis coli

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Mutation of Pten/Mmac1 in mice causes neoplasia in multiple organ systems

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

C2-domains, structure and function of a universal Ca2+-binding domain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Clinical and pathological features of breast disease in Cowden's syndrome: an underrecognized syndrome with an increased risk of breast cancer

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN expression causes feedback upregulation of insulin receptor substrate 2

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline mutation of the tumour suppressor PTEN in Proteus syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN modulates cell cycle progression and cell survival by regulating phosphatidylinositol 3,4,5,-trisphosphate and Akt/protein kinase B signaling pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Inhibition of cell migration, spreading, and focal adhesions by tumor suppressor PTEN

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN interactions with focal adhesion kinase and suppression of the extracellular matrix-dependent phosphatidylinositol 3-kinase/Akt cell survival pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Activation of a cryptic splice site of PTEN and loss of heterozygosity in benign skin lesions in Cowden disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

The role of MMAC1 mutations in early-onset breast cancer: causative in association with Cowden syndrome and excluded in BRCA1-negative cases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

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/10.1002%2FHUMU.10257

7 January 2021

Phosphorylation of the PTEN tail regulates protein stability and function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Protean PTEN: form and function

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

BMP2 exposure results in decreased PTEN protein degradation and increased PTEN levels

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Identification of a PTEN mutation in a family with Cowden syndrome and Bannayan-Zonana syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN coordinates G(1) arrest by down-regulating cyclin D1 via its protein phosphatase activity and up-regulating p27 via its lipid phosphatase activity in a breast cancer model

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN induces apoptosis and cell cycle arrest through phosphoinositol-3-kinase/Akt-dependent and -independent pathways

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Transient ectopic expression of PTEN in thyroid cancer cell lines induces cell cycle arrest and cell type-dependent cell death

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN inhibits insulin-stimulated MEK/MAPK activation and cell growth by blocking IRS-1 phosphorylation and IRS-1/Grb-2/Sos complex formation in a breast cancer model

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

PTEN blocks insulin-mediated ETS-2 phosphorylation through MAP kinase, independently of the phosphoinositide 3-kinase pathway

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Nuclear PTEN expression and clinicopathologic features in a population-based series of primary cutaneous melanoma

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Mutational analysis of the PTEN gene in gliomas: molecular and pathological correlations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Distinct PTEN mutational spectra in hereditary non-polyposis colon cancer syndrome-related endometrial carcinomas compared to sporadic microsatellite unstable tumors.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10257

7 January 2021

Identifiers

DOI

10.1002/HUMU.10257

1 reference

Consolidated OpenCitations Corpus – April 2017

3384796

3384796

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference