PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes. - Wikidata - wikimedia - TriplyDB

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

http://www.wikidata.org/entity/Q36008552

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Somatic mosaic activating mutations in PIK3CA cause CLOVES syndrome Type I to type II ovarian carcinoma progression: mutant Trp53 or Pik3ca confers a more aggressive tumor phenotype in a mouse model of ovarian cancer.Genodermatosis Affecting the Skin and Mucosa of the Head and Neck: Clinicopathologic, Genetic, and Molecular Aspect--PTEN-Hamartoma Tumor Syndrome/Cowden Syndrome.When Overgrowth Bumps Into Cancer: The PTEN-Opathies.Magnetic resonance imaging of pediatric soft-tissue vascular anomalies.Fat-containing soft-tissue masses in children.Mosaic Disorders of the PI3K/PTEN/AKT/TSC/mTORC1 Signaling Pathway.An Overview of Autosomal Dominant Tumour Syndromes with Prominent Features in the Oral and Maxillofacial Region.A rare presentation: A case report of osseous metaplasia and mature bone formation in a follicular adenoma of the thyroid.Lethal outcomes in Klippel-Trenaunay syndrome.Appendiceal hamartoma resembling PHTS of soft tissue in a patient with Cowden syndrome.PTEN hamartoma of the soft tissue: the initial manifestation of an underlying PTEN hamartoma tumor syndrome in a 4-year-old female.Classification of Vascular Anomalies: An Update.Clinical and sonographic features of pediatric soft-tissue vascular anomalies part 2: vascular malformations.New Treatment Approaches to Arteriovenous Malformations.Angioarchitecture of Hereditary Arteriovenous Malformations.When overgrowth bumps into cancer: the PTEN-opathies.Assessment of PTEN-associated vascular malformations in a patient with Bannayan-Riley-Ruvalcaba syndrome.The categories of cutaneous mosaicism: A proposed classification.Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome.Hamartoma-like lesions in the mouse retina: an animal model of Pten hamartoma tumour syndrome.

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P2860

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

http://www.wikidata.org/entity/Q36008552

description

2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

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2012年論文

@zh-tw

2012年论文

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2012年论文

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2012年论文

@zh-cn

name

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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type

label

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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prefLabel

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

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PAS.0B013E31824DD86C

P1433

The American Journal of Surgical Pathology

P1476

PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.

@en

P2093

Ahmad I Alomari

http://www.w3.org/2001/XMLSchema#string

Antonio R Perez-Atayde

http://www.w3.org/2001/XMLSchema#string

Cameron C Trenor

http://www.w3.org/2001/XMLSchema#string

Charis Eng

http://www.w3.org/2001/XMLSchema#string

David J Harris

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Emily Howard

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Harry P W Kozakewich

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John B Mulliken

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Joseph Upton

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Kim Chalache

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P2860

The PTEN/PI3K pathway governs normal vascular development and tumor angiogenesis

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

A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands

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

Loss of PTEN facilitates HIF-1-mediated gene expression

Venous malformations of skeletal muscle

Lipomatosis, angiomatosis, and macrencephalia. A previously undescribed congenital syndrome

The biology and clinical relevance of the PTEN tumor suppressor pathway

Bannayan-Zonana syndrome: a rare autosomal dominant syndrome with multiple lipomas and hemangiomas: a case report and review of literature

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

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671-687

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10.1097/PAS.0B013E31824DD86C

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