Results 21 to 30 of about 18,113 (219)

Gardner syndrome with giant abdominal desmoid tumor during pregnancy: a case report

open access: yesBMC Surgery, 2020
Background Gardner syndrome is a subtype of familial adenomatous polyposis (FAP), characterized by a combination of adenomatous intestinal polyps and extracolonic lesions such as multiple osteomas, dental abnormalities, and soft tissue tumors.
Liquan Jin   +6 more
doaj   +1 more source

Modeling APC mutagenesis and familial adenomatous polyposis using human iPS cells. [PDF]

open access: yesPLoS ONE, 2018
Mutations in the gene Adenomatous Polyposis Coli or APC appear in most sporadic cases of colorectal cancer and it is the most frequent mutation causing hereditary Familial Adenomatous Polyposis.
Cesar A Sommer   +7 more
doaj   +1 more source

The Somatic Mutation Hit on Top of Genetic APC mutations Cause Skin Tumor

open access: yesTranslational Oncology, 2020
Inactivation of the adenomatous polyposis coli (APC) gene is the initiating event in familial adenomatous polyposis (FAP) patients. Up to 90% of FAP patients show intestinal tumorsĀ and other extracolonic malignancies including hepatoblastomas, desmoid ...
Ting Niu   +8 more
doaj   +1 more source

Repurposing the FDA-approved pinworm drug pyrvinium as a novel chemotherapeutic agent for intestinal polyposis. [PDF]

open access: yesPLoS ONE, 2014
Mutations in the WNT-pathway regulator ADENOMATOUS POLYPOSIS COLI (APC) promote aberrant activation of the WNT pathway that is responsible for APC-associated diseases such as Familial Adenomatous Polyposis (FAP) and 85% of spontaneous colorectal cancers (
Bin Li   +13 more
doaj   +1 more source

Peutz-Jeghers Syndrome without Polyposis

open access: yesCanadian Journal of Gastroenterology, 1988
Peutz-Jeghers syndrome is generally considered a condition in which familial gastrointestinal polyposis is associated with a characteristic pigmentation of the skin and mucous membranes Two members of a family in which the characteristic pigmentation was
Anthony G. Catto-Smith   +2 more
doaj   +1 more source

Colonic Polyps in Children and Adolescents

open access: yesCanadian Journal of Gastroenterology, 2007
Colonic polyps most commonly present with rectal bleeding in children. The isolated juvenile polyp is the most frequent kind of polyp identified in children.
Carol A Durno
doaj   +1 more source

Altered Interactions between the Gut Microbiome and Colonic Mucosa Precede Polyposis in APCMin/+ Mice. [PDF]

open access: yesPLoS ONE, 2015
Mutation of the adenomatous polyposis coli (APC gene), an early event in the adenoma-carcinoma sequence, is present in 70-80% of sporadic human colorectal adenomas and carcinomas.
Joshua S Son   +12 more
doaj   +1 more source

Rofecoxib and cardiovascular adverse events in adjuvant treatment of colorectal cancer [PDF]

open access: yes, 2007
Background Selective cyclooxygenase inhibitors may retard the progression of cancer, but they have enhanced thrombotic potential. We report on cardiovascular adverse events in patients receiving rofecoxib to reduce rates of recurrence of colorectal ...
Christopher C. McConkey   +36 more
core   +1 more source

Serrated Polyposis Syndrome with a Synchronous Colon Adenocarcinoma Treated by an Endoscopic Mucosal Resection

open access: yesThe Korean Journal of Gastroenterology, 2020
Serrated polyposis syndrome (SPS) can transform to malignant lesions through the sessile serrated pathway and traditional serrated pathway. These pathways may cause rapid neoplastic progression compared to the adenoma-carcinoma sequence, which may cause ...
Sang Hoon Lee   +6 more
doaj   +1 more source

A targeted constitutive mutation in the APC tumor suppressor gene underlies mammary but not intestinal tumorigenesis. [PDF]

open access: yesPLoS Genetics, 2009
Germline mutations in the adenomatous polyposis coli (APC) gene are responsible for familial adenomatous polyposis (FAP), an autosomal dominant hereditary predisposition to the development of multiple colorectal adenomas and of a broad spectrum of extra ...
Claudia Gaspar   +6 more
doaj   +1 more source

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