A gene for familial juvenile polyposis maps to chromosome 18q21.1. - Test2 - elhamkhani - TriplyDB

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

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

http://www.wikidata.org/entity/Q34385458

about

Germline mutations in SMAD4 disrupt bone morphogenetic protein signaling Protean PTEN: form and function Hamartomatous polyposis syndromes Gastrointestinal tract cancers: Genetics, heritability and germ line mutations Mutational spectra of PTEN/MMAC1 gene: a tumor suppressor with lipid phosphatase activity.Clinical challenges in management of familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer.Hereditary hamartomatous polyposis syndromes: understanding the disease risks as children reach adulthood.A review of juvenile polyposis syndrome.Juvenile polyposis syndrome.Genetic profiling of colon cancer.Identification of the modifier of Min 2 (Mom2) locus, a new mutation that influences Apc-induced intestinal neoplasia.Analysis of genetic and phenotypic heterogeneity in juvenile polyposis.Juvenile polyposis and other intestinal polyposis syndromes with microdeletions of chromosome 10q22-23 Common deletion of SMAD4 in juvenile polyposis is a mutational hotspot.Mutation screening in juvenile polyposis syndrome Cellular and molecular regulation of hematopoietic and intestinal stem cell behavior.The real face of juvenile polyposis syndrome ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes A family with two consecutive nonsense mutations in BMPR1A causing juvenile polyposis.Immunohistochemical labeling for dpc4 mirrors genetic status in pancreatic adenocarcinomas : a new marker of DPC4 inactivation.Haploid loss of the tumor suppressor Smad4/Dpc4 initiates gastric polyposis and cancer in mice.Massive Gastric Juvenile Polyposis: A Clinicopathologic Study Using SMAD4 Immunohistochemistry.Common structural features characterize interstitial intrachromosomal Xp and 18q triplications.[Colorectal polyposis syndrome: a guide to diagnosis].Café au lait macules and juvénile polyps.Nuclear accumulation of beta-catenin occurs commonly in the epithelial cells of juvenile polyps.

P2860

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P2860

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

http://www.wikidata.org/entity/Q34385458

description

1998 nî lūn-bûn

@nan

1998 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի մայիսին հրատարակված գիտական հոդված

@hy

1998年の論文

@ja

1998年論文

@yue

1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

@zh-tw

1998年论文

@wuu

name

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

@ast

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

@en

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

@nl

type

label

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

@ast

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

@en

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

@nl

prefLabel

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

@ast

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

@en

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

@nl

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American Journal of Human Genetics

P1476

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

@en

P2093

Mitros FA

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Nishimura DY

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Ringold JC

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Summers RW

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P2860

Deleted in Colorectal Cancer (DCC) encodes a netrin receptor

MADR2 maps to 18q21 and encodes a TGFbeta-regulated MAD-related protein that is functionally mutated in colorectal carcinoma

A simple salting out procedure for extracting DNA from human nucleated cells

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

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

The DCC gene: structural analysis and mutations in colorectal carcinomas

Identification of a chromosome 18q gene that is altered in colorectal cancers

Genetic alterations during colorectal-tumor development

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

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

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1129-1136

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scholarly article

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10.1086/301840

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