CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study.
about
Signet-ring cell carcinoma of the stomach: Impact on prognosis and specific therapeutic challengeHereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers.Realizing the promise of cancer predisposition genes.Clinical impact of tumour biology in the management of gastroesophageal cancerGenetic screening analysis of patients with hereditary diffuse gastric cancer from northern and northeastern Brazil.A unified analytic framework for prioritization of non-coding variants of uncertain significance in heritable breast and ovarian cancer.Lobular breast cancer: molecular basis, mouse and cellular models.Prospective study of high-risk, BRCA1/2-mutation negative women: the 'negative study'Lobular breast cancer: incidence and genetic and non-genetic risk factors.CDH1 Missense Variant c.1679C>G (p.T560R) Completely Disrupts Normal Splicing through Creation of a Novel 5' Splice Site.Familial Gastric Cancers.Recurrent candidiasis and early-onset gastric cancer in a patient with a genetically defined partial MYD88 defectGermline CDH1 mutations in bilateral lobular carcinoma in situ.E-cadherin germline mutation carriers: clinical management and genetic implications.Testing for Hereditary Breast Cancer: Panel or Targeted Testing? Experience from a Clinical Cancer Genetics Practice.Recognition of and recent issues in hereditary diffuse gastric cancer.CDH1 germline mutations and hereditary lobular breast cancer.Histopathological, Molecular, and Genetic Profile of Hereditary Diffuse Gastric Cancer: Current Knowledge and Challenges for the Future.Hereditary breast and ovarian cancer: new genes in confined pathways.Quantification of mutant E-cadherin using bioimaging analysis of in situ fluorescence microscopy. A new approach to CDH1 missense variants.Alterations of type II classical cadherin, cadherin-10 (CDH10), is associated with pancreatic ductal adenocarcinomas.Epithelial-mesenchymal transition and nuclear β-catenin induced by conditional intestinal disruption of Cdh1 with Apc is E-cadherin EC1 domain dependent.Is there an association between invasive lobular carcinoma of the breast and a family history of gastric cancer?Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing.Complementary molecular approaches reveal heterogeneous CDH1 germline defects in Italian patients with hereditary diffuse gastric cancer (HDGC) syndrome.SSAT State-of-the-Art Conference: Current Surgical Management of Gastric Tumors.Prophylactic total gastrectomy in hereditary diffuse gastric cancer: identification of two novel CDH1 gene mutations-a clinical observational study.Characterizing Metastatic HER2-Positive Gastric Cancer at the CDH1 Haplotype.CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohort.Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility.Merging perspectives: genotype-directed molecular therapy for hereditary diffuse gastric cancer (HDGC) and E-cadherin-EGFR crosstalk.Revisiting breast cancer patients who previously tested negative for BRCA mutations using a 12-gene panel.Germline mutations in hereditary diffuse gastric cancer.
P2860
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P2860
CDH1 germline mutations and the hereditary diffuse gastric and lobular breast cancer syndrome: a multicentre study.
description
2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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2013年学术文章
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2013年学术文章
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@zh-hans
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@zh-my
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@zh-hant
name
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@en
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@nl
type
label
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@en
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@nl
prefLabel
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@en
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@nl
P2093
P2860
P50
P1476
CDH1 germline mutations and th ...... syndrome: a multicentre study.
@en
P2093
Alain Sezeur
Antoine De Pauw
Bruno Buecher
Camille Tlemsani
Catherine Noguès
Chrystelle Colas
David Malka
Diane Molière
Emmanuelle Fourme
Etienne Rouleau
P2860
P304
P356
10.1136/JMEDGENET-2012-101472
P407
P577
2013-05-25T00:00:00Z