EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis

<p style="text-align:justify;"> <b>Background:</b> Ephrin receptor B2 (EPHB2) has recently been proposed as a novel tumor suppressor gene in colorectal cancer (CRC). Inactivation of the gene has been shown to correlate with progression of colorectal tumorigenesis, and so...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Kokko, A, Laiho, P, Lehtonen, R, Korja, S, Carvajal-Carmona, L, Järvinen, H, Mecklin, J, Eng, C, Schleutker, J, Tomlinson, I, Vahteristo, P, Aaltonen, L
التنسيق:	Journal article
اللغة:	English
منشور في:	BioMed Central 2006

مواد مشابهة

<it>EPHB2 </it>germline variants in patients with colorectal cancer or hyperplastic polyposis
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Structure of the EphB6 receptor ectodomain.
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Prognostic Significance of EPHB2 Expression in Colorectal Cancer Progression
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Hyperplastic candidiases on dorsum of tongue
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Genome-wide allelotyping of 104 Finnish colorectal cancers reveals an excess of allelic imbalance in chromosome 20q in familial cases.
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The type of somatic mutation at APC in familial adenomatous polyposis is determined by the site of the germline mutation: a new facet to Knudson's 'two-hit' hypothesis.
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The differential expression of EphB2 and EphB4 receptor kinases in normal bladder and in transitional cell carcinoma of the bladder.
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Coinheritance of germline mutations in APC and MUTYH genes defines the clinical outcome of adenomatous polyposis syndromes
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A truncated protein product of the germline variant of the DUOX2 gene leads to adenomatous polyposis
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Hyperplastic Cardiac Sarcoma Recurrence
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Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas
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Whole-gene APC deletions cause classical familial adenomatous polyposis, but not attenuated polyposis or "multiple" colorectal adenomas.
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