نتایج جستجو برای: ژن tp63
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PURPOSE Lacrimo-auriculo-dento-digital (LADD) syndrome is an autosomal dominant disorder displaying variable expression of multiple congenital anomalies including hypoplasia or aplasia of the lacrimal and salivary systems causing abnormal tearing and dry mouth. Mutations in the FGF10, FGFR2, and FGFR3 genes were found to cause some cases of LADD syndrome in prior genetic studies. The goal of th...
Recently, the landscape of single base mutations in diffuse large B-cell lymphoma (DLBCL) was described. Here we report the discovery of a gene fusion between TBL1XR1 and TP63, the only recurrent somatic novel gene fusion identified in our analysis of transcriptome data from 96 DLBCL cases. Based on this cohort and a further 157 DLBCL cases analyzed by FISH, the incidence in de novo germinal ce...
سابقه و هدف : ژن tp63، بعنوان قدیمی ترین همولوگ tp53، دو واریانت n-ترمینالی اصلی را بوسیله ی پروموتور های مختلف کد می کند : واریانت tap63 با فعالیت سرکوبگری تومور و δnp63 با فعالیت انکوژنی. در اثر حذف اگزون شماره ی 4 هر یک از واریانت های مذکور، دو واریانت n-ترمینالی دیگر نیز در دهه ی گذشته برای p63 گزارش شد :d4tap63 و δnp73l ، اما همچنان عملکرد دقیق این واریانت ها در سلول های سالم و توموری مشخص...
BACKGROUND Germline apoptosis-related single nucleotide polymorphisms (SNPs) have been shown to contribute to the risk of developing non-small cell lung cancer (NSCLC). However, very few studies have looked specifically at apoptosis-related SNPs in a racially-stratified analysis of white and African-American women. METHODS We examined the risk of developing NSCLC associated with 98 germline S...
سابقه و هدف : ژن TP63، بعنوان قدیمی‌ترین همولوگ TP53، دو واریانت N-ترمینالی اصلی را بوسیله‌ی پروموتور‌های مختلف کد می‌کند : واریانت TAp63 با فعالیت سرکوبگری تومور و ΔNp63 با فعالیت انکوژنی. در اثر حذف اگزون شماره‌ی 4 هر یک از واریانت‌های مذکور، دو واریانت N-ترمینالی دیگر نیز در دهه‌ی گذشته برای p63 گزارش شد :d4TAp63 و ΔNp73L ، اما همچنان عملکرد دقیق این واریانت‌ها در سلول‌های سالم و توموری مشخ...
Lung carcinoma development is accompanied by field changes that may have diagnostic significance. We have previously shown the importance of chromosomal aneusomy in lung cancer progression. Here, we tested whether genomic gains in six specific loci, TP63 on 3q28, EGFR on 7p12, MYC on 8q24, 5p15.2, and centromeric regions for chromosomes 3 (CEP3) and 6 (CEP6), may provide further value in the pr...
BACKGROUND Chagas' disease is a human tropical parasitic illness and a subset of the chronic patients develop megaesophagus or megacolon. The esophagus dilation is known as chagasic megaesophagus (CM) and one of the severe late consequences of CM is the increased risk for esophageal carcinoma (ESCC). Based on the association between CM and ESCC, we investigated whether genes frequently showing ...
Non-coding microRNAs are involved in multiple regulatory mechanisms underlying response of cancer cells to stress leading to apoptosis, cell cycle arrest and autophagy. Many molecular layers are implicated in such cellular response including epigenetic regulation of transcription, RNA processing, metabolism, signaling. The molecular interrelationship between tumor protein (TP)-p53 family member...
Peripheral T-cell lymphomas (PTCLs) are aggressive malignancies of mature T lymphocytes with 5-year overall survival rates of only ∼ 35%. Improvement in outcomes has been stymied by poor understanding of the genetics and molecular pathogenesis of PTCL, with a resulting paucity of molecular targets for therapy. We developed bioinformatic tools to identify chromosomal rearrangements using genome-...
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