نتایج جستجو برای: cancer causing genes

تعداد نتایج: 1370181  

Journal: :Current Neurology and Neuroscience Reports 2017

Journal: :middle east journal of cancer 0
mozhgan rasti department of biochemistry, medical school, shiraz university of medical sciences, shiraz, iran rita arabsolghar department of biochemistry, medical school, shiraz university of medical sciences, shiraz, iran sajad azmand pharmaceutical science research center, shiraz university of medical sciences, shiraz, iran

background :many breast cancer tumor suppressor genes have been reported to undergo hypermethylation, including er, rassf1a, hic, cdh1, gspt1, apc, twist and ccnd2. we first determined the promoter methylation of the above eight tumor suppressor genes as epigenetic markers of breast cancer in three cell lines with different er status. methods : this study was an experimental study performed on ...

Journal: :Current medicinal chemistry 2010
Y Li T O Tollefsbol

It is well established that aberrant gene regulation by epigenetic mechanisms can develop as a result of pathological processes such as cancer. Methylation of CpG islands is an important component of the epigenetic code and a number of genes become abnormally methylated during tumorigenesis. Some bioactive food components have been shown to have cancer inhibition activities by reducing DNA hype...

Objective(s): Amyotrophic lateral sclerosis (ALS), a fatal progressive neurodegenerative disorder, is the most common motor neuron disease in European populations. Approximately 10% of ALS cases are familial (FALS) and the other patients are considered as sporadic ALS (SALS). Among many ALS causing genes that have been identified, mutations in SOD1 and C9orf72 are the most common genetic causes...

2012
Anna Noatynska Monica Gotta Patrick Meraldi

Correct alignment of the mitotic spindle during cell division is crucial for cell fate determination, tissue organization, and development. Mutations causing brain diseases and cancer in humans and mice have been associated with spindle orientation defects. These defects are thought to lead to an imbalance between symmetric and asymmetric divisions, causing reduced or excessive cell proliferati...

2012
Barbara Wappenschmidt Alexandra A. Becker Jan Hauke Ute Weber Stefanie Engert Juliane Köhler Karin Kast Norbert Arnold Kerstin Rhiem Eric Hahnen Alfons Meindl Rita K. Schmutzler

Screening for pathogenic mutations in breast and ovarian cancer genes such as BRCA1/2, CHEK2 and RAD51C is common practice for individuals from high-risk families. However, test results may be ambiguous due to the presence of unclassified variants (UCV) in the concurrent absence of clearly cancer-predisposing mutations. Especially the presence of intronic or exonic variants within these genes t...

Journal: :Biomedical Research and Therapy 2021

Triclosan (TCS) is present in toothpaste and other cosmetic products as an antibacterial anti-fungal agent. This manuscript highlights that TCS a potential oxidative stress-causing agent, estrogenic, mutagenic, cancer-causing genotoxic agent products. study also summarizes the therapeutic approach to overcome all of harmful effects. It popular current topic, new research needed find alternative...

Introduction: The imbalance of the microbial ecosystem causes biological changes associated with colorectal cancer and cell proliferation and their planned death, as well as the immune responses. The aim of this study was to determine the effect of probiotic bacteria on the expression of genes associated with growth, metastasis and apoptosis in cancer cells of the HT29 colon.   Materials & Me...

Rastgar Jazii

Gastric Cancer (GC) is the second most common cancer in the world and a leading cause of cancer-related mortality. Methylation of promoter CpG islands (CGIs) belonging to tumor suppressor genes causes transcriptional silencing of their corresponding genes leading to carcinogenesis and other disorders. Adenomatous Polyposis Coli (APC) a tumor suppressor gene is inactivated by methylation of prom...

Journal: :The New England journal of medicine 2000
P Lichtenstein N V Holm P K Verkasalo A Iliadou J Kaprio M Koskenvuo E Pukkala A Skytthe K Hemminki

BACKGROUND The contribution of hereditary factors to the causation of sporadic cancer is unclear. Studies of twins make it possible to estimate the overall contribution of inherited genes to the development of malignant diseases. METHODS We combined data on 44,788 pairs of twins listed in the Swedish, Danish, and Finnish twin registries in order to assess the risks of cancer at 28 anatomical ...

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