نتایج جستجو برای: basal core promoter double mutations

تعداد نتایج: 780868  

ژورنال: یافته 2017

Background : Infertility is a multifactorial disease. Hormonal disorders and genetic factors are important in female infertility. Development and maturation of ovulation are depending on the molecular signaling pathways in response to androgens. Over hundreds of mutations leading to resistance gene function in androgen receptor (AR) has been recorded. One of them is polymorphic region 5'UTR. Th...

F. Haghighi Reza Ghaderi,

Background: The most frequently mutated tumor suppressor gene found in human cancer is p53. In a normal situation, p53 is activated upon the induction of DNA damage to either arrest the cell cycle or to induce apoptosis. However, when mutated, p53 is no longer able to properly accomplish these functions. The aim of this study was to investigate the expression of p53 gene in cases of skin cancer...

Journal: :Antiviral therapy 2010
Karine Lacombe Anders Boyd Joel Gozlan Fabien Lavocat Pierre-Marie Girard Fabien Zoulim

HIV-HBV-coinfected patients require optimal control of viral replication in order to prevent the development of severe comorbidities, such as liver cirrhosis and hepatocellular carcinoma. The genetic diversity of HBV is a poorly investigated factor of such viral replication in HIV-infected hosts. HBV genome diversity can be differentiated into two major aspects: genotypic and phenotypic. Genoty...

Many recent studies have shown that glycosylation patterns of Agaricus bisporus are similar to those of mammalians, so that this organism is a good candidate for the expression of glycosylated pharmaceutical protein. To achieve constant interested gene expression in all cells of the organism, proper promoter isolation is necessary. To isolate this promoter, PCR with specific primers was perform...

2010
K. Lacombe A. Boyd J. Gozlan F. Lavocat PM Girard F Zoulim

HIV-HBV infected patients require optimal control of viral replication in order to prevent severe comorbidities, such as liver cirrhosis and hepatocellular carcinoma. The genetic diversity of HBV is a poorly investigated factor of such viral replication in HIV-infected hosts. HBV genome diversity can be differentiated in two major aspects: genotypic and phenotypic. Genotypic diversity is more r...

Journal: :Cancer letters 2009
Flor Helene Pujol Maria-Cristina Navas Pierre Hainaut Isabelle Chemin

Hepatitis B viruses (HBV) are responsible for over 50% of the worldwide attributable risk of hepatocellular carcinoma (HCC) and this figure increases even further in regions of high endemicity. Systematic sequencing of HBV genomes has identified that this common virus existed as eight distinct genotypes (denoted A-H), each regrouping variants with less than 8% divergence in their DNA sequence. ...

Journal: :Journal of medical virology 2013
Xiaodong Li Yan Liu Zhihui Xu Zhihong Wan Siyu Bai Panyong Mao Yuanli Mao Shaojie Xin Dongping Xu

This study investigated features and clinical implications of HBV mutations in patients with different clinical manifestations. In total, 516 patients were enrolled in this study, including 131 patients with acute hepatitis B, 239 patients with chronic hepatitis B, and 146 patients with acute-on-chronic liver failure. HBV genotypes and mutations were analyzed by direct sequencing of complete vi...

Journal: :Journal of medical virology 2009
Yong Fang Xu Teng Wei-Zhen Xu Di Li Hong-Wei Zhao Li-Juan Fu Feng-Min Zhang Hong-Xi Gu

Occult HBV infection is defined as the persistence of HBV DNA in individuals negative for HBV surface antigen (HBsAg), and many different mechanisms have been reported in different countries. However, in China, one of the endemic areas for HBV infection, no reports have been published on occult HBV infection. The present study investigated the virological features and the mechanism of occult HB...

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