نتایج جستجو برای: basal core promoter double mutations

تعداد نتایج: 780868  

2018
Yeshambel Belyhun Uwe Gerd Liebert Melanie Maier

BACKGROUND We recently reported complex hepatitis B virus (HBV) drug resistant and concomitant vaccine escape hepatitis B surface antigen (HBsAg) variants during human immunodeficiency virus (HIV) co-infection and antiretroviral therapy (ART) exposure in Ethiopia. As a continuation of this report using the HBV positive sera from the same study participants, the current study further analyzed th...

Journal: :Neuro-oncology 2022

Abstract Mutations in the TERT promoter are single most common non-coding mutation cancer and represent genetic underpinnings of tumor cell immortality. Beyond two point mutations, G228A G250A, which selectively recruit ETS factor GABP to activate TERT, significance other variants unknown. We identified duplications wildtype sequence within core region 7 different types that have strikingly sim...

Journal: :International journal of clinical and experimental pathology 2013
Weihua Li Guangyuan Chen Xianwen Yu Yongying Shi Miaoguan Peng Jianjun Wei

UNLABELLED Hepatitis B virus (HBV) genotype C is associated with the development of hepatocellular carcinoma (HCC). In addition, HBV subgenotype C1 is the major subgenotype in Southern China. The aim of this study was to investigate whether there was the specific mutation patterns in HBV/C1 associated with Southern Chinese patients with HCC. METHODS Mutations in HBV basal core promoter (BCP) ...

2015
Hua Dong Ziliang Qian Lan Zhang Yunqin Chen Zhenggang Ren Qunsheng Ji

Interaction between HBV and host genome integrations in hepatocellular carcinoma (HCC) development is a complex process and the mechanism is still unclear. Here we described in details the quality controls and data mining of aCGH and transcriptome sequencing data on 50 HCC samples from the Chinese patients, published by Dong et al. (2015) (GEO#: GSE65486). In additional to the HBV-MLL4 integrat...

Journal: :The Journal of biological chemistry 2001
T Albert J Wells J O Funk A Pullner E E Raschke G Stelzer M Meisterernst P J Farnham D Eick

The proto-oncogene c-myc is transcribed from a dual promoter P1/P2, with transcription initiation sites 160 base pairs apart. Here we have studied the transcriptional activation of both promoters on chromatin templates. c-myc chromatin was reconstituted on stably transfected, episomal, Epstein-Barr virus-derived vectors in a B cell line. Episomal P1 and P2 promoters showed only basal activity b...

Journal: :Plant physiology 2006
Kanti Kiran Suraiya A Ansari Rakesh Srivastava Niraj Lodhi Chandra Prakash Chaturvedi Samir V Sawant Rakesh Tuli

A prototype 13-bp TATA-box sequence, TCACTATATATAG, was mutated at each nucleotide position and examined for its function in the core promoter. Specific nucleotides in the first TATA, the second TATA, as well as the flanking sequences influenced promoter function in transient transformation of tobacco (Nicotiana tabacum var Petit Havana) leaves. The effect of a given mutation on reporter gene e...

Journal: :The Biochemical journal 2007
Ian Pearse Ying X Zhu Eleanor J Murray Pradeep K Dudeja Krishnamurthy Ramaswamy Jaleh Malakooti

We have previously cloned the human Na+/H+ exchanger NHE2 gene and its promoter region. In the present study, the regulatory elements responsible for the constitutive expression of NHE2 were studied. Transient transfection assays revealed that the -40/+150 promoter region contains the core promoter responsible for the optimal promoter activity. A smaller fragment, -10/+40, containing the TIS (t...

Journal: :Journal of virology 2007
Chaoyang Ye David J Pintel

In contrast to the prototype adeno-associated virus type 2 (AAV2), the capsid gene P41 promoter of AAV5, within viral constructs that lack inverted terminal repeat sequences, displays a high basal level of expression in 293 cells in the absence of coinfecting adenovirus. Here we demonstrate that this was due to differences in the relative strengths of the core promoter elements and to the prese...

Journal: :Journal of Investigative Dermatology 2023

Gorlin syndrome (also known as basal cell nevus syndrome) is a hereditary condition characterized by development of numerous epidermal and follicular tumors. Mutations in theSHH signaling pathway are key drivers this disease. It currently unknown whether SHH mutations non-epidermal types play role phenotypes, the tumor microenvironment, or altered skin development. Through lineage tracing using...

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