نتایج جستجو برای: ژن p15ink4b

تعداد نتایج: 15970  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه سیستان و بلوچستان - دانشکده علوم پایه 1391

معرفی: بیماری ناخنک چشم ، یک بافت پارانشیمی رگدار، در سطح چشم است ، که به صورت پیش رونده رشد کرده و گاهی بینایی را تهدید می نماید.دلایل بوجود آورنده این ضایعه هنوز به صورت واضح روشن نشده است.شواهد اخیر حاکی از آن است که ، این ضایعه بیشتر میتواند نوعی ایجاد بافت جدید باشد تا آسیب بافتی ، که در اثر اشعه uvموجود در نور خورشید بوجود می آید.مطالعه حاضر ، رابطه متیلاسیون پروموتور ژنهای p14 arf و p15i...

Amir Atashi Fatemeh Skandari Mehdi Azad Mehrdad Noruzinia, Mohammad Hosein Ahmadi Mohammad Shahjahani Naser Mobarra, Saeid Abroun Saeid Kaviani Shaban Alizadeh, Yousef Mortazavi, Zahra Zonoubi

  Objective(s): Stem cell differentiation into different cell lineages depends upon several factors, cell cycle control elements and intracellular signaling elements, including P15INK4b and P16INK4a genes. Epigenetics may be regarded as a control mechanism which is affected by these factors with respect to their promoter structure.   Materials and Methods: The CD34 + cord blood s...

Journal: :Blood 1996
A Hangaishi S Ogawa N Imamura S Miyawaki Y Miura N Uike C Shimazaki N Emi K Takeyama S Hirosawa N Kamada Y Kobayashi Y Takemoto T Kitani K Toyama S Ohtake Y Yazaki R Ueda H Hirai

It is now evident that the cell cycle machinery has a variety of elements negatively regulating cell cycle progression. However, among these negative regulators in cell cycle control, only 4 have been shown to be consistently involved in the development of human cancers as tumor suppressors: Rb (Retinoblastoma susceptibility protein), p53, and two recently identified cyclin-dependent kinase inh...

Journal: :European journal of haematology 2006
Anni Aggerholm Mette S Holm Per Guldberg Lene H Olesen Peter Hokland

The propensity of myelodysplastic syndrome (MDS) to transform into acute myeloid leukemia (AML) suggests the existence of common pathogenic components for these malignancies. Here, four genes implicated in the development of AML were examined for promoter CpG island hypermethylation in cells from 37 patients with different stages of MDS. Aberrant methylation was detected by polymerase chain rea...

Journal: :Molecular cancer research : MCR 2014
Katja Schuster Niranjan Venkateswaran Andrea Rabellino Luc Girard Samuel Peña-Llopis Pier Paolo Scaglioni

UNLABELLED Lung cancer commonly displays a number of recurrent genetic abnormalities, and about 30% of lung adenocarcinomas carry activating mutations in the Kras gene, often concomitantly with inactivation of tumor suppressor genes p16(INK4A) and p14(ARF) of the CDKN2AB locus. However, little is known regarding the function of p15INK4B translated from the same locus. To determine the frequency...

ژورنال: ارمغان دانش 2020

Background and aim: Lung cancer is one of the most leading causes of cancer death in males and females and the second leading cause of cancer death. Epigenetic alterations, including DNA hypermethylation, histone deacetylation, and miRNAs lead to the silencing of tumor suppressor genes (TSGs) resulting in tumorigenesis. This change has been reported in various cancers. The activity of DNA meth...

A. Khoshdel A. Movafagh A. Sayad K. Amini K. Majidzadeh-A M. A. Broumand M. D. Omrani M. Yari R. Mirfakhraie

Genome-Wide Association Studies (GWAS) have identified genetic variants contributing to the risk of cardiovascular disease (CVD) at the chromosome 9p21 locus. The chromosome 9p21 is an important susceptibility locus for several multifactorial diseases like ischemic stroke, aortic aneurysm, type 2 diabetes mellitus and coronary artery disease (CAD). F7 gene because of its role in activating the ...

Journal: :Cancer research 1995
M Gonzalez-Zulueta C M Bender A S Yang T Nguyen R W Beart J M Van Tornout P A Jones

Loss of heterozygosity on 9p21, where the p16/CDKN2 tumor suppressor and the p15INK4B cell cycle regulator genes are located, is a common genetic alteration in bladder cancer. However, it has been difficult to demonstrate homozygous deletions and intragenic mutations in either of these two genes in primary transitional cell carcinomas (TCC) of the bladder. Similarly, colon cancer-derived cell l...

Journal: :journal of sciences, islamic republic of iran 2016
m. yari a. movafagh a. sayad m. d. omrani m. a. broumand

genome-wide association studies (gwas) have identified genetic variants contributing to the risk of cardiovascular disease (cvd) at the chromosome 9p21 locus. the chromosome 9p21 is an important susceptibility locus for several multifactorial diseases like ischemic stroke, aortic aneurysm, type 2 diabetes mellitus and coronary artery disease (cad). f7 gene because of its role in activating the ...

2014
Na Shen Fei Yan Jiuxia Pang Lai-Chu Wu Aref Al-Kali Mark R. Litzow Shujun Liu

Nucleolin overexpression and DNA hypermethylation have been implicated in cancer pathogenesis, but whether and how these aberrations cooperate in controlling leukemia cell fate remains elusive. Here, we provide the first mechanistic insights into the role of nucleolin in leukemogenesis through creating a DNA hypermethylation profile in leukemia cells. We found that, in leukemia patients, nucleo...

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