نتایج جستجو برای: xpd gene

تعداد نتایج: 1141662  

2012
Yuan Yuan Hu Hua Yuan Guang Bing Jiang Ning Chen Li Wen Wei Dong Leng Xian Tao Zeng Yu Ming Niu

BACKGROUND To investigate the association between XPD Asp312Asn polymorphism and head and neck cancer risk through this meta-analysis. METHODS We performed a meta-analysis of 9 published case-control studies including 2,670 patients with head and neck cancer and 4,452 controls. An odds ratio (OR) with a 95% confidence interval (CI) was applied to assess the association between XPD Asp312Asn p...

2013
Zhi Qi Robert A Pugh Maria Spies Yann R Chemla

Helicases couple the chemical energy of ATP hydrolysis to directional translocation along nucleic acids and transient duplex separation. Understanding helicase mechanism requires that the basic physicochemical process of base pair separation be understood. This necessitates monitoring helicase activity directly, at high spatio-temporal resolution. Using optical tweezers with single base pair (b...

Journal: :Carcinogenesis 2005
Leah E Mechanic Aizen J Marrogi Judith A Welsh Elise D Bowman Mohammed A Khan Lindsey Enewold Yun-Ling Zheng Stephen Chanock Peter G Shields Curtis C Harris

The pattern of somatic mutations in TP53 is distinct for particular cancers and carcinogenic exposures, providing clues to disease etiology, e.g. G:C-->T:A mutations in TP53 are more frequently observed in smoking-associated lung cancers. In order to investigate possible causes and mechanisms of lung cancer susceptibility differences, the TP53 gene was sequenced in a case-only study of lung can...

Journal: :Circulation 2012
Matej Durik Maryam Kavousi Ingrid van der Pluijm Aaron Isaacs Caroline Cheng Koen Verdonk Annemarieke E Loot Hisko Oeseburg Usha Musterd Bhaggoe Frank Leijten Richard van Veghel René de Vries Goran Rudez Renata Brandt Yanto R Ridwan Elza D van Deel Martine de Boer Dennie Tempel Ingrid Fleming Gary F Mitchell Germaine C Verwoert Kirill V Tarasov Andre G Uitterlinden Albert Hofman Henricus J Duckers Cornelia M van Duijn Ben A Oostra Jacqueline C M Witteman Dirk J Duncker A H Jan Danser Jan H Hoeijmakers Anton J M Roks

BACKGROUND Vascular dysfunction in atherosclerosis and diabetes mellitus, as observed in the aging population of developed societies, is associated with vascular DNA damage and cell senescence. We hypothesized that cumulative DNA damage during aging contributes to vascular dysfunction. METHODS AND RESULTS In mice with genomic instability resulting from the defective nucleotide excision repair...

Journal: :International journal of cancer 2006
Valérie Le Morvan Michel Longy Catherine Bonaïti-Pellié Binh Bui Nadine Houédé Jean-Michel Coindre Jacques Robert Philippe Pourquier

There are more than 50 subtypes of soft tissue sarcomas, among which 30% are associated with specific genetic alterations, including translocations. Several studies have reported associations between cancer risk and polymorphisms of DNA repair genes from the nucleotide excision repair (NER) pathway. NER involves more than 20 proteins whose inactivation leads to xeroderma pigmentosum (XP) or coc...

2016
Julian Kunkel Eugen Betke

In contrast to disk or flash based storage solutions, throughput and latency of in-memory storage promises to be close to the best performance. Kove®’s XPD® offers pooled memory for cluster systems. However, the system does not expose access methods to treat the memory like a traditional parallel file system that offers POSIX or MPI-IO semantics. Contributions of this poster are: 1. Implementat...

2011
Sajeela Yousaf Muhammad Imran Khan Shazia Micheal Farah Akhtar Syeda Hafiza Benish Ali Moeen Riaz Mahmood Ali Pramila Lall Nadia Khalida Waheed Anneke I. den Hollander Asifa Ahmed Raheel Qamar

PURPOSE The present study was designed to determine the association of polymorphisms of the DNA repair genes X-ray cross-complementing group 1 (XRCC1) (c.1316G>A [rs25487]) and xeroderma pigmentosum complementation group D (XPD) (c.2298A>C [rs13181]) with primary open-angle glaucoma (POAG) and primary closed-angle glaucoma (PCAG). METHODS In this prospective case-control study, polymerase cha...

2015
Ling-I Hsu Meei-Maan Wu Yuan-Hung Wang Cheng-Yeh Lee Tse-Yen Yang Bo-Yu Hsiao Chien-Jen Chen

Deficiency in the capability of xenobiotic detoxification and arsenic methylation may be correlated with individual susceptibility to arsenic-related skin cancers. We hypothesized that glutathione S-transferase (GST M1, T1, and P1), reactive oxygen species (ROS) related metabolic genes (NQO1, EPHX1, and HO-1), and DNA repair genes (XRCC1, XPD, hOGG1, and ATM) together may play a role in arsenic...

Journal: :Carcinogenesis 2004
Pavel Vodicka Rajiv Kumar Rudolf Stetina Somali Sanyal Pavel Soucek Vincent Haufroid Maria Dusinska Miroslava Kuricova Maria Zamecnikova Ludovit Musak Jana Buchancova Hannu Norppa Ari Hirvonen Ludmila Vodickova Alessio Naccarati Zora Matousu Kari Hemminki

We analysed the associations between genetic polymorphisms in genes coding for DNA repair enzymes XPD (exon 23 A --> C, K751Q), XPG (exon 15 G --> C, D1104H), XPC (exon 15 A --> C, K939Q), XRCC1 (exon 10 G --> A, R399Q) and XRCC3 (exon 7 C --> T, T241 M) and the levels of chromosomal aberrations (CAs) and single-strand breaks (SSBs) in peripheral lymphocytes in a central European population. We...

2007
Katie M. Applebaum Margaret R. Karagas David J. Hunter Paul J. Catalano Steven H. Byler Steve Morris Heather H. Nelson

BACKGROUND Arsenic exposure may alter the efficiency of DNA repair. UV damage is specifically repaired by nucleotide excision repair (NER), and common genetic variants in NER may increase risk for non-melanoma skin cancer (NMSC). OBJECTIVE We tested whether polymorphisms in the NER genes XPA (A23G) and XPD (Asp312Asn and Lys751Gln) modify the association between arsenic and NMSC. METHODS In...

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