Polymorphisms of DNA repair genes XPD and XRCC1 and risk of cataract development

AI Ahmed, MYS Saif, AA Zayed - Comparative Clinical Pathology, 2012 - Springer

Age-related cataract is a leading cause of blindness throughout the world. Regular exposure
to sunlight increases the risk of cataract development. Ultraviolet light causes oxidative …

被引用次数：2 相关文章所有 10 个版本

[PDF] unam.mx

[PDF][PDF] “POLIMORFISMO rs13181 DEL GEN ERCC2 EN PACIENTES

CONC SENIL - 2021 - ru.dgb.unam.mx

Introducción: La catarata senil es la causa número uno de discapacidad visual y ceguera
reversible, el único tratamiento definitivo es la cirugía. Además de los factores ambientales …

[HTML] nih.gov

[HTML][HTML] Deoxyribonucleic acid repair gene X-ray repair cross-complementing group 1 polymorphisms and non-carcinogenic disease risk in different populations: A …

B Larijani, JM Asl, A Keshtkar, N Saki… - Indian Journal of …, 2013 - ncbi.nlm.nih.gov

PURPOSE: This study aims to assess a meta-analysis of the association of X-ray repair
cross-complementing group 1 (XRCC1) polymorphisms with the risk of various non …

被引用次数：1 相关文章所有 18 个版本

[HTML] docplayer.es

[HTML][HTML] Estudio genético de la

UEN OFTALMOLOGÍA, LAV DOS OJOS PARA TODA… - docplayer.es

Estudio genético de la catarata presenil DEPARTAMENTO DE CIRUGIA TESIS DOCTORAL
GLORIA LÓPEZ VALVERDE DIRECTORES: PROF. DR. D. FERNANDO CRUZ GONZÁLEZ …

[PDF] archive.org

The role of BER and NER gene polymorphisms and their expression in glaucoma pathogenesis.

M Gorczyca-Bojko, D Pytel, D Lewko… - Acta …, 2019 - search.ebscohost.com

Introduction: Glaucoma is the second most common cause of blindness globally. Glaucoma
development has been attributed to impaired base excision repair (BER) and, possibly …

[PDF][PDF] Investigation of DNA repair genes XPD and hOGG1 in type 2 Diabetes mellitus

N Yigitbasi, LM Yurdum, U Yilmaz, N Yilmaz… - …, 2018 - manage.effectpublishing.com

Increased oxidative stress in type 2 diabetes cause to the accumulation of DNA damage and
results diabetic complications. Xeroderma pigmentosum complementation group D (XPD) …

Meta-analysis of genetic polymorphisms and ophthalmologic disease risk in Asian populations: a case of DNA repair XRCC1 gene.

N Saki, H Galehdari, M Feghhi, FA Larijani… - Pakistan Journal of …, 2013 - europepmc.org

This study aimed to assess a meta-analysis of the association of XRCC1 polymorphisms
with the risk of various ophthalmologic diseases in Asian population. This meta-analysis was …

[引用][C] Gastrointestinal adenokarsinomaları ile bazı dna onarım genleri arasındaki ilişkinin araştırılması

AB Engin - platform.almanhal.com

منصة المنهل لقد انتهت الجلسة. يرجى العمل على إعادة تحديث الصفحة إعادة تحديث يرجى الانتظار...
يتم تحضير الملف الاستخدام المجاني إذا كنت ترغب في الوصول الكامل إلى هذا المحتوى وقاعدة …‎

[引用][C] Prematür ovaryan yetmezlikle XPD ve XRCC1 DNA tamir gen polimorfizminin ilişkisi

Ç Doğan - … Uzmanlık Tezi, İnönü Üniversitesi Tıp Fakültesi …, 2011 - platform.almanhal.com

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