نتایج جستجو برای: ercc5

تعداد نتایج: 216  

Journal: :The EMBO journal 2009
Lidija Staresincic Adebanke F Fagbemi Jacqueline H Enzlin Audrey M Gourdin Nils Wijgers Isabelle Dunand-Sauthier Giuseppina Giglia-Mari Stuart G Clarkson Wim Vermeulen Orlando D Schärer

Nucleotide excision repair (NER) requires the coordinated sequential assembly and actions of the involved proteins at sites of DNA damage. Following damage recognition, dual incision 5' to the lesion by ERCC1-XPF and 3' to the lesion by XPG leads to the removal of a lesion-containing oligonucleotide of about 30 nucleotides. The resulting single-stranded DNA (ssDNA) gap on the undamaged strand i...

2014
Salim Ziani Zita Nagy Sergey Alekseev Evi Soutoglou Jean-Marc Egly Frédéric Coin

In nucleotide excision repair (NER), damage recognition by XPC-hHR23b is described as a critical step in the formation of the preincision complex (PInC) further composed of TFIIH, XPA, RPA, XPG, and ERCC1-XPF. To obtain new molecular insights into the assembly of the PInC, we analyzed its formation independently of DNA damage by using the lactose operator/repressor reporter system. We observed ...

Journal: :The EMBO journal 1997
E Evans J Fellows A Coffer R D Wood

Human XPG nuclease makes the 3' incision during nucleotide excision repair of DNA. The enzyme cleaves model DNA bubble structures specifically near the junction of unpaired DNA with a duplex region. It is not yet known, however, whether an unpaired structure is an intermediate during actual DNA repair. We find here that XPG requires opening of >5 bp for efficient cleavage. To seek direct eviden...

Journal: :JAAD case reports 2015
Tao Wang Chen-Chen Xu Xi-Ping Zhou Jonathan J Lee Jun Shen Bill Q Lian Yue-Hua Liu Christine Guo Lian

CS: Cockayne syndrome ERCC5: Excision Repair Cross-complementing Rodent Repair Deficiency Complementation Group 5 gene NER: Nucleotide excision repair UV: Ultraviolet WES: Whole exome sequencing XP: Xeroderma pigmentosum XP-G: Xeroderma pigmentosum complementation group G INTRODUCTION Xeroderma pigmentosum (XP) is an autosomal recessive genodermatosis caused by a germline loss of function in DN...

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