Meltem Muftuoglu

Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates (2007)

Wong, Heng-Kuan, Muftuoglu, Meltem, Beck, Gad, Imam, Syed Z., Bohr, Vilhelm A., Wilson, David M.

The Cockayne syndrome B (CSB) protein—defective in a majority of patients suffering from the rare autosomal disorder CS—is a member of the SWI2/SNF2 family with roles in DNA repair and...

Cockayne syndrome group B protein has novel strand annealing and exchange activities (2006)

Muftuoglu, Meltem, Sharma, Sudha, Thorslund, Tina, Stevnsner, Tinna, Soerensen, Martin M., Brosh, Robert M., ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB)...

Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells (2002)

Selzer, Rebecca R., Nyaga, Simon, Tuo, Jingsheng, May, Alfred, Muftuoglu, Meltem, Christiansen, Mette, ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, developmental abnormalities and premature aging. The cellular and molecular phenotypes of CS include...

Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells

Selzer, Rebecca R., Nyaga, Simon, Tuo, Jingsheng, May, Alfred, Muftuoglu, Meltem, Christiansen, Mette, ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, developmental abnormalities and premature aging. The cellular and molecular phenotypes of CS include...

Cockayne syndrome group B protein has novel strand annealing and exchange activities

Muftuoglu, Meltem, Sharma, Sudha, Thorslund, Tina, Stevnsner, Tinna, Soerensen, Martin M., Brosh, Robert M., ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB)...

Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells

Selzer, Rebecca R., Nyaga, Simon, Tuo, Jingsheng, May, Alfred, Muftuoglu, Meltem, Christiansen, Mette, ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, developmental abnormalities and premature aging. The cellular and molecular phenotypes of CS include...

Cockayne syndrome group B protein has novel strand annealing and exchange activities

Muftuoglu, Meltem, Sharma, Sudha, Thorslund, Tina, Stevnsner, Tinna, Soerensen, Martin M., Brosh, Robert M., ...

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB)...

Cockayne syndrome B protein stimulates apurinic endonuclease 1 activity and protects against agents that introduce base excision repair intermediates

Wong, Heng-Kuan, Muftuoglu, Meltem, Beck, Gad, Imam, Syed Z., Bohr, Vilhelm A., Wilson, David M.

The Cockayne syndrome B (CSB) protein—defective in a majority of patients suffering from the rare autosomal disorder CS—is a member of the SWI2/SNF2 family with roles in DNA repair and...

Acetylation Regulates WRN Catalytic Activities and Affects Base Excision DNA Repair

Muftuoglu, Meltem, Kusumoto, Rika, Speina, Elzbieta, Beck, Gad, Cheng, Wen-Hsing, Bohr, Vilhelm A.

WRN Is Required for ATM Activation and the S-Phase Checkpoint in Response to Interstrand Cross-Link–Induced DNA Double-Strand Breaks

Cheng, Wen-Hsing, Muftic, Diana, Muftuoglu, Meltem, Dawut, Lale, Morris, Christa, Helleday, Thomas, ...

Werner syndrome (WS) is a human genetic disorder characterized by extensive clinical features of premature aging. Ataxia-telengiectasia (A-T) is a multisystem human genomic instability syndrome that...