Results for &quot;&quot;RecQ Helicases&quot;&quot;[mesh_terms]

Recognition and coacervation of G-quadruplexes by a multifunctional disordered region in RECQ4 helicase.

Anna C Papageorgiou, Michaela Pospisilova, Jakub Cibulka, Raghib Ashraf, Christopher A Waudby, Pavel Kadeřávek, Volha Maroz, Karel Kubicek, Zbynek Prokop, Lumir Krejci, Konstantinos Tripsianes

Nature communications 2023;14(1):6751

The structural and functional characterization of human RecQ4 reveals insights into its helicase mechanism.

Caroline Kisker, Florian Sauer, Sebastian Kaiser

Nature communications 2019;8():15907

The Genetic and Physical Interactomes of the Hrq1 Helicase.

Cody M Rogers, Elsbeth Sanders, Phoebe A Nguyen, Whitney Smith-Kinnaman, Amber L Mosley, Matthew L Bochman

G3 (Bethesda, Md.) 2021;10(12):4347-4357

RecQ and Fe-S helicases have unique roles in DNA metabolism dictated by their unwinding directionality, substrate specificity, and protein interactions.

Katrina N Estep, Robert M Brosh

Biochemical Society transactions 2018;46(1):77-95

Pathways and functions of the Werner syndrome protein.

Jae Wan Lee, Vilhelm A Bohr, Patricia L Opresko, Jeanine Harrigan

Mechanisms of ageing and development 2005;126(1):79-86

Selective interactions of cationic porphyrins with G-quadruplex structures.

H Han, D R Langley, A Rangan, L H Hurley

Journal of the American Chemical Society 2001;123(37):8902-13

The Human RecQ4 Helicase Contains a Functional RecQ C-terminal Region (RQC) That Is Essential for Activity.

Silvia Onesti, Francesca Marino, Matteo De March, Aditya Mojumdar

The Journal of biological chemistry 2017;292(10):4176-4184

Processing of DNA replication and repair intermediates by the concerted action of RecQ helicases and Rad2 structure-specific nucleases.

Joshua A Sommers, Robert M Brosh, Sudha Sharma

Protein and peptide letters 2008;15(1):89-102

Osteosarcoma development and stem cell differentiation.

Ni Tang, Wen-Xin Song, Jinyong Luo, Rex C Haydon, Tong-Chuan He

Clinical orthopaedics and related research 2008;466(9):2114-30

Interaction of Werner and Bloom syndrome genes with p53 in familial breast cancer.

Michael Wirtenberger, Bernd Frank, Kari Hemminki, Rüdiger Klaes, Rita K Schmutzler, Barbara Wappenschmidt, Alfons Meindl, Marion Kiechle, Norbert Arnold, Bernhard H F Weber, Dieter Niederacher, Claus R Bartram, Barbara Burwinkel

Carcinogenesis 2006;27(8):1655-60

Monopolar spindle 1 (MPS1) protein-dependent phosphorylation of RecQ-mediated genome instability protein 2 (RMI2) at serine 112 is essential for BLM-Topo III α-RMI1-RMI2 (BTR) protein complex function upon spindle assembly checkpoint (SAC) activation during mitosis.

Arun Pradhan, Thiyam Ramsing Singh, Abdullah Mahmood Ali, Kebola Wahengbam, Amom Ruhikanta Meetei

The Journal of biological chemistry 2014;288(47):33500-33508