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Results: 1 to 20 of 547

Similar articles for PubMed (Select 16150736)

1.

Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain.

Lee JW, Kusumoto R, Doherty KM, Lin GX, Zeng W, Cheng WH, von Kobbe C, Brosh RM Jr, Hu JS, Bohr VA.

J Biol Chem. 2005 Nov 25;280(47):39627-36. Epub 2005 Sep 7.

2.

In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication.

Sharma S, Sommers JA, Brosh RM Jr.

Hum Mol Genet. 2004 Oct 1;13(19):2247-61. Epub 2004 Jul 28.

3.

The three-dimensional structure of the HRDC domain and implications for the Werner and Bloom syndrome proteins.

Liu Z, Macias MJ, Bottomley MJ, Stier G, Linge JP, Nilges M, Bork P, Sattler M.

Structure. 1999 Dec 15;7(12):1557-66.

PMID:
10647186
4.

Werner syndrome protein contains three structure-specific DNA binding domains.

von Kobbe C, Thomä NH, Czyzewski BK, Pavletich NP, Bohr VA.

J Biol Chem. 2003 Dec 26;278(52):52997-3006. Epub 2003 Oct 8.

5.

Pathways and functions of the Werner syndrome protein.

Lee JW, Harrigan J, Opresko PL, Bohr VA.

Mech Ageing Dev. 2005 Jan;126(1):79-86. Review.

PMID:
15610765
6.

Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex.

Li B, Comai L.

J Biol Chem. 2001 Mar 30;276(13):9896-902. Epub 2001 Jan 4.

7.

POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates.

Opresko PL, Mason PA, Podell ER, Lei M, Hickson ID, Cech TR, Bohr VA.

J Biol Chem. 2005 Sep 16;280(37):32069-80. Epub 2005 Jul 18.

8.

WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.

Chen L, Huang S, Lee L, Davalos A, Schiestl RH, Campisi J, Oshima J.

Aging Cell. 2003 Aug;2(4):191-9.

PMID:
12934712
9.

Enzymatic mechanism of the WRN helicase/nuclease.

Brosh RM Jr, Opresko PL, Bohr VA.

Methods Enzymol. 2006;409:52-85.

PMID:
16793395
10.

Crystal structure of the HRDC domain of human Werner syndrome protein, WRN.

Kitano K, Yoshihara N, Hakoshima T.

J Biol Chem. 2007 Jan 26;282(4):2717-28. Epub 2006 Dec 4.

11.

Coordinate action of the helicase and 3' to 5' exonuclease of Werner syndrome protein.

Opresko PL, Laine JP, Brosh RM Jr, Seidman MM, Bohr VA.

J Biol Chem. 2001 Nov 30;276(48):44677-87. Epub 2001 Sep 25.

12.

Physical and functional mapping of the replication protein a interaction domain of the werner and bloom syndrome helicases.

Doherty KM, Sommers JA, Gray MD, Lee JW, von Kobbe C, Thoma NH, Kureekattil RP, Kenny MK, Brosh RM Jr.

J Biol Chem. 2005 Aug 19;280(33):29494-505. Epub 2005 Jun 17.

13.

The Werner syndrome helicase/exonuclease (WRN) disrupts and degrades D-loops in vitro.

Orren DK, Theodore S, Machwe A.

Biochemistry. 2002 Nov 19;41(46):13483-8.

PMID:
12427008
14.

Characterization and mutational analysis of the RecQ core of the bloom syndrome protein.

Janscak P, Garcia PL, Hamburger F, Makuta Y, Shiraishi K, Imai Y, Ikeda H, Bickle TA.

J Mol Biol. 2003 Jun 27;330(1):29-42.

PMID:
12818200
15.

DNA binding residues in the RQC domain of Werner protein are critical for its catalytic activities.

Tadokoro T, Kulikowicz T, Dawut L, Croteau DL, Bohr VA.

Aging (Albany NY). 2012 Jun;4(6):417-29.

16.

The N-terminal domain of the large subunit of human replication protein A binds to Werner syndrome protein and stimulates helicase activity.

Shen JC, Lao Y, Kamath-Loeb A, Wold MS, Loeb LA.

Mech Ageing Dev. 2003 Aug-Sep;124(8-9):921-30.

PMID:
14499497
17.

Analyses of the interaction of WRNIP1 with Werner syndrome protein (WRN) in vitro and in the cell.

Kawabe Y, Seki M, Yoshimura A, Nishino K, Hayashi T, Takeuchi T, Iguchi S, Kusa Y, Ohtsuki M, Tsuyama T, Imamura O, Matsumoto T, Furuichi Y, Tada S, Enomoto T.

DNA Repair (Amst). 2006 Jul 13;5(7):816-28.

PMID:
16769258
18.

Intrinsic ssDNA annealing activity in the C-terminal region of WRN.

Muftuoglu M, Kulikowicz T, Beck G, Lee JW, Piotrowski J, Bohr VA.

Biochemistry. 2008 Sep 30;47(39):10247-54. doi: 10.1021/bi800807n. Epub 2008 Sep 5.

PMID:
18771289
19.

Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases.

Opresko PL, von Kobbe C, Laine JP, Harrigan J, Hickson ID, Bohr VA.

J Biol Chem. 2002 Oct 25;277(43):41110-9. Epub 2002 Aug 13.

20.

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

Shen JC, Gray MD, Oshima J, Kamath-Loeb AS, Fry M, Loeb LA.

J Biol Chem. 1998 Dec 18;273(51):34139-44.

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