Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 217

1.

Bilateral retinal detachment in Werner syndrome.

Sasoh M, Tsukitome H, Matsui Y, Furuta M, Kondo M.

Retin Cases Brief Rep. 2014 Spring;8(2):92-4. doi: 10.1097/ICB.0000000000000011.

PMID:
25372317
2.

The Werner syndrome protein limits the error-prone 8-oxo-dG lesion bypass activity of human DNA polymerase kappa.

Maddukuri L, Ketkar A, Eddy S, Zafar MK, Eoff RL.

Nucleic Acids Res. 2014 Oct 29;42(19):12027-40. doi: 10.1093/nar/gku913. Epub 2014 Oct 7.

3.

Cellular deficiency of Werner syndrome protein or RECQ1 promotes genotoxic potential of hydroquinone and benzo[a]pyrene exposure.

Garige M, Sharma S.

Int J Toxicol. 2014 Sep-Oct;33(5):373-81. doi: 10.1177/1091581814547422. Epub 2014 Sep 15.

PMID:
25228686
4.

WRNIP1 functions upstream of DNA polymerase η in the UV-induced DNA damage response.

Yoshimura A, Kobayashi Y, Tada S, Seki M, Enomoto T.

Biochem Biophys Res Commun. 2014 Sep 12;452(1):48-52. doi: 10.1016/j.bbrc.2014.08.043. Epub 2014 Aug 16.

PMID:
25139235
5.

Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas.

Oshitari T, Kitahashi M, Mizuno S, Baba T, Kubota-Taniai M, Takemoto M, Yokote K, Yamamoto S, Roy S.

BMC Ophthalmol. 2014 Mar 12;14:31. doi: 10.1186/1471-2415-14-31.

6.

The FEN1 E359K germline mutation disrupts the FEN1-WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers.

Chung L, Onyango D, Guo Z, Jia P, Dai H, Liu S, Zhou M, Lin W, Pang I, Li H, Yuan YC, Huang Q, Zheng L, Lopes J, Nicolas A, Chai W, Raz D, Reckamp KL, Shen B.

Oncogene. 2015 Feb 12;34(7):902-11. doi: 10.1038/onc.2014.19. Epub 2014 Mar 10.

PMID:
24608430
7.

Serines 440 and 467 in the Werner syndrome protein are phosphorylated by DNA-PK and affects its dynamics in response to DNA double strand breaks.

Kusumoto-Matsuo R, Ghosh D, Karmakar P, May A, Ramsden D, Bohr VA.

Aging (Albany NY). 2014 Jan;6(1):70-81.

8.

Werner's syndrome: incidental finding during pregnancy.

Hurtarte Sandoval AR, Penate Dardón JD, Flores Robles BJ, Porres S.

BMJ Case Rep. 2013 Dec 3;2013. pii: bcr2013200931. doi: 10.1136/bcr-2013-200931.

PMID:
24302663
9.

Exploring the pathophysiology behind the more common genetic and acquired lipodystrophies.

Nolis T.

J Hum Genet. 2014 Jan;59(1):16-23. doi: 10.1038/jhg.2013.107. Epub 2013 Oct 24. Review.

PMID:
24152769
10.

Targeting an Achilles' heel of cancer with a WRN helicase inhibitor.

Aggarwal M, Banerjee T, Sommers JA, Brosh RM Jr.

Cell Cycle. 2013 Oct 15;12(20):3329-35. doi: 10.4161/cc.26320. Epub 2013 Sep 12.

11.

Decrease of fibulin-3 in hepatocellular carcinoma indicates poor prognosis.

Luo R, Zhang M, Liu L, Lu S, Zhang CZ, Yun J.

PLoS One. 2013 Aug 1;8(8):e70511. doi: 10.1371/journal.pone.0070511. Print 2013.

12.

Partial lipodystrophy with severe insulin resistance and adult progeria Werner syndrome.

Donadille B, D'Anella P, Auclair M, Uhrhammer N, Sorel M, Grigorescu R, Ouzounian S, Cambonie G, Boulot P, Laforêt P, Carbonne B, Christin-Maitre S, Bignon YJ, Vigouroux C.

Orphanet J Rare Dis. 2013 Jul 12;8:106. doi: 10.1186/1750-1172-8-106.

13.

Human RECQ1 interacts with Ku70/80 and modulates DNA end-joining of double-strand breaks.

Parvathaneni S, Stortchevoi A, Sommers JA, Brosh RM Jr, Sharma S.

PLoS One. 2013 May 1;8(5):e62481. doi: 10.1371/journal.pone.0062481. Print 2013.

14.

Telomere shortening in human diseases.

Kong CM, Lee XW, Wang X.

FEBS J. 2013 Jul;280(14):3180-93. doi: 10.1111/febs.12326. Epub 2013 Jun 24. Review.

PMID:
23647631
15.

Human RECQL5: guarding the crossroads of DNA replication and transcription and providing backup capability.

Popuri V, Tadokoro T, Croteau DL, Bohr VA.

Crit Rev Biochem Mol Biol. 2013 May-Jun;48(3):289-99. doi: 10.3109/10409238.2013.792770. Epub 2013 Apr 29. Review.

PMID:
23627586
16.

Functional deficit associated with a missense Werner syndrome mutation.

Tadokoro T, Rybanska-Spaeder I, Kulikowicz T, Dawut L, Oshima J, Croteau DL, Bohr VA.

DNA Repair (Amst). 2013 Jun 1;12(6):414-21. doi: 10.1016/j.dnarep.2013.03.004. Epub 2013 Apr 11.

17.

Leg ulcer in Werner syndrome (adult progeria): a case report.

Fumo G, Pau M, Patta F, Aste N, Atzori L.

Dermatol Online J. 2013 Mar 15;19(3):6.

18.

Chondrosarcoma of the mandibular condyle in a patient with Werner syndrome: a case report.

Goutzanis L, Kalfarentzos EF, Petsinis V, Papadogeorgakis N.

J Craniomaxillofac Surg. 2013 Oct;41(7):e170-4. doi: 10.1016/j.jcms.2012.11.045. Epub 2013 Jan 26.

PMID:
23357132
19.

Werner's syndrome may be lost in the shadow of the scleroderma.

Gonullu E, Bilge NS, Kaşifoğlu T, Korkmaz C.

Rheumatol Int. 2013 May;33(5):1309-12. doi: 10.1007/s00296-012-2564-4. Epub 2012 Nov 6.

PMID:
23129431
20.

Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis.

Niida Y, Kuroda M, Mitani Y, Okumura A, Yokoi A.

Mol Genet Metab. 2012 Nov;107(3):580-5. doi: 10.1016/j.ymgme.2012.09.008. Epub 2012 Sep 10.

PMID:
23022073
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk