Terms: = Bone cancer AND WRN, RECQL2, 7486, ENSG00000165392, Q14191, RECQ3
21 results:
1. Werner helicase is required for proliferation and DNA damage repair in multiple myeloma.
Akcora-Yildiz D; Ozkan T; Ozen M; Gunduz M; Sunguroglu A; Beksac M
Mol Biol Rep; 2023 Feb; 50(2):1565-1573. PubMed ID: 36515823
[TBL] [Abstract] [Full Text] [Related]
2. Identification and Analysis of Transcriptional Regulatory Networks of Osteosarcoma Microarray Data via Systems Biology.
Cai J; Tao Z; Chen X; Yi E
J Oleo Sci; 2022; 71(3):379-386. PubMed ID: 35236797
[TBL] [Abstract] [Full Text] [Related]
3. Severe metabolic disorders coexisting with Werner syndrome: a case report.
Li H; Yang M; Shen H; Wang S; Cai H
Endocr J; 2021 Mar; 68(3):261-267. PubMed ID: 33087645
[TBL] [Abstract] [Full Text] [Related]
4. Werner Syndrome Protein Expression in Breast cancer.
Savva C; Sadiq M; Sheikh O; Karim S; Trivedi S; Green AR; Rakha EA; Madhusudan S; Arora A
Clin Breast Cancer; 2021 Feb; 21(1):57-73.e7. PubMed ID: 32919863
[TBL] [Abstract] [Full Text] [Related]
5. RECQ DNA Helicases and Osteosarcoma.
Lu L; Jin W; Wang LL
Adv Exp Med Biol; 2020; 1258():37-54. PubMed ID: 32767233
[TBL] [Abstract] [Full Text] [Related]
6. Impact of the homogeneous and heterogeneous risk factors on the incidence and survival outcome of bone metastasis in NSCLC patients.
Song Q; Shang J; Zhang C; Zhang L; Wu X
J Cancer Res Clin Oncol; 2019 Mar; 145(3):737-746. PubMed ID: 30603904
[TBL] [Abstract] [Full Text] [Related]
7. [Hereditary bone tumors].
Baumhoer D
Pathologe; 2017 May; 38(3):179-185. PubMed ID: 28421271
[TBL] [Abstract] [Full Text] [Related]
8. Radiographic presentation of musculoskeletal involvement in Werner syndrome (adult progeria).
David A; Vincent M; Arrigoni PP; Barbarot S; Pistorius MA; Isidor B; Frampas E
Diagn Interv Imaging; 2017 May; 98(5):373-378. PubMed ID: 27931782
[TBL] [Abstract] [Full Text] [Related]
9. RECQ DNA helicases and osteosarcoma.
Lu L; Jin W; Liu H; Wang LL
Adv Exp Med Biol; 2014; 804():129-45. PubMed ID: 24924172
[TBL] [Abstract] [Full Text] [Related]
10. Werner syndrome helicase has a critical role in DNA damage responses in the absence of a functional fanconi anemia pathway.
Aggarwal M; Banerjee T; Sommers JA; Iannascoli C; Pichierri P; Shoemaker RH; Brosh RM
Cancer Res; 2013 Sep; 73(17):5497-507. PubMed ID: 23867477
[TBL] [Abstract] [Full Text] [Related]
11. Diagnostic criteria for Werner syndrome based on Japanese nationwide epidemiological survey.
Takemoto M; Mori S; Kuzuya M; Yoshimoto S; Shimamoto A; Igarashi M; Tanaka Y; Miki T; Yokote K
Geriatr Gerontol Int; 2013 Apr; 13(2):475-81. PubMed ID: 22817610
[TBL] [Abstract] [Full Text] [Related]
12. [Hereditary bone tumors].
Jundt G; Baumhoer D
Pathologe; 2010 Oct; 31(6):471-6. PubMed ID: 20960198
[TBL] [Abstract] [Full Text] [Related]
13. The human wrn and BLM RecQ helicases differentially regulate cell proliferation and survival after chemotherapeutic DNA damage.
Mao FJ; Sidorova JM; Lauper JM; Emond MJ; Monnat RJ
Cancer Res; 2010 Aug; 70(16):6548-55. PubMed ID: 20663905
[TBL] [Abstract] [Full Text] [Related]
14. Unrelated donor hematopoietic cell transplantation: factors associated with a better HLA match.
Dehn J; Arora M; Spellman S; Setterholm M; Horowitz M; Confer D; Weisdorf D
Biol Blood Marrow Transplant; 2008 Dec; 14(12):1334-40. PubMed ID: 19041054
[TBL] [Abstract] [Full Text] [Related]
15. wrn protects against topo I but not topo II inhibitors by preventing DNA break formation.
Christmann M; Tomicic MT; Gestrich C; Roos WP; Bohr VA; Kaina B
DNA Repair (Amst); 2008 Dec; 7(12):1999-2009. PubMed ID: 18805512
[TBL] [Abstract] [Full Text] [Related]
16. Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents.
Cabral RE; Queille S; Bodemer C; de Prost Y; Neto JB; Sarasin A; Daya-Grosjean L
Mutat Res; 2008 Aug; 643(1-2):41-7. PubMed ID: 18616953
[TBL] [Abstract] [Full Text] [Related]
17. Association of a missense single nucleotide polymorphism, Cys1367Arg of the wrn gene, with the risk of bone and soft tissue sarcomas in Japan.
Nakayama R; Sato Y; Masutani M; Ogino H; Nakatani F; Chuman H; Beppu Y; Morioka H; Yabe H; Hirose H; Sugimura H; Sakamoto H; Ohta T; Toyama Y; Yoshida T; Kawai A
Cancer Sci; 2008 Feb; 99(2):333-9. PubMed ID: 18271933
[TBL] [Abstract] [Full Text] [Related]
18. RECQL4, mutated in the Rothmund-Thomson and RAPADILINO syndromes, interacts with ubiquitin ligases UBR1 and UBR2 of the N-end rule pathway.
Yin J; Kwon YT; Varshavsky A; Wang W
Hum Mol Genet; 2004 Oct; 13(20):2421-30. PubMed ID: 15317757
[TBL] [Abstract] [Full Text] [Related]
19. Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
Siitonen HA; Kopra O; Kääriäinen H; Haravuori H; Winter RM; Säämänen AM; Peltonen L; Kestilä M
Hum Mol Genet; 2003 Nov; 12(21):2837-44. PubMed ID: 12952869
[TBL] [Abstract] [Full Text] [Related]
20. Genetic instability and hematologic disease risk in Werner syndrome patients and heterozygotes.
Moser MJ; Bigbee WL; Grant SG; Emond MJ; Langlois RG; Jensen RH; Oshima J; Monnat RJ
Cancer Res; 2000 May; 60(9):2492-6. PubMed ID: 10811130
[TBL] [Abstract] [Full Text] [Related]
[Next]
