374 related articles for article (PubMed ID: 33934394)
1. Cancer-associated POT1 mutations lead to telomere elongation without induction of a DNA damage response.
Kim WT; Hennick K; Johnson J; Finnerty B; Choo S; Short SB; Drubin C; Forster R; McMaster ML; Hockemeyer D
EMBO J; 2021 Jun; 40(12):e107346. PubMed ID: 33934394
[TBL] [Abstract][Full Text] [Related]
2. POT1 mutations cause differential effects on telomere length leading to opposing disease phenotypes.
Zade NH; Khattar E
J Cell Physiol; 2023 Jun; 238(6):1237-1255. PubMed ID: 37183325
[TBL] [Abstract][Full Text] [Related]
3. Pot1b -/- tumors activate G-quadruplex-induced DNA damage to promote telomere hyper-elongation.
Takasugi T; Gu P; Liang F; Staco I; Chang S
Nucleic Acids Res; 2023 Sep; 51(17):9227-9247. PubMed ID: 37560909
[TBL] [Abstract][Full Text] [Related]
4.
Shen E; Xiu J; Lopez GY; Bentley R; Jalali A; Heimberger AB; Bainbridge MN; Bondy ML; Walsh KM
J Med Genet; 2020 Oct; 57(10):664-670. PubMed ID: 31937561
[TBL] [Abstract][Full Text] [Related]
5. Structural insights into POT1-TPP1 interaction and POT1 C-terminal mutations in human cancer.
Chen C; Gu P; Wu J; Chen X; Niu S; Sun H; Wu L; Li N; Peng J; Shi S; Fan C; Huang M; Wong CC; Gong Q; Kumar-Sinha C; Zhang R; Pusztai L; Rai R; Chang S; Lei M
Nat Commun; 2017 Apr; 8():14929. PubMed ID: 28393832
[TBL] [Abstract][Full Text] [Related]
6. The enigma of excessively long telomeres in cancer: lessons learned from rare human POT1 variants.
Gong Y; Stock AJ; Liu Y
Curr Opin Genet Dev; 2020 Feb; 60():48-55. PubMed ID: 32155570
[TBL] [Abstract][Full Text] [Related]
7. Pot1 OB-fold mutations unleash telomere instability to initiate tumorigenesis.
Gu P; Wang Y; Bisht KK; Wu L; Kukova L; Smith EM; Xiao Y; Bailey SM; Lei M; Nandakumar J; Chang S
Oncogene; 2017 Apr; 36(14):1939-1951. PubMed ID: 27869160
[TBL] [Abstract][Full Text] [Related]
8. Replication stress conferred by POT1 dysfunction promotes telomere relocalization to the nuclear pore.
Pinzaru AM; Kareh M; Lamm N; Lazzerini-Denchi E; Cesare AJ; Sfeir A
Genes Dev; 2020 Dec; 34(23-24):1619-1636. PubMed ID: 33122293
[TBL] [Abstract][Full Text] [Related]
9. POT1 and Damage Response Malfunction Trigger Acquisition of Somatic Activating Mutations in the VEGF Pathway in Cardiac Angiosarcomas.
Calvete O; Garcia-Pavia P; Domínguez F; Mosteiro L; Pérez-Cabornero L; Cantalapiedra D; Zorio E; Ramón Y Cajal T; Crespo-Leiro MG; Teulé Á; Lázaro C; Morente MM; Urioste M; Benitez J
J Am Heart Assoc; 2019 Sep; 8(18):e012875. PubMed ID: 31510873
[TBL] [Abstract][Full Text] [Related]
10. The role of telomere binding molecules for normal and abnormal hematopoiesis.
Hosokawa K; Arai F
Int J Hematol; 2018 Jun; 107(6):646-655. PubMed ID: 29550946
[TBL] [Abstract][Full Text] [Related]
11. POT1 involved in telomeric DNA damage repair and genomic stability of cervical cancer cells in response to radiation.
Li Q; Wang X; Liu J; Wu L; Xu S
Mutat Res Genet Toxicol Environ Mutagen; 2023 Oct; 891():503670. PubMed ID: 37770150
[TBL] [Abstract][Full Text] [Related]
12. Familial Clonal Hematopoiesis in a Long Telomere Syndrome.
DeBoy EA; Tassia MG; Schratz KE; Yan SM; Cosner ZL; McNally EJ; Gable DL; Xiang Z; Lombard DB; Antonarakis ES; Gocke CD; McCoy RC; Armanios M
N Engl J Med; 2023 Jun; 388(26):2422-2433. PubMed ID: 37140166
[TBL] [Abstract][Full Text] [Related]
13. POT1 mutations cause telomere dysfunction in chronic lymphocytic leukemia.
Ramsay AJ; Quesada V; Foronda M; Conde L; Martínez-Trillos A; Villamor N; Rodríguez D; Kwarciak A; Garabaya C; Gallardo M; López-Guerra M; López-Guillermo A; Puente XS; Blasco MA; Campo E; López-Otín C
Nat Genet; 2013 May; 45(5):526-30. PubMed ID: 23502782
[TBL] [Abstract][Full Text] [Related]
14. Germ line mutations in shelterin complex genes are associated with familial chronic lymphocytic leukemia.
Speedy HE; Kinnersley B; Chubb D; Broderick P; Law PJ; Litchfield K; Jayne S; Dyer MJS; Dearden C; Follows GA; Catovsky D; Houlston RS
Blood; 2016 Nov; 128(19):2319-2326. PubMed ID: 27528712
[TBL] [Abstract][Full Text] [Related]
15. Nonsense mutations in the shelterin complex genes ACD and TERF2IP in familial melanoma.
Aoude LG; Pritchard AL; Robles-Espinoza CD; Wadt K; Harland M; Choi J; Gartside M; Quesada V; Johansson P; Palmer JM; Ramsay AJ; Zhang X; Jones K; Symmons J; Holland EA; Schmid H; Bonazzi V; Woods S; Dutton-Regester K; Stark MS; Snowden H; van Doorn R; Montgomery GW; Martin NG; Keane TM; López-Otín C; Gerdes AM; Olsson H; Ingvar C; Borg A; Gruis NA; Trent JM; Jönsson G; Bishop DT; Mann GJ; Newton-Bishop JA; Brown KM; Adams DJ; Hayward NK
J Natl Cancer Inst; 2015 Feb; 107(2):. PubMed ID: 25505254
[TBL] [Abstract][Full Text] [Related]
16. Germline POT1 Deregulation Can Predispose to Myeloid Malignancies in Childhood.
Michler P; Schedel A; Witschas M; Friedrich UA; Wagener R; Mehtonen J; Brozou T; Menzel M; Walter C; Nabi D; Pearce G; Erlacher M; Göhring G; Dugas M; Heinäniemi M; Borkhardt A; Stölzel F; Hauer J; Auer F
Int J Mol Sci; 2021 Oct; 22(21):. PubMed ID: 34769003
[TBL] [Abstract][Full Text] [Related]
17. Association of the POT1 Germline Missense Variant p.I78T With Familial Melanoma.
Wong K; Robles-Espinoza CD; Rodriguez D; Rudat SS; Puig S; Potrony M; Wong CC; Hewinson J; Aguilera P; Puig-Butille JA; Bressac-de Paillerets B; Zattara H; van der Weyden L; Fletcher CDM; Brenn T; Arends MJ; Quesada V; Newton-Bishop JA; Lopez-Otin C; Bishop DT; Harms PW; Johnson TM; Durham AB; Lombard DB; Adams DJ
JAMA Dermatol; 2019 May; 155(5):604-609. PubMed ID: 30586141
[TBL] [Abstract][Full Text] [Related]
18. Identification of a Cancer-Predisposing Germline
Jajosky AN; Mitchell AL; Akgul M; Shetty S; Yoest JM; Gerson SL; Sadri N; Oduro KA
Genes (Basel); 2022 Mar; 13(4):. PubMed ID: 35456397
[TBL] [Abstract][Full Text] [Related]
19. Investigation of conformational dynamics of Tyr89Cys mutation in protection of telomeres 1 gene associated with familial melanoma.
Amir M; Ahamad S; Mohammad T; Jairajpuri DS; Hasan GM; Dohare R; Islam A; Ahmad F; Hassan MI
J Biomol Struct Dyn; 2021 Jan; 39(1):35-44. PubMed ID: 31847782
[TBL] [Abstract][Full Text] [Related]
20. A mouse model for Li-Fraumeni-Like Syndrome with cardiac angiosarcomas associated to POT1 mutations.
Martínez P; Sánchez-Vázquez R; Ferrara-Romeo I; Serrano R; Flores JM; Blasco MA
PLoS Genet; 2022 Jun; 18(6):e1010260. PubMed ID: 35727838
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
