219 related articles for article (PubMed ID: 33986331)
1. Structural genomics approach to investigate deleterious impact of nsSNPs in conserved telomere maintenance component 1.
Choudhury A; Mohammad T; Samarth N; Hussain A; Rehman MT; Islam A; Alajmi MF; Singh S; Hassan MI
Sci Rep; 2021 May; 11(1):10202. PubMed ID: 33986331
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of telomere syndrome caused by CTC1 mutations.
Chen LY; Majerská J; Lingner J
Genes Dev; 2013 Oct; 27(19):2099-108. PubMed ID: 24115768
[TBL] [Abstract][Full Text] [Related]
3. Structural and functional impact of non-synonymous SNPs in the CST complex subunit TEN1: structural genomics approach.
Amir M; Kumar V; Mohammad T; Dohare R; Rehman MT; Alajmi MF; Hussain A; Ahmad F; Hassan MI
Biosci Rep; 2019 May; 39(5):. PubMed ID: 31028137
[TBL] [Abstract][Full Text] [Related]
4. Structural and functional analysis of an OB-fold in human Ctc1 implicated in telomere maintenance and bone marrow syndromes.
Shastrula PK; Rice CT; Wang Z; Lieberman PM; Skordalakes E
Nucleic Acids Res; 2018 Jan; 46(2):972-984. PubMed ID: 29228254
[TBL] [Abstract][Full Text] [Related]
5. Functional characterization of human CTC1 mutations reveals novel mechanisms responsible for the pathogenesis of the telomere disease Coats plus.
Gu P; Chang S
Aging Cell; 2013 Dec; 12(6):1100-9. PubMed ID: 23869908
[TBL] [Abstract][Full Text] [Related]
6. CTC1-STN1 coordinates G- and C-strand synthesis to regulate telomere length.
Gu P; Jia S; Takasugi T; Smith E; Nandakumar J; Hendrickson E; Chang S
Aging Cell; 2018 Aug; 17(4):e12783. PubMed ID: 29774655
[TBL] [Abstract][Full Text] [Related]
7. Investigation of deleterious effects of nsSNPs in the POT1 gene: a structural genomics-based approach to understand the mechanism of cancer development.
Amir M; Kumar V; Mohammad T; Dohare R; Hussain A; Rehman MT; Alam P; Alajmi MF; Islam A; Ahmad F; Hassan MI
J Cell Biochem; 2019 Jun; 120(6):10281-10294. PubMed ID: 30556179
[TBL] [Abstract][Full Text] [Related]
8. CTC1-STN1 terminates telomerase while STN1-TEN1 enables C-strand synthesis during telomere replication in colon cancer cells.
Feng X; Hsu SJ; Bhattacharjee A; Wang Y; Diao J; Price CM
Nat Commun; 2018 Jul; 9(1):2827. PubMed ID: 30026550
[TBL] [Abstract][Full Text] [Related]
9. Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
Anderson BH; Kasher PR; Mayer J; Szynkiewicz M; Jenkinson EM; Bhaskar SS; Urquhart JE; Daly SB; Dickerson JE; O'Sullivan J; Leibundgut EO; Muter J; Abdel-Salem GM; Babul-Hirji R; Baxter P; Berger A; Bonafé L; Brunstom-Hernandez JE; Buckard JA; Chitayat D; Chong WK; Cordelli DM; Ferreira P; Fluss J; Forrest EH; Franzoni E; Garone C; Hammans SR; Houge G; Hughes I; Jacquemont S; Jeannet PY; Jefferson RJ; Kumar R; Kutschke G; Lundberg S; Lourenço CM; Mehta R; Naidu S; Nischal KK; Nunes L; Ounap K; Philippart M; Prabhakar P; Risen SR; Schiffmann R; Soh C; Stephenson JB; Stewart H; Stone J; Tolmie JL; van der Knaap MS; Vieira JP; Vilain CN; Wakeling EL; Wermenbol V; Whitney A; Lovell SC; Meyer S; Livingston JH; Baerlocher GM; Black GC; Rice GI; Crow YJ
Nat Genet; 2012 Jan; 44(3):338-42. PubMed ID: 22267198
[TBL] [Abstract][Full Text] [Related]
10. CTC1 OB-B interaction with TPP1 terminates telomerase and prevents telomere overextension.
Wang H; Ma T; Zhang X; Chen W; Lan Y; Kuang G; Hsu SJ; He Z; Chen Y; Stewart J; Bhattacharjee A; Luo Z; Price C; Feng X
Nucleic Acids Res; 2023 Jun; 51(10):4914-4928. PubMed ID: 37021555
[TBL] [Abstract][Full Text] [Related]
11. Human TEN1 maintains telomere integrity and functions in genome-wide replication restart.
Kasbek C; Wang F; Price CM
J Biol Chem; 2013 Oct; 288(42):30139-30150. PubMed ID: 24025336
[TBL] [Abstract][Full Text] [Related]
12. Pathogenic CTC1 mutations cause global genome instabilities under replication stress.
Wang Y; Chai W
Nucleic Acids Res; 2018 May; 46(8):3981-3992. PubMed ID: 29481669
[TBL] [Abstract][Full Text] [Related]
13. Patient-Derived iPSCs Reveal Evidence of Telomere Instability and DNA Repair Deficiency in Coats Plus Syndrome.
Oudrhiri N; M'kacher R; Chaker D; Colicchio B; Borie C; Jeandidier E; Dieterlen A; Griscelli F; Bennaceur-Griscelli A; Turhan AG
Genes (Basel); 2022 Aug; 13(8):. PubMed ID: 36011306
[TBL] [Abstract][Full Text] [Related]
14. Mutations in the telomere capping complex in bone marrow failure and related syndromes.
Walne AJ; Bhagat T; Kirwan M; Gitiaux C; Desguerre I; Leonard N; Nogales E; Vulliamy T; Dokal IS
Haematologica; 2013 Mar; 98(3):334-8. PubMed ID: 22899577
[TBL] [Abstract][Full Text] [Related]
15. Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation.
Netravathi M; Kumari R; Kapoor S; Dakle P; Dwivedi MK; Roy SD; Pandey P; Saini J; Ramakrishna A; Navalli D; Satishchandra P; Pal PK; Kumar A; Faruq M
BMC Med Genet; 2015 Feb; 16():5. PubMed ID: 25928698
[TBL] [Abstract][Full Text] [Related]
16. CTC1-mediated C-strand fill-in is an essential step in telomere length maintenance.
Feng X; Hsu SJ; Kasbek C; Chaiken M; Price CM
Nucleic Acids Res; 2017 May; 45(8):4281-4293. PubMed ID: 28334750
[TBL] [Abstract][Full Text] [Related]
17. A novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung disease.
Liu L; Luo H; Sheng Y; Kang X; Peng H; Luo H; Fan LL
Hereditas; 2023 Nov; 160(1):37. PubMed ID: 37978541
[TBL] [Abstract][Full Text] [Related]
18. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures.
Sargolzaeiaval F; Zhang J; Schleit J; Lessel D; Kubisch C; Precioso DR; Sillence D; Hisama FM; Dorschner M; Martin GM; Oshima J
Mol Genet Genomic Med; 2018 Nov; 6(6):1148-1156. PubMed ID: 30393977
[TBL] [Abstract][Full Text] [Related]
19. Emerging roles of CST in maintaining genome stability and human disease.
Stewart JA; Wang Y; Ackerson SM; Schuck PL
Front Biosci (Landmark Ed); 2018 Mar; 23(8):1564-1586. PubMed ID: 29293451
[TBL] [Abstract][Full Text] [Related]
20. The human CTC1/STN1/TEN1 complex regulates telomere maintenance in ALT cancer cells.
Huang C; Jia P; Chastain M; Shiva O; Chai W
Exp Cell Res; 2017 Jun; 355(2):95-104. PubMed ID: 28366536
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
