275 related articles for article (PubMed ID: 34758190)
1. POGZ promotes homology-directed DNA repair in an HP1-dependent manner.
Heath J; Cheyou ES; Findlay S; Luo VM; Carpio EP; Lee J; Djerir B; Chen X; Morin T; Lebeau B; Karam M; Bagci H; Grapton D; Ursini-Siegel J; Côté JF; Witcher M; Richard S; Maréchal A; Orthwein A
EMBO Rep; 2022 Jan; 23(1):e51041. PubMed ID: 34758190
[TBL] [Abstract][Full Text] [Related]
2. Hepatoma-derived growth factor-related protein 2 promotes DNA repair by homologous recombination.
Baude A; Aaes TL; Zhai B; Al-Nakouzi N; Oo HZ; Daugaard M; Rohde M; Jäättelä M
Nucleic Acids Res; 2016 Mar; 44(5):2214-26. PubMed ID: 26721387
[TBL] [Abstract][Full Text] [Related]
3. Human POGZ modulates dissociation of HP1alpha from mitotic chromosome arms through Aurora B activation.
Nozawa RS; Nagao K; Masuda HT; Iwasaki O; Hirota T; Nozaki N; Kimura H; Obuse C
Nat Cell Biol; 2010 Jul; 12(7):719-27. PubMed ID: 20562864
[TBL] [Abstract][Full Text] [Related]
4. CHAMP1-POGZ counteracts the inhibitory effect of 53BP1 on homologous recombination and affects PARP inhibitor resistance.
Fujita H; Ikeda M; Ui A; Ouchi Y; Mikami Y; Kanno SI; Yasui A; Tanaka K
Oncogene; 2022 May; 41(19):2706-2718. PubMed ID: 35393543
[TBL] [Abstract][Full Text] [Related]
5. HP1 regulates the localization of FANCJ at sites of DNA double-strand breaks.
Wu W; Togashi Y; Johmura Y; Miyoshi Y; Nobuoka S; Nakanishi M; Ohta T
Cancer Sci; 2016 Oct; 107(10):1406-1415. PubMed ID: 27399284
[TBL] [Abstract][Full Text] [Related]
6. HP1 promotes tumor suppressor BRCA1 functions during the DNA damage response.
Lee YH; Kuo CY; Stark JM; Shih HM; Ann DK
Nucleic Acids Res; 2013 Jun; 41(11):5784-98. PubMed ID: 23589625
[TBL] [Abstract][Full Text] [Related]
7. A case of White-Sutton syndrome arising from a maternally-inherited mutation in POGZ.
Liu S; Yan Z; Huang Y; Zheng W; Deng Y; Zou Y; Xie H
Psychiatr Genet; 2021 Aug; 31(4):135-139. PubMed ID: 34133408
[TBL] [Abstract][Full Text] [Related]
8. Kruppel-associated Box (KRAB)-associated co-repressor (KAP-1) Ser-473 phosphorylation regulates heterochromatin protein 1β (HP1-β) mobilization and DNA repair in heterochromatin.
Bolderson E; Savage KI; Mahen R; Pisupati V; Graham ME; Richard DJ; Robinson PJ; Venkitaraman AR; Khanna KK
J Biol Chem; 2012 Aug; 287(33):28122-31. PubMed ID: 22715096
[TBL] [Abstract][Full Text] [Related]
9. The nuclear oncogene SET controls DNA repair by KAP1 and HP1 retention to chromatin.
Kalousi A; Hoffbeck AS; Selemenakis PN; Pinder J; Savage KI; Khanna KK; Brino L; Dellaire G; Gorgoulis VG; Soutoglou E
Cell Rep; 2015 Apr; 11(1):149-63. PubMed ID: 25818296
[TBL] [Abstract][Full Text] [Related]
10. A novel patient with White-Sutton syndrome refines the mutational and clinical repertoire of the POGZ-related phenotype and suggests further observations.
Pascolini G; Agolini E; Fleischer N; Gulotta E; Cesario C; D'Elia G; Novelli A; Majore S; Grammatico P
Am J Med Genet A; 2020 Jul; 182(7):1791-1795. PubMed ID: 32359026
[TBL] [Abstract][Full Text] [Related]
11. The Role of
Yannuzzi I; Butler MA; Fernandez J; LaRocque JR
Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573412
[TBL] [Abstract][Full Text] [Related]
12. Differential contribution of HP1 proteins to DNA end resection and homology-directed repair.
Soria G; Almouzni G
Cell Cycle; 2013 Feb; 12(3):422-9. PubMed ID: 23287531
[TBL] [Abstract][Full Text] [Related]
13. Heterochromatin protein 1 is recruited to various types of DNA damage.
Luijsterburg MS; Dinant C; Lans H; Stap J; Wiernasz E; Lagerwerf S; Warmerdam DO; Lindh M; Brink MC; Dobrucki JW; Aten JA; Fousteri MI; Jansen G; Dantuma NP; Vermeulen W; Mullenders LH; Houtsmuller AB; Verschure PJ; van Driel R
J Cell Biol; 2009 May; 185(4):577-86. PubMed ID: 19451271
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome).
Assia Batzir N; Posey JE; Song X; Akdemir ZC; Rosenfeld JA; Brown CW; Chen E; Holtrop SG; Mizerik E; Nieto Moreno M; Payne K; Raas-Rothschild A; Scott R; Vernon HJ; Zadeh N; ; Lupski JR; Sutton VR
Am J Med Genet A; 2020 Jan; 182(1):38-52. PubMed ID: 31782611
[TBL] [Abstract][Full Text] [Related]
15. A novel, de novo intronic variant in POGZ causes White-Sutton syndrome.
Merriweather A; Murdock DR; Rosenfeld JA; Dai H; Ketkar S; Emrick L; Nicholas S; Lewis RA; ; Bacino CA; Scott DA; Lee B; Sutton VR; Potocki L; Burrage LC
Am J Med Genet A; 2022 Jul; 188(7):2198-2203. PubMed ID: 35396900
[TBL] [Abstract][Full Text] [Related]
16. Double strand break (DSB) repair in heterochromatin and heterochromatin proteins in DSB repair.
Lemaître C; Soutoglou E
DNA Repair (Amst); 2014 Jul; 19():163-8. PubMed ID: 24754998
[TBL] [Abstract][Full Text] [Related]
17. CHAMP1 binds to REV7/FANCV and promotes homologous recombination repair.
Li F; Sarangi P; Iyer DR; Feng H; Moreau L; Nguyen H; Clairmont C; D'Andrea AD
Cell Rep; 2022 Aug; 40(9):111297. PubMed ID: 36044844
[TBL] [Abstract][Full Text] [Related]
18. Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Garde A; Cornaton J; Sorlin A; Moutton S; Nicolas C; Juif C; Geneviève D; Perrin L; Khau-Van-Kien P; Smol T; Vincent-Delorme C; Isidor B; Cogné B; Afenjar A; Keren B; Coubes C; Prieur F; Toutain A; Trousselet Y; Bourgouin S; Gonin-Olympiade C; Giraudat K; Piton A; Gérard B; Odent S; Tessier F; Lemasson L; Heide S; Gelineau AC; Sarret C; Miret A; Schaefer E; Piard J; Mathevet R; Boucon M; Bruel AL; Mau-Them FT; Chevarin M; Vitobello A; Philippe C; Thauvin-Robinet C; Faivre L
Clin Genet; 2021 Mar; 99(3):407-417. PubMed ID: 33277917
[TBL] [Abstract][Full Text] [Related]
19. Repair of DNA Double-Strand Breaks in Heterochromatin.
Watts FZ
Biomolecules; 2016 Dec; 6(4):. PubMed ID: 27999260
[TBL] [Abstract][Full Text] [Related]
20. The impact of heterochromatin on DSB repair.
Goodarzi AA; Noon AT; Jeggo PA
Biochem Soc Trans; 2009 Jun; 37(Pt 3):569-76. PubMed ID: 19442252
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]