201 related articles for article (PubMed ID: 35603789)
1. Hypomorphic GINS3 variants alter DNA replication and cause Meier-Gorlin syndrome.
McQuaid ME; Ahmed K; Tran S; Rousseau J; Shaheen R; Kernohan KD; Yuki KE; Grover P; Dreseris ES; Ahmed S; Dupuis L; Stimec J; Shago M; Al-Hassnan ZN; Tremblay R; Maass PG; Wilson MD; Grunebaum E; Boycott KM; Boisvert FM; Maddirevula S; Faqeih EA; Almanjomi F; Khan ZU; Alkuraya FS; Campeau PM; Kannu P; Campos EI; Wurtele H
JCI Insight; 2022 May; 7(10):. PubMed ID: 35603789
[TBL] [Abstract][Full Text] [Related]
2. Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis.
Fenwick AL; Kliszczak M; Cooper F; Murray J; Sanchez-Pulido L; Twigg SR; Goriely A; McGowan SJ; Miller KA; Taylor IB; Logan C; ; Bozdogan S; Danda S; Dixon J; Elsayed SM; Elsobky E; Gardham A; Hoffer MJ; Koopmans M; McDonald-McGinn DM; Santen GW; Savarirayan R; de Silva D; Vanakker O; Wall SA; Wilson LC; Yuregir OO; Zackai EH; Ponting CP; Jackson AP; Wilkie AO; Niedzwiedz W; Bicknell LS
Am J Hum Genet; 2016 Jul; 99(1):125-38. PubMed ID: 27374770
[TBL] [Abstract][Full Text] [Related]
3. DONSON facilitates Cdc45 and GINS chromatin association and is essential for DNA replication initiation.
Kingsley G; Skagia A; Passaretti P; Fernandez-Cuesta C; Reynolds-Winczura A; Koscielniak K; Gambus A
Nucleic Acids Res; 2023 Oct; 51(18):9748-9763. PubMed ID: 37638758
[TBL] [Abstract][Full Text] [Related]
4. Tissue-Specific DNA Replication Defects in
McDaniel SL; Hollatz AJ; Branstad AM; Gaskill MM; Fox CA; Harrison MM
Genetics; 2020 Feb; 214(2):355-367. PubMed ID: 31818869
[TBL] [Abstract][Full Text] [Related]
5. Biallelic
Nabais Sá MJ; Miller KA; McQuaid M; Koelling N; Wilkie AOM; Wurtele H; de Brouwer APM; Oliveira J
J Med Genet; 2022 Aug; 59(8):776-780. PubMed ID: 34353863
[TBL] [Abstract][Full Text] [Related]
6. Defective replication initiation results in locus specific chromosome breakage and a ribosomal RNA deficiency in yeast.
Sanchez JC; Kwan EX; Pohl TJ; Amemiya HM; Raghuraman MK; Brewer BJ
PLoS Genet; 2017 Oct; 13(10):e1007041. PubMed ID: 29036220
[TBL] [Abstract][Full Text] [Related]
7. Zebrafish cdc6 hypomorphic mutation causes Meier-Gorlin syndrome-like phenotype.
Yao L; Chen J; Wu X; Jia S; Meng A
Hum Mol Genet; 2017 Nov; 26(21):4168-4180. PubMed ID: 28985365
[TBL] [Abstract][Full Text] [Related]
8. Functional studies in yeast confirm the pathogenicity of a new GINS3 Meier-Gorlin syndrome variant.
Mehrjoo Y; Campeau PM; Al Abdi L; Aldowaish A; Abouyousef O; Alkuraya FS; Codina-Solà M; Cueto-González AM; Wurtele H
Clin Genet; 2024 May; ():. PubMed ID: 38773883
[TBL] [Abstract][Full Text] [Related]
9. MCM complex members MCM3 and MCM7 are associated with a phenotypic spectrum from Meier-Gorlin syndrome to lipodystrophy and adrenal insufficiency.
Knapp KM; Jenkins DE; Sullivan R; Harms FL; von Elsner L; Ockeloen CW; de Munnik S; Bongers EMHF; Murray J; Pachter N; Denecke J; Kutsche K; Bicknell LS
Eur J Hum Genet; 2021 Jul; 29(7):1110-1120. PubMed ID: 33654309
[TBL] [Abstract][Full Text] [Related]
10. MCM5: a new actor in the link between DNA replication and Meier-Gorlin syndrome.
Vetro A; Savasta S; Russo Raucci A; Cerqua C; Sartori G; Limongelli I; Forlino A; Maruelli S; Perucca P; Vergani D; Mazzini G; Mattevi A; Stivala LA; Salviati L; Zuffardi O
Eur J Hum Genet; 2017 May; 25(5):646-650. PubMed ID: 28198391
[TBL] [Abstract][Full Text] [Related]
11. Helicase Subunit Cdc45 Targets the Checkpoint Kinase Rad53 to Both Replication Initiation and Elongation Complexes after Fork Stalling.
Can G; Kauerhof AC; Macak D; Zegerman P
Mol Cell; 2019 Feb; 73(3):562-573.e3. PubMed ID: 30595439
[TBL] [Abstract][Full Text] [Related]
12. The ORC/Cdc6/MCM2–7 complex, a new power player for regulated helicase loading.
Riera A; Fernández-Cid A; Speck C
Cell Cycle; 2013 Jul; 12(14):2155-6. PubMed ID: 23803736
[No Abstract] [Full Text] [Related]
13. The Eukaryotic CMG Helicase at the Replication Fork: Emerging Architecture Reveals an Unexpected Mechanism.
Li H; O'Donnell ME
Bioessays; 2018 Mar; 40(3):. PubMed ID: 29405332
[TBL] [Abstract][Full Text] [Related]
14. Cdt1 variants reveal unanticipated aspects of interactions with cyclin/CDK and MCM important for normal genome replication.
Pozo PN; Matson JP; Cole Y; Kedziora KM; Grant GD; Temple B; Cook JG
Mol Biol Cell; 2018 Dec; 29(25):2989-3002. PubMed ID: 30281379
[TBL] [Abstract][Full Text] [Related]
15. Linked-read genome sequencing identifies biallelic pathogenic variants in
Knapp KM; Sullivan R; Murray J; Gimenez G; Arn P; D'Souza P; Gezdirici A; Wilson WG; Jackson AP; Ferreira C; Bicknell LS
J Med Genet; 2020 Mar; 57(3):195-202. PubMed ID: 31784481
[TBL] [Abstract][Full Text] [Related]
16. Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome.
Stiff T; Alagoz M; Alcantara D; Outwin E; Brunner HG; Bongers EM; O'Driscoll M; Jeggo PA
PLoS Genet; 2013; 9(3):e1003360. PubMed ID: 23516378
[TBL] [Abstract][Full Text] [Related]
17. DONSON is required for CMG helicase assembly in the mammalian cell cycle.
Evrin C; Alvarez V; Ainsworth J; Fujisawa R; Alabert C; Labib KP
EMBO Rep; 2023 Nov; 24(11):e57677. PubMed ID: 37781960
[TBL] [Abstract][Full Text] [Related]
18. Drosophila model of Meier-Gorlin syndrome based on the mutation in a conserved C-Terminal domain of Orc6.
Balasov M; Akhmetova K; Chesnokov I
Am J Med Genet A; 2015 Nov; 167A(11):2533-40. PubMed ID: 26139588
[TBL] [Abstract][Full Text] [Related]
19. Dpb11 protein helps control assembly of the Cdc45·Mcm2-7·GINS replication fork helicase.
Dhingra N; Bruck I; Smith S; Ning B; Kaplan DL
J Biol Chem; 2015 Mar; 290(12):7586-601. PubMed ID: 25659432
[TBL] [Abstract][Full Text] [Related]
20. Dormant origins, the licensing checkpoint, and the response to replicative stresses.
McIntosh D; Blow JJ
Cold Spring Harb Perspect Biol; 2012 Oct; 4(10):. PubMed ID: 22904560
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
