307 related articles for article (PubMed ID: 35792828)
1. Human iPSC-derived cerebral organoids model features of Leigh syndrome and reveal abnormal corticogenesis.
Romero-Morales AI; Robertson GL; Rastogi A; Rasmussen ML; Temuri H; McElroy GS; Chakrabarty RP; Hsu L; Almonacid PM; Millis BA; Chandel NS; Cartailler JP; Gama V
Development; 2022 Oct; 149(20):. PubMed ID: 35792828
[TBL] [Abstract][Full Text] [Related]
2. Defective metabolic programming impairs early neuronal morphogenesis in neural cultures and an organoid model of Leigh syndrome.
Inak G; Rybak-Wolf A; Lisowski P; Pentimalli TM; Jüttner R; Glažar P; Uppal K; Bottani E; Brunetti D; Secker C; Zink A; Meierhofer D; Henke MT; Dey M; Ciptasari U; Mlody B; Hahn T; Berruezo-Llacuna M; Karaiskos N; Di Virgilio M; Mayr JA; Wortmann SB; Priller J; Gotthardt M; Jones DP; Mayatepek E; Stenzel W; Diecke S; Kühn R; Wanker EE; Rajewsky N; Schuelke M; Prigione A
Nat Commun; 2021 Mar; 12(1):1929. PubMed ID: 33771987
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial Dysfunction and Calcium Dysregulation in Leigh Syndrome Induced Pluripotent Stem Cell Derived Neurons.
Galera-Monge T; Zurita-Díaz F; Canals I; Hansen MG; Rufián-Vázquez L; Ehinger JK; Elmér E; Martin MA; Garesse R; Ahlenius H; Gallardo ME
Int J Mol Sci; 2020 Apr; 21(9):. PubMed ID: 32366037
[TBL] [Abstract][Full Text] [Related]
4. Human Cytomegalovirus Compromises Development of Cerebral Organoids.
Brown RM; Rana PSJB; Jaeger HK; O'Dowd JM; Balemba OB; Fortunato EA
J Virol; 2019 Sep; 93(17):. PubMed ID: 31217239
[TBL] [Abstract][Full Text] [Related]
5. Metabolic Signature of MELAS/Leigh Overlap Syndrome in Patient-specific Induced Pluripotent Stem Cells Model.
Hattori T; Hamazaki T; Kudo S; Shintaku H
Osaka City Med J; 2016 Dec; 62(2):69-76. PubMed ID: 30721581
[TBL] [Abstract][Full Text] [Related]
6. Cytochrome C oxydase deficiency: SURF1 gene investigation in patients with Leigh syndrome.
Maalej M; Kammoun T; Alila-Fersi O; Kharrat M; Ammar M; Felhi R; Mkaouar-Rebai E; Keskes L; Hachicha M; Fakhfakh F
Biochem Biophys Res Commun; 2018 Mar; 497(4):1043-1048. PubMed ID: 29481804
[TBL] [Abstract][Full Text] [Related]
7. Generation of a human iPSC line from a patient with Leigh syndrome caused by a mutation in the MT-ATP6 gene.
Galera-Monge T; Zurita-Díaz F; González-Páramos C; Moreno-Izquierdo A; Fraga MF; Fernández AF; Garesse R; Gallardo ME
Stem Cell Res; 2016 May; 16(3):766-9. PubMed ID: 27346203
[No Abstract] [Full Text] [Related]
8. Metabolic rescue in pluripotent cells from patients with mtDNA disease.
Ma H; Folmes CD; Wu J; Morey R; Mora-Castilla S; Ocampo A; Ma L; Poulton J; Wang X; Ahmed R; Kang E; Lee Y; Hayama T; Li Y; Van Dyken C; Gutierrez NM; Tippner-Hedges R; Koski A; Mitalipov N; Amato P; Wolf DP; Huang T; Terzic A; Laurent LC; Izpisua Belmonte JC; Mitalipov S
Nature; 2015 Aug; 524(7564):234-8. PubMed ID: 26176921
[TBL] [Abstract][Full Text] [Related]
9. Generation of four iPSC lines from four patients with Leigh syndrome carrying homoplasmic mutations m.8993T > G or m.8993T > C in the mitochondrial gene MT-ATP6.
Lorenz C; Zink A; Henke MT; Staege S; Mlody B; Bünning M; Wanker E; Diecke S; Schuelke M; Prigione A
Stem Cell Res; 2022 May; 61():102742. PubMed ID: 35279592
[TBL] [Abstract][Full Text] [Related]
10. Genotype-phenotype analysis of MT-ATP6-associated Leigh syndrome.
Na JH; Lee YM
Acta Neurol Scand; 2022 Apr; 145(4):414-422. PubMed ID: 34877647
[TBL] [Abstract][Full Text] [Related]
11. mRNA Reprogramming of T8993G Leigh's Syndrome Fibroblast Cells to Create Induced Pluripotent Stem Cell Models for Mitochondrial Disorders.
Grace HE; Galdun P; Lesnefsky EJ; West FD; Iyer S
Stem Cells Dev; 2019 Jul; 28(13):846-859. PubMed ID: 31017045
[TBL] [Abstract][Full Text] [Related]
12. Metabolic rescue ameliorates mitochondrial encephalo-cardiomyopathy in murine and human iPSC models of Leigh syndrome.
Yoon JY; Daneshgar N; Chu Y; Chen B; Hefti M; Vikram A; Irani K; Song LS; Brenner C; Abel ED; London B; Dai DF
Clin Transl Med; 2022 Jul; 12(7):e954. PubMed ID: 35872650
[TBL] [Abstract][Full Text] [Related]
13. Generation of two mother-child pairs of iPSCs from maternally inherited Leigh syndrome patients with m.8993 T > G and m.9176 T > G MT-ATP6 mutations.
Henke MT; Zink A; Diecke S; Prigione A; Schuelke M
Stem Cell Res; 2023 Mar; 67():103030. PubMed ID: 36669241
[TBL] [Abstract][Full Text] [Related]
14. Comparative Transcriptomic Analysis of Cerebral Organoids and Cortical Neuron Cultures Derived from Human Induced Pluripotent Stem Cells.
Kathuria A; Lopez-Lengowski K; Watmuff B; Karmacharya R
Stem Cells Dev; 2020 Nov; 29(21):1370-1381. PubMed ID: 32862797
[TBL] [Abstract][Full Text] [Related]
15. Generation of an induced pluripotent stem cell line (IUFi002-A) from a Leigh syndrome patient carrying mutations in the NDUFS1 gene.
Valente O; Dobner J; Ramachandran H; Hildebrandt B; Distelmaier F; Ventura N; Rossi A
Stem Cell Res; 2022 Dec; 65():102971. PubMed ID: 36403546
[TBL] [Abstract][Full Text] [Related]
16. The NAD
Hong Y; Zhang Z; Yangzom T; Chen A; Lundberg BC; Fang EF; Siller R; Sullivan GJ; Zeman J; Tzoulis C; Bindoff LA; Liang KX
Int J Biol Sci; 2024; 20(4):1194-1217. PubMed ID: 38385069
[TBL] [Abstract][Full Text] [Related]
17. Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
Iannetti EF; Smeitink JAM; Willems PHGM; Beyrath J; Koopman WJH
Cell Death Dis; 2018 Nov; 9(11):1135. PubMed ID: 30429455
[TBL] [Abstract][Full Text] [Related]
18. A novel neuronal organoid model mimicking glioblastoma (GBM) features from induced pluripotent stem cells (iPSC).
Hwang JW; Loisel-Duwattez J; Desterke C; Latsis T; Pagliaro S; Griscelli F; Bennaceur-Griscelli A; Turhan AG
Biochim Biophys Acta Gen Subj; 2020 Apr; 1864(4):129540. PubMed ID: 31978452
[TBL] [Abstract][Full Text] [Related]
19. Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations.
Yu XL; Yan CZ; Ji KQ; Lin PF; Xu XB; Dai TJ; Li W; Zhao YY
Chin Med J (Engl); 2018 Nov; 131(22):2705-2712. PubMed ID: 30425197
[TBL] [Abstract][Full Text] [Related]
20. Gene correction of the CLN3 c.175G>A variant in patient-derived induced pluripotent stem cells prevents pathological changes in retinal organoids.
Zhang X; Zhang D; Thompson JA; Chen SC; Huang Z; Jennings L; McLaren TL; Lamey TM; De Roach JN; Chen FK; McLenachan S
Mol Genet Genomic Med; 2021 Mar; 9(3):e1601. PubMed ID: 33497524
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]