These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 36403546)
1. 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]
2. Generation of an induced pluripotent stem cell line (IUFi001) from a Cockayne syndrome patient carrying a mutation in the ERCC6 gene. Martins S; Hacheney I; Teichweyde N; Hildebrandt B; Krutmann J; Rossi A Stem Cell Res; 2021 Aug; 55():102456. PubMed ID: 34271225 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Generation of two induced pluripotent stem cells lines from a Mucopolysaccharydosis IIIB (MPSIIIB) patient. Vallejo-Diez S; Fleischer A; Martín-Fernández JM; Sánchez-Gilabert A; Bachiller D Stem Cell Res; 2018 Dec; 33():180-184. PubMed ID: 30408744 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. Generation of a human iPSC line from a patient with Leigh syndrome. Galera T; Zurita F; González-Páramos C; Moreno-Izquierdo A; Fraga MF; Fernández AF; Garesse R; Gallardo ME Stem Cell Res; 2016 Jan; 16(1):63-6. PubMed ID: 27345786 [TBL] [Abstract][Full Text] [Related]
7. Self-replicative mRNA-mediated generation of induced pluripotent stem cell line from a 1-year-old Leigh syndrome patient with mitochondrial DNA cytochrome b mutation. Son D; Zheng J; Kim IY; You S Stem Cell Res; 2021 Jul; 54():102392. PubMed ID: 34091428 [TBL] [Abstract][Full Text] [Related]
8. Generation of induced pluripotent stem cells (iPSCs) IRMBi002-A from an Alzheimer's disease patient carrying a D694N mutation in the APP gene. Auboyer L; Monzo C; Wallon D; Rovelet-Lecrux A; Gabelle A; Gazagne I; Cacheux V; Lehmann S; Crozet C Stem Cell Res; 2019 May; 37():101438. PubMed ID: 31004935 [TBL] [Abstract][Full Text] [Related]
9. Generation of a human induced pluripotent stem cell line NTUHi004-A from a patient with Leigh syndrome harboring a homozygous missense mutation c.836 T > G (p.Met279Arg) in NDUFAF5 gene. Ou-Yang CH; Chen PS; Lin CH Stem Cell Res; 2024 Apr; 76():103379. PubMed ID: 38458030 [TBL] [Abstract][Full Text] [Related]
10. Fibroblast-derived integration-free iPSC line ISRM-NBS1 from an 18-year-old Nijmegen Breakage Syndrome patient carrying the homozygous NBN c.657_661del5 mutation. Martins S; Bohndorf M; Graffmann N; Wruck W; Chrzanowska KH; Adjaye J Stem Cell Res; 2019 Jan; 34():101372. PubMed ID: 30616142 [TBL] [Abstract][Full Text] [Related]
12. Generation of a Crigler-Najjar Syndrome Type I patient-derived induced pluripotent stem cell line CNS705 (HHUUKDi005-A). Graffmann N; Martins S; Ljubikj T; Matte JC; Bohndorf M; Wruck W; Adjaye J Stem Cell Res; 2021 Mar; 51():102167. PubMed ID: 33485181 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Leigh syndrome associated with mitochondrial complex I deficiency due to a novel mutation in the NDUFS1 gene. Martín MA; Blázquez A; Gutierrez-Solana LG; Fernández-Moreira D; Briones P; Andreu AL; Garesse R; Campos Y; Arenas J Arch Neurol; 2005 Apr; 62(4):659-61. PubMed ID: 15824269 [TBL] [Abstract][Full Text] [Related]
15. Generation of induced pluripotent stem cells (IRMBi001-A) from an Alzheimer's disease patient carrying a G217D mutation in the PSEN1 gene. Auboyer L; Monzo C; Wallon D; Rovelet-Lecrux A; Gabelle A; Gazagne I; Cacheux V; Lehmann S; Crozet C Stem Cell Res; 2019 Jan; 34():101381. PubMed ID: 30677723 [TBL] [Abstract][Full Text] [Related]
16. Generation of an induced pluripotent stem cell line (UBCi001-A) from a presymptomatic individual carrying the R418X progranulin gene mutation. Frew J; Wu X; Hsiung GY; Feldman HH; Mackenzie IR; Nygaard HB Stem Cell Res; 2019 Dec; 41():101582. PubMed ID: 31707213 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene. López-Márquez A; Alonso-Barroso E; Cerro-Tello G; Bravo-Alonso I; Arribas-Carreira L; Briso-Montiano Á; Navarrete R; Pérez-Cerdá C; Ugarte M; Pérez B; Desviat LR; Richard E Stem Cell Res; 2019 Jul; 38():101469. PubMed ID: 31132581 [TBL] [Abstract][Full Text] [Related]
19. Establishment of transgene-free induced pluripotent stem cells reprogrammed from human stem cells of apical papilla for neural differentiation. Zou XY; Yang HY; Yu Z; Tan XB; Yan X; Huang GT Stem Cell Res Ther; 2012 Oct; 3(5):43. PubMed ID: 23095454 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]