306 related articles for article (PubMed ID: 35792828)
21. The mutation m.13513G>A impairs cardiac function, favoring a neuroectoderm commitment, in a mutant-load dependent way.
Galera-Monge T; Zurita-Díaz F; Garesse R; Gallardo ME
J Cell Physiol; 2019 Nov; 234(11):19511-19522. PubMed ID: 30950033
[TBL] [Abstract][Full Text] [Related]
22. Early infantile-onset Leigh syndrome complicated with infantile spasms associated with the m.9185 T > C variant in the MT-ATP6 gene: Expanding the clinical spectrum.
Takada R; Tozawa T; Kondo H; Kizaki Z; Kishita Y; Okazaki Y; Murayama K; Ohtake A; Chiyonobu T
Brain Dev; 2020 Jan; 42(1):69-72. PubMed ID: 31500933
[TBL] [Abstract][Full Text] [Related]
23. Leigh syndrome caused by mitochondrial DNA-maintenance defects revealed by whole exome sequencing.
Souza PVS; Bortholin T; Teixeira CAC; Seneor DD; Marin VDGB; Dias RB; Farias IB; Badia BML; Silva LHL; Pinto WBVR; Oliveira ASB; DiMauro S
Mitochondrion; 2019 Nov; 49():25-34. PubMed ID: 31271879
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Heteroplasmic Mutant Load Differences in Mitochondrial DNA-Associated Leigh Syndrome.
Na JH; Lee YM
Pediatr Neurol; 2023 Jan; 138():27-32. PubMed ID: 36335839
[TBL] [Abstract][Full Text] [Related]
26. Generation of improved human cerebral organoids from single copy DYRK1A knockout induced pluripotent stem cells in trisomy 21: hypothetical solutions for neurodevelopmental models and therapeutic alternatives in down syndrome.
Çağlayan ES
Cell Biol Int; 2016 Dec; 40(12):1256-1270. PubMed ID: 27743462
[TBL] [Abstract][Full Text] [Related]
27. Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.
Zhang Y; Yang YL; Sun F; Cai X; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Zhang YH; Jiang YW; Qin J; Wu XR
J Inherit Metab Dis; 2007 Apr; 30(2):265. PubMed ID: 17323145
[TBL] [Abstract][Full Text] [Related]
28. Transcriptome analysis and functional characterization of cerebral organoids in bipolar disorder.
Kathuria A; Lopez-Lengowski K; Vater M; McPhie D; Cohen BM; Karmacharya R
Genome Med; 2020 Apr; 12(1):34. PubMed ID: 32306996
[TBL] [Abstract][Full Text] [Related]
29. Human iPSC-Derived Neural Progenitors Are an Effective Drug Discovery Model for Neurological mtDNA Disorders.
Lorenz C; Lesimple P; Bukowiecki R; Zink A; Inak G; Mlody B; Singh M; Semtner M; Mah N; Auré K; Leong M; Zabiegalov O; Lyras EM; Pfiffer V; Fauler B; Eichhorst J; Wiesner B; Huebner N; Priller J; Mielke T; Meierhofer D; Izsvák Z; Meier JC; Bouillaud F; Adjaye J; Schuelke M; Wanker EE; Lombès A; Prigione A
Cell Stem Cell; 2017 May; 20(5):659-674.e9. PubMed ID: 28132834
[TBL] [Abstract][Full Text] [Related]
30. Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders.
Gabriel E; Gopalakrishnan J
J Vis Exp; 2017 Apr; (122):. PubMed ID: 28448044
[TBL] [Abstract][Full Text] [Related]
31. Transcriptomic Landscape and Functional Characterization of Induced Pluripotent Stem Cell-Derived Cerebral Organoids in Schizophrenia.
Kathuria A; Lopez-Lengowski K; Jagtap SS; McPhie D; Perlis RH; Cohen BM; Karmacharya R
JAMA Psychiatry; 2020 Jul; 77(7):745-754. PubMed ID: 32186681
[TBL] [Abstract][Full Text] [Related]
32. Loss of function of the mitochondrial peptidase PITRM1 induces proteotoxic stress and Alzheimer's disease-like pathology in human cerebral organoids.
Pérez MJ; Ivanyuk D; Panagiotakopoulou V; Di Napoli G; Kalb S; Brunetti D; Al-Shaana R; Kaeser SA; Fraschka SA; Jucker M; Zeviani M; Viscomi C; Deleidi M
Mol Psychiatry; 2021 Oct; 26(10):5733-5750. PubMed ID: 32632204
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Human iPSC-Derived Neural Models for Studying Alzheimer's Disease: from Neural Stem Cells to Cerebral Organoids.
Barak M; Fedorova V; Pospisilova V; Raska J; Vochyanova S; Sedmik J; Hribkova H; Klimova H; Vanova T; Bohaciakova D
Stem Cell Rev Rep; 2022 Feb; 18(2):792-820. PubMed ID: 35107767
[TBL] [Abstract][Full Text] [Related]
35. DSCAM/PAK1 pathway suppression reverses neurogenesis deficits in iPSC-derived cerebral organoids from patients with Down syndrome.
Tang XY; Xu L; Wang J; Hong Y; Wang Y; Zhu Q; Wang D; Zhang XY; Liu CY; Fang KH; Han X; Wang S; Wang X; Xu M; Bhattacharyya A; Guo X; Lin M; Liu Y
J Clin Invest; 2021 Jun; 131(12):. PubMed ID: 33945512
[TBL] [Abstract][Full Text] [Related]
36. A Protocol to Study Mitochondrial Function in Human Neural Progenitors and iPSC-Derived Astrocytes.
Assis-de-Lemos G; Ledur PF; Karmirian K; Rehen SK; Galina A
Curr Protoc Toxicol; 2020 Sep; 85(1):e97. PubMed ID: 32881422
[TBL] [Abstract][Full Text] [Related]
37. Mutations in SURF1 are important genetic causes of Leigh syndrome in Slovak patients.
Danis D; Brennerova K; Skopkova M; Kurdiova T; Ukropec J; Stanik J; Kolnikova M; Gasperikova D
Endocr Regul; 2018 Apr; 52(2):110-118. PubMed ID: 29715184
[TBL] [Abstract][Full Text] [Related]
38. Abnormal mitochondria in Down syndrome iPSC-derived GABAergic interneurons and organoids.
Xu L; Huo HQ; Lu KQ; Tang XY; Hong Y; Han X; Fu ZX; Fang KH; Xu M; Guo X; Liu Y
Biochim Biophys Acta Mol Basis Dis; 2022 Jun; 1868(6):166388. PubMed ID: 35301086
[TBL] [Abstract][Full Text] [Related]
39. Clinical and laboratory survey of 65 Chinese patients with Leigh syndrome.
Yang YL; Sun F; Zhang Y; Qian N; Yuan Y; Wang ZX; Qi Y; Xiao JX; Wang XY; Qi ZY; Zhang YH; Jiang YW; Bao XH; Qin J; Wu XR
Chin Med J (Engl); 2006 Mar; 119(5):373-7. PubMed ID: 16542579
[TBL] [Abstract][Full Text] [Related]
40. Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case report.
Sun D; Liu Z; Liu Y; Wu M; Fang F; Deng X; Liu Z; Song L; Murayama K; Zhang C; Zhu Y
BMC Med Genet; 2020 Jul; 21(1):149. PubMed ID: 32677908
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]