149 related articles for article (PubMed ID: 32761840)
1. RAB39B's role in membrane traffic, autophagy, and associated neuropathology.
Tang BL
J Cell Physiol; 2021 Mar; 236(3):1579-1592. PubMed ID: 32761840
[TBL] [Abstract][Full Text] [Related]
2. Cerebral organoid and mouse models reveal a RAB39b-PI3K-mTOR pathway-dependent dysregulation of cortical development leading to macrocephaly/autism phenotypes.
Zhang W; Ma L; Yang M; Shao Q; Xu J; Lu Z; Zhao Z; Chen R; Chai Y; Chen JF
Genes Dev; 2020 Apr; 34(7-8):580-597. PubMed ID: 32115408
[TBL] [Abstract][Full Text] [Related]
3. Rabs, Membrane Dynamics, and Parkinson's Disease.
Tang BL
J Cell Physiol; 2017 Jul; 232(7):1626-1633. PubMed ID: 27925204
[TBL] [Abstract][Full Text] [Related]
4. The intellectual disability protein RAB39B selectively regulates GluA2 trafficking to determine synaptic AMPAR composition.
Mignogna ML; Giannandrea M; Gurgone A; Fanelli F; Raimondi F; Mapelli L; Bassani S; Fang H; Van Anken E; Alessio M; Passafaro M; Gatti S; Esteban JA; Huganir R; D'Adamo P
Nat Commun; 2015 Mar; 6():6504. PubMed ID: 25784538
[TBL] [Abstract][Full Text] [Related]
5. RAB39B-mediated trafficking of the GluA2-AMPAR subunit controls dendritic spine maturation and intellectual disability-related behaviour.
Mignogna ML; Musardo S; Ranieri G; Gelmini S; Espinosa P; Marra P; Belloli S; Murtaj V; Moresco RM; Bellone C; D'Adamo P
Mol Psychiatry; 2021 Nov; 26(11):6531-6549. PubMed ID: 34035473
[TBL] [Abstract][Full Text] [Related]
6. Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly.
Giannandrea M; Bianchi V; Mignogna ML; Sirri A; Carrabino S; D'Elia E; Vecellio M; Russo S; Cogliati F; Larizza L; Ropers HH; Tzschach A; Kalscheuer V; Oehl-Jaschkowitz B; Skinner C; Schwartz CE; Gecz J; Van Esch H; Raynaud M; Chelly J; de Brouwer AP; Toniolo D; D'Adamo P
Am J Hum Genet; 2010 Feb; 86(2):185-95. PubMed ID: 20159109
[TBL] [Abstract][Full Text] [Related]
7. Dysfunction of RAB39B-Mediated Vesicular Trafficking in Lewy Body Diseases.
Koss DJ; Campesan S; Giorgini F; Outeiro TF
Mov Disord; 2021 Aug; 36(8):1744-1758. PubMed ID: 33939203
[TBL] [Abstract][Full Text] [Related]
8. Clinical characterization of a novel RAB39B nonstop mutation in a family with ASD and severe ID causing RAB39B downregulation and study of a Rab39b knock down mouse model.
Mignogna ML; Ficarella R; Gelmini S; Marzulli L; Ponzi E; Gabellone A; Peschechera A; Alessio M; Margari L; Gentile M; D'Adamo P
Hum Mol Genet; 2022 May; 31(9):1389-1406. PubMed ID: 34761259
[TBL] [Abstract][Full Text] [Related]
9. Mutations in
Woodbury-Smith M; Deneault E; Yuen RKC; Walker S; Zarrei M; Pellecchia G; Howe JL; Hoang N; Uddin M; Marshall CR; Chrysler C; Thompson A; Szatmari P; Scherer SW
Mol Autism; 2017; 8():59. PubMed ID: 29152164
[TBL] [Abstract][Full Text] [Related]
10. Increased level of RAB39B leads to neuronal dysfunction and behavioural changes in mice.
Wang Z; Niu M; Zheng N; Meng J; Jiang Y; Yang D; Yao P; Yao T; Luo H; Xu H; Ge Y; Zhang YW; Zhang X
J Cell Mol Med; 2023 May; 27(9):1214-1226. PubMed ID: 36977207
[TBL] [Abstract][Full Text] [Related]
11. Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology.
Wilson GR; Sim JC; McLean C; Giannandrea M; Galea CA; Riseley JR; Stephenson SE; Fitzpatrick E; Haas SA; Pope K; Hogan KJ; Gregg RG; Bromhead CJ; Wargowski DS; Lawrence CH; James PA; Churchyard A; Gao Y; Phelan DG; Gillies G; Salce N; Stanford L; Marsh AP; Mignogna ML; Hayflick SJ; Leventer RJ; Delatycki MB; Mellick GD; Kalscheuer VM; D'Adamo P; Bahlo M; Amor DJ; Lockhart PJ
Am J Hum Genet; 2014 Dec; 95(6):729-35. PubMed ID: 25434005
[TBL] [Abstract][Full Text] [Related]
12. Distribution of Parkinson's disease associated RAB39B in mouse brain tissue.
Gao Y; Wilson GR; Stephenson SEM; Oulad-Abdelghani M; Charlet-Berguerand N; Bozaoglu K; McLean CA; Thomas PQ; Finkelstein DI; Lockhart PJ
Mol Brain; 2020 Mar; 13(1):52. PubMed ID: 32228644
[TBL] [Abstract][Full Text] [Related]
13. RAB39B Deficiency Impairs Learning and Memory Partially Through Compromising Autophagy.
Niu M; Zheng N; Wang Z; Gao Y; Luo X; Chen Z; Fu X; Wang Y; Wang T; Liu M; Yao T; Yao P; Meng J; Zhou Y; Ge Y; Wang Z; Ma Q; Xu H; Zhang YW
Front Cell Dev Biol; 2020; 8():598622. PubMed ID: 33364235
[No Abstract] [Full Text] [Related]
14. Clinical and Neuropathological Features Associated With Loss of RAB39B.
Gao Y; Martínez-Cerdeño V; Hogan KJ; McLean CA; Lockhart PJ
Mov Disord; 2020 Apr; 35(4):687-693. PubMed ID: 31951675
[TBL] [Abstract][Full Text] [Related]
15. X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.
Ciammola A; Carrera P; Di Fonzo A; Sassone J; Villa R; Poletti B; Ferrari M; Girotti F; Monfrini E; Buongarzone G; Silani V; Cinnante CM; Mignogna ML; D'Adamo P; Bonati MT
Parkinsonism Relat Disord; 2017 Nov; 44():142-146. PubMed ID: 28851564
[TBL] [Abstract][Full Text] [Related]
16. A novel RAB39B mutation and concurrent de novo NF1 mutation in a boy with neurofibromatosis type 1, intellectual disability, and autism: a case report.
Santoro C; Giugliano T; Bernardo P; Palladino F; Torella A; Del Vecchio Blanco F; Onore ME; Carotenuto M; Nigro V; Piluso G
BMC Neurol; 2020 Sep; 20(1):327. PubMed ID: 32873259
[TBL] [Abstract][Full Text] [Related]
17. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease.
Yuan L; Deng X; Song Z; Yang Z; Ni B; Chen Y; Deng H
Neurobiol Aging; 2015 Oct; 36(10):2907.e11-2. PubMed ID: 26163985
[TBL] [Abstract][Full Text] [Related]
18. Novel RAB39B loss-of-function mutation in patient with typical early-onset Parkinson's disease.
Jacobson JR; Piat C; Aksamit AJ; Patane' G; Ross OA; Savica R
Parkinsonism Relat Disord; 2024 Jun; 123():106038. PubMed ID: 38503262
[TBL] [Abstract][Full Text] [Related]
19. The emerging role of Rab GTPases in the pathogenesis of Parkinson's disease.
Gao Y; Wilson GR; Stephenson SEM; Bozaoglu K; Farrer MJ; Lockhart PJ
Mov Disord; 2018 Feb; 33(2):196-207. PubMed ID: 29315801
[TBL] [Abstract][Full Text] [Related]
20. C9orf72's Interaction with Rab GTPases-Modulation of Membrane Traffic and Autophagy.
Tang BL
Front Cell Neurosci; 2016; 10():228. PubMed ID: 27774051
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
