171 related articles for article (PubMed ID: 35289477)
1. Human cerebral organoids reveal progenitor pathology in EML1-linked cortical malformation.
Jabali A; Hoffrichter A; Uzquiano A; Marsoner F; Wilkens R; Siekmann M; Bohl B; Rossetti AC; Horschitz S; Koch P; Francis F; Ladewig J
EMBO Rep; 2022 May; 23(5):e54027. PubMed ID: 35289477
[TBL] [Abstract][Full Text] [Related]
2. Mutations in the Heterotopia Gene Eml1/EML1 Severely Disrupt the Formation of Primary Cilia.
Uzquiano A; Cifuentes-Diaz C; Jabali A; Romero DM; Houllier A; Dingli F; Maillard C; Boland A; Deleuze JF; Loew D; Mancini GMS; Bahi-Buisson N; Ladewig J; Francis F
Cell Rep; 2019 Aug; 28(6):1596-1611.e10. PubMed ID: 31390572
[TBL] [Abstract][Full Text] [Related]
3. A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects.
Markus F; Kannengießer A; Näder P; Atigbire P; Scholten A; Vössing C; Bültmann E; Korenke GC; Owczarek-Lipska M; Neidhardt J
J Hum Genet; 2021 Dec; 66(12):1159-1167. PubMed ID: 34211111
[TBL] [Abstract][Full Text] [Related]
4. Cerebral organoids to unravel the mechanisms underlying malformations of human cortical development.
Krefft O; Koch P; Ladewig J
Semin Cell Dev Biol; 2021 Mar; 111():15-22. PubMed ID: 32741653
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human.
Kielar M; Tuy FP; Bizzotto S; Lebrand C; de Juan Romero C; Poirier K; Oegema R; Mancini GM; Bahi-Buisson N; Olaso R; Le Moing AG; Boutourlinsky K; Boucher D; Carpentier W; Berquin P; Deleuze JF; Belvindrah R; Borrell V; Welker E; Chelly J; Croquelois A; Francis F
Nat Neurosci; 2014 Jul; 17(7):923-33. PubMed ID: 24859200
[TBL] [Abstract][Full Text] [Related]
7. Cell-to-Cell Adhesion and Neurogenesis in Human Cortical Development: A Study Comparing 2D Monolayers with 3D Organoid Cultures.
Scuderi S; Altobelli GG; Cimini V; Coppola G; Vaccarino FM
Stem Cell Reports; 2021 Feb; 16(2):264-280. PubMed ID: 33513360
[TBL] [Abstract][Full Text] [Related]
8. Distinctive genomic signature of neural and intestinal organoids from familial Parkinson's disease patient-derived induced pluripotent stem cells.
Son MY; Sim H; Son YS; Jung KB; Lee MO; Oh JH; Chung SK; Jung CR; Kim J
Neuropathol Appl Neurobiol; 2017 Dec; 43(7):584-603. PubMed ID: 28235153
[TBL] [Abstract][Full Text] [Related]
9. Eml1 loss impairs apical progenitor spindle length and soma shape in the developing cerebral cortex.
Bizzotto S; Uzquiano A; Dingli F; Ershov D; Houllier A; Arras G; Richards M; Loew D; Minc N; Croquelois A; Houdusse A; Francis F
Sci Rep; 2017 Dec; 7(1):17308. PubMed ID: 29229923
[TBL] [Abstract][Full Text] [Related]
10. Establishing Cerebral Organoids as Models of Human-Specific Brain Evolution.
Pollen AA; Bhaduri A; Andrews MG; Nowakowski TJ; Meyerson OS; Mostajo-Radji MA; Di Lullo E; Alvarado B; Bedolli M; Dougherty ML; Fiddes IT; Kronenberg ZN; Shuga J; Leyrat AA; West JA; Bershteyn M; Lowe CB; Pavlovic BJ; Salama SR; Haussler D; Eichler EE; Kriegstein AR
Cell; 2019 Feb; 176(4):743-756.e17. PubMed ID: 30735633
[TBL] [Abstract][Full Text] [Related]
11. Dynamic behaviour of human neuroepithelial cells in the developing forebrain.
Subramanian L; Bershteyn M; Paredes MF; Kriegstein AR
Nat Commun; 2017 Jan; 8():14167. PubMed ID: 28139695
[TBL] [Abstract][Full Text] [Related]
12. EML1-associated brain overgrowth syndrome with ribbon-like heterotopia.
Oegema R; McGillivray G; Leventer R; Le Moing AG; Bahi-Buisson N; Barnicoat A; Mandelstam S; Francis D; Francis F; Mancini GMS; Savelberg S; van Haaften G; Mankad K; Lequin MH
Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):627-637. PubMed ID: 31710781
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. An Organoid-Based Model of Cortical Development Identifies Non-Cell-Autonomous Defects in Wnt Signaling Contributing to Miller-Dieker Syndrome.
Iefremova V; Manikakis G; Krefft O; Jabali A; Weynans K; Wilkens R; Marsoner F; Brändl B; Müller FJ; Koch P; Ladewig J
Cell Rep; 2017 Apr; 19(1):50-59. PubMed ID: 28380362
[TBL] [Abstract][Full Text] [Related]
15. A deletion in Eml1 leads to bilateral subcortical heterotopia in the tish rat.
Grosenbaugh DK; Joshi S; Fitzgerald MP; Lee KS; Wagley PK; Koeppel AF; Turner SD; McConnell MJ; Goodkin HP
Neurobiol Dis; 2020 Jul; 140():104836. PubMed ID: 32179177
[TBL] [Abstract][Full Text] [Related]
16. [Mutations in Eml1/EML1 lead to ectopic progenitors and neuronal heterotopia in mouse and human].
Kielar M; Phan Dinh Tuy F; Bizzotto S; Belvindrah R; Croquelois A; Francis F
Med Sci (Paris); 2014 Dec; 30(12):1087-90. PubMed ID: 25537038
[No Abstract] [Full Text] [Related]
17. Shared effects of DISC1 disruption and elevated WNT signaling in human cerebral organoids.
Srikanth P; Lagomarsino VN; Muratore CR; Ryu SC; He A; Taylor WM; Zhou C; Arellano M; Young-Pearse TL
Transl Psychiatry; 2018 Apr; 8(1):77. PubMed ID: 29643329
[TBL] [Abstract][Full Text] [Related]
18. The neuroanatomy of Eml1 knockout mice, a model of subcortical heterotopia.
Collins SC; Uzquiano A; Selloum M; Wendling O; Gaborit M; Osipenko M; Birling MC; Yalcin B; Francis F
J Anat; 2019 Sep; 235(3):637-650. PubMed ID: 31173351
[TBL] [Abstract][Full Text] [Related]
19. Ethanol exposure disrupted the formation of radial glial processes and impaired the generation and migration of outer radial glial cells in forebrain organoids derived from human embryonic stem cells.
Lü L; Yuan F; Fan H; Li Y; Liu J; Feng W; Zhang HG; Chen SY
Exp Neurol; 2023 Apr; 362():114325. PubMed ID: 36669750
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
