Papers associated with olig2

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	Hox3 genes coordinate mechanisms of genetic suppression and activation in the generation of branchial and somatic motoneurons., Gaufo GO, Thomas KR, Capecchi MR., Development. November 1, 2003; 130 (21): 5191-201.
	Identification of mutants in inbred Xenopus tropicalis., Grammer TC, Khokha MK, Lane MA, Lam K, Harland RM., Mech Dev. March 1, 2005; 122 (3): 263-72.
	The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis., Bronchain OJ, Pollet N, Ymlahi-Ouazzani Q, Dhorne-Pollet S, Helbling JC, Lecarpentier JE, Percheron K, Wegnez M., Dev Genes Evol. July 1, 2007; 217 (7): 485-97.
	From fish to man: understanding endogenous remyelination in central nervous system demyelinating diseases., Dubois-Dalcq M, Williams A, Stadelmann C, Stankoff B, Zalc B, Lubetzki C., Brain. July 1, 2008; 131 (Pt 7): 1686-700.
	Sponge genes provide new insight into the evolutionary origin of the neurogenic circuit., Richards GS, Simionato E, Perron M, Adamska M, Vervoort M, Degnan BM., Curr Biol. August 5, 2008; 18 (15): 1156-61.
	Olig2 lineage cells generate GABAergic neurons in the prethalamic nuclei, including the zona incerta, ventral lateral geniculate nucleus and reticular thalamic nucleus., Inamura N, Ono K, Takebayashi H, Zalc B, Ikenaka K., Dev Neurosci. January 1, 2011; 33 (2): 118-29.
	Ascl1/Mash1 promotes brain oligodendrogenesis during myelination and remyelination., Nakatani H, Martin E, Hassani H, Clavairoly A, Maire CL, Viadieu A, Kerninon C, Delmasure A, Frah M, Weber M, Nakafuku M, Zalc B, Thomas JL, Guillemot F, Nait-Oumesmar B, Parras C., J Neurosci. June 5, 2013; 33 (23): 9752-9768.
	Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus., Roberts NA, Woolf AS, Stuart HM, Thuret R, McKenzie EA, Newman WG, Hilton EN., Hum Mol Genet. August 15, 2014; 23 (16): 4302-14.
	Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination., He D, Marie C, Zhao C, Kim B, Wang J, Deng Y, Clavairoly A, Frah M, Wang H, He X, Hmidan H, Jones BV, Witte D, Zalc B, Zhou X, Choo DI, Martin DM, Parras C, Lu QR., Nat Neurosci. May 1, 2016; 19 (5): 678-89.
	Zebrafish cyclin Dx is required for development of motor neuron progenitors, and its expression is regulated by hypoxia-inducible factor 2α., Lien HW, Yuan RY, Chou CM, Chen YC, Hung CC, Hu CH, Hwang SP, Hwang PP, Shen CN, Chen CL, Cheng CH, Huang CJ., Sci Rep. June 21, 2016; 6 28297.
	Heterogeneity of the astrocytic AMPA-receptor transcriptome., Mölders A, Koch A, Menke R, Klöcker N., Glia. December 1, 2018; 66 (12): 2604-2616.
	Nervous NDRGs: the N-myc downstream-regulated gene family in the central and peripheral nervous system., Schonkeren SL, Massen M, van der Horst R, Koch A, Vaes N, Melotte V., Neurogenetics. October 1, 2019; 20 (4): 173-186.
	Hes5.9 Coordinate FGF and Notch Signaling to Modulate Gastrulation via Regulating Cell Fate Specification and Cell Migration in Xenopus tropicalis., Huang X, Zhang L, Yang S, Zhang Y, Wu M, Chen P., Genes (Basel). November 18, 2020; 11 (11):
	Parallel in vivo analysis of large-effect autism genes implicates cortical neurogenesis and estrogen in risk and resilience., Willsey HR, Exner CRT, Xu Y, Xu Y, Everitt A, Sun N, Wang B, Dea J, Schmunk G, Zaltsman Y, Teerikorpi N, Kim A, Anderson AS, Shin D, Seyler M, Nowakowski TJ, Harland RM, Willsey AJ, State MW., Neuron. March 3, 2021; 109 (5): 788-804.e8.
	Teriflunomide Promotes Oligodendroglial 8,9-Unsaturated Sterol Accumulation and CNS Remyelination., Martin E, Aigrot MS, Lamari F, Bachelin C, Lubetzki C, Nait Oumesmar B, Zalc B, Stankoff B., Neurol Neuroimmunol Neuroinflamm. November 1, 2021; 8 (6):
	Cell landscape of larval and adult Xenopus laevis at single-cell resolution., Liao Y, Ma L, Guo Q, E W, Fang X, Yang L, Ruan F, Wang J, Zhang P, Sun Z, Chen H, Lin Z, Wang X, Wang X, Sun H, Fang X, Zhou Y, Chen M, Shen W, Guo G, Han X., Nat Commun. July 25, 2022; 13 (1): 4306.
	Deleterious functional consequences of perfluoroalkyl substances accumulation into the myelin sheath., Butruille L, Jubin P, Martin E, Aigrot MS, Lhomme M, Fini JB, Demeneix B, Stankoff B, Lubetzki C, Zalc B, Remaud S., Environ Int. October 1, 2023; 180 108211.
	Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders., Kaiyrzhanov R, Rad A, Lin SJ, Bertoli-Avella A, Kallemeijn WW, Godwin A, Zaki MS, Huang K, Lau T, Petree C, Efthymiou S, Karimiani EG, Hempel M, Normand EA, Rudnik-Schöneborn S, Schatz UA, Baggelaar MP, Ilyas M, Sultan T, Alvi JR, Ganieva M, Fowler B, Aanicai R, Tayfun GA, Al Saman A, Alswaid A, Amiri N, Asilova N, Shotelersuk V, Yeetong P, Azam M, Babaei M, Monajemi GB, Mohammadi P, Samie S, Banu SH, Pinto Basto J, Kortüm F, Bauer M, Bauer P, Beetz C, Garshasbi M, Issa AH, Eyaid W, Ahmed H, Hashemi N, Hassanpour K, Herman I, Ibrohimov S, Abdul-Majeed BA, Imdad M, Isrofilov M, Kaiyal Q, Khan S, Kirmse B, Koster J, Lourenço CM, Mitani T, Moldovan O, Murphy D, Najafi M, Pehlivan D, Rocha ME, Salpietro V, Schmidts M, Shalata A, Mahroum M, Talbeya JK, Taylor RW, Vazquez D, Vetro A, Waterham HR, Zaman M, Schrader TA, Chung WK, Guerrini R, Lupski JR, Gleeson J, Suri M, Jamshidi Y, Bhatia KP, Vona B, Schrader M, Severino M, Guille M, Tate EW, Varshney GK, Houlden H, Maroofian R., Brain. April 4, 2024; 147 (4): 1436-1456.

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