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Journal Abstract Search

237 related items for PubMed ID: 25995483

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  • 4. The Prdm13 histone methyltransferase encoding gene is a Ptf1a-Rbpj downstream target that suppresses glutamatergic and promotes GABAergic neuronal fate in the dorsal neural tube.
    Hanotel J, Bessodes N, Thélie A, Hedderich M, Parain K, Van Driessche B, Brandão Kde O, Kricha S, Jorgensen MC, Grapin-Botton A, Serup P, Van Lint C, Perron M, Pieler T, Henningfeld KA, Bellefroid EJ.
    Dev Biol; 2014 Feb 15; 386(2):340-57. PubMed ID: 24370451
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  • 7. Ectopic transgene expression in the retina of four transgenic mouse lines.
    Gábriel R, Erdélyi F, Szabó G, Lawrence JJ, Wilhelm M.
    Brain Struct Funct; 2016 Sep 15; 221(7):3729-41. PubMed ID: 26563404
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  • 8. Ptf1a is essential for the differentiation of GABAergic and glycinergic amacrine cells and horizontal cells in the mouse retina.
    Nakhai H, Sel S, Favor J, Mendoza-Torres L, Paulsen F, Duncker GI, Schmid RM.
    Development; 2007 Mar 15; 134(6):1151-60. PubMed ID: 17301087
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  • 10. Commentary: "Prdm13 regulates subtype specification of retinal amacrine interneurons and modulates visual sensitivity".
    Bowrey HE, James MH.
    Front Cell Neurosci; 2015 Mar 15; 9():424. PubMed ID: 26578884
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  • 12. Role of the Barhl2 homeobox gene in the specification of glycinergic amacrine cells.
    Mo Z, Li S, Yang X, Xiang M.
    Development; 2004 Apr 15; 131(7):1607-18. PubMed ID: 14998930
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  • 14. Transcription factor LIM homeobox 7 (Lhx7) maintains subtype identity of cholinergic interneurons in the mammalian striatum.
    Lopes R, Verhey van Wijk N, Neves G, Pachnis V.
    Proc Natl Acad Sci U S A; 2012 Feb 21; 109(8):3119-24. PubMed ID: 22315402
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  • 16. Immunocytochemical localization of cholinergic amacrine cells in the bat retina.
    Park EB, Gu YN, Jeon CJ.
    Acta Histochem; 2017 May 21; 119(4):428-437. PubMed ID: 28483062
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  • 17. Transcription factor PRDM8 is required for rod bipolar and type 2 OFF-cone bipolar cell survival and amacrine subtype identity.
    Jung CC, Atan D, Ng D, Ploder L, Ross SE, Klein M, Birch DG, Diez E, McInnes RR.
    Proc Natl Acad Sci U S A; 2015 Jun 09; 112(23):E3010-9. PubMed ID: 26023183
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  • 18. A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia.
    Whittaker DE, Oleari R, Gregory LC, Le Quesne-Stabej P, Williams HJ, GOSgene, Torpiano JG, Formosa N, Cachia MJ, Field D, Lettieri A, Ocaka LA, Paganoni AJ, Rajabali SH, Riegman KL, De Martini LB, Chaya T, Robinson IC, Furukawa T, Cariboni A, Basson MA, Dattani MT.
    J Clin Invest; 2021 Dec 15; 131(24):. PubMed ID: 34730112
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