| 1 | NTNG1, NTNG2
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| Diversification of behavior and postsynaptic properties by netrin-G presynaptic adhesion family proteins.
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| Zhang Q, Goto H, Akiyoshi-Nishimura S, Prosselkov P, Sano C, Matsukawa H, Yaguchi K, Nakashiba T, Itohara S.
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| Mol Brain 9:6. doi: 10.1186/s13041-016-0187-5.
2016
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| 2 | LRRC4, LRRC4C, NTNG1, NTNG2
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| Netrin-G/NGL complexes encode functional synaptic diversification.
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| Matsukawa H, Akiyoshi-Nishimura S, Zhang Q, Luján R, Yamaguchi K, Goto H, Yaguchi K, Hashikawa T, Sano C, Shigemoto R, Nakashiba T, Itohara S.
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| J Neurosci 34(47):15779-92. doi: 10.1523/JNEUROSCI.1141-14.2014. 2014
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| 3 | NTNG1, NTNG2
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| Identification of transcriptional regulatory elements for Ntng1 and Ntng2 genes in mice.
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| Yaguchi K, Nishimura-Akiyoshi S, Kuroki S, Onodera T, Itohara S.
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| Mol Brain 7:19. doi: 10.1186/1756-6606-7-19.
2014
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| 4 | DCC, EPHB1, NTNG1, SEMA5A, SLIT3
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| Axon guidance and synaptic maintenance: preclinical markers for neurodegenerative disease and therapeutics.
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| Lin L, Lesnick TG, Maraganore DM, Isacson O.
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| Trends Neurosci 32(3):142-9. Epub 2009 Jan 21. Review.PMID: 19162339 2009
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| 5 | NTNG1, NTNG2
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| Decreased mRNA expression of netrin-G1 and netrin-G2 in the temporal lobe in schizophrenia and bipolar disorder.
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| Eastwood SL, Harrison PJ.
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| Neuropsychopharmacology 33(4):933-45. Epub 2007 May 16.PMID: 17507910 2008
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| 6 | DEL1PP, NTNG1, WNT2B
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| Interstitial deletion of the short arm of chromosome 1 (1p13.1p21.1) in a girl with mental retardation, short stature and colobomata.
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| Bisgaard AM, Rasmussen LN, Moller HU, Kirchhoff M, Bryndorf T.
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| Clin Dysmorphol 16(2):109-12. 2007
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| 7 | NTNG1, RTT
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| Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy.
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| Nectoux J, Girard B, Bahi-Buisson N, Prieur F, Afenjar A, Rosas-Vargas H, Chelly J, Bienvenu T.
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| Pediatr Neurol 37(4):270-4.
2007
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| 8 | NTNG1
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| NTNG1 mutations are a rare cause of Rett syndrome.
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| Archer HL, Evans JC, Millar DS, Thompson PW, Kerr AM, Leonard H, Christodoulou J, Ravine D, Lazarou L, Grove L, Verity C, Whatley SD, Pilz DT, Sampson JR, Clarke AJ.
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| Am J Med Genet A 140(7):691-4.PMID: 16502428 2006
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| 9 | NTNG1
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| A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia.
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| Aoki-Suzuki M, Yamada K, Meerabux J, Iwayama-Shigeno Y, Ohba H, Iwamoto K, Takao H, Toyota T, Suto Y, Nakatani N, Dean B, Nishimura S, Seki K, Kato T, Itohara S, Nishikawa T, Yoshikawa T.
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| Biol Psychiatry 57(4):382-93. 2005
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| 10 | NTNG1, NTNG2
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| Human netrin-G1 isoforms show evidence of differential expression.
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| Meerabux JM, Ohba H, Fukasawa M, Suto Y, Aoki-Suzuki M, Nakashiba T, Nishimura S, Itohara S, Yoshikawa T.
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| Genomics 86(1):112-6. 2005
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| 11 | NTNG1
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| Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome.
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| Borg I, Freude K, Kubart S, Hoffmann K, Menzel C, Laccone F, Firth H, Ferguson-Smith MA, Tommerup N, Ropers HH, Sargan D, Kalscheuer VM.
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| Eur J Hum Genet 13(8):921-7. 2005
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| 12 | NTNG1
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| Case-control association study of human netrin G1 gene in Japanese schizophrenia.
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| Fukasawa M, Aoki M, Yamada K, Iwayama-Shigeno Y, Takao H, Meerabux J, Toyota T, Nishikawa T, Yoshikawa T.
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| J Med Dent Sci 51(2):121-8. 2004
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| 13 | NTNG1, LRRC4, LRRC4C
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| The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons.
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| Lin JC, Ho WH, Gurney A, Rosenthal A.
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| Nat Neurosci 6(12):1270-6. Epub 2003 Nov 2. 2003
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| 14 | NTNG1
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| Netrin-G1: a novel glycosyl phosphatidylinositol-linked mammalian netrin that is functionally divergent from classical netrins.
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| Nakashiba T, Ikeda T, Nishimura S, Tashiro K, Honjo T, Culotti JG, Itohara S.
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| J Neurosci 20(17):6540-50. 2000
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