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