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Literature DB >> 22048335

The clasp between NetrinG and NGL becomes crystal clear.

Jennifer S Goldman¹, Timothy E Kennedy.

Abstract

Entities: Gene

Mesh：

Substances：

Year: 2011 PMID： 22048335 PMCID： PMC3230384 DOI： 10.1038/emboj.2011.375

Source DB: PubMed Journal: EMBO J ISSN： 0261-4189 Impact factor: 11.598

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References

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11 in total

1. Complementary expression and neurite outgrowth activity of netrin-G subfamily members.

Authors: Toshiaki Nakashiba; Sachiko Nishimura; Toshio Ikeda; Shigeyoshi Itohara
Journal: Mech Dev Date: 2002-02 Impact factor: 1.882

2. NTNG1 mutations are a rare cause of Rett syndrome.

Authors: Hayley L Archer; Julie C Evans; David S Millar; Peter W Thompson; Alison M Kerr; Helen Leonard; John Christodoulou; David Ravine; Lazarus Lazarou; Lucy Grove; Christopher Verity; Sharon D Whatley; Daniela T Pilz; Julian R Sampson; Angus J Clarke
Journal: Am J Med Genet A Date: 2006-04-01 Impact factor: 2.802

3. Human netrin-G1 isoforms show evidence of differential expression.

Authors: Joanne M A Meerabux; Hisako Ohba; Masayuki Fukasawa; Yumiko Suto; Mika Aoki-Suzuki; Toshiaki Nakashiba; Sachiko Nishimura; Shigeyoshi Itohara; Takeo Yoshikawa
Journal: Genomics Date: 2005-07 Impact factor: 5.736

4. NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation.

Authors: Seho Kim; Alain Burette; Hye Sun Chung; Seok-Kyu Kwon; Jooyeon Woo; Hyun Woo Lee; Karam Kim; Hyun Kim; Richard J Weinberg; Eunjoon Kim
Journal: Nat Neurosci Date: 2006-09-17 Impact factor: 24.884

5. A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia.

Authors: Mika Aoki-Suzuki; Kazuo Yamada; Joanne Meerabux; Yoshimi Iwayama-Shigeno; Hisako Ohba; Kazuya Iwamoto; Hitomi Takao; Tomoko Toyota; Yumiko Suto; Noriaki Nakatani; Brian Dean; Sachiko Nishimura; Kenjiro Seki; Tadafumi Kato; Shigeyoshi Itohara; Toru Nishikawa; Takeo Yoshikawa
Journal: Biol Psychiatry Date: 2005-02-15 Impact factor: 13.382

6. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.

Authors: T Ohtsuki; Y Horiuchi; M Koga; H Ishiguro; T Inada; N Iwata; N Ozaki; H Ujike; Y Watanabe; T Someya; T Arinami
Journal: Neurosci Lett Date: 2008-02-29 Impact factor: 3.046

The clasp between NetrinG and NGL becomes crystal clear.

1. Complementary expression and neurite outgrowth activity of netrin-G subfamily members.

2. NTNG1 mutations are a rare cause of Rett syndrome.

3. Human netrin-G1 isoforms show evidence of differential expression.

4. NGL family PSD-95-interacting adhesion molecules regulate excitatory synapse formation.

5. A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia.

6. Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations.

7. Netrin-G2 and netrin-G2 ligand are both required for normal auditory responsiveness.

8. Axonal netrin-Gs transneuronally determine lamina-specific subdendritic segments.

Review 9. The NGL family of leucine-rich repeat-containing synaptic adhesion molecules.

10. Decreased mRNA expression of netrin-G1 and netrin-G2 in the temporal lobe in schizophrenia and bipolar disorder.