PubMed for id: 9783

Year	Number of Results
1996	1
2000	1
2002	1
2003	1
2004	2
2006	2
2008	1
2009	2
2010	1
2011	4
2014	1
2017	2
2019	1
2020	2
2021	1
2024	0

1

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB. Kumar RA, et al. J Med Genet. 2010 Feb;47(2):81-90. doi: 10.1136/jmg.2008.065821. Epub 2009 Jun 21. J Med Genet. 2010. PMID: 19546099 Free PMC article.

2

Investigation of the expression of genes affecting cytomatrix active zone function in the amygdala in schizophrenia: effects of antipsychotic drugs.

Weidenhofer J, Scott RJ, Tooney PA. Weidenhofer J, et al. J Psychiatr Res. 2009 Jan;43(3):282-90. doi: 10.1016/j.jpsychires.2008.04.001. Epub 2008 May 19. J Psychiatr Res. 2009. PMID: 18490030

3

Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease.

Huang XF, Mao JY, Huang ZQ, Rao FQ, Cheng FF, Li FF, Wang QF, Jin ZB. Huang XF, et al. Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):424-429. doi: 10.1167/iovs.16-20705. Invest Ophthalmol Vis Sci. 2017. PMID: 28118666

4

The RIM/NIM family of neuronal C2 domain proteins. Interactions with Rab3 and a new class of Src homology 3 domain proteins.

Wang Y, Sugita S, Sudhof TC. Wang Y, et al. J Biol Chem. 2000 Jun 30;275(26):20033-44. doi: 10.1074/jbc.M909008199. J Biol Chem. 2000. PMID: 10748113 Free article.

5

Genomic definition of RIM proteins: evolutionary amplification of a family of synaptic regulatory proteins.

Wang Y, Südhof TC. Wang Y, et al. Genomics. 2003 Feb;81(2):126-37. doi: 10.1016/s0888-7543(02)00024-1. Genomics. 2003. PMID: 12620390

6

The synaptic vesicle cycle.

Sudhof TC. Sudhof TC. Annu Rev Neurosci. 2004;27:509-47. doi: 10.1146/annurev.neuro.26.041002.131412. Annu Rev Neurosci. 2004. PMID: 15217342 Review.

7

Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain.

Nagase T, Seki N, Ishikawa K, Ohira M, Kawarabayasi Y, Ohara O, Tanaka A, Kotani H, Miyajima N, Nomura N. Nagase T, et al. DNA Res. 1996 Oct 31;3(5):321-9, 341-54. doi: 10.1093/dnares/3.5.321. DNA Res. 1996. PMID: 9039502 Free article.

8

Image-based genome-wide siRNA screen identifies selective autophagy factors.

Orvedahl A, Sumpter R Jr, Xiao G, Ng A, Zou Z, Tang Y, Narimatsu M, Gilpin C, Sun Q, Roth M, Forst CV, Wrana JL, Zhang YE, Luby-Phelps K, Xavier RJ, Xie Y, Levine B. Orvedahl A, et al. Nature. 2011 Dec 1;480(7375):113-7. doi: 10.1038/nature10546. Nature. 2011. PMID: 22020285 Free PMC article.

9

DCAF8, a novel MuRF1 interaction partner, promotes muscle atrophy.

Nowak M, Suenkel B, Porras P, Migotti R, Schmidt F, Kny M, Zhu X, Wanker EE, Dittmar G, Fielitz J, Sommer T. Nowak M, et al. J Cell Sci. 2019 Sep 6;132(17):jcs233395. doi: 10.1242/jcs.233395. J Cell Sci. 2019. PMID: 31391242

10

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

Corominas R, Yang X, Lin GN, Kang S, Shen Y, Ghamsari L, Broly M, Rodriguez M, Tam S, Wanamaker SA, Fan C, Yi S, Tasan M, Lemmens I, Kuang X, Zhao N, Malhotra D, Michaelson JJ, Vacic V, Calderwood MA, Roth FP, Tavernier J, Horvath S, Salehi-Ashtiani K, Korkin D, Sebat J, Hill DE, Hao T, Vidal M, Iakoucheva LM. Corominas R, et al. Nat Commun. 2014 Apr 11;5:3650. doi: 10.1038/ncomms4650. Nat Commun. 2014. PMID: 24722188 Free PMC article.

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