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Year | Number of Results |
---|---|
1998 | 1 |
2001 | 1 |
2003 | 2 |
2022 | 2 |
2024 | 0 |
PubMed (cited) for id: 300561
6 results
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Page 1
SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
Nat Commun. 2022 Jul 15;13(1):4112. doi: 10.1038/s41467-022-31566-z.
Nat Commun. 2022.
PMID: 35840571
Free PMC article.
Slitrk2 deficiency causes hyperactivity with altered vestibular function and serotonergic dysregulation.
Katayama KI, Morimura N, Kobayashi K, Corbett D, Okamoto T, Ornthanalai VG, Matsunaga H, Fujita W, Matsumoto Y, Akagi T, Hashikawa T, Yamada K, Murphy NP, Nagao S, Aruga J.
Katayama KI, et al.
iScience. 2022 Jun 14;25(7):104604. doi: 10.1016/j.isci.2022.104604. eCollection 2022 Jul 15.
iScience. 2022.
PMID: 35789858
Free PMC article.
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Human SLITRK family genes: genomic organization and expression profiling in normal brain and brain tumor tissue.
Aruga J, Yokota N, Mikoshiba K.
Aruga J, et al.
Gene. 2003 Oct 2;315:87-94. doi: 10.1016/s0378-1119(03)00715-7.
Gene. 2003.
PMID: 14557068
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Identification and characterization of Slitrk, a novel neuronal transmembrane protein family controlling neurite outgrowth.
Aruga J, Mikoshiba K.
Aruga J, et al.
Mol Cell Neurosci. 2003 Sep;24(1):117-29. doi: 10.1016/s1044-7431(03)00129-5.
Mol Cell Neurosci. 2003.
PMID: 14550773
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Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T, Nakayama M, Nakajima D, Kikuno R, Ohara O.
Nagase T, et al.
DNA Res. 2001 Apr 27;8(2):85-95. doi: 10.1093/dnares/8.2.85.
DNA Res. 2001.
PMID: 11347906
Free article.
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Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampus.
Redolfi E, Montagna C, Mumm S, Affer M, Susani L, Reinbold R, Hol F, Vezzoni P, Cimino M, Zucchi I.
Redolfi E, et al.
DNA Cell Biol. 1998 Dec;17(12):1009-16. doi: 10.1089/dna.1998.17.1009.
DNA Cell Biol. 1998.
PMID: 9881668
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