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Year | Number of Results |
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PubMed (GeneRIF) for id: 55558
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Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome.
Pediatr Neurol. 2022 Jan;126:65-73. doi: 10.1016/j.pediatrneurol.2021.10.008. Epub 2021 Oct 18.
Pediatr Neurol. 2022.
PMID: 34740135
Free article.
PLXNA3 Variant rs5945430 is Associated with Severe Clinical Course in Male Multiple Sclerosis Patients.
Qureshi M, Hatem M, Alroughani R, Jacob SP, Al-Temaimi RA.
Qureshi M, et al.
Neuromolecular Med. 2017 Sep;19(2-3):286-292. doi: 10.1007/s12017-017-8443-0. Epub 2017 May 23.
Neuromolecular Med. 2017.
PMID: 28536997
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PlexinA polymorphisms mediate the developmental trajectory of human corpus callosum microstructure.
Belyk M, Kraft SJ, Brown S; Pediatric Imaging, Neurocognition and Genetics Study.
Belyk M, et al.
J Hum Genet. 2015 Mar;60(3):147-50. doi: 10.1038/jhg.2014.107. Epub 2014 Dec 18.
J Hum Genet. 2015.
PMID: 25518740
Free PMC article.
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Semaphorin-plexin signalling genes associated with human breast tumourigenesis.
Gabrovska PN, Smith RA, Tiang T, Weinstein SR, Haupt LM, Griffiths LR.
Gabrovska PN, et al.
Gene. 2011 Dec 10;489(2):63-9. doi: 10.1016/j.gene.2011.08.024. Epub 2011 Sep 2.
Gene. 2011.
PMID: 21925246
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Expression and function of semaphorin 3A and its receptors in human monocyte-derived macrophages.
Ji JD, Park-Min KH, Ivashkiv LB.
Ji JD, et al.
Hum Immunol. 2009 Apr;70(4):211-7. doi: 10.1016/j.humimm.2009.01.026. Epub 2009 Feb 7.
Hum Immunol. 2009.
PMID: 19480842
Free PMC article.
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