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  • Search Condition : Filter (MeSH = Nerve Tissue Proteins / genetics*)
Species Resource Title
Zebrafish pT2ZUASRFP HeterozygousKIDINS220/ARMSnonsense variants cause spastic paraplegia, intellectual disability, nystagmus, and obesity
C.intestinalis / (O.japonicus) Wild C. int Ciona intestinalis Noto4 contains a phosphotyrosine interaction domain and is involved in the midline intercalation of notochord cells.
Drosophila DGRC#115336 Short and long sleeping mutants reveal links between sleep and macroautophagy.
Human and Animal Cells MCF7(RCB1904) Anti-apoptotic effects of PCP4/PEP19 in human breast cancer cell lines: a novel oncotarget.
DNA material p1.21 (RDB01838) , p2.10 (RDB01839) , p4.1 (RDB01840) , p5.1 (RDB01841) , p6.2 (RDB01842) , p7.5 (RDB01843) , p8.21 (RDB01844) , p9.2 (RDB01845) , pR1.40 (RDB01846) , pR2IIIb-1 (RDB01847) , ... Expression of the fibroblast growth factor family and their receptor family genes during mouse brain development.
Human and Animal Cells 409B2(HPS0076) NGN2 induces diverse neuron types from human pluripotency.
Zebrafish vglut2:dsRed Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.
Zebrafish RIKEN WT Characterization of the RNA-binding protein Musashi1 in zebrafish.
C.elegans tm5210 Reduction of WDR81 impairs autophagic clearance of aggregated proteins and cell viability in neurodegenerative phenotypes.
C.elegans tm6403 OSM-9 and OCR-2 TRPV channels are accessorial warm receptors in Caenorhabditis elegans temperature acclimatisation.
Drosophila DGRC#140892 , DGRC#205074 Abnormal Social Interactions in a Drosophila Mutant of an Autism Candidate Gene: Neuroligin 3.
Mice RBRC02189 , RBRC02933 The olfactory critical period is determined by activity-dependent Sema7A/PlxnC1 signaling within glomeruli.
Mice GSC0036 ENU-mutagenesis mice with a non-synonymous mutation in Grin1 exhibit abnormal anxiety-like behaviors, impaired fear memory, and decreased acoustic startle response.
Human and Animal Cells Atg5^(+/+)MEF(RCB2710) , Atg5^(-/-)MEF(RCB2711) Fbxo2 mediates clearance of damaged lysosomes and modifies neurodegeneration in the Niemann-Pick C brain.
DNA material pGL4-phGLI1 (RDB07902) , pcDNA3.1-His-hGLI3 (RDB08066) Novel GLI3 pathogenic variants in complex pre- and postaxial polysyndactyly and Greig cephalopolysyndactyly syndrome.
Human and Animal Cells MtT/S(RCB0528) , MtT/SM(RCB0530) Infrequent detectable somatic mutations of the RET and glial cell line-derived neurotrophic factor (GDNF) genes in human pituitary adenomas.
Human and Animal Cells Ca9-22(RCB1976) , Sa3(RCB0980) , HSC-2(RCB1945) , HSC-4(RCB1902) Persephin: A potential key component in human oral cancer progression through the RET receptor tyrosine kinase-mitogen-activated protein kinase signaling pathway.
Drosophila Glial cell lineage expression of mutant ataxin-1 and huntingtin induces developmental and late-onset neuronal pathologies in Drosophila models.
Zebrafish Tg(vglut2a:loxP-DsRed-loxP-GFP) Intestinal dysmotility in a zebrafish (Danio rerio) shank3a;shank3b mutant model of autism.
C.elegans tm1301 , tm1860 henn-1/HEN1 Promotes Germline Immortality in Caenorhabditis elegans.