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  • Search Condition : Filter (MeSH = Reelin Protein)
Species Resource Title
Mice RBRC06344 Single-cell multiregion dissection of Alzheimer's disease.
Zebrafish aldoca:gap43-Venus , hspGFFDMC90A , hspGFFDMC28C , hspzGFFgDMC156A , SAGFF(LF)251A , UAS:GFP Role of Reelin in cell positioning in the cerebellum and the cerebellum-like structure in zebrafish.
DNA material Genome Network Project Human cDNA clone W01A072L02 (HGE029066) In Vitro Modeling of the Bipolar Disorder and Schizophrenia Using Patient-Derived Induced Pluripotent Stem Cells with Copy Number Variations of PCDH15 and RELN.
Mice RBRC00063 Genetic and animal model analyses reveal the pathogenic role of a novel deletion of RELN in schizophrenia.
Human and Animal Cells 201B7(HPS0063) Single-cell trajectory analysis of human homogenous neurons carrying a rare RELN variant.
Mice RBRC01834 Secreted Metalloproteinase ADAMTS-3 Inactivates Reelin.
Human and Animal Cells 201B7(HPS0063) A novel strategy for enrichment and isolation of osteoprogenitor cells from induced pluripotent stem cells based on surface marker combination.
Human and Animal Cells P19 Reelin signals survival through Src-family kinases that inactivate BAD activity.
Zebrafish rw0 Identification of alternatively spliced dab1 isoforms in zebrafish.
Rats KZC/Tky(strainID=20) Rat neurological disease creeping is caused by a mutation in the reelin gene.