换一批
第一作者：
Wiljan J A J,Hendriks
第一单位：
Department of Cell Biology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. w.hendriks@ncmls.ru.nl
作者：
关键词
AURKABand 4.1/Ezrin/Radixin/MoesinCAMCDCMTCell signalingCharcot–Marie–ToothCrohn's diseaseDEP-1DUSPDensity-enhanced phosphatase-1Disease susceptibilityEYAFERMFNIIIGLEPP1HPEHTTIRIgJMMLKINDMAP kinase phosphataseMKPMSMTMRNSNoonan syndromePDZPHTSPI(3,4,5)P3PRLPSD95/Dlg/ZO-1PTENPTEN hamartoma tumor syndromesPTPPhosphotyrosine dephosphorylationPost-translational modificationRARLSRPTPRTKSCIDSFKSH2SLESNPSTEPSrc homology type 2Src-family tyrosine kinaseX-linked myotubular myopathyXLMTMaurora kinase Acell adhesion moleculedual-specificity PTPeyes absentfibronectin type IIIglomerular epithelial protein 1hereditary haemorrhagic telangiectasiaholoprosencephalyimmunoglobulininsulin receptorjuvenile myelomonocytic leukemiakinase non-catalytic C-lobe domainmultiple sclerosismyotubularin-related proteinphosphatase and tensin homologphosphatase of regenerating liverphosphatidylinositol 3,4,5-triphosphateprotein tyrosine phosphatasereceptor tyrosine kinasereceptor-type PTPrestless legs syndromerheumatoid arthritissevere combined immunodeficiencysingle nucleotide polymorphismstriatal-enriched PTPsystemic lupus erythematosus
医学主题词
遗传性疾病, 先天性(Genetic Diseases, Inborn);疾病遗传易感性(Genetic Predisposition to Disease);人类(Humans);同工酶类(Isoenzymes);蛋白质酪氨酸磷酸酶类(Protein Tyrosine Phosphatases)
DOI
10.1016/j.bbadis.2013.05.022
PMID
23707412
发布时间
2016-11-26
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