VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q42151883 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000037.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q42151883‏
024 ‎‡a 0000-0002-4379-3616‏ ‎‡2 orcid‏
024 ‎‡a 56695460500‏ ‎‡2 scopus‏
035 ‎‡a (OCoLC)Q42151883‏
100 0 ‎‡a Jun Zhang‏ ‎‡9 ast‏ ‎‡9 nl‏ ‎‡9 es‏ ‎‡9 sl‏
400 0 ‎‡a Jun Zhang‏ ‎‡c researcher ORCID: 0000-0002-4379-3616‏ ‎‡9 en‏
670 ‎‡a Author's Alternatively spliced isoforms reveal a novel type of PTB domain in CCM2 protein‏
670 ‎‡a Author's Ccm1 assures microvascular integrity during angiogenesis‏
670 ‎‡a Author's Ccm1 Regulates Microvascular Morphogenesis during Angiogenesis‏
670 ‎‡a Author's Circulating Blood Prognostic Biomarker Signatures for Hemorrhagic Cerebral Cavernous Malformations (CCMs)‏
670 ‎‡a Author's Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy‏
670 ‎‡a Author's Comparative omics of CCM signaling complex (CSC)‏
670 ‎‡a Author's Crohn's disease may be differentiated into 2 distinct biotypes based on the detection of bacterial genomic sequences and virulence genes within submucosal tissues‏
670 ‎‡a Author's Epidemiology of intracranial aneurysms of Mississippi: a 10-year‏
670 ‎‡a Author's Epidemiology of intracranial aneurysms of Mississippi: a 10-year (1997-2007) retrospective study‏
670 ‎‡a Author's Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus‏
670 ‎‡a Author's Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus‏
670 ‎‡a Author's Genetics of human hydrocephalus.‏
670 ‎‡a Author's Genome-wide linkage scan maps ETINPH gene to chromosome 19q12-13.31.‏
670 ‎‡a Author's Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH)‏
670 ‎‡a Author's Identification of a new form of autosomal dominant spastic paraplegia‏
670 ‎‡a Author's Identification of candidate regions for familial idiopathic scoliosis‏
670 ‎‡a Author's Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation‏
670 ‎‡a Author's Interaction between krit1 and malcavernin: implications for the pathogenesis of cerebral cavernous malformations.‏
670 ‎‡a Author's Krit1 modulates beta 1-integrin-mediated endothelial cell proliferation‏
670 ‎‡a Author's Metabolic syndrome associated with ischemic stroke among the Mexican Hispanic population in the El Paso/US-Mexico border region‏
670 ‎‡a Author's Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblings.‏
670 ‎‡a Author's Recent advances in cerebral cavernous malformation research‏
670 ‎‡a Author's Risk factors of congenital hydrocephalus: a 10 year retrospective study‏
670 ‎‡a Author's Systems-wide analysis unravels the new roles of CCM signal complex (CSC)‏
670 ‎‡a Author's The Biological Significance and Regulatory Mechanism of c-Myc Binding Protein 1‏
670 ‎‡a Author's The Biological Significance and Regulatory Mechanism of c-Myc Binding Protein 1 (MBP-1)‏
670 ‎‡a Author's The cardiovascular triad of dysfunctional angiogenesis.‏
909 ‎‡a (orcid) 0000000243793616‏ ‎‡9 1‏
909 ‎‡a (scopus) 56695460500‏ ‎‡9 1‏
919 ‎‡a epidemiologyofintracranialaneurysmsofmississippia10year19972007retrospectivestudy‏ ‎‡A Epidemiology of intracranial aneurysms of Mississippi: a 10-year (1997-2007) retrospective study‏ ‎‡9 1‏
919 ‎‡a familialidiopathicscoliosisevidenceofan10linkedsusceptibilitylocus‏ ‎‡A Familial idiopathic scoliosis: evidence of an X-linked susceptibility locus‏ ‎‡9 1‏
919 ‎‡a geneticlinkageofanovelautosomaldominantrestrictivecardiomyopathylocus‏ ‎‡A Genetic linkage of a novel autosomal dominant restrictive cardiomyopathy locus‏ ‎‡9 1‏
919 ‎‡a geneticsofhumanhydrocephalus‏ ‎‡A Genetics of human hydrocephalus.‏ ‎‡9 1‏
919 ‎‡a genomewidelinkagescanmapsetinphgenetochromosome19q121331‏ ‎‡A Genome-wide linkage scan maps ETINPH gene to chromosome 19q12-13.31.‏ ‎‡9 1‏
919 ‎‡a heritableessentialtremoridiopathicnormalpressurehydrocephalusetinph‏ ‎‡A Heritable essential tremor-idiopathic normal pressure hydrocephalus (ETINPH)‏ ‎‡9 1‏
919 ‎‡a identificationofanewformofautosomaldominantspasticparaplegia‏ ‎‡A Identification of a new form of autosomal dominant spastic paraplegia‏ ‎‡9 1‏
919 ‎‡a identificationofcandidateregionsforfamilialidiopathicscoliosis‏ ‎‡A Identification of candidate regions for familial idiopathic scoliosis‏ ‎‡9 1‏
919 ‎‡a interactionbetweenkrit1andicap1alphainfersperturbationofintegrinbeta1mediatedangiogenesisinthepathogenesisofcerebralcavernousmalformation‏ ‎‡A Interaction between krit1 and icap1alpha infers perturbation of integrin beta1-mediated angiogenesis in the pathogenesis of cerebral cavernous malformation‏ ‎‡9 1‏
919 ‎‡a interactionbetweenkrit1andmalcaverninimplicationsforthepathogenesisofcerebralcavernousmalformations‏ ‎‡A Interaction between krit1 and malcavernin: implications for the pathogenesis of cerebral cavernous malformations.‏ ‎‡9 1‏
919 ‎‡a krit1modulatesbeta1integrinmediatedendothelialcellproliferation‏ ‎‡A Krit1 modulates beta 1-integrin-mediated endothelial cell proliferation‏ ‎‡9 1‏
919 ‎‡a metabolicsyndromeassociatedwithischemicstrokeamongthemexicanhispanicpopulationintheelpasousmexicoborderregion‏ ‎‡A Metabolic syndrome associated with ischemic stroke among the Mexican Hispanic population in the El Paso/US-Mexico border region‏ ‎‡9 1‏
919 ‎‡a phenotypicalmanifestationsofpartialtrisomy9andmonosomy4in2siblings‏ ‎‡A Phenotypical manifestations of partial trisomy 9 and monosomy 4 in two siblings.‏ ‎‡9 1‏
919 ‎‡a recentadvancesincerebralcavernousmalformationresearch‏ ‎‡A Recent advances in cerebral cavernous malformation research‏ ‎‡9 1‏
919 ‎‡a riskfactorsofcongenitalhydrocephalusa10yearretrospectivestudy‏ ‎‡A Risk factors of congenital hydrocephalus: a 10 year retrospective study‏ ‎‡9 1‏
919 ‎‡a systemswideanalysisunravelsthenewrolesofccmsignalcomplexcsc‏ ‎‡A Systems-wide analysis unravels the new roles of CCM signal complex (CSC)‏ ‎‡9 1‏
919 ‎‡a biologicalsignificanceandregulatorymechanismof100mycbindingprotein1‏ ‎‡A The Biological Significance and Regulatory Mechanism of c-Myc Binding Protein 1‏ ‎‡9 1‏
919 ‎‡a biologicalsignificanceandregulatorymechanismof100mycbindingprotein1mbp1‏ ‎‡A The Biological Significance and Regulatory Mechanism of c-Myc Binding Protein 1 (MBP-1)‏ ‎‡9 1‏
919 ‎‡a cardiovasculartriadofdysfunctionalangiogenesis‏ ‎‡A The cardiovascular triad of dysfunctional angiogenesis.‏ ‎‡9 1‏
919 ‎‡a alternativelysplicedisoformsrevealanoveltypeofptbdomaininccm2protein‏ ‎‡A Alternatively spliced isoforms reveal a novel type of PTB domain in CCM2 protein‏ ‎‡9 1‏
919 ‎‡a ccm1assuresmicrovascularintegrityduringangiogenesis‏ ‎‡A Ccm1 assures microvascular integrity during angiogenesis‏ ‎‡9 1‏
919 ‎‡a ccm1regulatesmicrovascularmorphogenesisduringangiogenesis‏ ‎‡A Ccm1 Regulates Microvascular Morphogenesis during Angiogenesis‏ ‎‡9 1‏
919 ‎‡a circulatingbloodprognosticbiomarkersignaturesforhemorrhagiccerebralcavernousmalformationsccms‏ ‎‡A Circulating Blood Prognostic Biomarker Signatures for Hemorrhagic Cerebral Cavernous Malformations (CCMs)‏ ‎‡9 1‏
919 ‎‡a clinicalandmolecularstudiesofalargefamilywithdesminassociatedrestrictivecardiomyopathy‏ ‎‡A Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy‏ ‎‡9 1‏
919 ‎‡a comparativeomicsofccmsignalingcomplexcsc‏ ‎‡A Comparative omics of CCM signaling complex (CSC)‏ ‎‡9 1‏
919 ‎‡a crohnsdiseasemaybedifferentiatedinto2distinctbiotypesbasedonthedetectionofbacterialgenomicsequencesandvirulencegeneswithinsubmucosaltissues‏ ‎‡A Crohn's disease may be differentiated into 2 distinct biotypes based on the detection of bacterial genomic sequences and virulence genes within submucosal tissues‏ ‎‡9 1‏
919 ‎‡a epidemiologyofintracranialaneurysmsofmississippia10year‏ ‎‡A Epidemiology of intracranial aneurysms of Mississippi: a 10-year‏ ‎‡9 1‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏
998 ‎‡a Jun, Zhang‏ ‎‡2 J9U|987007322067605171‏ ‎‡3 exact name‏
998 ‎‡a Jun, Zhang‏ ‎‡2 DBC|87097991157756‏ ‎‡3 exact name‏
998 ‎‡a Jun, Zhang‏ ‎‡2 CAOONL|ncf11564154‏ ‎‡3 exact name‏
998 ‎‡a Jun, Zhang‏ ‎‡2 LC|no2009159205‏ ‎‡3 exact name‏