Search
Leader | 00000nz a2200037n 45 0 | ||
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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 |