VIAF

Virtual International Authority File

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Leader     00000nz a2200037n 45 0
001     WKP|Q58339500  (VIAF cluster)  (Authority/Source Record)
003     WKP
005     20241221010722.0
008     241221nneanz||abbn n and d
035 ‎‡a  (WKP)Q58339500‏
024 ‎‡a  0000-0002-3043-8797‏ ‎‡2  orcid‏
024 ‎‡a  6504669524‏ ‎‡2  scopus‏
035 ‎‡a  (OCoLC)Q58339500‏
100 0 ‎‡a  Luis Federico Batiz‏ ‎‡c  researcher, ORCID id # 0000-0002-3043-8797‏ ‎‡9  en‏
375 ‎‡a  1‏ ‎‡2  iso5218‏
400 0 ‎‡a  Luis Federico Batiz‏ ‎‡c  wetenschapper‏ ‎‡9  nl‏
670 ‎‡a  Author's A cell junction pathology of neural stem cells leads to abnormal neurogenesis and hydrocephalus.‏
670 ‎‡a  Author's A Role for mir-26a in Stress: A Potential sEV Biomarker and Modulator of Excitatory Neurotransmission‏
670 ‎‡a  Author's A simple PCR-based genotyping method for M105I mutation of alpha-SNAP enhances the study of early pathological changes in hyh phenotype.‏
670 ‎‡a  Author's Aging restricts the ability of mesenchymal stem cells to promote the generation of oligodendrocytes during remyelination‏
670 ‎‡a  Author's Astrocytes at the Hub of the Stress Response: Potential Modulation of Neurogenesis by miRNAs in Astrocyte-Derived Exosomes.‏
670 ‎‡a  Author's Cellular mechanisms involved in the stenosis and obliteration of the cerebral aqueduct of hyh mutant mice developing congenital hydrocephalus.‏
670 ‎‡a  Author's Defects in cell-cell junctions lead to neuroepithelial/ependymal denudation in the telencephalon of human hydrocephalic foetuses‏
670 ‎‡a  Author's Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia‏
670 ‎‡a  Author's Disruption of the neurogenic niche in the subventricular zone of postnatal hydrocephalic hyh mice.‏
670 ‎‡a  Author's Heterogeneous expression of hydrocephalic phenotype in the hyh mice carrying a point mutation in alpha-SNAP.‏
670 ‎‡a  Author's Molecular mechanisms underlying neuroepithelial/ependymal denudation in the hydrocephalic hyh mutant: spatial and temporal expression of alpha-SNAP and N-cadherin.‏
670 ‎‡a  Author's Neuroependymal denudation is in progress in full-term human foetal spina bifida aperta‏
670 ‎‡a  Author's New ependymal cells are born postnatally in two discrete regions of the mouse brain and support ventricular enlargement in hydrocephalus.‏
670 ‎‡a  Author's Patterned neuropathologic events occurring in hyh congenital hydrocephalic mutant mice.‏
670 ‎‡a  Author's Publisher Correction: α-SNAP is expressed in mouse ovarian granulosa cells and plays a key role in folliculogenesis and female fertility‏
670 ‎‡a  Author's Role of adherens junctions and apical-basal polarity of neural stem/progenitor cells in the pathogenesis of neurodevelopmental disorders: a novel perspective on congenital Zika syndrome‏
670 ‎‡a  Author's Sperm from hyh mice carrying a point mutation in alphaSNAP have a defect in acrosome reaction‏
670 ‎‡a  Author's α-SNAP is expressed in mouse ovarian granulosa cells and plays a key role in folliculogenesis and female fertility‏
909 ‎‡a  (scopus) 6504669524‏ ‎‡9  1‏
909 ‎‡a  (orcid) 0000000230438797‏ ‎‡9  1‏
919 ‎‡a  αsnapisexpressedinmouseovariangranulosacellsandplaysakeyroleinfolliculogenesisandfemalefertility‏ ‎‡A  α-SNAP is expressed in mouse ovarian granulosa cells and plays a key role in folliculogenesis and female fertility‏ ‎‡9  1‏
919 ‎‡a  roleofadherensjunctionsandapicalbasalpolarityofneuralstemprogenitorcellsinthepathogenesisofneurodevelopmentaldisordersanovelperspectiveoncongenitalzikasyndrome‏ ‎‡A  Role of adherens junctions and apical-basal polarity of neural stem/progenitor cells in the pathogenesis of neurodevelopmental disorders: a novel perspective on congenital Zika syndrome‏ ‎‡9  1‏
919 ‎‡a  publishercorrectionαsnapisexpressedinmouseovariangranulosacellsandplaysakeyroleinfolliculogenesisandfemalefertility‏ ‎‡A  Publisher Correction: α-SNAP is expressed in mouse ovarian granulosa cells and plays a key role in folliculogenesis and female fertility‏ ‎‡9  1‏
919 ‎‡a  patternedneuropathologiceventsoccurringinhyhcongenitalhydrocephalicmutantmice‏ ‎‡A  Patterned neuropathologic events occurring in hyh congenital hydrocephalic mutant mice.‏ ‎‡9  1‏
919 ‎‡a  newependymalcellsarebornpostnatallyin2discreteregionsofthemousebrainandsupportventricularenlargementinhydrocephalus‏ ‎‡A  New ependymal cells are born postnatally in two discrete regions of the mouse brain and support ventricular enlargement in hydrocephalus.‏ ‎‡9  1‏
919 ‎‡a  neuroependymaldenudationisinprogressinfulltermhumanfoetalspinabifidaaperta‏ ‎‡A  Neuroependymal denudation is in progress in full-term human foetal spina bifida aperta‏ ‎‡9  1‏
919 ‎‡a  molecularmechanismsunderlyingneuroepithelialependymaldenudationinthehydrocephalichyhmutantspatialandtemporalexpressionofalphasnapandncadherin‏ ‎‡A  Molecular mechanisms underlying neuroepithelial/ependymal denudation in the hydrocephalic hyh mutant: spatial and temporal expression of alpha-SNAP and N-cadherin.‏ ‎‡9  1‏
919 ‎‡a  heterogeneousexpressionofhydrocephalicphenotypeinthehyhmicecarryingapointmutationinalphasnap‏ ‎‡A  Heterogeneous expression of hydrocephalic phenotype in the hyh mice carrying a point mutation in alpha-SNAP.‏ ‎‡9  1‏
919 ‎‡a  disruptionoftheneurogenicnicheinthesubventricularzoneofpostnatalhydrocephalichyhmice‏ ‎‡A  Disruption of the neurogenic niche in the subventricular zone of postnatal hydrocephalic hyh mice.‏ ‎‡9  1‏
919 ‎‡a  disruptionofneuralprogenitorsalongtheventricularandsubventricularzonesinperiventricularheterotopia‏ ‎‡A  Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia‏ ‎‡9  1‏
919 ‎‡a  defectsincellcelljunctionsleadtoneuroepithelialependymaldenudationinthetelencephalonofhumanhydrocephalicfoetuses‏ ‎‡A  Defects in cell-cell junctions lead to neuroepithelial/ependymal denudation in the telencephalon of human hydrocephalic foetuses‏ ‎‡9  1‏
919 ‎‡a  cellularmechanismsinvolvedinthestenosisandobliterationofthecerebralaqueductofhyhmutantmicedevelopingcongenitalhydrocephalus‏ ‎‡A  Cellular mechanisms involved in the stenosis and obliteration of the cerebral aqueduct of hyh mutant mice developing congenital hydrocephalus.‏ ‎‡9  1‏
919 ‎‡a  astrocytesatthehubofthestressresponsepotentialmodulationofneurogenesisbymirnasinastrocytederivedexosomes‏ ‎‡A  Astrocytes at the Hub of the Stress Response: Potential Modulation of Neurogenesis by miRNAs in Astrocyte-Derived Exosomes.‏ ‎‡9  1‏
919 ‎‡a  agingrestrictstheabilityofmesenchymalstemcellstopromotethegenerationofoligodendrocytesduringremyelination‏ ‎‡A  Aging restricts the ability of mesenchymal stem cells to promote the generation of oligodendrocytes during remyelination‏ ‎‡9  1‏
919 ‎‡a  simplepcrbasedgenotypingmethodform105imutationofalphasnapenhancesthestudyofearlypathologicalchangesinhyhphenotype‏ ‎‡A  A simple PCR-based genotyping method for M105I mutation of alpha-SNAP enhances the study of early pathological changes in hyh phenotype.‏ ‎‡9  1‏
919 ‎‡a  roleformir26ainstressapotentialsevbiomarkerandmodulatorofexcitatoryneurotransmission‏ ‎‡A  A Role for mir-26a in Stress: A Potential sEV Biomarker and Modulator of Excitatory Neurotransmission‏ ‎‡9  1‏
919 ‎‡a  celljunctionpathologyofneuralstemcellsleadstoabnormalneurogenesisandhydrocephalus‏ ‎‡A  A cell junction pathology of neural stem cells leads to abnormal neurogenesis and hydrocephalus.‏ ‎‡9  1‏
919 ‎‡a  spermfromhyhmicecarryingapointmutationinalphasnaphaveadefectinacrosomereaction‏ ‎‡A  Sperm from hyh mice carrying a point mutation in alphaSNAP have a defect in acrosome reaction‏ ‎‡9  1‏
946 ‎‡a  b‏ ‎‡9  1‏
996 ‎‡2  J9U|987007426668605171
996 ‎‡2  ISNI|0000000116734285
996 ‎‡2  LNB|LNC10-000156960
996 ‎‡2  NII|DA04487053
996 ‎‡2  BIBSYS|90127846
996 ‎‡2  LC|n 84030769
996 ‎‡2  DNB|131427407
996 ‎‡2  NTA|071878947
996 ‎‡2  RERO|A003749644
996 ‎‡2  CAOONL|ncf11716351
996 ‎‡2  SUDOC|078699835
996 ‎‡2  NUKAT|n 01029962
996 ‎‡2  BNCHL|10000000000000000271025
997 ‎‡a  0 0 lived 0 0‏ ‎‡9  1‏