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