about
Alternative promoters and polyadenylation regulate tissue-specific expression of Hemogen isoforms during hematopoiesis and spermatogenesisCNS myelin paranodes require Nkx6-2 homeoprotein transcriptional activity for normal structureDistinct subdomain organization and molecular composition of a tight junction with adherens junction featuresMicrotubule deacetylases, SirT2 and HDAC6, in the nervous systemClaudin 11 deficiency in mice results in loss of the Sertoli cell epithelial phenotype in the testis.Claudin Proteins And Neuronal Function.Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins.A model of tight junction function in central nervous system myelinated axonsThe unfolded protein response in protein aggregating diseases.Claudin-11 Tight Junctions in Myelin Are a Barrier to Diffusion and Lack Strong Adhesive Properties.The unfolded protein response modulates disease severity in Pelizaeus-Merzbacher disease.Minimal role for caspase 12 in the unfolded protein response in oligodendrocytes in vivo.Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function.Disrupted proteolipid protein trafficking results in oligodendrocyte apoptosis in an animal model of Pelizaeus-Merzbacher disease.Intracellular distribution of transgenic bacterial beta-galactosidase in central nervous system neurons and neuroglia.Tight junctions potentiate the insulative properties of small CNS myelinated axons.Overexpression of CHOP in Myelinating Cells Does Not Confer a Significant Phenotype under Normal or Metabolic Stress Conditions.Myelin sheaths are formed with proteins that originated in vertebrate lineages.Potential For Cell-mediated Immune Responses In Mouse Models Of Pelizaeus-Merzbacher Disease.Neuroradiologic correlates of clinical disability and progression in the X-linked leukodystrophy Pelizaeus-Merzbacher diseaseDevelopmental window of sensorineural deafness in biotinidase-deficient mice.Dimethyl fumarate ameliorates myoclonus stemming from protein misfolding in oligodendrocytes.A cellular mechanism governing the severity of Pelizaeus-Merzbacher disease.Many naturally occurring mutations of myelin proteolipid protein impair its intracellular transport.Intracellular transport and sorting of the oligodendrocyte transmembrane proteolipid protein.Phenotyping the claudin 11 deficiency in testis: from histology to immunohistochemistry.Myelinogenesis and axonal recognition by oligodendrocytes in brain are uncoupled in Olig1-null mice.Neuregulin1 modulation of experimental autoimmune encephalomyelitis (EAE).Absence of Claudin 11 in CNS Myelin Perturbs Behavior and Neurotransmitter Levels in Mice.Equilibrium binding of myristoyllysophosphatidylcholine to bovine myelin basic protein: an example of ligand-mediated acceptor association.Corticohippocampal Dysfunction In The OBiden Mouse Model Of Primary OligodendrogliopathyInteractions between bovine myelin basic protein and zwitterionic lysophospholipidsPressure-induced dissociation of aggregates of myelin proteolipid proteinIntracellular transport of the DM-20 bearing shaking pup (shp) mutation and its possible phenotypic consequencesMinimal role for activating transcription factor 3 in the oligodendrocyte unfolded protein response in vivoNovel Role for Claudin-11 in the Regulation of Osteoblasts via Modulation of ADAM10-Mediated Notch SignalingOnecut-dependent Nkx6.2 transcription factor expression is required for proper formation and activity of spinal locomotor circuits
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Alexander Gow
@ast
Alexander Gow
@en
Alexander Gow
@es
Alexander Gow
@nl
type
label
Alexander Gow
@ast
Alexander Gow
@en
Alexander Gow
@es
Alexander Gow
@nl
prefLabel
Alexander Gow
@ast
Alexander Gow
@en
Alexander Gow
@es
Alexander Gow
@nl
P106
P1153
7006168340
P31
P496
0000-0001-7446-8990