about
Localization of LRRK2 to membranous and vesicular structures in mammalian brainImmunohistochemical localisation of mGluR7 protein in the rodent and human cerebellar cortex using subtype specific antibodiesIsoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor, and mutation analysis in hyperekplexiaDistribution of gephyrin in the human brain: an immunohistochemical analysisGPR105, a novel Gi/o-coupled UDP-glucose receptor expressed on brain glia and peripheral immune cells, is regulated by immunologic challenge: possible role in neuroimmune functionComparative cellular distribution of GABAA and GABAB receptors in the human basal ganglia: immunohistochemical colocalization of the alpha 1 subunit of the GABAA receptor, and the GABABR1 and GABABR2 receptor subunitsLocalization of glycine receptors in the human forebrain, brainstem, and cervical spinal cord: an immunohistochemical reviewAssociation of gephyrin and glycine receptors in the human brainstem and spinal cord: an immunohistochemical analysis.Immunohistochemical staining of post-mortem adult human brain sections.An ovine transgenic Huntington's disease model.Huntington's disease accelerates epigenetic aging of human brain and disrupts DNA methylation levels.Striosomes and mood dysfunction in Huntington's disease.Loss of SNAP-25 and rabphilin 3a in sensory-motor cortex in Huntington's disease.A second trigeminal CGRP receptor: function and expression of the AMY1 receptor.Metabolic disruption identified in the Huntington's disease transgenic sheep model.Graded perturbations of metabolism in multiple regions of human brain in Alzheimer's disease: Snapshot of a pervasive metabolic disorderElevation of brain glucose and polyol-pathway intermediates with accompanying brain-copper deficiency in patients with Alzheimer's disease: metabolic basis for dementia.Dissociated expression of mitochondrial and cytosolic creatine kinases in the human brain: a new perspective on the role of creatine in brain energy metabolism.Striatal parvalbuminergic neurons are lost in Huntington's disease: implications for dystoniaNew Perspectives on the Neuropathology in Huntington's Disease in the Human Brain and its Relation to Symptom Variation.The Neuropathology of Huntington's Disease.The diversity of GABA(A) receptor subunit distribution in the normal and Huntington's disease human brain.Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's disease.The role of the human globus pallidus in Huntington's disease.Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.Functional and immunocytochemical characterization of the creatine transporter in rat hippocampal neurons.String Vessel Formation is Increased in the Brain of Parkinson Disease.GABA(B) receptor heterodimer-component localisation in human brain.Localization of the type VI voltage-gated sodium channel protein in human CNS.The histamine H4 receptor is functionally expressed on neurons in the mammalian CNSTowards a Better Understanding of GABAergic Remodeling in Alzheimer's Disease.Cannabinoid (CB(1)), GABA(A) and GABA(B) receptor subunit changes in the globus pallidus in Huntington's disease.Immunohistochemical localisation of the creatine transporter in the rat brain.Cortical interneuron loss and symptom heterogeneity in Huntington disease.Widespread heterogeneous neuronal loss across the cerebral cortex in Huntington's disease.Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease.Chemical and anatomical changes in the striatum and substantia nigra following quinolinic acid lesions in the striatum of the rat: a detailed time course of the cellular and GABA(A) receptor changes.Symptom heterogeneity in Huntington's disease correlates with neuronal degeneration in the cerebral cortex.Glycine receptors in the striatum, globus pallidus, and substantia nigra of the human brain: an immunohistochemical study.Up-regulation of the isoenzymes MAO-A and MAO-B in the human basal ganglia and pons in Huntington's disease revealed by quantitative enzyme radioautography.
P50
Q24318643-BF4951EB-D810-462A-8F51-CC918DB78C14Q24336594-18E52809-A63A-42C5-966F-D34AD3945E52Q28189818-3723D54B-0C00-4F08-9A5E-B30EEF95243BQ28204151-B9D133F6-E060-4733-985A-FEAFCF4CFDABQ28209874-4BDD1156-4538-47B1-8517-4983259E150FQ28245019-4C6C148C-A37E-4F63-BDD9-9930C7E1133AQ30886039-4FDEB854-D8A5-4327-BDB5-E1372B317FB4Q33195106-D7B48064-FC17-44EC-AFB1-3309707ADFF1Q33280976-4B0C7FC7-AA1D-411D-BD29-3BAFDF064926Q33815561-935607F4-6709-4F94-AF06-AA6EF528328DQ34535959-4FB93CBF-80B8-449D-944D-6C288D10397EQ34573861-50E0A1DF-3359-4078-9285-88AC06970154Q34689527-0C92887D-38A4-4253-B851-5DC7ED283E36Q35777253-668AF052-2193-4E17-B63B-C8CCAC459461Q36569413-526238F5-80A4-4135-86FC-4684B6EC9D3DQ36869854-5FB79B4F-4615-4099-9672-CBD4D60410D8Q36985886-9D722EA9-BD67-428B-8F2E-156D6A72DDA3Q37073432-7D25A73C-458E-4AB0-A4B8-E95C981C2DB0Q37265881-08FDCA34-E537-4E17-BB7E-5B659D4012F7Q38234070-C48A0366-8733-4C81-B85A-3436E54314D0Q38258620-85B15615-18A8-456C-976E-E49EA1AE27A6Q38338483-4BD25F5E-F0F9-498E-BFDD-D4983F0A9ED3Q38925490-2B2CBDFE-B9D5-43CB-AE02-D9E039B643C9Q38928744-09A1BE4C-5C72-42A8-AD03-B52BC32CC8C1Q39631653-8D0AF34E-CD36-4984-8287-541EDC6F8955Q39753878-29DB9E5A-BADF-4C6B-9116-95E791FAA32BQ40458640-18922C83-1128-4FBB-B12F-71EE53CA756DQ40879309-C07FE0BC-C3B1-445B-ABFA-9EF6F51C8FDAQ40908703-8CA91C0E-7341-48F2-8C61-0907CC209C62Q41420104-FBB9776F-7E0C-4ED8-B3A5-DD0EA501BF7AQ41574564-5C2F2E27-1221-4129-AECB-4FA9DF4EFB1EQ42454539-926B2875-3278-4127-9B44-C1F160321140Q42456481-9CEA4028-476D-4EFF-8F88-0B904EFD3DD8Q42458049-43C0964A-61AD-4F9D-8CF8-795FD28658BEQ42462939-7AE78EE2-7D1F-4178-9288-941A78B04D00Q42469950-83EEF2EC-7AF6-4FE0-BFBB-EFC7918767ECQ42480737-E0FBAC6A-CA51-46FC-BC63-8900A72AA72CQ42498289-5ABE4BD8-1605-4DDD-B56E-BC55ADFE5EF7Q42511378-4926BD3F-96D5-4078-B0E5-C756195A2416Q42817778-FB4FB93E-A306-4B06-B343-3160B7DC9F5E
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Henry J. Waldvogel
@ast
Henry J. Waldvogel
@en
Henry J. Waldvogel
@es
Henry J. Waldvogel
@nl
Henry J. Waldvogel
@sl
type
label
Henry J. Waldvogel
@ast
Henry J. Waldvogel
@en
Henry J. Waldvogel
@es
Henry J. Waldvogel
@nl
Henry J. Waldvogel
@sl
altLabel
Henry Waldvogel
@en
prefLabel
Henry J. Waldvogel
@ast
Henry J. Waldvogel
@en
Henry J. Waldvogel
@es
Henry J. Waldvogel
@nl
Henry J. Waldvogel
@sl
P1053
D-6691-2012
P106
P1153
7003784228
P21
P31
P3829
P496
0000-0003-2165-8568