Detalhe da pesquisa
1.
A protein quality control pathway regulated by linear ubiquitination.
EMBO J
; 38(9)2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30886048
2.
Patterns of CAG repeat instability in the central nervous system and periphery in Huntington's disease and in spinocerebellar ataxia type 1.
Hum Mol Genet
; 29(15): 2551-2567, 2020 08 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-32761094
3.
Reelin signaling modulates GABAB receptor function in the neocortex.
J Neurochem
; 156(5): 589-603, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32083308
4.
Lateralization of increased density of Iba1-immunopositive microglial cells in the anterior midcingulate cortex of schizophrenia and bipolar disorder.
Eur Arch Psychiatry Clin Neurosci
; 270(7): 819-828, 2020 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-32062729
5.
Correction to: Lateralization of increased density of Iba1-immunopositive microglial cells in the anterior midcingulate cortex of schizophrenia and bipolar disorder.
Eur Arch Psychiatry Clin Neurosci
; 272(1): 171, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34642774
6.
Postsynaptic NO/cGMP increases NMDA receptor currents via hyperpolarization-activated cyclic nucleotide-gated channels in the hippocampus.
Cereb Cortex
; 24(7): 1923-36, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23448871
7.
A novel transgenic rat model for spinocerebellar ataxia type 17 recapitulates neuropathological changes and supplies in vivo imaging biomarkers.
J Neurosci
; 33(21): 9068-81, 2013 May 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-23699518
8.
Inactivation of ceramide synthase 6 in mice results in an altered sphingolipid metabolism and behavioral abnormalities.
J Biol Chem
; 288(29): 21433-21447, 2013 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-23760501
9.
Association of variation in the LAMA3 gene, encoding the alpha-chain of laminin 5, with atopic dermatitis in a German case-control cohort.
BMC Dermatol
; 14: 17, 2014 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363238
10.
A novel BACHD transgenic rat exhibits characteristic neuropathological features of Huntington disease.
J Neurosci
; 32(44): 15426-38, 2012 Oct 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-23115180
11.
Ccdc66 null mutation causes retinal degeneration and dysfunction.
Hum Mol Genet
; 20(18): 3620-31, 2011 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21680557
12.
Theta-burst transcranial magnetic stimulation alters cortical inhibition.
J Neurosci
; 31(4): 1193-203, 2011 Jan 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21273404
13.
Selective hippocampal neurodegeneration in transgenic mice expressing small amounts of truncated Aß is induced by pyroglutamate-Aß formation.
J Neurosci
; 31(36): 12790-801, 2011 Sep 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21900558
14.
Signal transducer and activator of transcription 3-mediated regulation of miR-199a-5p links cardiomyocyte and endothelial cell function in the heart: a key role for ubiquitin-conjugating enzymes.
Eur Heart J
; 32(10): 1287-97, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20965886
15.
Corrigendum: Postnatal Developmental Expression Profile Classifies the Indusium Griseum as a Distinct Subfield of the Hippocampal Formation.
Front Cell Dev Biol
; 10: 856519, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35309921
16.
Olfactory neuron-specific expression of A30P α-synuclein exacerbates dopamine deficiency and hyperactivity in a novel conditional model of early Parkinson's disease stages.
Neurobiol Dis
; 44(2): 192-204, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21767644
17.
First appraisal of brain pathology owing to A30P mutant alpha-synuclein.
Ann Neurol
; 67(5): 684-9, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20437567
18.
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.
Neurogenetics
; 11(2): 163-74, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19777273
19.
Von Economo neuron density in the anterior cingulate cortex is reduced in early onset schizophrenia.
Acta Neuropathol
; 119(6): 771-8, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20309567
20.
Generalized progressive retinal atrophy in the Irish Glen of Imaal Terrier is associated with a deletion in the ADAM9 gene.
Mol Cell Probes
; 24(6): 357-63, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20691256