Search details
1.
APC7 mediates ubiquitin signaling in constitutive heterochromatin in the developing mammalian brain.
Mol Cell
; 82(1): 90-105.e13, 2022 01 06.
Article
in English
| MEDLINE | ID: mdl-34942119
2.
Ectopic Fibrous Dysplasia Presenting As a Well-Circumscribed Orbital Mass.
Ophthalmic Plast Reconstr Surg
; 39(2): e40-e43, 2023.
Article
in English
| MEDLINE | ID: mdl-36700847
3.
Acute Posterior Multifocal Placoid Pigment Epitheliopathy Complicated by Fatal Cerebral Vasculitis.
J Neuroophthalmol
; 39(2): 260-267, 2019 Jun.
Article
in English
| MEDLINE | ID: mdl-30676416
4.
Rapid Clinical and Radiographic Response With Combined Dabrafenib and Trametinib in Adults With BRAF-Mutated High-Grade Glioma.
J Natl Compr Canc Netw
; 16(1): 4-10, 2018 01.
Article
in English
| MEDLINE | ID: mdl-29295876
5.
Focal traumatic rupture of a dermoid cyst in a pediatric patient: case report and literature review.
Childs Nerv Syst
; 34(12): 2485-2490, 2018 12.
Article
in English
| MEDLINE | ID: mdl-29961083
6.
Modulation of synaptic function by VAC14, a protein that regulates the phosphoinositides PI(3,5)P2 and PI(5)P.
EMBO J
; 31(16): 3442-56, 2012 Aug 15.
Article
in English
| MEDLINE | ID: mdl-22842785
7.
Pathogenic mechanism of the FIG4 mutation responsible for Charcot-Marie-Tooth disease CMT4J.
PLoS Genet
; 7(6): e1002104, 2011 Jun.
Article
in English
| MEDLINE | ID: mdl-21655088
8.
The Hao-Fountain syndrome protein USP7 regulates neuronal connectivity in the brain via a novel p53-independent ubiquitin signaling pathway.
bioRxiv
; 2024 Jan 13.
Article
in English
| MEDLINE | ID: mdl-37961719
9.
The anaphase-promoting complex controls a ubiquitination-phosphoprotein axis in chromatin during neurodevelopment.
Dev Cell
; 58(23): 2666-2683.e9, 2023 Dec 04.
Article
in English
| MEDLINE | ID: mdl-37875116
10.
Congenital CNS hypomyelination in the Fig4 null mouse is rescued by neuronal expression of the PI(3,5)P(2) phosphatase Fig4.
J Neurosci
; 31(48): 17736-51, 2011 Nov 30.
Article
in English
| MEDLINE | ID: mdl-22131434
11.
Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4.
Brain
; 134(Pt 7): 1959-71, 2011 Jul.
Article
in English
| MEDLINE | ID: mdl-21705420
12.
Defective autophagy in neurons and astrocytes from mice deficient in PI(3,5)P2.
Hum Mol Genet
; 18(24): 4868-78, 2009 Dec 15.
Article
in English
| MEDLINE | ID: mdl-19793721
13.
CHARGE syndrome protein CHD7 regulates epigenomic activation of enhancers in granule cell precursors and gyrification of the cerebellum.
Nat Commun
; 12(1): 5702, 2021 09 29.
Article
in English
| MEDLINE | ID: mdl-34588434
14.
Autoimmune Encephalitis With Multiple Autoantibodies: A Diagnostic and Therapeutic Challenge.
Neurologist
; 23(2): 55-59, 2018 Mar.
Article
in English
| MEDLINE | ID: mdl-29494437
15.
Epidermal Growth Factor Receptor Extracellular Domain Mutations in Glioblastoma Present Opportunities for Clinical Imaging and Therapeutic Development.
Cancer Cell
; 34(1): 163-177.e7, 2018 07 09.
Article
in English
| MEDLINE | ID: mdl-29990498
16.
Role of the phosphoinositide phosphatase FIG4 gene in familial epilepsy with polymicrogyria.
Neurology
; 82(12): 1068-75, 2014 Mar 25.
Article
in English
| MEDLINE | ID: mdl-24598713
17.
Teaching NeuroImages: Cerebral amyloid angiopathy-related inflammation presenting with isolated leptomeningitis.
Neurology
; 89(6): e66-e67, 2017 08 08.
Article
in English
| MEDLINE | ID: mdl-28784645
18.
PtdIns(3,5)P2 and autophagy in mouse models of neurodegeneration.
Autophagy
; 6(1): 170-1, 2010 Jan.
Article
in English
| MEDLINE | ID: mdl-20009544
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