Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
about
Nuclear transport of galectin-3 and its therapeutic implicationsThe nuclear envelope: an intriguing focal point for neurogenetic diseaseMolecular Architecture of the Transport Channel of the Nuclear Pore ComplexMutations in nuclear pore genes NUP93, NUP205 and XPO5 cause steroid-resistant nephrotic syndromeNucleoporin Nup62 maintains centrosome homeostasisA mutation in the nucleoporin-107 gene causes XX gonadal dysgenesisBrain mechanisms of acoustic communication in humans and nonhuman primates: an evolutionary perspective.Neurological Disorders Associated with Striatal Lesions: Classification and Diagnostic Approach.Degenerative Encephalopathy in Nova Scotia Duck Tolling Retrievers Presenting with a Rapid Eye Movement Sleep Behavior Disorder.Diseases of the nuclear envelope.Oxidative stress and adrenocortical insufficiency.A change in nuclear pore complex composition regulates cell differentiationRegulation of mRNA trafficking by nuclear pore complexes.Role for NUP62 depletion and PYK2 redistribution in dendritic retraction resulting from chronic stressNucleoporin 62-like protein activates canonical Wnt signaling through facilitating the nuclear import of β-catenin in zebrafish.Nuclear envelope and genome interactions in cell fate.The functions of the nuclear envelope in mediating the molecular crosstalk between the nucleus and the cytoplasm.Poreless eggshellsLoss of zygotic NUP107 protein causes missing of pharyngeal skeleton and other tissue defects with impaired nuclear pore function in zebrafish embryos.Neural expression of the transcription factor THAP1 during development in rat.Gene silencing at the nuclear periphery.Till disassembly do us part: a happy marriage of nuclear envelope and chromatin.The role of nuclear pores in gene regulation, development and diseaseDeficiency of ALADIN impairs redox homeostasis in human adrenal cells and inhibits steroidogenesis.Astrocyte-specific overexpressed gene signatures in response to methamphetamine exposure in vitro.Leigh map: A novel computational diagnostic resource for mitochondrial disease.Signaling from the cytoplasm to the nucleus in striatal medium-sized spiny neuronsMutant Huntingtin Disrupts the Nuclear Pore Complex.Nucleoporin genes in human diseases.The roles of the nuclear pore complex in cellular dysfunction, aging and disease.Modification of spectral features by nonhuman primatesAnalysis of the Lotus japonicus nuclear pore NUP107-160 subcomplex reveals pronounced structural plasticity and functional redundancy.Cerebrospinal fluid analysis in children with seizures from respiratory syncytial virus infection.MED20 mutation associated with infantile basal ganglia degeneration and brain atrophy.A type I interferon signature identifies bilateral striatal necrosis due to mutations in ADAR1.Bilateral striatal necrosis in two subjects with Aicardi-Goutières syndrome due to mutations in ADAR1 (AGS6).STRUCTURAL BIOLOGY. Locking down the core of the pore.
P2860
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P2860
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@en
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@nl
type
label
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@en
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@nl
prefLabel
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@en
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@nl
P2093
P2860
P356
P1433
P1476
Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis.
@en
P2093
Amos J Simon
Christopher A Walsh
Ellen Taub
Gideon Rechavi
Hanna Shalev
Limor Rainshtein
Liora Muncher
Metsada Pasmanik-Chor
Michal Yahav
Mordechai Shohat
P2860
P304
P356
10.1002/ANA.20902
P577
2006-08-01T00:00:00Z