Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype.
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Selective inner hair cell loss in prematurity: a temporal bone study of infants from a neonatal intensive care unitMice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organsMicroRNA-183 Family in Inner Ear: Hair Cell Development and Deafness.N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient mice.Perinatal thiamine deficiency causes cochlear innervation abnormalities in mice.Selective deletion of cochlear hair cells causes rapid age-dependent changes in spiral ganglion and cochlear nucleus neuronsFactors Affecting the Variation of Maximum Speech Intelligibility in Patients With Sensorineural Hearing Loss Other Than Apparent Retrocochlear Lesions.FGF23 deficiency leads to mixed hearing loss and middle ear malformation in mice.Inner hair cells are not required for survival of spiral ganglion neurons in the adult cochlea.MicroRNAs in hair cell development and deafness.Peripheral auditory processing changes seasonally in Gambel's white-crowned sparrow.Interactions of hearing loss and diabetes mellitus in the middle age CBA/CaJ mouse model of presbycusis.RNA microarray analysis in prenatal mouse cochlea reveals novel IGF-I target genes: implication of MEF2 and FOXM1 transcription factors.Thiamine-responsive megaloblastic anemia: identification of novel compound heterozygotes and mutation update.Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?The role of insulin-like growth factor-I in the physiopathology of hearing.A novel homozygous SLC19A2 mutation in a Portuguese patient with diabetes mellitus and thiamine-responsive megaloblastic anaemia.Adenosine A1 Receptor Protects Against Cisplatin Ototoxicity by Suppressing the NOX3/STAT1 Inflammatory Pathway in the Cochlea.Identification of a SLC19A2 nonsense mutation in Persian families with thiamine-responsive megaloblastic anemia.Neurotrophic support and oxidative stress: converging effects in the normal and diseased nervous system.Understanding auditory neuropathy spectrum disorder: a systematic review in transgenic mouse models.Auditory neuropathy--neural and synaptic mechanisms.Treatment of genetic defects of thiamine transport and metabolism.Selective hair cell ablation and noise exposure lead to different patterns of changes in the cochlea and the cochlear nucleus.Unraveling the pathophysiology of alcohol-induced thiamin deficiency.The efficacy of red ginseng in type 1 and type 2 diabetes in animals.Leber's congenital amaurosis as the retinal degenerative phenotype in thiamine responsive megaloblastic anemia: a case report.Thiamine responsive megaloblastic anemia: the puzzling phenotype.Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia.Auditory system dysfunction due to infantile thiamine deficiency: long-term auditory sequelae.Thiamine responsive megaloblastic anemia: a novel SLC19A2 compound heterozygous mutation in two siblings.Cochlear implant and thiamine-responsive megaloblastic anemia syndrome.
P2860
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P2860
Deletion of SLC19A2, the high affinity thiamine transporter, causes selective inner hair cell loss and an auditory neuropathy phenotype.
description
2006 nî lūn-bûn
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2006 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@ast
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@en
type
label
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@ast
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@en
prefLabel
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@ast
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@en
P2093
P2860
P1433
P1476
Deletion of SLC19A2, the high ...... auditory neuropathy phenotype.
@en
P2093
E J Neufeld
E Tartaglini
J C Fleming
M C Liberman
P2860
P2888
P304
P356
10.1007/S10162-006-0035-X
P577
2006-04-27T00:00:00Z
P5875
P6179
1033212937