Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems.
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Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin.A model of the development of the brain as a construct of the thyroid system.Influence of neonatal hypothyroidism on hepatic gene expression and lipid metabolism in adulthoodOtoferlin couples to clathrin-mediated endocytosis in mature cochlear inner hair cellsMice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss.Deletion of the Ca2+-activated potassium (BK) alpha-subunit but not the BKbeta1-subunit leads to progressive hearing lossThyroid hormone is required for the pruning of afferent type II spiral ganglion neurons in the mouse cochlea.BDNF in Lower Brain Parts Modifies Auditory Fiber Activity to Gain Fidelity but Increases the Risk for Generation of Central Noise After Injury.Functional Role of γ-Crystallin N in the Auditory Hindbrain.Associations between prenatal and recent postnatal methylmercury exposure and auditory function at age 19 years in the Seychelles Child Development Study.Specific synaptopathies diversify brain responses and hearing disorders: you lose the gain from early life.Developmental neurotoxicity of 3,3',4,4'-tetrachloroazobenzene with thyroxine deficit: Sensitivity of glia and dentate granule neurons in the absence of behavioral changes.Gestational and early postnatal hypothyroidism alters VGluT1 and VGAT bouton distribution in the neocortex and hippocampus, and behavior in rats.Effect of maternal care on hearing onset induced by developmental changes in the auditory peripheryNeurophysiologic measures of auditory function in fish consumers: associations with long chain polyunsaturated fatty acids and methylmercury.Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.Complete activation of thyroid hormone receptor β by T3 is essential for normal cochlear function and morphology in mice.Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.The reduced cochlear output and the failure to adapt the central auditory response causes tinnitus in noise exposed rats.Critical role for cochlear hair cell BK channels for coding the temporal structure and dynamic range of auditory information for central auditory processingGenetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.Elementary properties of CaV1.3 Ca(2+) channels expressed in mouse cochlear inner hair cells.The influence of thyroid hormone deficiency on the development of cochlear nonlinearities.Deafness in TRbeta mutants is caused by malformation of the tectorial membrane.Developmental exposure to PCBs, MeHg, or both: long-term effects on auditory function.Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.Development and function of the voltage-gated sodium current in immature mammalian cochlear inner hair cells.Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease.Thyroid hormone increases fibroblast growth factor receptor expression and disrupts cell mechanics in the developing organ of cortiExpression of prestin-homologous solute carrier (SLC26) in auditory organs of nonmammalian vertebrates and insects.Hearing impairment in congenitally hypothyroid patientsThe effect of maternal thyroid disorders (hypothyroidism and hyperthyroidism) during pregnancy and lactation on skin development in wistar rat newbornsDevelopmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.Structure and development of cochlear afferent innervation in mammals.Altered phenotype of the vestibular organ in GLAST-1 null mice.Auditory brainstem evoked potentials in early-treated congenital hypothyroidism.A rat neurodevelopmental evaluation of offspring, including evaluation of adult and neonatal thyroid, from mothers treated with ammonium perchlorate in drinking water.GC-B Deficient Mice With Axon Bifurcation Loss Exhibit Compromised Auditory Processing
P2860
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P2860
Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
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@yue
2000年學術文章
@zh-hant
name
Thyroid hormone deficiency bef ...... and central auditory systems.
@en
Thyroid hormone deficiency bef ...... and central auditory systems.
@nl
type
label
Thyroid hormone deficiency bef ...... and central auditory systems.
@en
Thyroid hormone deficiency bef ...... and central auditory systems.
@nl
prefLabel
Thyroid hormone deficiency bef ...... and central auditory systems.
@en
Thyroid hormone deficiency bef ...... and central auditory systems.
@nl
P2093
P1476
Thyroid hormone deficiency bef ...... and central auditory systems.
@en
P2093
I Köpschall
M Praetorius
U Zimmermann
P304
P356
10.1152/JN.2000.83.5.3101
P407
P577
2000-05-01T00:00:00Z