Pages that link to "Q28292052"
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The following pages link to Thyroid hormone receptor beta-dependent expression of a potassium conductance in inner hair cells at the onset of hearing (Q28292052):
Displaying 50 items.
- Thyroid hormone is a critical determinant for the regulation of the cochlear motor protein prestin (Q24531197) (← links)
- Characterization of the chicken inward rectifier K channel IRK1/Kir2.1 gene (Q24808677) (← links)
- A model of the development of the brain as a construct of the thyroid system. (Q24812027) (← links)
- Divergent roles for thyroid hormone receptor beta isoforms in the endocrine axis and auditory system (Q28140997) (← links)
- Neurodevelopmental control by thyroid hormone receptors (Q28203265) (← links)
- Tissue-specific actions of thyroid hormone: insights from animal models (Q28204857) (← links)
- Rac and Rho mediate opposing hormonal regulation of the ether-a-go-go-related potassium channel (Q28215456) (← links)
- The two thyroid hormone receptor genes have opposite effects on estrogen-stimulated sex behaviors (Q28590413) (← links)
- Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss (Q28590867) (← links)
- Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems (Q29026493) (← links)
- Morphological and physiological development of auditory synapses (Q30413035) (← links)
- Distinct behavioral phenotypes in male mice lacking the thyroid hormone receptor α1 or β isoforms (Q30439089) (← links)
- Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. (Q30445850) (← links)
- A coregulatory network of NR2F1 and microRNA-140 (Q30445915) (← links)
- Complete activation of thyroid hormone receptor β by T3 is essential for normal cochlear function and morphology in mice (Q30451822) (← links)
- Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment (Q30469465) (← links)
- Bisphenol A induces otolith malformations during vertebrate embryogenesis (Q30476934) (← links)
- The influence of thyroid hormone deficiency on the development of cochlear nonlinearities (Q30484949) (← links)
- Deafness in TRbeta mutants is caused by malformation of the tectorial membrane (Q30486540) (← links)
- Thyroid hormone action in the absence of thyroid hormone receptor DNA-binding in vivo (Q30532205) (← links)
- A thyroid hormone receptor that is required for the development of green cone photoreceptors (Q31804576) (← links)
- Research on ageing in Germany (Q33930325) (← links)
- Brain glucose utilization in mice with a targeted mutation in the thyroid hormone alpha or beta receptor gene (Q33934516) (← links)
- Genetics of sensory mechanotransduction (Q34158811) (← links)
- CaV1.3 channels are essential for development and presynaptic activity of cochlear inner hair cells. (Q34279866) (← links)
- Maturation of ribbon synapses in hair cells is driven by thyroid hormone (Q34611014) (← links)
- Distinct requirements for TrkB and TrkC signaling in target innervation by sensory neurons (Q35005769) (← links)
- Type 2 iodothyronine deiodinase expression in the cochlea before the onset of hearing (Q35016845) (← links)
- Mice devoid of all known thyroid hormone receptors are viable but exhibit disorders of the pituitary-thyroid axis, growth, and bone maturation (Q35197215) (← links)
- The emotional ear in stress (Q35541524) (← links)
- Functional development of hair cells. (Q35607427) (← links)
- The rat thyroid hormone receptor (TR) Deltabeta3 displays cell-, TR isoform-, and thyroid hormone response element-specific actions (Q37189670) (← links)
- Maternal thyroid hormones are transcriptionally active during embryo-foetal development: results from a novel transgenic mouse model (Q37295374) (← links)
- Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland (Q37663895) (← links)
- Structure and development of cochlear afferent innervation in mammals (Q37900809) (← links)
- Neural circuit development in the mammalian cochlea (Q38002837) (← links)
- The deiodinases and the control of intracellular thyroid hormone signaling during cellular differentiation. (Q38013541) (← links)
- Making sense with thyroid hormone--the role of T(3) in auditory development (Q38093043) (← links)
- Generation of somatic electromechanical force by outer hair cells may be influenced by prestin-CASK interaction at the basal junction with the Deiter's cell. (Q42436471) (← links)
- Thyroid hormone-deficient period prior to the onset of hearing is associated with reduced levels of beta-tectorin protein in the tectorial membrane: implication for hearing loss (Q43698986) (← links)
- Thyroid hormone is not necessary for the development of outer hair cell electromotility (Q44277679) (← links)
- Thyroid hormone receptors: lessons from knockout and knock-in mutant mice (Q44318983) (← links)
- Thyroid hormone receptor beta gene mutation (P453A) in a family producing resistance to thyroid hormone (Q46534371) (← links)
- An emilin family extracellular matrix protein identified in the cochlear basilar membrane (Q48264857) (← links)
- Retardation of cochlear maturation and impaired hair cell function caused by deletion of all known thyroid hormone receptors. (Q48692469) (← links)
- Evaluation of hearing loss in patients with Graves’ disease (Q50433180) (← links)
- Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells (Q50457425) (← links)
- Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2 and K channels in rodent inner hair cells. (Q50458423) (← links)
- Tmc1 is necessary for normal functional maturation and survival of inner and outer hair cells in the mouse cochlea (Q50465515) (← links)
- Hearing loss in congenital hypothalamic hypothyroidism: a wide therapeutic window (Q50486249) (← links)