| Q35297950 | A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice |
| Q42028039 | Altered phenotype of the vestibular organ in GLAST-1 null mice. |
| Q52649632 | Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness. |
| Q30374321 | BDNF in Lower Brain Parts Modifies Auditory Fiber Activity to Gain Fidelity but Increases the Risk for Generation of Central Noise After Injury. |
| Q60313143 | Central Hypothyroidism and Novel Clinical Phenotypes in Hemizygous Truncation of |
| Q30445850 | Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants. |
| Q30486540 | Deafness in TRbeta mutants is caused by malformation of the tectorial membrane |
| Q33632192 | Deciphering direct and indirect influence of thyroid hormone with mouse genetics. |
| Q30364788 | Developmental PCB Exposure Increases Audiogenic Seizures and Decreases Glutamic Acid Decarboxylase in the Inferior Colliculus. |
| Q35590745 | Developmental and cell-specific expression of thyroid hormone transporters in the mouse cochlea |
| Q50434868 | Effects of retinoic acid and butyric acid on the expression of prestin and Gata-3 in organotypic cultures of the organ of corti of newborn rats |
| Q39131790 | Exploring regulatory networks of miR-96 in the developing inner ear |
| Q42436471 | 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. |
| Q30469465 | Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment |
| Q36637419 | Genome-wide analysis of thyroid hormone receptors shared and specific functions in neural cells |
| Q37514901 | Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase gene |
| Q38113895 | Iodine deficiency, thyroid function and hearing deficit: a review |
| Q30501104 | Lateral wall protein content mediates alterations in cochlear outer hair cell mechanics before and after hearing onset |
| Q47252265 | Mechanisms involved in hearing disorders of thyroid ontogeny: a literature review |
| Q36793594 | Multigenic control of thyroid hormone functions in the nervous system |
| Q36350118 | Pseudo-immortalization of postnatal cochlear progenitor cells yields a scalable cell line capable of transcriptionally regulating mature hair cell genes |
| Q24648887 | Rapid cell-cycle reentry and cell death after acute inactivation of the retinoblastoma gene product in postnatal cochlear hair cells |
| Q91496580 | Redox activation of JNK2α2 mediates thyroid hormone-stimulated proliferation of neonatal murine cardiomyocytes |
| Q84215036 | Severe impairment of cerebellum development in mice expressing a dominant-negative mutation inactivating thyroid hormone receptor alpha1 isoform |
| Q34317893 | Specification of skeletal muscle differentiation by repressor element-1 silencing transcription factor (REST)-regulated Kv7.4 potassium channels |
| Q37900809 | Structure and development of cochlear afferent innervation in mammals |
| Q34359558 | The Specific Slow Afterhyperpolarization Inhibitor UCL2077 Is a Subtype-Selective Blocker of the Epilepsy Associated KCNQ Channels |
| Q30484949 | The influence of thyroid hormone deficiency on the development of cochlear nonlinearities |
| Q43268823 | The significance of stress: its role in the auditory system and the pathogenesis of tinnitus |
| Q50455106 | Therapeutic use of stem cells |
| Q50458423 | Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. |
| Q50457425 | Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells |
| Q34107422 | Thyroid hormone receptor beta (TRbeta) and liver X receptor (LXR) regulate carbohydrate-response element-binding protein (ChREBP) expression in a tissue-selective manner |
| Q58783095 | Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function |
| Q30451832 | Transcriptional regulation of the pendrin gene |
| Q37366609 | Use of a new model of transgenic mice to clarify the respective functions of thyroid hormone receptors in vivo |
| Q50431784 | cGMP-Prkg1 signaling and Pde5 inhibition shelter cochlear hair cells and hearing function |