Weiwei Guo

Inflammasome activation in mouse inner ear in response to MCMV induced hearing loss.

[A report on a large family with X-linked recessive nonsyndromic hereditary low frequency neuropathic hearing impairment].

Correlation of cochlear blood supply with mitochondrial DNA common deletion in presbyacusis.

[The saccular function in Meniere's disease].

[The significance of the interaural latency difference of VEMP].

[Establishment of conditionally immortalized rat cochlear greater epithelial ridge and lesser epithelial ridge cell lines using a retrovirus-mediated gene transfer technique].

Expression and clinical significance of cathepsin B and stefin A in laryngeal cancer.

Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.

Tonotopic reorganization and spontaneous firing in inferior colliculus during both short and long recovery periods after noise overexposure.

De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome.

Hydrogen-saturated saline protects intensive narrow band noise-induced hearing loss in guinea pigs through an antioxidant effect.

Profiles of the auditory epithelia related microRNA expression in neonatal and adult rats.

Spontaneous and Partial Repair of Ribbon Synapse in Cochlear Inner Hair Cells After Ototoxic Withdrawal.

The morphology and electrophysiology of the cochlea of the miniature pig.

Overexpression of ROCK1 and ROCK2 inhibits human laryngeal squamous cell carcinoma.

SMAD4 Defect Causes Auditory Neuropathy Via Specialized Disruption of Cochlear Ribbon Synapses in Mice.

DAPT mediates atoh1 expression to induce hair cell-like cells.

A de novo silencer causes elimination of MITF-M expression and profound hearing loss in pigs.

Aminoglycoside Increases Permeability of Osseous Spiral Laminae of Cochlea by Interrupting MMP-2 and MMP-9 Balance.

Transplantation of human umbilical cord mesenchymal stem cells in cochlea to repair sensorineural hearing.

Miniature pigs: a large animal model of cochlear implantation.

Establishing the standard method of cochlear implant in Rongchang pig.

The morphological and functional development of the stria vascularis in miniature pigs.

Adeno-associated virus transformation into the normal miniature pig and the normal guinea pigs cochlea via scala tympani.

Matrix metalloproteinase-2 and -9 contribute to functional integrity and noise‑induced damage to the blood-labyrinth-barrier.

Pilot study of large-scale production of mutant pigs by ENU mutagenesis.

Transcription analysis of cochlear development in minipigs.

Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesis.

NLRP3-inflammasomes are triggered by age-related hearing loss in the inner ear of mice.

Cochlear morphology in the developing inner ear of the porcine model of spontaneous deafness.

Differential fates of tissue macrophages in the cochlea during postnatal development.

Transcript variants and expression profiles analysis of gene in minipigs.

Advantages of a miniature pig model in research on human hereditary hearing loss.

Rapid analysis of neomycin in cochlear perilymph of guinea pigs using disposable SPE cartridges and high performance liquid chromatography-tandem mass spectrometry.

Degeneration of saccular hair cells caused by MITF gene mutation.

Establishment of a large animal model for Eustachian tube functional study in miniature pigs.

Transplantation and Tracking of the Human Umbilical Cord Mesenchymal Stem Cell Labeled with Superparamagnetic Iron Oxide in Deaf Pigs.

The characteristics of vHIT gain and PR score in peripheral vestibular disorders.

Air and bone-conducted vestibular evoked myogenic potentials in children with large vestibular aqueduct syndrome.

KIT gene mutation causes deafness and hypopigmentation in Bama miniature pigs.

Phenotypic similarities in pigs with SOX10 and SOX10 mutations implied the correlation of SOX10 haploinsufficiency with Waardenburg syndrome.

Oridonin ameliorates noise-induced hearing loss by blocking NLRP3 - NEK7 mediated inflammasome activation.

Electrophysiological and histomorphological changes of cochlea in miniature pigs after abrasion of round window niches.

CRISPR/Cas9-mediated correction of homozygous point mutation in a Waardenburg syndrome 2A pig model.

Exploratory saccades data analysis of video head impulse test in different Meniere's disease stages.

Sox10 Gene Is Required for the Survival of Saccular and Utricular Hair Cells in a Porcine Model.

Correction to: Sox10 Gene Is Required for the Survival of Saccular and Utricular Hair Cells in a Porcine Model.

Head and neck radiotherapy causes significant disruptions of cochlear ribbon synapses and consequent sensorineural hearing loss.

LDL receptor-related protein 1 (LRP1), a novel target for opening the blood-labyrinth barrier (BLB).