Research graph
References from Altered vestibular-related reflex responses in Npc1−/− mice. Local targets link to admitted publications; unresolved targets remain external evidence.
Evaluation of age of death in Niemann-Pick disease, type C: Utility of disease support group websites to understand natural history
10.1016/j.ymgme.2019.02.004 · 2019 · External reference
Insights into the molecular mechanisms of cholesterol binding to the NPC1 and NPC2 Proteins
10.1007/978-3-030-14265-0_8 · 2019 · External reference
Selective neurodegeneration, without neurofibrillary tangles, in a mouse model of Niemann-Pick C disease
10.1002/cne.1149 · 2001 · External reference
Gender‐specific effects of two treatment strategies in a mouse model of Niemann‐pick disease type c1
10.3390/ijms22052539 · 2021 · External reference
Genetic variation in the mouse model of Niemann pick C1 affects female, as well as male, adiposity, and hepatic bile transporters but has indeterminate effects on caveolae
10.1016/j.gene.2011.10.010 · 2012 · External reference
Hearing loss is an early consequence of Npc1 gene deletion in the mouse model of Niemann-Pick disease, type C
10.1007/s10162-014-0459-7 · 2014 · External reference
Auditory phenotype of Niemann-Pick disease, type C1
10.1097/aud.0b013e3182a362b8 · 2014 · External reference
Mitochonic acid 5 mitigates age-related hearing loss progression by targeting defective 2-methylthiolation in mitochondrial transfer RNAs
10.3389/fncel.2025.1541347 · 2025 · External reference
adding Insult to injury: cochlear nerve degeneration after “temporary” noise-induced hearing loss
10.1523/jneurosci.2845-09.2009 · 2009 · External reference
Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene
10.1126/science.277.5323.232 · 1997 · External reference
Brainstem neuropathology in a mouse model of Niemann-Pick disease type C
10.1016/j.jns.2007.11.018 · 2008 · External reference
Tsukushi is essential for the formation of the posterior semicircular canal that detects gait performance
10.1007/s12079-021-00627-1 · 2021 · External reference
Long-term exposure to high-concentration dexamethasone in the inner ear via intratympanic administration
10.1016/j.steroids.2022.109152 · 2023 · External reference
Development of a vestibular implant for otolith stimulation: a mouse model study
10.1016/j.anl.2025.06.007 · 2025 · External reference
Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss
10.1038/mt.2013.62 · 2013 · External reference
Intranasal drug delivery into mouse nasal mucosa and brain utilizing arginine-rich cell-penetrating peptide-mediated protein transduction
10.1007/s10989-019-09971-8 · 2020 · External reference
N 1 -methylnicotinamide promotes age-related cochlear damage via the overexpression of SIRT1
2025 · External reference
Spiral ligament dysfunction and endocochlear potential loss drive hearing impairment in Niemann–Pick C1 mice
10.1016/j.brainresbull.2026.111846 · 2026 · External reference
The unique electrical properties in an extracellular fluid of the mammalian cochlea; their functional roles, homeostatic processes, and pathological significance
10.1007/s00424-016-1871-0 · 2016 · External reference
Neurodegeneration in Niemann-Pick type C disease mice
10.1007/s002210100870 · 2001 · External reference
Niemann-Pick disease Type C [WWW Document]
2020 · External reference
On the role of fibrocytes and the extracellular matrix in the physiology and pathophysiology of the spiral ligament
10.3389/fneur.2020.580639 · 2020 · External reference
Prenatal electroporation-mediated gene transfer restores Slc26a4 knock-out mouse hearing and vestibular function
10.1038/s41598-019-54262-3 · 2019 · External reference
Synaptopathy as a mechanism for age-related vestibular dysfunction in mice
10.3389/fnagi.2019.00156 · 2019 · External reference
Quantitative analysis and correlative evaluation of video-oculography, micro-computed tomography, and histopathology in Pendrin-null mice
10.1016/j.nbd.2023.106194 · 2023 · External reference
Different solubilizing ability of cyclodextrin derivatives for cholesterol in Niemann-Pick disease type C treatment
10.1002/ctm2.1350 · 2023 · External reference
Differential mode of cholesterol inclusion with 2-hydroxypropyl-cyclodextrins increases safety margin in treatment of Niemann-Pick disease type C
10.1111/bph.15464 · 2021 · External reference
Fine-tuned cholesterol solubilizer, mono-6-O-α-D-maltosyl-γ-cyclodextrin, ameliorates experimental Niemann–Pick disease type C without hearing loss
10.1016/j.biopha.2022.113698 · 2022 · External reference
