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A New Kind of Naturally Occurring Mouse Model for Usher Syndrome Generated by Crossing with Cba/J Mice

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inferredcites →https://doi.org/10.1002/advs.202205993openalex-extracted
Deafness‐Associated ADGRV1 Mutation Impairs USH2A Stability through Improper Phosphorylation of WHRN and WDSUB1 Recruitment
inferredcites →https://doi.org/10.1007/s00221-020-06032-1openalex-extracted
Effects of acquired vestibular pathology on the organization of mouse exploratory behavior
inferredcites →https://doi.org/10.1007/s00439-021-02324-wopenalex-extracted
Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2
inferredcites →https://doi.org/10.1007/s10162-010-0228-1openalex-extracted
Divergent Aging Characteristics in CBA/J and CBA/CaJ Mouse Cochleae
inferredcites →https://doi.org/10.1007/s10633-022-09872-0openalex-extracted
ISCEV Standard for full-field clinical electroretinography (2022 update)
inferredcites →https://doi.org/10.1007/s12031-012-9911-5openalex-extracted
The Very Large G Protein Coupled Receptor (Vlgr1) in Hair Cells
inferredcites →https://doi.org/10.1016/0378-5955(92)90094-4openalex-extracted
Incidence of otitis media in CBA/J and CBA/CaJ mice
inferredcites →https://doi.org/10.1016/j.cell.2023.08.020openalex-extracted
Spatiotemporal insight into early pregnancy governed by immune-featured stromal cells
inferredcites →https://doi.org/10.1016/j.exer.2020.108330openalex-extracted
USH2A-retinopathy: From genetics to therapeutics
inferredcites →https://doi.org/10.1016/j.heares.2008.06.001openalex-extracted
Age-related auditory pathology in the CBA/J mouse
inferredcites →https://doi.org/10.1016/j.heares.2020.107932openalex-extracted
Disease mechanisms and gene therapy for Usher syndrome
inferredcites →https://doi.org/10.1016/j.neubiorev.2021.05.005openalex-extracted
Anxiety and Alzheimer’s disease: Behavioral analysis and neural basis in rodent models of Alzheimer’s-related neuropathology
inferredcites →https://doi.org/10.1016/s0378-5955(99)00003-9openalex-extracted
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses
inferredcites →https://doi.org/10.1038/ejhg.2016.99openalex-extracted
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
inferredcites →https://doi.org/10.1080/17482631.2019.1656790openalex-extracted
Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study
inferredcites →https://doi.org/10.1080/21655979.2021.2003676openalex-extracted
Paeoniflorin ameliorates chronic stress-induced depression-like behavior in mice model by affecting ERK1/2 pathway
inferredcites →https://doi.org/10.1086/381685openalex-extracted
Mutations in the VLGR1 Gene Implicate G-Protein Signaling in the Pathogenesis of Usher Syndrome Type II
inferredcites →https://doi.org/10.1089/humc.2013.037openalex-extracted
Preclinical Potency and Safety Studies of an AAV2-Mediated Gene Therapy Vector for the Treatment of MERTK Associated Retinitis Pigmentosa
inferredcites →https://doi.org/10.1093/nar/gkm961openalex-extracted
The Mouse Genome Database (MGD): mouse biology and model systems
inferredcites →https://doi.org/10.1093/nar/gkx1006openalex-extracted
Mouse Genome Database (MGD)-2018: knowledgebase for the laboratory mouse
inferredcites →https://doi.org/10.1093/nar/gky1056openalex-extracted
Mouse Genome Database (MGD) 2019
inferredcites →https://doi.org/10.1097/aud.0000000000001066openalex-extracted
Review of Genotype-Phenotype Correlations in Usher Syndrome
inferredcites →https://doi.org/10.1097/mao.0000000000001441openalex-extracted
Cochlear Implantation in Patients With Usher Syndrome Type IIa Increases Performance and Quality of Life
inferredcites →https://doi.org/10.1097/mop.0000000000000690openalex-extracted
Retinitis pigmentosa: recent advances and future directions in diagnosis and management
inferredcites →https://doi.org/10.1121/1.5132550openalex-extracted
Mouse methods and models for studies in hearing
inferredcites →https://doi.org/10.1136/jmg.2008.060947openalex-extracted
A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family
inferredcites →https://doi.org/10.1159/000491068openalex-extracted
A Natural Occurring Mouse Model with Adgrv1 Mutation of Usher Syndrome 2C and Characterization of its Recombinant Inbred Strains
inferredcites →https://doi.org/10.1177/00034894931020s101openalex-extracted
Cochlear Pathology in Presbycusis
inferredcites →https://doi.org/10.1186/s10194-019-0963-6openalex-extracted
Behavioral and cognitive animal models in headache research
inferredcites →https://doi.org/10.1371/journal.pone.0094272openalex-extracted
EIAV-Based Retinal Gene Therapy in the shaker1 Mouse Model for Usher Syndrome Type 1B: Development of UshStat
inferredcites →https://doi.org/10.1371/journal.pone.0155619openalex-extracted
The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome
inferredcites →https://doi.org/10.3109/00206098009070071openalex-extracted
Genotypic Differences in Behavioral, Physiological and Anatomical Expressions of Age-Related Hearing Loss in the Laboratory Mouse: Original Papers Travaux originaux
inferredcites →https://doi.org/10.3233/wor-182731openalex-extracted
Health, work, social trust, and financial situation in persons with Usher syndrome type 1
inferredcites →https://doi.org/10.3390/cells11182790openalex-extracted
The Adhesion GPCR VLGR1/ADGRV1 Regulates the Ca2+ Homeostasis at Mitochondria-Associated ER Membranes
inferredcites →https://doi.org/10.3390/genes10040287openalex-extracted
Adeno-Associated Viral Vectors as a Tool for Large Gene Delivery to the Retina
inferredcites →https://doi.org/10.3390/genes12060805openalex-extracted
Generation and Genetic Correction of USH2A c.2299delG Mutation in Patient-Derived Induced Pluripotent Stem Cells
inferredcites →https://doi.org/10.3390/ijms21124197openalex-extracted
Recombinant Adeno-Associated Viral Vectors (rAAV)-Vector Elements in Ocular Gene Therapy Clinical Trials and Transgene Expression and Bioactivity Assays
inferredcites →https://doi.org/10.3390/ijms22136723openalex-extracted
Usher Syndrome: Genetics of a Human Ciliopathy
inferredcites →https://doi.org/10.3390/ijms24087603openalex-extracted
A Review of CRISPR Tools for Treating Usher Syndrome: Applicability, Safety, Efficiency, and In Vivo Delivery
inferredcites →https://doi.org/10.3390/nu12072036openalex-extracted
High-Fat Diet Enhances Working Memory in the Y-Maze Test in Male C57BL/6J Mice with Less Anxiety in the Elevated Plus Maze Test
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