Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions
Published 2019 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Spontaneous mutations of the Zpld1 gene in mice cause semicircular canal dysfunction but do not impair gravity receptor or hearing functions
Authors
Keywords
-
Journal
Scientific Reports
Volume 9, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2019-08-27
DOI
10.1038/s41598-019-48835-5
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide
- (2017) Sarath Vijayakumar et al. HUMAN MOLECULAR GENETICS
- Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere’s disease
- (2016) Carmen Martín-Sierra et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease
- (2016) Carmen Martín-Sierra et al. HUMAN MOLECULAR GENETICS
- Genetics of vestibular disorders: pathophysiological insights
- (2016) Lidia Frejo et al. JOURNAL OF NEUROLOGY
- Vestibular animal models: contributions to understanding physiology and disease
- (2016) Hans Straka et al. JOURNAL OF NEUROLOGY
- Epidemiology of Dizziness and Balance Problems in Children in the United States: A Population-Based Study
- (2016) Chuan-Ming Li et al. JOURNAL OF PEDIATRICS
- Differential effects of Cdh23 753A on auditory and vestibular functional aging in C57BL/6J mice
- (2016) Bruce E. Mock et al. NEUROBIOLOGY OF AGING
- Deletion of Shank1 has minimal effects on the molecular composition and function of glutamatergic afferent postsynapses in the mouse inner ear
- (2015) Jeremy P. Braude et al. HEARING RESEARCH
- Vestibular dysfunction, altered macular structure and trait localization in A/J inbred mice
- (2015) Sarath Vijayakumar et al. MAMMALIAN GENOME
- Identification of two novel mutations in FAM136A and DTNA genes in autosomal-dominant familial Meniere's disease
- (2014) T. Requena et al. HUMAN MOLECULAR GENETICS
- Genetics of Peripheral Vestibular Dysfunction: Lessons from Mutant Mouse Strains
- (2014) Sherri M. Jones et al. Journal of the American Academy of Audiology
- Cupulin Is a Zona Pellucida-Like Domain Protein and Major Component of the Cupula from the Inner Ear
- (2014) Jens Dernedde et al. PLoS One
- A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunction
- (2013) Sue I. Lee et al. HEARING RESEARCH
- Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane
- (2013) P. K. Legan et al. HUMAN MOLECULAR GENETICS
- Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia
- (2012) Kenneth R. Johnson et al. PLoS One
- Genetics of Recurrent Vertigo and Vestibular Disorders
- (2011) Irene Gazquez et al. CURRENT GENOMICS
- Genetic disorders of the vestibular system
- (2011) Robert W. Eppsteiner et al. Current Opinion in Otolaryngology & Head and Neck Surgery
- Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice
- (2011) Kelly L. Kane et al. HEARING RESEARCH
- RNAscope
- (2011) Fay Wang et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Gravity Receptor Aging in the CBA/CaJ Strain: A Comparison to Auditory Aging
- (2010) Bruce Mock et al. JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY
- From A to Z: apical structures and zona pellucida-domain proteins
- (2010) Serge Plaza et al. TRENDS IN CELL BIOLOGY
- Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology
- (2009) Amiel A. Dror et al. Annual Review of Genetics
- Burden of Dizziness and Vertigo in the Community
- (2008) Hannelore K. Neuhauser et al. ARCHIVES OF INTERNAL MEDICINE
- A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
- (2008) G. Lefevre et al. DEVELOPMENT
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started