A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
出版年份 2017 全文链接
标题
A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
作者
关键词
-
出版物
Nature Communications
Volume 8, Issue 1, Pages -
出版商
Springer Nature
发表日期
2017-10-06
DOI
10.1038/s41467-017-00595-4
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Absence of Neuroplastin-65 Affects Synaptogenesis in Mouse Inner Hair Cells and Causes Profound Hearing Loss
- (2016) L. Carrott et al. JOURNAL OF NEUROSCIENCE
- Neuroplastin Isoform Np55 Is Expressed in the Stereocilia of Outer Hair Cells and Required for Normal Outer Hair Cell Function
- (2016) W.-Z. Zeng et al. JOURNAL OF NEUROSCIENCE
- High-throughput discovery of novel developmental phenotypes
- (2016) Mary E. Dickinson et al. NATURE
- g:Profiler—a web server for functional interpretation of gene lists (2016 update)
- (2016) Jüri Reimand et al. NUCLEIC ACIDS RESEARCH
- Novel gene function revealed by mouse mutagenesis screens for models of age-related disease
- (2016) Paul K. Potter et al. Nature Communications
- Non-syndromic hearing loss gene identification: A brief history and glimpse into the future
- (2015) Barbara Vona et al. MOLECULAR AND CELLULAR PROBES
- Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics
- (2015) Martin Hrabě de Angelis et al. NATURE GENETICS
- Genetics of Hearing Loss
- (2015) Tal Koffler et al. OTOLARYNGOLOGIC CLINICS OF NORTH AMERICA
- PhenStat: A Tool Kit for Standardized Analysis of High Throughput Phenotypic Data
- (2015) Natalja Kurbatova et al. PLoS One
- Applying the ARRIVE Guidelines to an In Vivo Database
- (2015) Natasha A. Karp et al. PLOS BIOLOGY
- Neuropilin-2/Semaphorin-3F-mediated repulsion promotes inner hair cell innervation by spiral ganglion neurons
- (2015) Thomas M Coate et al. eLife
- STRING v10: protein–protein interaction networks, integrated over the tree of life
- (2014) Damian Szklarczyk et al. NUCLEIC ACIDS RESEARCH
- Spinster Homolog 2 (Spns2) Deficiency Causes Early Onset Progressive Hearing Loss
- (2014) Jing Chen et al. PLoS Genetics
- Genome-wide Generation and Systematic Phenotyping of Knockout Mice Reveals New Roles for Many Genes
- (2013) Jacqueline K. White et al. CELL
- Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource
- (2013) Edward Ryder et al. MAMMALIAN GENOME
- Mcph1-Deficient Mice Reveal a Role for MCPH1 in Otitis Media
- (2013) Jing Chen et al. PLoS One
- Advantages of a Mouse Model for Human Hearing Impairment
- (2012) Yoshiaki Kikkawa et al. EXPERIMENTAL ANIMALS
- The International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping
- (2012) Steve D. M. Brown et al. MAMMALIAN GENOME
- Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project
- (2012) Abdel Ayadi et al. MAMMALIAN GENOME
- 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
- A conditional knockout resource for the genome-wide study of mouse gene function
- (2011) William C. Skarnes et al. NATURE
- A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment
- (2010) Rachel E Hardisty-Hughes et al. Nature Protocols
- Hearing Impairment: A Panoply of Genes and Functions
- (2010) Amiel A. Dror et al. NEURON
- ENU Mutagenesis, a Way Forward to Understand Gene Function
- (2008) Abraham Acevedo-Arozena et al. Annual Review of Genomics and Human Genetics
- Quiet as a mouse: dissecting the molecular and genetic basis of hearing
- (2008) Steve D. M. Brown et al. NATURE REVIEWS GENETICS
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