标题
Zebrafish Models of Autosomal Dominant Ataxias
作者
关键词
-
出版物
Cells
Volume 10, Issue 2, Pages 421
出版商
MDPI AG
发表日期
2021-02-18
DOI
10.3390/cells10020421
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。- Hyperactivity, Memory Defects, and Craniofacial Abnormalities in Zebrafish fmr1 Mutant Larvae
- (2020) Jia Hu et al. BEHAVIOR GENETICS
- Infant and adult SCA13 mutations differentially affect Purkinje cell excitability, maturation, and viability in vivo
- (2020) Jui-Yi Hsieh et al. eLife
- Altered brain-wide auditory networks in a zebrafish model of fragile X syndrome
- (2020) Lena Constantin et al. BMC BIOLOGY
- Modeling neurodegenerative Spinocerebellar Ataxia type 13 in zebrafish using a Purkinje neuron specific tunable co-expression system
- (2019) Kazuhiko Namikawa et al. JOURNAL OF NEUROSCIENCE
- Role of Reelin in cell positioning in the cerebellum and the cerebellum-like structure in zebrafish
- (2019) Takayuki Nimura et al. DEVELOPMENTAL BIOLOGY
- Reelin Signaling Controls the Preference for Social Novelty in Zebrafish
- (2019) Elisa Dalla Vecchia et al. Frontiers in Behavioral Neuroscience
- The Zebrafish Visual System: From Circuits to Behavior
- (2019) Johann H. Bollmann Annual Review of Vision Science
- The RNA binding protein fragile X mental retardation protein promotes myelin sheath growth
- (2019) Caleb A. Doll et al. GLIA
- Bi-allelic variants in RNF170 are associated with hereditary spastic paraplegia
- (2019) Matias Wagner et al. Nature Communications
- Genetic and epigenetic control of retinal development in zebrafish
- (2019) Pawat Seritrakul et al. CURRENT OPINION IN NEUROBIOLOGY
- Phenotypic Characterization of Larval Zebrafish (Danio rerio) with Partial Knockdown of the cacna1a Gene
- (2019) Kinga Gawel et al. MOLECULAR NEUROBIOLOGY
- A DNAzyme based knockdown model for Fragile-X syndrome in zebrafish reveals a critical window for therapeutic intervention
- (2019) Raghavender Medishetti et al. JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS
- A novel metabolism-based phenotypic drug discovery platform in zebrafish uncovers HDACs 1 and 3 as a potential combined anti-seizure drug target
- (2018) Kingsley Ibhazehiebo et al. BRAIN
- An Attractive Reelin Gradient Establishes Synaptic Lamination in the Vertebrate Visual System
- (2018) Vincenzo Di Donato et al. NEURON
- Animal models of neurodegenerative diseases
- (2018) Ted M. Dawson et al. NATURE NEUROSCIENCE
- Loss of zebrafish Ataxin-7, a SAGA subunit responsible for SCA7 retinopathy, causes ocular coloboma and malformation of photoreceptors
- (2018) Samantha Carrillo-Rosas et al. HUMAN MOLECULAR GENETICS
- Single copy/knock-in models of ALS SOD1 in C. elegans suggest loss and gain of function have different contributions to cholinergic and glutamatergic neurodegeneration
- (2018) Saba N. Baskoylu et al. PLoS Genetics
- Calpain Inhibition Is Protective in Machado–Joseph Disease Zebrafish Due to Induction of Autophagy
- (2017) Maxinne Watchon et al. JOURNAL OF NEUROSCIENCE
- Genome editing using CRISPR/Cas9-based knock-in approaches in zebrafish
- (2017) Shahad Albadri et al. METHODS
- Antisense oligonucleotide therapy for spinocerebellar ataxia type 2
- (2017) Daniel R. Scoles et al. NATURE
- Fragile X Mental Retardation-1 Knockout Zebrafish Shows Precocious Development in Social Behavior
- (2017) Yao-Ju Wu et al. Zebrafish
- CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing
- (2017) Miguel A. Moreno-Mateos et al. Nature Communications
- Guidelines for morpholino use in zebrafish
- (2017) Didier Y. R. Stainier et al. PLoS Genetics
- The most prevalent genetic cause of ALS-FTD, C9orf72 synergizes the toxicity of ATXN2 intermediate polyglutamine repeats through the autophagy pathway
- (2016) Sorana Ciura et al. Autophagy
- Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin‐2 to induce motor neuron dysfunction and cell death
- (2016) Chantal Sellier et al. EMBO JOURNAL
- Quantification of the Relative Contributions of Loss-of-function and Gain-of-function Mechanisms in TAR DNA-binding Protein 43 (TDP-43) Proteinopathies
- (2016) Roberta Cascella et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Fragile X-associated tremor/ataxia syndrome — features, mechanisms and management
- (2016) Randi J. Hagerman et al. Nature Reviews Neurology
- The Machado–Joseph Disease Deubiquitinase Ataxin-3 Regulates the Stability and Apoptotic Function of p53
- (2016) Hongmei Liu et al. PLOS BIOLOGY
- Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish
- (2016) Robert A. Kozol et al. Frontiers in Molecular Neuroscience
- Epilepsy, Behavioral Abnormalities, and Physiological Comorbidities in Syntaxin-Binding Protein 1 (STXBP1) Mutant Zebrafish
- (2016) Brian P. Grone et al. PLoS One
- CACNA1A haploinsufficiency causes cognitive impairment, autism and epileptic encephalopathy with mild cerebellar symptoms
- (2015) Lena Damaj et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- The N17 domain mitigates nuclear toxicity in a novel zebrafish Huntington’s disease model
- (2015) Matthew B. Veldman et al. Molecular Neurodegeneration
- Evaluating the relationship between reelin gene variants (rs7341475 and rs262355) and schizophrenia: A meta-analysis
- (2015) Wei Li et al. NEUROSCIENCE LETTERS
- Fmrp Interacts with Adar and Regulates RNA Editing, Synaptic Density and Locomotor Activity in Zebrafish
- (2015) Adi Shamay-Ramot et al. PLoS Genetics
- Pharmacological Characterization of an Antisense Knockdown Zebrafish Model of Dravet Syndrome: Inhibition of Epileptic Seizures by the Serotonin Agonist Fenfluramine
- (2015) Yifan Zhang et al. PLoS One
- Reelin Signaling Pathway Genotypes and Alzheimer Disease in a Spanish Population
- (2014) Enric Bufill et al. ALZHEIMER DISEASE & ASSOCIATED DISORDERS
- Reelin gene variants and risk of autism spectrum disorders: An integrated meta-analysis
- (2014) Zhenling Wang et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
- Identification and characterization of PKCγ, a kinase associated with SCA14, as an amyloidogenic protein
- (2014) Hideyuki Takahashi et al. HUMAN MOLECULAR GENETICS
- The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability
- (2014) Katherine E Hekman et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Direct Binding of Ataxin-2 to Distinct Elements in 3′ UTRs Promotes mRNA Stability and Protein Expression
- (2014) Moe Yokoshi et al. MOLECULAR CELL
- Huntington disease: Can a zebrafish trail leave more than a ripple?
- (2014) Sambit Das et al. NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
- Anxiety, hyperactivity and stereotypy in a zebrafish model of fragile X syndrome and autism spectrum disorder
- (2014) Lily Kim et al. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY
- Zebrafish models of human motor neuron diseases: Advantages and limitations
- (2014) Patrick J. Babin et al. PROGRESS IN NEUROBIOLOGY
- The new frontier of genome engineering with CRISPR-Cas9
- (2014) J. A. Doudna et al. SCIENCE
- Insights From Cerebellar Transcriptomic Analysis Into the Pathogenesis of Ataxia
- (2014) Conceição Bettencourt et al. JAMA Neurology
- Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias
- (2013) A. Matilla-Dueñas et al. CEREBELLUM
- Optical coherence tomography findings in spinocerebellar ataxia-3
- (2013) G Alvarez et al. EYE
- Hereditary ataxias: overview
- (2013) Suman Jayadev et al. GENETICS IN MEDICINE
- Zebrafish Calls for Reinterpretation for the Roles of P/Q Calcium Channels in Neuromuscular Transmission
- (2013) H. Wen et al. JOURNAL OF NEUROSCIENCE
- The zebrafish reference genome sequence and its relationship to the human genome
- (2013) Kerstin Howe et al. NATURE
- Genome engineering using the CRISPR-Cas9 system
- (2013) F Ann Ran et al. Nature Protocols
- Behavioral and Synaptic Circuit Features in a Zebrafish Model of Fragile X Syndrome
- (2013) Ming-Chong Ng et al. PLoS One
- Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development
- (2012) F. A. Issa et al. Disease Models & Mechanisms
- Touch responsiveness in zebrafish requires voltage-gated calcium channel 2.1b
- (2012) Sean E. Low et al. JOURNAL OF NEUROPHYSIOLOGY
- Requirement for Zebrafish Ataxin-7 in Differentiation of Photoreceptors and Cerebellar Neurons
- (2012) Constantin Yanicostas et al. PLoS One
- Auditory change detection in fragile X syndrome males: A brain potential study
- (2011) M.J.W. Van der Molen et al. CLINICAL NEUROPHYSIOLOGY
- Spinocerebellar Ataxia Type 13 Mutant Potassium Channel Alters Neuronal Excitability and Causes Locomotor Deficits in Zebrafish
- (2011) F. A. Issa et al. JOURNAL OF NEUROSCIENCE
- Retinal Nerve Fibre Layer and Macular Thinning in Spinocerebellar Ataxia and Cerebellar Multisystem Atrophy
- (2011) John H. Pula et al. NEURO-OPHTHALMOLOGY
- The Genetic Variation of RELN Expression in Schizophrenia and Bipolar Disorder
- (2011) Galit Ovadia et al. PLoS One
- Toward understanding Machado–Joseph disease
- (2011) Maria do Carmo Costa et al. PROGRESS IN NEUROBIOLOGY
- The long adventurous journey of rhombic lip cells in jawed vertebrates: a comparative developmental analysis
- (2011) Mario Wullimann Frontiers in Neuroanatomy
- Functional effects of spinocerebellar ataxia type 13 mutations are conserved in zebrafish Kv3.3 channels
- (2010) Allan F Mock et al. BMC NEUROSCIENCE
- A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
- (2010) Paul N. Valdmanis et al. BRAIN
- Protein kinase Cγ is a signaling molecule required for the developmental speeding of α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate receptor kinetics
- (2010) Shunmoogum A. Patten et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Mutant protein kinase C gamma that causes spinocerebellar ataxia type 14 (SCA14) is selectively degraded by autophagy
- (2010) Kazuhiro Yamamoto et al. GENES TO CELLS
- Genetic and functional characterisation of the P/Q calcium channel in episodic ataxia with epilepsy
- (2010) Sanjeev Rajakulendran et al. JOURNAL OF PHYSIOLOGY-LONDON
- Cerebellar ataxias
- (2009) Mario Manto et al. CURRENT OPINION IN NEUROLOGY
- Mutations in VLDLR as a Cause for Autosomal Recessive Cerebellar Ataxia With Mental Retardation (Dysequilibrium Syndrome)
- (2009) Kym M. Boycott et al. JOURNAL OF CHILD NEUROLOGY
- Generation and Characterization of Fmr1 Knockout Zebrafish
- (2009) Marjo J. den Broeder et al. PLoS One
- PKC -induced trafficking of AMPA receptors in embryonic zebrafish depends on NSF and PICK1
- (2009) S. A. Patten et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- SCA13
- (2008) M. F. Waters et al. CEREBELLUM
- Spinocerebellar ataxia 2 (SCA2)
- (2008) Isabel Lastres-Becker et al. CEREBELLUM
- SCA3: Neurological features, pathogenesis and animal models
- (2008) Olaf Riess et al. CEREBELLUM
- Characterization of the Zebrafishatxn1/axhGene Family
- (2008) Kerri M. Carlson et al. JOURNAL OF NEUROGENETICS
- Ca2+ channel-independent requirement for MAGUK family CACNB4 genes in initiation of zebrafish epiboly
- (2008) A. M. Ebert et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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