Ana Quelle-Regaldie, Daniel Sobrido-Cameán, Antón Barreiro-Iglesias, María Jesús Sobrido, Laura Sánchez. Cells 2021
Times Cited: 3
Times Cited: 3
Times Cited
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Function Over Form: Modeling Groups of Inherited Neurological Conditions in Zebrafish.
Robert A Kozol, Alexander J Abrams, David M James, Elena Buglo, Qing Yan, Julia E Dallman. Front Mol Neurosci 2016
Robert A Kozol, Alexander J Abrams, David M James, Elena Buglo, Qing Yan, Julia E Dallman. Front Mol Neurosci 2016
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Characterization of the zebrafish atxn1/axh gene family.
Kerri M Carlson, Laura Melcher, Shaojuan Lai, Huda Y Zoghbi, H Brent Clark, Harry T Orr. J Neurogenet 2009
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Zebrafish: Housing and husbandry recommendations.
Peter Aleström, Livia D'Angelo, Paul J Midtlyng, Daniel F Schorderet, Stefan Schulte-Merker, Frederic Sohm, Susan Warner. Lab Anim 2020
Peter Aleström, Livia D'Angelo, Paul J Midtlyng, Daniel F Schorderet, Stefan Schulte-Merker, Frederic Sohm, Susan Warner. Lab Anim 2020
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Pathogenic mechanisms of a polyglutamine-mediated neurodegenerative disease, spinocerebellar ataxia type 1.
Huda Y Zoghbi, Harry T Orr. J Biol Chem 2009
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The zebrafish reference genome sequence and its relationship to the human genome.
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The complex clinical and genetic classification of inherited ataxias. II. Autosomal recessive ataxias.
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Genome engineering using the CRISPR-Cas9 system.
F Ann Ran, Patrick D Hsu, Jason Wright, Vineeta Agarwala, David A Scott, Feng Zhang. Nat Protoc 2013
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Differential requirement for ptf1a in endocrine and exocrine lineages of developing zebrafish pancreas.
John W Lin, Andrew V Biankin, Marko E Horb, Bidyut Ghosh, Nijaguna B Prasad, Nelson S Yee, Michael A Pack, Steven D Leach. Dev Biol 2004
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Zebrafish cancer: the state of the art and the path forward.
Richard White, Kristin Rose, Leonard Zon. Nat Rev Cancer 2013
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Graded levels of Ptf1a differentially regulate endocrine and exocrine fates in the developing pancreas.
P Duc Si Dong, Elayne Provost, Steven D Leach, Didier Y R Stainier. Genes Dev 2008
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Cell senescence contributes to tissue regeneration in zebrafish.
Sabela Da Silva-Álvarez, Jorge Guerra-Varela, Daniel Sobrido-Cameán, Ana Quelle, Antón Barreiro-Iglesias, Laura Sánchez, Manuel Collado. Aging Cell 2020
Sabela Da Silva-Álvarez, Jorge Guerra-Varela, Daniel Sobrido-Cameán, Ana Quelle, Antón Barreiro-Iglesias, Laura Sánchez, Manuel Collado. Aging Cell 2020
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PNPLA6 mutations cause Boucher-Neuhauser and Gordon Holmes syndromes as part of a broad neurodegenerative spectrum.
Matthis Synofzik, Michael A Gonzalez, Charles Marques Lourenco, Marie Coutelier, Tobias B Haack, Adriana Rebelo, Didier Hannequin, Tim M Strom, Holger Prokisch, Christoph Kernstock,[...]. Brain 2014
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Mutations in a novel gene encoding a CRAL-TRIO domain cause human Cayman ataxia and ataxia/dystonia in the jittery mouse.
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A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies.
Hemant Khanna, Erica E Davis, Carlos A Murga-Zamalloa, Alejandro Estrada-Cuzcano, Irma Lopez, Anneke I den Hollander, Marijke N Zonneveld, Mohammad I Othman, Naushin Waseem, Christina F Chakarova,[...]. Nat Genet 2009
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Loss of wwox expression in zebrafish embryos causes edema and alters Ca(2+) dynamics.
Yusuke Tsuruwaka, Masataka Konishi, Eriko Shimada. PeerJ 2015
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The Ciliopathy Gene ahi1 Is Required for Zebrafish Cone Photoreceptor Outer Segment Morphogenesis and Survival.
Emma M Lessieur, Joseph Fogerty, Robert J Gaivin, Ping Song, Brian D Perkins. Invest Ophthalmol Vis Sci 2017
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Clinical features and molecular genetics of autosomal recessive cerebellar ataxias.
Brent L Fogel, Susan Perlman. Lancet Neurol 2007
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Zebrafish lacking functional DNA polymerase gamma survive to juvenile stage, despite rapid and sustained mitochondrial DNA depletion, altered energetics and growth.
Jennifer J Rahn, Jennifer E Bestman, Krista D Stackley, Sherine S L Chan. Nucleic Acids Res 2015
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Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome.
Tawfeg Ben-Omran, Somayyeh Fahiminiya, Natalie Sorfazlian, Mariam Almuriekhi, Zafar Nawaz, Javad Nadaf, Kitam Abu Khadija, Samiha Zaineddin, Hussein Kamel, Jacek Majewski,[...]. J Med Genet 2015
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The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenance.
Irene Ojeda Naharros, Flavia B Cristian, Jingjing Zang, Matthias Gesemann, Philip W Ingham, Stephan C F Neuhauss, Ruxandra Bachmann-Gagescu. Sci Rep 2018
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laminin alpha 1 gene is essential for normal lens development in zebrafish.
Natalya S Zinkevich, Dmitry V Bosenko, Brian A Link, Elena V Semina. BMC Dev Biol 2006
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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder.
Alexander J Abrams, Robert B Hufnagel, Adriana Rebelo, Claudia Zanna, Neville Patel, Michael A Gonzalez, Ion J Campeanu, Laurie B Griffin, Saskia Groenewald, Alleene V Strickland,[...]. Nat Genet 2015
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Arl13b Interacts With Vangl2 to Regulate Cilia and Photoreceptor Outer Segment Length in Zebrafish.
Ping Song, Lynn Dudinsky, Joseph Fogerty, Robert Gaivin, Brian D Perkins. Invest Ophthalmol Vis Sci 2016
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POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness.
M Mancuso, M Filosto, M Bellan, R Liguori, P Montagna, A Baruzzi, S DiMauro, V Carelli. Neurology 2004
M Mancuso, M Filosto, M Bellan, R Liguori, P Montagna, A Baruzzi, S DiMauro, V Carelli. Neurology 2004
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Wwox-Brca1 interaction: role in DNA repair pathway choice.
M S Schrock, B Batar, J Lee, T Druck, B Ferguson, J H Cho, K Akakpo, H Hagrass, N A Heerema, F Xia,[...]. Oncogene 2017
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Zebrafish models for personalized psychiatry: Insights from individual, strain and sex differences, and modeling gene x environment interactions.
Andrey D Volgin, Oleg A Yakovlev, Konstantin A Demin, Murilo S de Abreu, Polina A Alekseeva, Ashton J Friend, Anton M Lakstygal, Tamara G Amstislavskaya, Wandong Bao, Cai Song,[...]. J Neurosci Res 2019
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Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency.
Ming-Yang Chang, Tsu-Lin Ma, Cheng-Chieh Hung, Ya-Chung Tian, Yung-Chang Chen, Chih-Wei Yang, Yi-Chuan Cheng. Sci Rep 2017
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A familial late‑onset hereditary ataxia mimicking pontocerebellar hypoplasia caused by a novel TSEN54 mutation.
Yi Qian, Haiyong Wang, Tao Jin, Yiqing Wang, Lizheng Fang, Yuhao Chen, Liying Chen. Mol Med Rep 2014
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Serotonin Promotes Development and Regeneration of Spinal Motor Neurons in Zebrafish.
Antón Barreiro-Iglesias, Karolina S Mysiak, Angela L Scott, Michell M Reimer, Yujie Yang, Catherina G Becker, Thomas Becker. Cell Rep 2015
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The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4.
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Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia.
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Gain-of-function defects of astrocytic Kir4.1 channels in children with autism spectrum disorders and epilepsy.
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Autophagy regulates cytoplasmic remodeling during cell reprogramming in a zebrafish model of muscle regeneration.
Alfonso Saera-Vila, Phillip E Kish, Ke'ale W Louie, Steven J Grzegorski, Daniel J Klionsky, Alon Kahana. Autophagy 2016
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Up-regulation of autophagy-related gene 5 (ATG5) protects dopaminergic neurons in a zebrafish model of Parkinson's disease.
Zhan-Ying Hu, Bo Chen, Jing-Pu Zhang, Yuan-Yuan Ma. J Biol Chem 2017
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SLC25A46 mutations underlie progressive myoclonic ataxia with optic atrophy and neuropathy.
Gavin Charlesworth, Bettina Balint, Niccolò E Mencacci, Lucinda Carr, Nicholas W Wood, Kailash P Bhatia. Mov Disord 2016
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Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
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A zebrafish model of CLN2 disease is deficient in tripeptidyl peptidase 1 and displays progressive neurodegeneration accompanied by a reduction in proliferation.
Fahad Mahmood, Sonia Fu, Jennifer Cooke, Stephen W Wilson, Jonathan D Cooper, Claire Russell. Brain 2013
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Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy.
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Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes.
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Basal body stability and ciliogenesis requires the conserved component Poc1.
Chad G Pearson, Daniel P S Osborn, Thomas H Giddings, Philip L Beales, Mark Winey. J Cell Biol 2009
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Modeling Niemann-Pick disease type C1 in zebrafish: a robust platform for in vivo screening of candidate therapeutic compounds.
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Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.
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Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease).
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Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration.
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Genetic compensation in a stable slc25a46 mutant zebrafish: A case for using F0 CRISPR mutagenesis to study phenotypes caused by inherited disease.
Elena Buglo, Evan Sarmiento, Nicole Belliard Martuscelli, David W Sant, Matt C Danzi, Alexander J Abrams, Julia E Dallman, Stephan Züchner. PLoS One 2020
Elena Buglo, Evan Sarmiento, Nicole Belliard Martuscelli, David W Sant, Matt C Danzi, Alexander J Abrams, Julia E Dallman, Stephan Züchner. PLoS One 2020
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CA8 mutations cause a novel syndrome characterized by ataxia and mild mental retardation with predisposition to quadrupedal gait.
Seval Türkmen, Gao Guo, Masoud Garshasbi, Katrin Hoffmann, Amjad J Alshalah, Claudia Mischung, Andreas Kuss, Nicholas Humphrey, Stefan Mundlos, Peter N Robinson. PLoS Genet 2009
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Evolutionary conserved role of ptf1a in the specification of exocrine pancreatic fates.
Elisabetta Zecchin, Anastasia Mavropoulos, Nathalie Devos, Alida Filippi, Natascia Tiso, Dirk Meyer, Bernard Peers, Marino Bortolussi, Francesco Argenton. Dev Biol 2004
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.