메뉴 건너뛰기




Volumn 26, Issue 8, 2010, Pages 373-381

In the swim of things: Recent insights to neurogenetic disorders from zebrafish

Author keywords

[No Author keywords available]

Indexed keywords

SURVIVAL MOTOR NEURON PROTEIN 1; TAR DNA BINDING PROTEIN;

EID: 77955089579     PISSN: 01689525     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tig.2010.05.004     Document Type: Review
Times cited : (47)

References (75)
  • 1
    • 47849103448 scopus 로고    scopus 로고
    • Zebrafish: an in vivo model for the study of neurological diseases
    • Best J.D., Alderton W.K. Zebrafish: an in vivo model for the study of neurological diseases. Neuropsychiatr. Dis. Treat. 2008, 4:567-576.
    • (2008) Neuropsychiatr. Dis. Treat. , vol.4 , pp. 567-576
    • Best, J.D.1    Alderton, W.K.2
  • 2
    • 63149158008 scopus 로고    scopus 로고
    • The power of the zebrafish for disease analysis
    • Ingham P.W. The power of the zebrafish for disease analysis. Hum. Mol. Genet. 2009, 18:R107-112.
    • (2009) Hum. Mol. Genet. , vol.18
    • Ingham, P.W.1
  • 3
    • 0033550061 scopus 로고    scopus 로고
    • Zebrafish (Danio rerio) presenilin promotes aberrant amyloid beta-peptide production and requires a critical aspartate residue for its function in amyloidogenesis
    • Leimer U., et al. Zebrafish (Danio rerio) presenilin promotes aberrant amyloid beta-peptide production and requires a critical aspartate residue for its function in amyloidogenesis. Biochemistry 1999, 38:13602-13609.
    • (1999) Biochemistry , vol.38 , pp. 13602-13609
    • Leimer, U.1
  • 4
    • 70349786368 scopus 로고    scopus 로고
    • Amyloid precursor protein is required for convergent-extension movements during Zebrafish development
    • Joshi P., et al. Amyloid precursor protein is required for convergent-extension movements during Zebrafish development. Dev. Biol. 2009, 335:1-11.
    • (2009) Dev. Biol. , vol.335 , pp. 1-11
    • Joshi, P.1
  • 5
    • 59649109467 scopus 로고    scopus 로고
    • Decreased BDNF levels are a major contributor to the embryonic phenotype of huntingtin knockdown zebrafish
    • Diekmann H., et al. Decreased BDNF levels are a major contributor to the embryonic phenotype of huntingtin knockdown zebrafish. J. Neurosci. 2009, 29:1343-1349.
    • (2009) J. Neurosci. , vol.29 , pp. 1343-1349
    • Diekmann, H.1
  • 6
    • 33751100104 scopus 로고    scopus 로고
    • Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis
    • Carrel T.L., et al. Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis. J. Neurosci. 2006, 26:11014-11022.
    • (2006) J. Neurosci. , vol.26 , pp. 11014-11022
    • Carrel, T.L.1
  • 7
    • 42549088649 scopus 로고    scopus 로고
    • Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
    • Oprea G.E., et al. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science 2008, 320:524-527.
    • (2008) Science , vol.320 , pp. 524-527
    • Oprea, G.E.1
  • 8
    • 58149152976 scopus 로고    scopus 로고
    • Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord
    • Montpetit A., et al. Disruption of AP1S1, causing a novel neurocutaneous syndrome, perturbs development of the skin and spinal cord. PLoS Genet. 2008, 4:e1000296.
    • (2008) PLoS Genet. , vol.4
    • Montpetit, A.1
  • 9
    • 0036810510 scopus 로고    scopus 로고
    • Development of the locomotor network in zebrafish
    • Drapeau P., et al. Development of the locomotor network in zebrafish. Prog. Neurobiol. 2002, 68:85-111.
    • (2002) Prog. Neurobiol. , vol.68 , pp. 85-111
    • Drapeau, P.1
  • 10
    • 34548740744 scopus 로고    scopus 로고
    • Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish
    • Lemmens R., et al. Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish. Hum. Mol. Genet. 2007, 16:2359-2365.
    • (2007) Hum. Mol. Genet. , vol.16 , pp. 2359-2365
    • Lemmens, R.1
  • 11
    • 33751250197 scopus 로고    scopus 로고
    • Genetics of familial and sporadic amyotrophic lateral sclerosis
    • Gros-Louis F., et al. Genetics of familial and sporadic amyotrophic lateral sclerosis. Biochim. Biophys. Acta 2006, 1762:956-972.
    • (2006) Biochim. Biophys. Acta , vol.1762 , pp. 956-972
    • Gros-Louis, F.1
  • 12
    • 49649085351 scopus 로고    scopus 로고
    • Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish
    • Gros-Louis F., et al. Als2 mRNA splicing variants detected in KO mice rescue severe motor dysfunction phenotype in Als2 knock-down zebrafish. Hum. Mol. Genet. 2008, 17:2691-2702.
    • (2008) Hum. Mol. Genet. , vol.17 , pp. 2691-2702
    • Gros-Louis, F.1
  • 13
    • 31144448704 scopus 로고    scopus 로고
    • Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking
    • Hadano S., et al. Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking. Hum. Mol. Genet. 2006, 15:233-250.
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 233-250
    • Hadano, S.1
  • 14
    • 58749097964 scopus 로고    scopus 로고
    • Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration
    • Simpson C.L., et al. Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration. Hum. Mol. Genet. 2009, 18:472-481.
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 472-481
    • Simpson, C.L.1
  • 15
    • 42649120983 scopus 로고    scopus 로고
    • TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
    • Kabashi E., et al. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis. Nat. Genet. 2008, 40:572-574.
    • (2008) Nat. Genet. , vol.40 , pp. 572-574
    • Kabashi, E.1
  • 16
    • 41149180753 scopus 로고    scopus 로고
    • TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
    • Sreedharan J., et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science 2008, 319:1668-1672.
    • (2008) Science , vol.319 , pp. 1668-1672
    • Sreedharan, J.1
  • 17
    • 33749632259 scopus 로고    scopus 로고
    • Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
    • Neumann M., et al. Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Science 2006, 314:130-133.
    • (2006) Science , vol.314 , pp. 130-133
    • Neumann, M.1
  • 18
    • 77950360176 scopus 로고    scopus 로고
    • Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo
    • Kabashi E., et al. Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo. Hum. Mol. Genet. 2010, 19:671-683.
    • (2010) Hum. Mol. Genet. , vol.19 , pp. 671-683
    • Kabashi, E.1
  • 19
    • 55549094109 scopus 로고    scopus 로고
    • Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms
    • Salinas S., et al. Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol. 2008, 7:1127-1138.
    • (2008) Lancet Neurol. , vol.7 , pp. 1127-1138
    • Salinas, S.1
  • 20
    • 33845991876 scopus 로고    scopus 로고
    • Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
    • Valdmanis P.N., et al. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia. Am. J. Hum. Genet. 2007, 80:152-161.
    • (2007) Am. J. Hum. Genet. , vol.80 , pp. 152-161
    • Valdmanis, P.N.1
  • 21
    • 57649084368 scopus 로고    scopus 로고
    • A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42)
    • Lin P., et al. A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). Am. J. Hum. Genet. 2008, 83:752-759.
    • (2008) Am. J. Hum. Genet. , vol.83 , pp. 752-759
    • Lin, P.1
  • 22
    • 33748747401 scopus 로고    scopus 로고
    • The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo
    • Wood J.D., et al. The microtubule-severing protein Spastin is essential for axon outgrowth in the zebrafish embryo. Hum. Mol. Genet. 2006, 15:2763-2771.
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 2763-2771
    • Wood, J.D.1
  • 23
    • 33845353014 scopus 로고    scopus 로고
    • A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition
    • Tarrade A., et al. A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. Hum. Mol. Genet. 2006, 15:3544-3558.
    • (2006) Hum. Mol. Genet. , vol.15 , pp. 3544-3558
    • Tarrade, A.1
  • 24
    • 0042887389 scopus 로고    scopus 로고
    • Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
    • McWhorter M.L., et al. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J. Cell Biol. 2003, 162:919-931.
    • (2003) J. Cell Biol. , vol.162 , pp. 919-931
    • McWhorter, M.L.1
  • 25
    • 66149118977 scopus 로고    scopus 로고
    • A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice
    • Workman E., et al. A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice. Hum. Mol. Genet. 2009, 18:2215-2229.
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 2215-2229
    • Workman, E.1
  • 26
    • 70350754456 scopus 로고    scopus 로고
    • Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects
    • Boon K.L., et al. Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects. Hum. Mol. Genet. 2009, 18:3615-3625.
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 3615-3625
    • Boon, K.L.1
  • 27
    • 58749114020 scopus 로고    scopus 로고
    • Disrupted-in-schizophrenia 1 and neuregulin 1 are required for the specification of oligodendrocytes and neurones in the zebrafish brain
    • Wood J.D., et al. Disrupted-in-schizophrenia 1 and neuregulin 1 are required for the specification of oligodendrocytes and neurones in the zebrafish brain. Hum. Mol. Genet. 2009, 18:391-404.
    • (2009) Hum. Mol. Genet. , vol.18 , pp. 391-404
    • Wood, J.D.1
  • 28
    • 70349783599 scopus 로고    scopus 로고
    • The autism susceptibility gene met regulates zebrafish cerebellar development and facial motor neuron migration
    • Elsen G.E., et al. The autism susceptibility gene met regulates zebrafish cerebellar development and facial motor neuron migration. Dev. Biol. 2009, 335:78-92.
    • (2009) Dev. Biol. , vol.335 , pp. 78-92
    • Elsen, G.E.1
  • 29
    • 63449111560 scopus 로고    scopus 로고
    • Novel de novo SHANK3 mutation in autistic patients
    • B
    • Gauthier J., et al. Novel de novo SHANK3 mutation in autistic patients. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2009, 150B:421-424.
    • (2009) Am. J. Med. Genet. B Neuropsychiatr. Genet. , vol.150 , pp. 421-424
    • Gauthier, J.1
  • 30
    • 17044378032 scopus 로고    scopus 로고
    • Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons
    • Roussignol G., et al. Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons. J. Neurosci. 2005, 25:3560-3570.
    • (2005) J. Neurosci. , vol.25 , pp. 3560-3570
    • Roussignol, G.1
  • 31
    • 77952374703 scopus 로고    scopus 로고
    • De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proc. Natl. Acad. Sci. U. S. A.
    • Gauthier, J. et al. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia. Proc. Natl. Acad. Sci. U. S. A. 107, 7863-7868.
    • , vol.107 , pp. 7863-7868
    • Gauthier, J.1
  • 32
    • 0034625631 scopus 로고    scopus 로고
    • Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport
    • Setou M., et al. Kinesin superfamily motor protein KIF17 and mLin-10 in NMDA receptor-containing vesicle transport. Science 2000, 288:1796-1802.
    • (2000) Science , vol.288 , pp. 1796-1802
    • Setou, M.1
  • 33
    • 40949162296 scopus 로고    scopus 로고
    • The homodimeric kinesin, Kif17, is essential for vertebrate photoreceptor sensory outer segment development
    • Insinna C., et al. The homodimeric kinesin, Kif17, is essential for vertebrate photoreceptor sensory outer segment development. Dev. Biol. 2008, 316:160-170.
    • (2008) Dev. Biol. , vol.316 , pp. 160-170
    • Insinna, C.1
  • 34
    • 77956943158 scopus 로고    scopus 로고
    • doi:10.1016/j.biopsych.2010.04.018, De Novo Truncating Mutation in Kinesin 17 Associated with Schizophrenia. Biol. Psychiatry
    • Tarabeux, J. et al. De Novo Truncating Mutation in Kinesin 17 Associated with Schizophrenia. Biol. Psychiatry, doi:10.1016/j.biopsych.2010.04.018.
    • Tarabeux, J.1
  • 35
    • 0842324801 scopus 로고    scopus 로고
    • The mechanisms of vesicle budding and fusion
    • Bonifacino J.S., Glick B.S. The mechanisms of vesicle budding and fusion. Cell 2004, 116:153-166.
    • (2004) Cell , vol.116 , pp. 153-166
    • Bonifacino, J.S.1    Glick, B.S.2
  • 36
    • 33847723997 scopus 로고    scopus 로고
    • P53-dependent neuronal cell death in a DJ-1-deficient zebrafish model of Parkinson's disease
    • Bretaud S., et al. p53-dependent neuronal cell death in a DJ-1-deficient zebrafish model of Parkinson's disease. J. Neurochem. 2007, 100:1626-1635.
    • (2007) J. Neurochem. , vol.100 , pp. 1626-1635
    • Bretaud, S.1
  • 37
    • 34247869645 scopus 로고    scopus 로고
    • Identification of anti-prion compounds as efficient inhibitors of polyglutamine protein aggregation in a zebrafish model
    • Schiffer N.W., et al. Identification of anti-prion compounds as efficient inhibitors of polyglutamine protein aggregation in a zebrafish model. J. Biol. Chem. 2007, 282:9195-9203.
    • (2007) J. Biol. Chem. , vol.282 , pp. 9195-9203
    • Schiffer, N.W.1
  • 38
    • 40449088986 scopus 로고    scopus 로고
    • The use of microarray technology in nonmammalian vertebrate systems
    • Sipe C.W., Saha M.S. The use of microarray technology in nonmammalian vertebrate systems. Methods Mol. Biol. 2007, 382:1-16.
    • (2007) Methods Mol. Biol. , vol.382 , pp. 1-16
    • Sipe, C.W.1    Saha, M.S.2
  • 39
    • 44949176174 scopus 로고    scopus 로고
    • Genomewide expression analysis in zebrafish mind bomb alleles with pancreas defects of different severity identifies putative Notch responsive genes
    • Hegde A., et al. Genomewide expression analysis in zebrafish mind bomb alleles with pancreas defects of different severity identifies putative Notch responsive genes. PLoS One 2008, 3:e1479.
    • (2008) PLoS One , vol.3
    • Hegde, A.1
  • 40
  • 41
    • 62649165022 scopus 로고    scopus 로고
    • Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation
    • Yeh J.R., et al. Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation. Nat. Chem. Biol. 2009, 5:236-243.
    • (2009) Nat. Chem. Biol. , vol.5 , pp. 236-243
    • Yeh, J.R.1
  • 42
    • 41949098854 scopus 로고    scopus 로고
    • Deciphering arterial identity through gene expression, genetics, and chemical biology
    • Mukhopadhyay A., Peterson R.T. Deciphering arterial identity through gene expression, genetics, and chemical biology. Curr. Opin. Hematol. 2008, 15:221-227.
    • (2008) Curr. Opin. Hematol. , vol.15 , pp. 221-227
    • Mukhopadhyay, A.1    Peterson, R.T.2
  • 43
    • 58149380087 scopus 로고    scopus 로고
    • Chemobehavioural phenomics and behaviour-based psychiatric drug discovery in the zebrafish
    • Kokel D., Peterson R.T. Chemobehavioural phenomics and behaviour-based psychiatric drug discovery in the zebrafish. Brief Funct. Genomic. Proteomic. 2008, 7:483-490.
    • (2008) Brief Funct. Genomic. Proteomic. , vol.7 , pp. 483-490
    • Kokel, D.1    Peterson, R.T.2
  • 44
    • 74549126594 scopus 로고    scopus 로고
    • Zebrafish behavioral profiling links drugs to biological targets and rest/wake regulation
    • Rihel J., et al. Zebrafish behavioral profiling links drugs to biological targets and rest/wake regulation. Science 2010, 327:348-351.
    • (2010) Science , vol.327 , pp. 348-351
    • Rihel, J.1
  • 45
    • 42249106042 scopus 로고    scopus 로고
    • Novel targets for Huntington's disease in an mTOR-independent autophagy pathway
    • Williams A., et al. Novel targets for Huntington's disease in an mTOR-independent autophagy pathway. Nat. Chem. Biol. 2008, 4:295-305.
    • (2008) Nat. Chem. Biol. , vol.4 , pp. 295-305
    • Williams, A.1
  • 46
    • 66449115032 scopus 로고    scopus 로고
    • A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation
    • Paquet D., et al. A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation. J. Clin. Invest. 2009, 119:1382-1395.
    • (2009) J. Clin. Invest. , vol.119 , pp. 1382-1395
    • Paquet, D.1
  • 47
    • 58549090296 scopus 로고    scopus 로고
    • Identification of zebrafish A2 adenosine receptors and expression in developing embryos
    • Boehmler W., et al. Identification of zebrafish A2 adenosine receptors and expression in developing embryos. Gene Expr. Patterns 2009, 9:144-151.
    • (2009) Gene Expr. Patterns , vol.9 , pp. 144-151
    • Boehmler, W.1
  • 48
    • 38549143712 scopus 로고    scopus 로고
    • Visualization of monoaminergic neurons and neurotoxicity of MPTP in live transgenic zebrafish
    • Wen L., et al. Visualization of monoaminergic neurons and neurotoxicity of MPTP in live transgenic zebrafish. Dev. Biol. 2008, 314:84-92.
    • (2008) Dev. Biol. , vol.314 , pp. 84-92
    • Wen, L.1
  • 49
    • 0033780376 scopus 로고    scopus 로고
    • Effective targeted gene 'knockdown' in zebrafish
    • Nasevicius A., Ekker S.C. Effective targeted gene 'knockdown' in zebrafish. Nat. Genet. 2000, 26:216-220.
    • (2000) Nat. Genet. , vol.26 , pp. 216-220
    • Nasevicius, A.1    Ekker, S.C.2
  • 50
    • 70349243477 scopus 로고    scopus 로고
    • Transgenesis in zebrafish with the tol2 transposon system
    • Suster M.L., et al. Transgenesis in zebrafish with the tol2 transposon system. Methods. Mol. Biol. 2009, 561:41-63.
    • (2009) Methods. Mol. Biol. , vol.561 , pp. 41-63
    • Suster, M.L.1
  • 51
    • 0035119846 scopus 로고    scopus 로고
    • Transgenic zebrafish for studying nervous system development and regeneration
    • Goldman D., et al. Transgenic zebrafish for studying nervous system development and regeneration. Transgenic Res. 2001, 10:21-33.
    • (2001) Transgenic Res. , vol.10 , pp. 21-33
    • Goldman, D.1
  • 52
    • 0037114674 scopus 로고    scopus 로고
    • Transgenic zebrafish model of neurodegeneration
    • Tomasiewicz H.G., et al. Transgenic zebrafish model of neurodegeneration. J. Neurosci. Res. 2002, 70:734-745.
    • (2002) J. Neurosci. Res. , vol.70 , pp. 734-745
    • Tomasiewicz, H.G.1
  • 53
    • 0034303585 scopus 로고    scopus 로고
    • Neuronal specification in the spinal cord: inductive signals and transcriptional codes
    • Jessell T.M. Neuronal specification in the spinal cord: inductive signals and transcriptional codes. Nat. Rev. Genet. 2000, 1:20-29.
    • (2000) Nat. Rev. Genet. , vol.1 , pp. 20-29
    • Jessell, T.M.1
  • 54
    • 22144446344 scopus 로고    scopus 로고
    • Identification of a conserved 125 base-pair Hb9 enhancer that specifies gene expression to spinal motor neurons
    • Nakano T., et al. Identification of a conserved 125 base-pair Hb9 enhancer that specifies gene expression to spinal motor neurons. Dev. Biol. 2005, 283:474-485.
    • (2005) Dev. Biol. , vol.283 , pp. 474-485
    • Nakano, T.1
  • 55
    • 0034001073 scopus 로고    scopus 로고
    • Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer
    • Higashijima S., et al. Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. J. Neurosci. 2000, 20:206-218.
    • (2000) J. Neurosci. , vol.20 , pp. 206-218
    • Higashijima, S.1
  • 56
    • 58149186547 scopus 로고    scopus 로고
    • A novel conserved evx1 enhancer links spinal interneuron morphology and cis-regulation from fish to mammals
    • Suster M.L., et al. A novel conserved evx1 enhancer links spinal interneuron morphology and cis-regulation from fish to mammals. Dev. Biol. 2009, 325:422-433.
    • (2009) Dev. Biol. , vol.325 , pp. 422-433
    • Suster, M.L.1
  • 57
    • 0036333606 scopus 로고    scopus 로고
    • A novel positive transcriptional feedback loop in midbrain-hindbrain boundary development is revealed through analysis of the zebrafish pax2.1 promoter in transgenic lines
    • Picker A., et al. A novel positive transcriptional feedback loop in midbrain-hindbrain boundary development is revealed through analysis of the zebrafish pax2.1 promoter in transgenic lines. Development 2002, 129:3227-3239.
    • (2002) Development , vol.129 , pp. 3227-3239
    • Picker, A.1
  • 58
    • 33847384708 scopus 로고    scopus 로고
    • A topographic map of recruitment in spinal cord
    • McLean D.L., et al. A topographic map of recruitment in spinal cord. Nature 2007, 446:71-75.
    • (2007) Nature , vol.446 , pp. 71-75
    • McLean, D.L.1
  • 59
    • 33744975862 scopus 로고    scopus 로고
    • Alx, a zebrafish homolog of Chx10, marks ipsilateral descending excitatory interneurons that participate in the regulation of spinal locomotor circuits
    • Kimura Y., et al. alx, a zebrafish homolog of Chx10, marks ipsilateral descending excitatory interneurons that participate in the regulation of spinal locomotor circuits. J. Neurosci. 2006, 26:5684-5697.
    • (2006) J. Neurosci. , vol.26 , pp. 5684-5697
    • Kimura, Y.1
  • 60
    • 0037307776 scopus 로고    scopus 로고
    • Multiple regulatory elements with spatially and temporally distinct activities control neurogenin1 expression in primary neurons of the zebrafish embryo
    • Blader P., et al. Multiple regulatory elements with spatially and temporally distinct activities control neurogenin1 expression in primary neurons of the zebrafish embryo. Mech. Dev. 2003, 120:211-218.
    • (2003) Mech. Dev. , vol.120 , pp. 211-218
    • Blader, P.1
  • 61
    • 25844505439 scopus 로고    scopus 로고
    • Formation of the digestive system in zebrafish. III. Intestinal epithelium morphogenesis
    • Ng A.N., et al. Formation of the digestive system in zebrafish. III. Intestinal epithelium morphogenesis. Dev. Biol. 2005, 286:114-135.
    • (2005) Dev. Biol. , vol.286 , pp. 114-135
    • Ng, A.N.1
  • 62
    • 0346458920 scopus 로고    scopus 로고
    • Neural cell fate analysis in zebrafish using olig2 BAC transgenics
    • Shin J., et al. Neural cell fate analysis in zebrafish using olig2 BAC transgenics. Methods Cell Sci. 2003, 25:7-14.
    • (2003) Methods Cell Sci. , vol.25 , pp. 7-14
    • Shin, J.1
  • 63
    • 33845245652 scopus 로고    scopus 로고
    • In vivo time-lapse imaging shows dynamic oligodendrocyte progenitor behavior during zebrafish development
    • Kirby B.B., et al. In vivo time-lapse imaging shows dynamic oligodendrocyte progenitor behavior during zebrafish development. Nat. Neurosci. 2006, 9:1506-1511.
    • (2006) Nat. Neurosci. , vol.9 , pp. 1506-1511
    • Kirby, B.B.1
  • 64
    • 70449729803 scopus 로고    scopus 로고
    • Transposon-mediated BAC transgenesis in zebrafish and mice
    • Suster M.L., et al. Transposon-mediated BAC transgenesis in zebrafish and mice. BMC Genomics 2009, 10:477.
    • (2009) BMC Genomics , vol.10 , pp. 477
    • Suster, M.L.1
  • 65
    • 0026628045 scopus 로고
    • A transgene containing lacZ is expressed in primary sensory neurons in zebrafish
    • Bayer T.A., Campos-Ortega J.A. A transgene containing lacZ is expressed in primary sensory neurons in zebrafish. Development 1992, 115:421-426.
    • (1992) Development , vol.115 , pp. 421-426
    • Bayer, T.A.1    Campos-Ortega, J.A.2
  • 66
    • 45549103009 scopus 로고    scopus 로고
    • Gal4/UAS transgenic tools and their application to zebrafish
    • Halpern M.E., et al. Gal4/UAS transgenic tools and their application to zebrafish. Zebrafish 2008, 5:97-110.
    • (2008) Zebrafish , vol.5 , pp. 97-110
    • Halpern, M.E.1
  • 67
    • 16644387777 scopus 로고    scopus 로고
    • Transgene manipulation in zebrafish by using recombinases
    • Dong J., Stuart G.W. Transgene manipulation in zebrafish by using recombinases. Methods Cell Biol. 2004, 77:363-379.
    • (2004) Methods Cell Biol. , vol.77 , pp. 363-379
    • Dong, J.1    Stuart, G.W.2
  • 68
    • 58149385745 scopus 로고    scopus 로고
    • Reverse genetics in zebrafish by TILLING
    • Moens C.B., et al. Reverse genetics in zebrafish by TILLING. Brief Funct. Genomic. Proteomic. 2008, 7:454-459.
    • (2008) Brief Funct. Genomic. Proteomic. , vol.7 , pp. 454-459
    • Moens, C.B.1
  • 69
    • 84861409753 scopus 로고    scopus 로고
    • Rapid mutation of endogenous zebrafish genes using zinc finger nucleases made by Oligomerized Pool ENgineering (OPEN)
    • Foley J.E., et al. Rapid mutation of endogenous zebrafish genes using zinc finger nucleases made by Oligomerized Pool ENgineering (OPEN). PLoS One 2009, 4:e4348.
    • (2009) PLoS One , vol.4
    • Foley, J.E.1
  • 70
    • 0042162816 scopus 로고    scopus 로고
    • Developmental control of Presenilin1 expression, endoproteolysis, and interaction in zebrafish embryos
    • Nornes S., et al. Developmental control of Presenilin1 expression, endoproteolysis, and interaction in zebrafish embryos. Exp Cell Res 2003, 289:124-132.
    • (2003) Exp Cell Res , vol.289 , pp. 124-132
    • Nornes, S.1
  • 71
    • 33645101015 scopus 로고    scopus 로고
    • Zebrafish lacking Alzheimer presenilin enhancer 2 (Pen-2) demonstrate excessive p53-dependent apoptosis and neuronal loss
    • Campbell W.A., et al. Zebrafish lacking Alzheimer presenilin enhancer 2 (Pen-2) demonstrate excessive p53-dependent apoptosis and neuronal loss. J Neurochem 2006, 96:1423-1440.
    • (2006) J Neurochem , vol.96 , pp. 1423-1440
    • Campbell, W.A.1
  • 72
    • 51149105923 scopus 로고    scopus 로고
    • Loss of PINK1 function affects development and results in neurodegeneration in zebrafish
    • Anichtchik O., et al. Loss of PINK1 function affects development and results in neurodegeneration in zebrafish. J Neurosci 2008, 28:8199-8207.
    • (2008) J Neurosci , vol.28 , pp. 8199-8207
    • Anichtchik, O.1
  • 73
    • 0344121266 scopus 로고    scopus 로고
    • Cloning and expression analysis of a Parkinson's disease gene, uch-L1, and its promoter in zebrafish
    • Son O.L., et al. Cloning and expression analysis of a Parkinson's disease gene, uch-L1, and its promoter in zebrafish. Biochem Biophys Res Commun 2003, 312:601-607.
    • (2003) Biochem Biophys Res Commun , vol.312 , pp. 601-607
    • Son, O.L.1
  • 74
    • 67649413521 scopus 로고    scopus 로고
    • Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio)
    • Flinn L., et al. Complex I deficiency and dopaminergic neuronal cell loss in parkin-deficient zebrafish (Danio rerio). Brain 2009, 132:1613-1623.
    • (2009) Brain , vol.132 , pp. 1613-1623
    • Flinn, L.1
  • 75
    • 69049098972 scopus 로고    scopus 로고
    • Disc1 regulates foxd3 and sox10 expression, affecting neural crest migration and differentiation
    • Drerup C.M., et al. Disc1 regulates foxd3 and sox10 expression, affecting neural crest migration and differentiation. Development 2009, 136:2623-2632.
    • (2009) Development , vol.136 , pp. 2623-2632
    • Drerup, C.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.