Drosophila cholinergic neurons and processes visualized with Gal4/UAS-GFP.

PubWeight™: 1.79‹?› | Rank: Top 3%

🔗 View Article (PMID 15018821)

Published in Brain Res Gene Expr Patterns on August 01, 2001

Authors

P M Salvaterra1, T Kitamoto

Author Affiliations

1: Division of Neuroscience, Beckman Research Institute of the City of Hope, 1450 E. Duarte Road, Duarte, CA 91010, USA. psalv@coh.org

Articles citing this

Cell-type-specific TEV protease cleavage reveals cohesin functions in Drosophila neurons. Dev Cell (2008) 2.82

Refined spatial manipulation of neuronal function by combinatorial restriction of transgene expression. Neuron (2006) 2.57

Neural circuitry underlying Drosophila female postmating behavioral responses. Curr Biol (2012) 2.17

SMN is required for sensory-motor circuit function in Drosophila. Cell (2012) 1.68

Abeta42-induced neurodegeneration via an age-dependent autophagic-lysosomal injury in Drosophila. PLoS One (2009) 1.61

Tuning of RNA editing by ADAR is required in Drosophila. EMBO J (2005) 1.39

Glutamate, GABA and acetylcholine signaling components in the lamina of the Drosophila visual system. PLoS One (2008) 1.27

Midline signalling systems direct the formation of a neural map by dendritic targeting in the Drosophila motor system. PLoS Biol (2009) 1.25

The development of motor coordination in Drosophila embryos. Development (2008) 1.22

JNK/FOXO-mediated neuronal expression of fly homologue of peroxiredoxin II reduces oxidative stress and extends life span. J Biol Chem (2009) 1.21

Structural homeostasis: compensatory adjustments of dendritic arbor geometry in response to variations of synaptic input. PLoS Biol (2008) 1.20

Three-dimensional imaging of Drosophila melanogaster. PLoS One (2007) 1.20

Plug-and-play genetic access to drosophila cell types using exchangeable exon cassettes. Cell Rep (2015) 1.19

Sperm-storage defects and live birth in Drosophila females lacking spermathecal secretory cells. PLoS Biol (2011) 1.18

A large population of diverse neurons in the Drosophila central nervous system expresses short neuropeptide F, suggesting multiple distributed peptide functions. BMC Neurosci (2008) 1.16

A nucleostemin family GTPase, NS3, acts in serotonergic neurons to regulate insulin signaling and control body size. Genes Dev (2008) 1.14

Analysis of functional neuronal connectivity in the Drosophila brain. J Neurophysiol (2012) 1.13

Dedicated olfactory neurons mediating attraction behavior to ammonia and amines in Drosophila. Proc Natl Acad Sci U S A (2013) 1.13

Optical dissection of neural circuits responsible for Drosophila larval locomotion with halorhodopsin. PLoS One (2011) 1.10

The octopamine receptor OAMB mediates ovulation via Ca2+/calmodulin-dependent protein kinase II in the Drosophila oviduct epithelium. PLoS One (2009) 1.07

Immunolocalization of the vesicular acetylcholine transporter in larval and adult Drosophila neurons. Neurosci Lett (2017) 1.07

Genetic modifiers of MeCP2 function in Drosophila. PLoS Genet (2008) 1.01

Four GABAergic interneurons impose feeding restraint in Drosophila. Neuron (2014) 1.00

Adenosine-to-inosine genetic recoding is required in the adult stage nervous system for coordinated behavior in Drosophila. J Biol Chem (2009) 0.99

The chemical component of the mixed GF-TTMn synapse in Drosophila melanogaster uses acetylcholine as its neurotransmitter. Eur J Neurosci (2007) 0.98

Seizure suppression by gain-of-function escargot mutations. Genetics (2005) 0.96

The genetic analysis of functional connectomics in Drosophila. Adv Genet (2012) 0.95

Peristalsis in the junction region of the Drosophila larval midgut is modulated by DH31 expressing enteroendocrine cells. BMC Physiol (2010) 0.94

The Drosophila TRPA channel, Painless, regulates sexual receptivity in virgin females. Genes Brain Behav (2009) 0.94

Functional conservation in human and Drosophila of Metazoan ADAR2 involved in RNA editing: loss of ADAR1 in insects. Nucleic Acids Res (2011) 0.93

Reduced growth of Drosophila neurofibromatosis 1 mutants reflects a non-cell-autonomous requirement for GTPase-Activating Protein activity in larval neurons. Genes Dev (2006) 0.93

Genetics and neurobiology of aggression in Drosophila. Fly (Austin) (2012) 0.91

The actions of the neonicotinoid imidacloprid on cholinergic neurons of Drosophila melanogaster. Invert Neurosci (2006) 0.90

The fundamentals of flying: simple and inexpensive strategies for employing Drosophila genetics in neuroscience teaching laboratories. J Undergrad Neurosci Educ (2012) 0.89

Retrograde signaling from the brain to the retina modulates the termination of the light response in Drosophila. Proc Natl Acad Sci U S A (2005) 0.89

Seizure sensitivity is ameliorated by targeted expression of K+-Cl- cotransporter function in the mushroom body of the Drosophila brain. Genetics (2009) 0.88

Control of directional change after mechanical stimulation in Drosophila. Mol Brain (2012) 0.83

Feminizing cholinergic neurons in a male Drosophila nervous system enhances aggression. Fly (Austin) (2009) 0.82

The dystrophin Dp186 isoform regulates neurotransmitter release at a central synapse in Drosophila. J Neurosci (2008) 0.81

The Drosophila transcription factor Adf-1 (nalyot) regulates dendrite growth by controlling FasII and Staufen expression downstream of CaMKII and neural activity. J Neurosci (2013) 0.80

A central neural pathway controlling odor tracking in Drosophila. J Neurosci (2015) 0.80

Odd-skipped labels a group of distinct neurons associated with the mushroom body and optic lobe in the adult Drosophila brain. J Comp Neurol (2013) 0.80

Neuronal fiber tracts connecting the brain and ventral nerve cord of the early Drosophila larva. J Comp Neurol (2009) 0.80

Intracellular calcium deficits in Drosophila cholinergic neurons expressing wild type or FAD-mutant presenilin. PLoS One (2009) 0.80

Interaction with a kinesin-2 tail propels choline acetyltransferase flow towards synapse. Traffic (2012) 0.80

A dopamine receptor contributes to paraquat-induced neurotoxicity in Drosophila. Hum Mol Genet (2014) 0.79

Behavioral and electrophysiological outcomes of tissue-specific Smn knockdown in Drosophila melanogaster. Brain Res (2012) 0.79

Systematic analysis of fly models with multiple drivers reveals different effects of ataxin-1 and huntingtin in neuron subtype-specific expression. PLoS One (2014) 0.78

Organization of descending neurons in Drosophila melanogaster. Sci Rep (2016) 0.77

A neural command circuit for grooming movement control. Elife (2015) 0.77

Anaplastic Lymphoma Kinase Acts in the Drosophila Mushroom Body to Negatively Regulate Sleep. PLoS Genet (2015) 0.76

Synaptic transmission parallels neuromodulation in a central food-intake circuit. Elife (2016) 0.76

Interallelic Transcriptional Enhancement as an in Vivo Measure of Transvection in Drosophila melanogaster. G3 (Bethesda) (2016) 0.75

The sox gene Dichaete is expressed in local interneurons and functions in development of the Drosophila adult olfactory circuit. Dev Neurobiol (2012) 0.75

Central neural alterations predominate in an insect model of nociceptive sensitization. J Comp Neurol (2016) 0.75

Anterograde Transport of Rab4-Associated Vesicles Regulates Synapse Organization in Drosophila. Cell Rep (2017) 0.75

Seizure control through genetic and pharmacological manipulation of Pumilio: a key component of neuronal homeostasis. Dis Model Mech (2016) 0.75

Regulation of Drosophila hematopoietic sites by Activin-β from active sensory neurons. Nat Commun (2017) 0.75

Serotonergic Modulation Enables Pathway-Specific Plasticity in a Developing Sensory Circuit in Drosophila. Neuron (2017) 0.75

Articles by these authors

(truncated to the top 100)

Activation of the estrogen receptor through phosphorylation by mitogen-activated protein kinase. Science (1995) 6.37

Formic acid pretreatment enhances immunostaining of cerebral and systemic amyloids. Lab Invest (1987) 4.98

Disruption of neurotransmission in Drosophila mushroom body blocks retrieval but not acquisition of memory. Nature (2001) 2.93

Beta-protein amyloid is widely distributed in the central nervous system of patients with Alzheimer's disease. Am J Pathol (1989) 2.61

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome. Biochem Biophys Res Commun (1989) 2.35

Intestinal pseudo-obstruction in patients with amyloidosis: clinicopathologic differences between chemical types of amyloid protein. Gut (1993) 2.31

The amnesiac gene product is expressed in two neurons in the Drosophila brain that are critical for memory. Cell (2000) 2.10

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein. Ann Neurol (1999) 1.98

Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP. Proc Natl Acad Sci U S A (1996) 1.94

Amyloid plaques in Creutzfeldt-Jakob disease stain with prion protein antibodies. Ann Neurol (1986) 1.85

Typing prion isoforms. Nature (1997) 1.82

Hydrated autoclave pretreatment enhances tau immunoreactivity in formalin-fixed normal and Alzheimer's disease brain tissues. Lab Invest (1991) 1.78

The sequential development of abnormal prion protein accumulation in mice with Creutzfeldt-Jakob disease. Am J Pathol (1992) 1.66

Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents. Neurology (1996) 1.54

Sporadic Creutzfeldt-Jakob disease with MM1-type prion protein and plaques. Neurology (2003) 1.49

Inherited prion diseases and transmission to rodents. Brain Pathol (1995) 1.39

Changes in expression of sensory organ-specific microRNAs in rat dorsal root ganglia in association with mechanical hypersensitivity induced by spinal nerve ligation. Neuroscience (2009) 1.38

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease. Ann Neurol (1998) 1.37

Immunochemical, molecular genetic, and transmission studies on a case of Gerstmann-Sträussler-Scheinker syndrome. Neurology (1990) 1.20

Clinical features of Creutzfeldt-Jakob disease with V180I mutation. Neurology (2004) 1.20

The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype. Brain Pathol (1995) 1.19

p300 mediates functional synergism between AF-1 and AF-2 of estrogen receptor alpha and beta by interacting directly with the N-terminal A/B domains. J Biol Chem (2000) 1.17

Increased tau accumulation in senile plaques as a hallmark in Alzheimer's disease. Am J Pathol (1989) 1.16

CJD discrepancy. Nature (1991) 1.16

Ferritin immunohistochemistry as a marker for microglia. Acta Neuropathol (1989) 1.15

Clinical features and diagnosis of dura mater graft associated Creutzfeldt Jakob disease. Neurology (2007) 1.10

Interaction of aluminum with PHFtau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method. Am J Pathol (1999) 1.10

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease. Neurology (2005) 1.10

Protective prion protein polymorphisms against sporadic Creutzfeldt-Jakob disease. Lancet (1998) 1.09

Alzheimer's amyloid precursor protein accumulates within axonal swellings in human brain lesions. Neurosci Lett (1992) 1.05

Intron retention generates a novel isoform of the murine vitamin D receptor that acts in a dominant negative way on the vitamin D signaling pathway. Mol Cell Biol (1996) 1.02

An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity. Neurology (1999) 1.00

Creutzfeldt-Jakob disease patients with congophilic kuru plaques have the missense variant prion protein common to Gerstmann-Sträussler syndrome. Ann Neurol (1990) 1.00

Increased senile plaques without microglia in Alzheimer's disease. Acta Neuropathol (1991) 1.00

Aging and cerebral amyloid: early detection of amyloid in the human brain using biochemical extraction and immunostain. J Gerontol (1988) 0.99

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome. Brain Res Mol Brain Res (1995) 0.99

Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting. Arch Neurol (1999) 0.98

First experimental transmission of fatal familial insomnia. Nature (1995) 0.98

A new method to classify amyloid fibril proteins. Acta Neuropathol (1985) 0.98

Gerstmann-Sträussler-Scheinker disease: immunohistological and experimental studies. Ann Neurol (1988) 0.97

Colocalization of prion protein and beta protein in the same amyloid plaques in patients with Gerstmann-Sträussler syndrome. Acta Neuropathol (1992) 0.96

Detection of human T lymphotrophic virus type I (HTLV-I) proviral DNA and analysis of T cell receptor V beta CDR3 sequences in spinal cord lesions of HTLV-I-associated myelopathy/tropical spastic paraparesis. J Exp Med (1994) 0.96

Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene. Neurology (1994) 0.94

The Drosophila TRPA channel, Painless, regulates sexual receptivity in virgin females. Genes Brain Behav (2009) 0.94

MIB1 staining index and scoring of histologic features in meningioma. Indicators for the prediction of biologic potential and postoperative management. Cancer (1994) 0.92

Accumulation of abnormal prion protein in mice infected with Creutzfeldt-Jakob disease via intraperitoneal route: a sequential study. Am J Pathol (1993) 0.92

Localization of choline acetyltransferase-expressing neurons in the larval visual system of Drosophila melanogaster. Cell Tissue Res (1995) 0.92

Renal amyloidosis. Correlations between morphology, chemical types of amyloid protein and clinical features. Virchows Arch A Pathol Anat Histopathol (1988) 0.92

Expression of neurofibromatosis 2 protein in human brain tumors: an immunohistochemical study. Acta Neuropathol (1997) 0.91

Prion disease with 144 base pair insertion in a Japanese family line. Acta Neuropathol (1995) 0.90

A comparative immunohistochemical study of Kuru and senile plaques with a special reference to glial reactions at various stages of amyloid plaque formation. Am J Pathol (1991) 0.90

Increased 9,13-di-cis-retinoic acid in rat hepatic fibrosis: implication for a potential link between retinoid loss and TGF-beta mediated fibrogenesis in vivo. J Hepatol (1999) 0.90

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations. Acta Neuropathol (1992) 0.90

Successful transmission of Creutzfeldt-Jakob disease from human to mouse verified by prion protein accumulation in mouse brains. Brain Res (1992) 0.90

[A case of Creutzfeldt-Jakob disease (CJD) started with monoparesis of the left arm]. Rinsho Shinkeigaku (1996) 0.90

The MM2-cortical form of sporadic Creutzfeldt-Jakob disease presenting with visual disturbance. Neurology (2006) 0.89

Amyloid beta-protein (Abeta) 1-40 but not Abeta1-42 contributes to the experimental formation of Alzheimer disease amyloid fibrils in rat brain. J Neurosci (1997) 0.89

ERC-55, a binding protein for the papilloma virus E6 oncoprotein, specifically interacts with vitamin D receptor among nuclear receptors. Biochem Biophys Res Commun (1997) 0.89

Immunocytochemical study of choline acetyltransferase in Drosophila melanogaster: an analysis of cis-regulatory regions controlling expression in the brain of cDNA-transformed flies. J Comp Neurol (1995) 0.88

Practical methods for chemical inactivation of Creutzfeldt-Jakob disease pathogen. Microbiol Immunol (1991) 0.88

Less protease-resistant PrP in a patient with sporadic CJD treated with intraventricular pentosan polysulphate. Acta Neurol Scand (2009) 0.87

Massive accumulation of modified tau and severe depletion of normal tau characterize the cerebral cortex and white matter of Alzheimer's disease. Demonstration using the hydrated autoclaving method. Am J Pathol (1992) 0.86

Molecular mechanism of a cross-talk between estrogen and growth-factor signaling pathways. Oncology (1998) 0.86

Choroid plexus papillomas: an immunohistochemical study with particular reference to the coexpression of prealbumin. Neurosurgery (1988) 0.86

TNF-beta produced by human T lymphotropic virus type I-infected cells influences the proliferation of human endothelial cells and fibroblasts. J Immunol (1994) 0.86

Scrapie-associated fibrils (SAF) purification method yields amyloid proteins from systemic and cerebral amyloidosis. Biosci Rep (1986) 0.85

[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease]. Rev Neurol (Paris) (1991) 0.85

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease. Neurology (1993) 0.85

A variant of Gerstmann-Sträussler-Scheinker disease carrying codon 105 mutation with codon 129 polymorphism of the prion protein gene: a clinicopathological study. J Neurol Sci (1994) 0.85

Variant Gerstmann-Sträussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles. Acta Neuropathol (1999) 0.85

Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease. Neuroradiology (2000) 0.84

Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study. Acta Neuropathol (1996) 0.84

Involvement of the peripheral nervous system in human prion diseases including dural graft associated Creutzfeldt-Jakob disease. J Neurol Neurosurg Psychiatry (2005) 0.84

Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes. J Hum Genet (2001) 0.84

Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu. Neurosci Lett (2000) 0.84

Differential regulation of choline acetyltransferase expression in adult Drosophila melanogaster brain. J Neurobiol (1996) 0.84

Immunoreactivity of cerebral amyloidosis is enhanced by protein denaturation treatments. Acta Neuropathol (1991) 0.83

Immunohistochemical distribution of amyloid precursor protein during normal rat development. Brain Res Dev Brain Res (1993) 0.83

Alpha-2-macroglobulin-like protease inhibitor from the egg white of cuban crocodile (Crocodylus rhombifer). J Biochem (1983) 0.83

The coexistence of Alzheimer's disease and Creutzfeldt-Jakob disease in a patient with dementia of long duration. Acta Neuropathol (1992) 0.83

A chicken monoclonal antibody with specificity for the N-terminal of human prion protein. FEMS Immunol Med Microbiol (1999) 0.83

Novel histochemical approaches to the prealbumin-related senile and familial forms of systemic amyloidosis. Am J Pathol (1986) 0.82

A case-control study of Creutzfeldt-Jakob disease in Japan: transplantation of cadaveric dura mater was a risk factor. J Epidemiol (2000) 0.81

Serial MRI in early Creutzfeldt-Jacob disease with a point mutation of prion protein at codon 180. Neuroradiology (1995) 0.81

Alzheimer's amyloid precursor protein-positive degenerative neurites exist even within kuru plaques not specific to Alzheimer's disease. Am J Pathol (1991) 0.81

Scrapie removal using Planova virus removal filters. Biologicals (2001) 0.81

Immunhistological evaluation of Creutzfeldt-Jakob disease with reference to the type PrPres deposition. Clin Neuropathol (1997) 0.81

Hen egg white ovomacroglobulin has a protease inhibitory activity. J Biochem (1982) 0.80

[An autopsy-verified case of Creutzfeldt-Jakob disease with codon 129 polymorphism and codon 180 point mutation]. Rinsho Shinkeigaku (1995) 0.80

Allelic variation of apolipoprotein E in Japanese sporadic Creutzfeldt-Jakob disease patients. Neurosci Lett (1995) 0.80

Creutzfeldt-Jakob disease with amyloid angiopathy: diagnosis by immunological analyses and transmission experiments. Acta Neuropathol (1992) 0.80

Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype. Acta Neuropathol (1997) 0.80

Construction of recombinant monoclonal antibodies from a chicken hybridoma line secreting specific antibody. Cytotechnology (2000) 0.80

Severe brain atrophy in a case of thalamic variant of sporadic CJD with plaque-like PrP deposition. Neuropathology (2001) 0.80

Widespread distribution of tau in the astrocytic elements of glial tumors. Acta Neuropathol (1993) 0.80

Modified tau is present in younger nondemented persons: a study of subcortical nuclei in Alzheimer's disease and progressive supranuclear palsy. Acta Neuropathol (1991) 0.80

Urocortin expression in the human central nervous system. Clin Endocrinol (Oxf) (1999) 0.79

MRI characteristics of sporadic CJD with valine homozygosity at codon 129 of the prion protein gene and PrPSc type 2 in Japan. J Neurol Neurosurg Psychiatry (2004) 0.79

[Gerstmann-Sträussler-Scheinker disease with heterozygous codon change at prion protein codon 129]. Rinsho Shinkeigaku (1992) 0.79

Apolipoprotein E in Creutzfeldt-Jakob disease. Lancet (1995) 0.79