2020 - Fellow of the American Academy of Arts and Sciences
2020 - Member of the National Academy of Sciences
Hugo J. Bellen mainly investigates Cell biology, Genetics, Synaptic vesicle, Neurotransmission and Gene. The concepts of his Cell biology study are interwoven with issues in STX1A, Mutant, Anatomy, Endocytosis and Neuromuscular junction. Within one scientific family, Hugo J. Bellen focuses on topics pertaining to Synaptotagmin 1 under STX1A, and may sometimes address concerns connected to Synaptotagmin I and Synapse.
His Genome, Drosophila Protein, Drosophila melanogaster, Enhancer and Drosophilidae study are his primary interests in Genetics. Hugo J. Bellen has researched Synaptic vesicle in several fields, including Subcellular localization, Conserved sequence and Dynamin. His work carried out in the field of Neurotransmission brings together such families of science as Neurotransmitter and Syntaxin.
His main research concerns Cell biology, Genetics, Gene, Drosophila melanogaster and Phenotype. The Cell biology study combines topics in areas such as Endocytosis, Synaptic vesicle, Neurodegeneration and Neurotransmission. His biological study spans a wide range of topics, including Neurotransmitter, Synapse, Neuromuscular junction, Neuroscience and Syntaxin.
His study in Drosophila Protein, Genome, Allele, Transcription factor and Mutant is carried out as part of his Genetics studies. His work is dedicated to discovering how Gene, Computational biology are connected with Model organism and CRISPR and other disciplines. As a part of the same scientific family, Hugo J. Bellen mostly works in the field of Phenotype, focusing on Hypotonia and, on occasion, Missense mutation and Ataxia.
The scientist’s investigation covers issues in Cell biology, Gene, Computational biology, Phenotype and Genetics. Hugo J. Bellen interconnects Oxidative stress and Neurodegeneration in the investigation of issues within Cell biology. His studies in Neurodegeneration integrate themes in fields like Reactive oxygen species and Mode of action.
His Computational biology research incorporates themes from Model organism, Genome editing, Genome, CRISPR and Function. The various areas that Hugo J. Bellen examines in his Phenotype study include Mutant and Cytoskeleton. His study in Drosophila is interdisciplinary in nature, drawing from both Evolutionary biology, Vertebrate and Cochlea.
His scientific interests lie mostly in Cell biology, Gene, Computational biology, Genetics and Phenotype. His Cell biology study incorporates themes from Cell and Lysosome. His Gene research includes elements of Interferon and Virology.
Hugo J. Bellen combines subjects such as Genome editing, CRISPR, Homologous recombination, Drosophila melanogaster and Genomics with his study of Computational biology. His Drosophila melanogaster study combines topics from a wide range of disciplines, such as Genetic model and Genome. Hugo J. Bellen regularly ties together related areas like Developmental disorder in his Genetics studies.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Math1: an essential gene for the generation of inner ear hair cells.
Nessan A. Bermingham;Bassem A. Hassan;Steven D. Price;Melissa A. Vollrath.
Science (1999)
The BDGP gene disruption project: single transposon insertions associated with 40% of Drosophila genes.
Hugo J. Bellen;Robert W. Levis;Guochun Liao;Yuchun He.
Genetics (2004)
P-element-mediated enhancer detection: a versatile method to study development in Drosophila.
Hugo J. Bellen;Cahir J. O'Kane;Clive Wilson;Ueli Grossniklaus.
Genes & Development (1989)
Synaptic Mitochondria Are Critical for Mobilization of Reserve Pool Vesicles at Drosophila Neuromuscular Junctions
Patrik Verstreken;Patrik Verstreken;Cindy V. Ly;Koen J.T. Venken;Tong-Wey Koh.
Neuron (2005)
P[acman]: A BAC Transgenic Platform for Targeted Insertion of Large DNA Fragments in D. melanogaster
Koen J. T. Venken;Yuchun He;Roger A. Hoskins;Hugo J. Bellen.
Science (2006)
Math1 is essential for genesis of cerebellar granule neurons.
Nissim Ben-Arie;Hugo J. Bellen;Dawna L. Armstrong;Alanna E. McCall.
Nature (1997)
Axon-Glia Interactions and the Domain Organization of Myelinated Axons Requires Neurexin IV/Caspr/Paranodin
Manzoor A. Bhat;Jose C. Rios;Yue Lu;German P. Garcia-Fresco.
Neuron (2001)
Senseless, a Zn finger transcription factor, is necessary and sufficient for sensory organ development in Drosophila.
Riitta Nolo;Lois A Abbott;Hugo J Bellen.
Cell (2000)
Mutational analysis of Drosophila synaptotagmin demonstrates its essential role in Ca2+-activated neurotransmitter release
J.Troy Littleton;Michael Stern;Karen Schulze;Mark Perin.
Cell (1993)
MiMIC: a highly versatile transposon insertion resource for engineering Drosophila melanogaster genes.
Koen J T Venken;Karen L Schulze;Nele A Haelterman;Hongling Pan.
Nature Methods (2011)
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