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One or more keywords matched the following properties of Lundell, Martha
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overview The research in Dr. Lundell’s lab is primarily focused on how neurons in the CNS of Drosophila acquire unique cell fates during neurogenesis. In particular, they are examining the specification of neurons that synthesize serotonin. Serotonin is a neurotransmitter conserved throughout the animal kingdom and has been associated with locomotion, learning, memory and several human neural disorders. The serotonin cell lineage includes six cells: two serotonin producing neurons, a neuron that produces the neuropeptide corazonin, a motor neuron and two cells that undergo apoptosis. Using a combination of molecular genetics, immunohistochemistry and confocal microscopy, the lab has characterized a number of genes that are essential in specifying these different cell fates and are investigating genetic interactions between these genes to establish a mechanism for serotonin cell specification. An understanding of the mechanism that leads to differentiation of serotonin neurons will provide molecular tools that can be used to investigate the physiological function of serotonin by altering serotonin levels in the CNS and examine the effect on fly behavior using various behavior paradigms. In a separate collaborative project with Dr. Jan Vijg (Albert Einstein College of Medicine), the lab has been examining the mechanisms of mutagenesis in Drosophila and the relationship of mutagenesis to aging. This project uses a plasmid-based lacZ report system that allows selective retrieval of genome integrated lacZ genes that have undergone mutation. This reporter system permits both the measurement of mutation frequencies and the analysis of the different types of mutations that are acquired during development of the transformed animal.
One or more keywords matched the following items that are connected to Lundell, Martha
Item TypeName
Academic Article Age- and temperature-dependent somatic mutation accumulation in Drosophila melanogaster.
Academic Article Loss of the bloom syndrome helicase increases DNA ligase 4-independent genome rearrangements and tumorigenesis in aging Drosophila.
Academic Article The zfh-2 gene product is a potential regulator of neuron-specific dopa decarboxylase gene expression in Drosophila.
Academic Article A new visible light DNA fluorochrome for confocal microscopy.
Academic Article The regulation of apoptosis by Numb/Notch signaling in the serotonin lineage of Drosophila.
Academic Article A model system for analyzing somatic mutations in Drosophila melanogaster.
Academic Article Temporal and spatial development of serotonin and dopamine neurons in the Drosophila CNS.
Academic Article Detection and analysis of somatic mutations at a lacZ reporter locus in higher organisms: application to Mus musculus and Drosophila melanogaster.
Academic Article Differentiation of the Drosophila serotonergic lineage depends on the regulation of Zfh-1 by Notch and Eagle.
Academic Article The engrailed and huckebein genes are essential for development of serotonin neurons in the Drosophila CNS.
Academic Article Lifespan extension by dietary restriction is not linked to protection against somatic DNA damage in Drosophila melanogaster.
Academic Article eagle is required for the specification of serotonin neurons and other neuroblast 7-3 progeny in the Drosophila CNS.
Academic Article Molecular characterization of Pegarn: a Drosophila homolog of UNC-51 kinase.
Concept Drosophila
Concept Drosophila melanogaster
Concept Drosophila Proteins
Academic Article Zfh-2 facilitates Notch-induced apoptosis in the CNS and appendages of Drosophila melanogaster.
Academic Article Hunchback prevents notch-induced apoptosis in the serotonergic lineage of Drosophila Melanogaster.
Academic Article ZFH-2 is required for Drosophila ovarian follicle development and is expressed at the band/interband boundaries of polytene chromosomes.
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  • Drosophila
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