Anderson, David

Combined from CaltechAUTHORS

• Nair, Aditya and Karigo, Tomomi, et el. (2023) An approximate line attractor in the hypothalamus encodes an aggressive state; Cell; Vol. 186; No. 1; 178-193; PMCID PMC9990527; 10.1016/j.cell.2022.11.027
• Yang, Bin and Karigo, Tomomi, et el. (2022) Transformations of neural representations in a social behaviour network; Nature; Vol. 608; No. 7924; 741-749; PMCID PMC9529293; 10.1038/s41586-022-05057-6
• Hu, Rongfeng K. and Chen, Patrick B., et el. (2022) Improved Version of ChETA Promotes Aggression in the Medial Amygdala; 10.1101/2022.06.05.493862
• Nair, Aditya and Karigo, Tomomi, et el. (2022) An approximate line attractor in the hypothalamus that encodes an aggressive internal state; 10.1101/2022.04.19.488776
• Liu, Mengyu and Kim, Dong-Wook, et el. (2022) Make war not love: The neural substrate underlying a state-dependent switch in female social behavior; Neuron; Vol. 110; No. 5; 841-856; PMCID PMC8897222; 10.1016/j.neuron.2021.12.002
• Sun, Jennifer J. and Ryou, Serim, et el. (2022) Self-Supervised Keypoint Discovery in Behavioral Videos; 10.48550/arXiv.2112.05121
• Ichiki, Takako and Wang, Tongtong, et el. (2022) Sensory representation and detection mechanisms of gut osmolality change; Nature; Vol. 602; No. 7897; 468-474; 10.1038/s41586-021-04359-5
• Segalin, Cristina and Williams, Jalani, et el. (2021) The Mouse Action Recognition System (MARS) software pipeline for automated analysis of social behaviors in mice; eLife; Vol. 10; Art. No. e63720; PMCID PMC8631946; 10.7554/eLife.63720
• Chari, Tara and Weissbourd, Brandon, et el. (2021) Whole-animal multiplexed single-cell RNA-seq reveals transcriptional shifts across Clytia medusa cell types; Science Advances; Vol. 7; No. 48; Art. No. eabh1683; PMCID PMC8626072; 10.1126/sciadv.abh1683
• Weissbourd, Brandon and Momose, Tsuyoshi, et el. (2021) A genetically tractable jellyfish model for systems and evolutionary neuroscience; Cell; Vol. 184; No. 24; 5854-5868; PMCID PMC8629132; 10.1016/j.cell.2021.10.021
• Sun, Jennifer J. and Kennedy, Ann, et el. (2021) Task Programming: Learning Data Efficient Behavior Representations; ISBN 978-1-6654-4509-2; 2021 IEEE/CVF Conference on Computer Vision and Pattern Recognition (CVPR); 2875-2884; 10.1109/CVPR46437.2021.00290
• Sun, Jennifer J. and Karigo, Tomomi, et el. (2021) The Multi-Agent Behavior Dataset: Mouse Dyadic Social Interactions; 10.48550/arXiv.2104.02710
• Weissbourd, Brandon and Momose, Tsuyoshi, et el. (2021) Functional modules within a distributed neural network control feeding in a model medusa; 10.1101/2021.02.22.432372
• Chiu, Hui and Hoopfer, Eric D., et el. (2021) A circuit logic for sexually shared and dimorphic aggressive behaviors in Drosophila; Cell; Vol. 184; No. 2; 507-520; PMCID PMC7856078; 10.1016/j.cell.2020.11.048
• Karigo, Tomomi and Kennedy, Ann, et el. (2021) Distinct hypothalamic control of same- and opposite-sex mounting behaviour in mice; Nature; Vol. 589; No. 7841; 258-263; 10.1038/s41586-020-2995-0
• Kennedy, Ann and Kunwar, Prabhat S., et el. (2020) Stimulus-specific hypothalamic encoding of a persistent defensive state; Nature; Vol. 586; No. 7831; 730-734; PMCID PMC7606611; 10.1038/s41586-020-2728-4
• Stagkourakis, Stefanos and Spigolon, Giada, et el. (2020) Experience-dependent plasticity in an innate social behavior is mediated by hypothalamic LTP; Proceedings of the National Academy of Sciences of the United States of America; Vol. 117; No. 41; 25789-25799; PMCID PMC7568289; 10.1073/pnas.2011782117
• Jung, Yonil and Kennedy, Ann, et el. (2020) Neurons that Function within an Integrator to Promote a Persistent Behavioral State in Drosophila; Neuron; Vol. 105; No. 2; 322-333; PMCID PMC6981076; 10.1016/j.neuron.2019.10.028
• Kim, Dong-Wook and Yao, Zizhen, et el. (2019) Multimodal Analysis of Cell Types in a Hypothalamic Node Controlling Social Behavior; Cell; Vol. 179; No. 3; 713-728; PMCID PMC7534821; 10.1016/j.cell.2019.09.020
• Datta, Sandeep Robert and Anderson, David J., et el. (2019) Computational Neuroethology: A Call to Action; Neuron; Vol. 104; No. 1; 11-24; PMCID PMC6981239; 10.1016/j.neuron.2019.09.038
• Ding, Keke and Han, Yifu, et el. (2019) Imaging neuropeptide release at synapses with a genetically engineered reporter; eLife; Vol. 8; Art. no. e46421; PMCID PMC6609332; 10.7554/eLife.46421
• Lo, Liching and Yao, Shenqin, et el. (2019) Connectional architecture of a mouse hypothalamic circuit node controlling social behavior; Proceedings of the National Academy of Sciences of the United States of America; Vol. 116; No. 15; 7503-7512; PMCID PMC6462064; 10.1073/pnas.1817503116
• Duistermars, Brian J. and Pfeiffer, Barret D., et el. (2018) A Brain Module for Scalable Control of Complex, Multi-motor Threat Displays; Neuron; Vol. 100; No. 6; 1474-1490; PMCID PMC6314657; 10.1016/j.neuron.2018.10.027
• Zelikowsky, Moriel and Hui, May, et el. (2018) The Neuropeptide Tac2 Controls a Distributed Brain State Induced by Chronic Social Isolation Stress; Cell; Vol. 173; No. 5; 1265-1279; PMCID PMC5967263; 10.1016/j.cell.2018.03.037
• Walter, Peter and Anderson, David (2018) Günter Blobel (1936–2018); Science; Vol. 360; No. 6387; 383; 10.1126/science.aat7913
• Anderson, David J. and Hoelz, André, et el. (2018) Günter Blobel: Pioneer of molecular cell biology (1936–2018); Journal of Cell Biology; Vol. 217; No. 4; 1163-1167; PMCID PMC5881517; 10.1083/jcb.201803048
• Zelikowsky, Moriel and Ding, Keke, et el. (2018) Neuropeptidergic Control of an Internal Brain State Produced by Prolonged Social Isolation Stress; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 83; 97-103; 10.1101/sqb.2018.83.038109
• Remedios, Ryan and Kennedy, Ann, et el. (2017) Social behaviour shapes hypothalamic neural ensemble representations of conspecific sex; Nature; Vol. 550; No. 7676; 388-392; PMCID PMC5674977; 10.1038/nature23885
• Watanabe, Kiichi and Chiu, Hui, et el. (2017) A Circuit Node that Integrates Convergent Input from Neuromodulatory and Social Behavior-Promoting Neurons to Control Aggression in Drosophila; Neuron; Vol. 95; No. 5; 1112-1128; PMCID PMC5588916; 10.1016/j.neuron.2017.08.017
• Hong, Weizhe and Anderson, David J., et el. (2017) Systems and Methods for Behavior Detection Using 3D Tracking and Machine Learning
• Ting, Alice and Segal, Rosalind, et el. (2016) Opportunities for Technology and Tool Development; Neuron; Vol. 92; No. 3; 564-566; 10.1016/j.neuron.2016.10.042
• Anderson, David J. (2016) Circuit modules linking internal states and social behaviour in flies and mice; Nature Reviews Neuroscience; Vol. 17; No. 11; 692-704; 10.1038/nrn.2016.125
• Anderson, David J. (2016) Social behavior circuits in flies and mice; Chemical Senses; Vol. 41; No. 9; E111; 10.1093/chemse/bjw091
• Hoopfer, Eric D. and Jung, Yonil, et el. (2015) P1 interneurons promote a persistent internal state that enhances inter-male aggression in Drosophila; eLife; Vol. 4; Art. No. 11346; PMCID PMC4749567; 10.7554/eLife.11346
• Hong, Weizhe and Kennedy, Ann, et el. (2015) Automated measurement of mouse social behaviors using depth sensing, video tracking, and machine learning; Proceedings of the National Academy of Sciences; Vol. 112; No. 38; E5351-E5360; PMCID PMC4603510; 10.1073/pnas.1515982112
• Gibson, William T. and Gonzalez, Carlos R., et el. (2015) Behavioral Responses to a Repetitive Visual Threat Stimulus Express a Persistent State of Defensive Arousal in Drosophila; Current Biology; Vol. 25; No. 11; 1401-1415; PMCID PMC4452410; 10.1016/j.cub.2015.03.058
• Jorgenson, Lyric A. and Newsom, William T., et el. (2015) The BRAIN Initiative: developing technology to catalyse neuroscience discovery; Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences; Vol. 370; No. 1668; Art. No. 20140164; PMCID PMC4387507; 10.1098/rstb.2014.0164
• Kunwar, Prabhat S. and Zelikowsky, Moriel, et el. (2015) Ventromedial hypothalamic neurons control a defensive emotion state; eLife; Vol. 4; Art. No. e06633; PMCID PMC4379496; 10.7554/eLife.06633
• Inagaki, Hidehiko K. and Panse, Ketaki M., et el. (2014) Independent, Reciprocal Neuromodulatory Control of Sweet and Bitter Taste Sensitivity during Starvation in Drosophila; Neuron; Vol. 84; No. 4; 806-820; PMCID PMC4365050; 10.1016/j.neuron.2014.09.032
• Anderson, David J. and Perona, Pietro (2014) Toward a Science of Computational Ethology; Neuron; Vol. 84; No. 1; 18-31; 10.1016/j.neuron.2014.09.005
• Hong, Weizhe and Kim, Dong-Wook, et el. (2014) Antagonistic Control of Social versus Repetitive Self-Grooming Behaviors by Separable Amygdala Neuronal Subsets; Cell; Vol. 158; No. 6; 1348-1361; PMCID PMC4167378; 10.1016/j.cell.2014.07.049
• Anderson, David J. (2014) Paul Patterson: In Memoriam; Neuron; Vol. 83; No. 5; 1040-1042; 10.1016/j.neuron.2014.08.024
• Cai, Haijiang and Haubensak, Wulf, et el. (2014) Central amygdala PKC-δ^+ neurons mediate the influence of multiple anorexigenic signals; Nature Neuroscience; Vol. 17; No. 9; 1240-1248; PMCID PMC4146747; 10.1038/nn.3767
• Lim, Rod S. and Eyjolfsdottir, Eyrun, et el. (2014) How Food Controls Aggression in Drosophila; PLoS ONE; Vol. 9; No. 8; Art. No. e105626; PMCID PMC4146546; 10.1371/journal.pone.0105626
• Lee, Hyosang and Kim, Dong-Wook, et el. (2014) Scalable control of mounting and attack by Esr1^+ neurons in the ventromedial hypothalamus; Nature; Vol. 509; No. 7502; 627-632; PMCID PMC4069208; 10.1038/nature13169
• Falkner, Annegret L. and Dollar, Piotr, et el. (2014) Decoding Ventromedial Hypothalamic Neural Activity during Male Mouse Aggression; Journal of Neuroscience; Vol. 34; No. 17; 5971-5984; PMCID PMC3996217; 10.1523/JNEUROSCI.5109-13.2014
• Anderson, David J. and Adolphs, Ralph (2014) A Framework for Studying Emotions across Species; Cell; Vol. 157; No. 1; 187-200; PMCID PMC4098837; 10.1016/j.cell.2014.03.003
• Anthony, Todd E. and Dee, Nick, et el. (2014) Control of Stress-Induced Persistent Anxiety by an Extra-Amygdala Septohypothalamic Circuit; Cell; Vol. 156; No. 3; 522-536; PMCID PMC3982923; 10.1016/j.cell.2013.12.040
• Asahina, Kenta and Watanabe, Kiichi, et el. (2014) Tachykinin-Expressing Neurons Control Male-Specific Aggressive Arousal in Drosophila; Cell; Vol. 156; No. 1-2; 221-235; PMCID PMC3978814; 10.1016/j.cell.2013.11.045
• Kennedy, Ann and Asahina, Kenta, et el. (2014) Internal States and Behavioral Decision-Making: Toward an Integration of Emotion and Cognition; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 79; 199-210; 10.1101/sqb.2014.79.024984
• Eyjolfsdottir, Eyrun and Branson, Steve, et el. (2014) Detecting Social Actions of Fruit Flies; ISBN 978-3-319-10604-5; Computer Vision – ECCV 2014; 772-787; 10.1007/978-3-319-10605-2_50
• Inagaki, Hidehiko K. and Jung, Yonil, et el. (2013) Optogenetic control of Drosophila using a red-shifted channelrhodopsin reveals experience-dependent influences on courtship; Nature Methods; Vol. 11; No. 3; 325-332; PMCID PMC4151318; 10.1038/nmeth.2765
• Adolphs, Ralph and Anderson, David (2013) Social and emotional neuroscience; Current Opinion in Neurobiology; Vol. 23; No. 3; 291-293; 10.1016/j.conb.2013.04.011
• Vrontou, Sophia and Wong, Allan M., et el. (2013) Genetic identification of C fibres that detect massage-like stroking of hairy skin in vivo; Nature; Vol. 493; No. 7434; 669-673; PMCID PMC3563425; 10.1038/nature11810
• Tayler, Timothy D. and Pacheco, Diego A., et el. (2012) A neuropeptide circuit that coordinates sperm transfer and copulation duration in Drosophila; Proceedings of the National Academy of Sciences of the United States of America; Vol. 109; No. 50; 20697-20702; PMCID PMC3528491; 10.1073/pnas.1218246109
• Anderson, David J. (2012) Optogenetics, Sex, and Violence in the Brain: Implications for Psychiatry; Biological Psychiatry; Vol. 71; No. 12; 1081-1089; PMCID PMC3380604; 10.1016/j.biopsych.2011.11.012
• Burgos-Artizzu, Xavier P. and Dollár, Piotr, et el. (2012) Social behavior recognition in continuous video; ISBN 978-1-4673-1226-4; 2012 IEEE Conference on Computer Vision and Pattern Recognition (CVPR); 1322-1329; 10.1109/CVPR.2012.6247817
• Avula, Leela R. and Buckinx, Roeland, et el. (2012) Expression and involvement of the Mas-related gene receptor MrgD in intestinal inflammation in the mouse; FASEB Journal; Vol. 26; Art. No. 727.2
• Hergarden, Anne Christina and Tayler, Timothy D., et el. (2012) Allatostatin-A neurons inhibit feeding behavior in adult Drosophila; Proceedings of the National Academy of Sciences of the United States of America; Vol. 109; No. 10; 3967-3972; PMCID PMC3309792; 10.1073/pnas.1200778109
• Inagaki, Hidehiko K. and Ben-Tabou de-Leon, Shlomo, et el. (2012) Visualizing Neuromodulation In Vivo: TANGO-Mapping of Dopamine Signaling Reveals Appetite Control of Sugar Sensing; Cell; Vol. 148; No. 3; 583-595; PMCID PMC3295637; 10.1016/j.cell.2011.12.022
• Lo, Liching and Anderson, David J. (2011) A Cre-Dependent, Anterograde Transsynaptic Viral Tracer for Mapping Output Pathways of Genetically Marked Neurons; Neuron; Vol. 72; No. 6; 938-950; PMCID PMC3275419; 10.1016/j.neuron.2011.12.002
• Lukaszewicz, Agnès I. and Anderson, David J. (2011) Cyclin D1 promotes neurogenesis in the developing spinal cord in a cell cycle-independent manner; Proceedings of the National Academy of Sciences of the United States of America; Vol. 108; No. 28; 11632-11637; PMCID PMC3136279; 10.1073/pnas.1106230108
• Lukaszewicz, A. I. and Anderson, D. J. (2011) Cyclin D1 promotes neurogenesis in the developing spinal cord in a cell cycle-independent manner; Proceedings of the National Academy of Sciences of the United States of America; Vol. 108; No. 28; 11632-11637; PMCID PMC3136279; 10.1073/pnas.1106230108
• Wang, Liming and Han, Xiaoqing, et el. (2011) Hierarchical chemosensory regulation of male-male social interactions in Drosophila; Nature Neuroscience; Vol. 14; No. 6; 757-762; PMCID PMC3102769; 10.1038/nn.2800
• Lin, Dayu and Boyle, Maureen P., et el. (2011) Functional identification of an aggression locus in the mouse hypothalamus; Nature; Vol. 470; No. 7333; 221-226; PMCID PMC3075820; 10.1038/nature09736
• Haubensak, Wulf and Kunwar, Prabhat S., et el. (2010) Genetic dissection of an amygdala microcircuit that gates conditioned fear; Nature; Vol. 468; No. 7321; 270-276; PMCID PMC3597095; 10.1038/nature09553
• Shields, Shannon D. and Cavanaugh, Daniel J., et el. (2010) Pain behavior in the formalin test persists after ablation of the great majority of C-fiber nociceptors; Pain; Vol. 151; No. 2; 422-429; 10.1016/j.pain.2010.08.001
• Guan, Yun and Liu, Qin, et el. (2010) Mas-related G-protein–coupled receptors inhibit pathological pain in mice; Proceedings of the National Academy of Sciences of the United States of America; Vol. 107; No. 36; 15933-15938; PMCID PMC2936626; 10.1073/pnas.1011221107
• Gleick, P. H. and Anderson, D. J., et el. (2010) Climate Change and the Integrity of Science; Science; Vol. 328; No. 5979; 689-690; PMCID PMC5125622; 10.1126/science.328.5979.689
• Wang, Liming and Anderson, David J. (2010) Identification of an aggression-promoting pheromone and its receptor neurons in Drosophila; Nature; Vol. 463; No. 7278; 227-231; PMCID PMC2999963; 10.1038/nature08678
• Liu, Qin and Tang, Zongxiang, et el. (2009) Sensory Neuron-Specific GPCR Mrgprs Are Itch Receptors Mediating Chloroquine-Induced Pruritus; Cell; Vol. 139; No. 7; 1353-1365; PMCID PMC2989405; 10.1016/j.cell.2009.11.034
• Lebestky, Tim and Chang, Jung-Sook C., et el. (2009) Two Different Forms of Arousal in Drosophila Are Oppositely Regulated by the Dopamine D1 Receptor Ortholog DopR via Distinct Neural Circuits; Neuron; Vol. 64; No. 4; 522-536; PMCID PMC2908595; 10.1016/j.neuron.2009.09.031
• Imamachi, Noritaka and Park, Goon Ho, et el. (2009) TRPV1-expressing primary afferents generate behavioral responses to pruritogens via multiple mechanisms; Proceedings of the National Academy of Sciences of the United States of America; Vol. 106; No. 27; 11330-11335; PMCID PMC2708751; 10.1073/pnas.0905605106
• Rau, Kristofer K. and McIlwrath, Sabrina L., et el. (2009) Mrgprd Enhances Excitability in Specific Populations of Cutaneous Murine Polymodal Nociceptors; Journal of Neuroscience; Vol. 29; No. 26; 8612-8619; PMCID PMC2756673; 10.1523/JNEUROSCI.1057-09.2009
• Cavanaugh, Daniel J. and Lee, Hyosang, et el. (2009) Distinct subsets of unmyelinated primary sensory fibers mediate behavioral responses to noxious thermal and mechanical stimuli; Proceedings of the National Academy of Sciences of the United States of America; Vol. 106; No. 22; 9075-9080; PMCID PMC2683885; 10.1073/pnas.0901507106
• Dankert, Heiko and Wang, Liming, et el. (2009) Automated monitoring and analysis of social behavior in Drosophila; Nature Methods; Vol. 6; No. 4; 297-303; PMCID PMC2679418; 10.1038/NMETH.1310
• Yorozu, Suzuko and Wong, Allan, et el. (2009) Distinct sensory representations of wind and near-field sound in the Drosophila brain; Nature; Vol. 458; No. 7235; 201-205; PMCID PMC2755041; 10.1038/nature07843
• Ng, Lydia and Bernard, Amy, et el. (2009) An anatomic gene expression atlas of the adult mouse brain; Nature Neuroscience; Vol. 12; No. 3; 356-362; 10.1038/nn.2281
• Hochstim, Christian and Deneen, Benjamin, et el. (2008) Identification of Positionally Distinct Astrocyte Subtypes whose Identities Are Specified by a Homeodomain Code; Cell; Vol. 133; No. 3; 510-522; PMCID PMC2394859; 10.1016/j.cell.2008.02.046
• Wang, Liming and Dankert, Heiko, et el. (2008) A common genetic target for environmental and heritable influences on aggressiveness in Drosophila; Proceedings of the National Academy of Sciences of the United States of America; Vol. 105; No. 15; 5657-5663; PMCID PMC2311352; 10.1073/pnas.0801327105
• Dussor, G. and Zylka, M. J., et el. (2008) Cutaneous Sensory Neurons Expressing the Mrgprd Receptor Sense Extracellular ATP and Are Putative Nociceptors; Journal of Neurophysiology; Vol. 99; No. 4; 1581-1589; 10.1152/jn.01396.2007
• Anderson, David and Brenner, Sydney (2008) Seymour Benzer (1921-2007) - Obituary; Nature; Vol. 451; No. 7175; 139; 10.1038/451139a
• Liu, Yang and Yang, Fu-Chia, et el. (2008) Mechanisms of Compartmentalized Expression of Mrg Class G-Protein-Coupled Sensory Receptors; Journal of Neuroscience; Vol. 28; No. 1; 125-132; PMCID PMC6671167; 10.1523/JNEUROSCI.4472-07.2008
• Liu, Qin and Vrontou, Sophia, et el. (2007) Molecular genetic visualization of a rare subset of unmyelinated sensory neurons that may detect gentle touch; Nature Neuroscience; Vol. 10; No. 8; 946-948; 10.1038/nn1937
• Suh, Greg S. B. and Ben-Tabou de Leon, Shlomo, et el. (2007) Light Activation of an Innate Olfactory Avoidance Response in Drosophila; Current Biology; Vol. 17; No. 10; 905-908; 10.1016/j.cub.2007.04.046
• Lerchner, Walter and Xiao, Cheng, et el. (2007) Reversible Silencing of Neuronal Excitability in Behaving Mice by a Genetically Targeted, Ivermectin-Gated Cl^− Channel; Neuron; Vol. 54; No. 1; 35-49; 10.1016/j.neuron.2007.02.030
• Zhang, Chengkang and Ng, Kwan L., et el. (2007) Prokineticin 2 Is a Target Gene of Proneural Basic Helix-Loop-Helix Factors for Olfactory Bulb Neurogenesis; Journal of Biological Chemistry; Vol. 282; No. 10; 6917-6921; 10.1074/jbc.C600290200
• Ligon, Keith L. and Huillard, Emmanuelle, et el. (2007) Olig2-Regulated Lineage-Restricted Pathway Controls Replication Competence in Neural Stem Cells and Malignant Glioma; Neuron; Vol. 53; No. 4; 503-517; 10.1016/j.neuron.2007.01.009
• Deneen, Benjamin and Ho, Ritchie, et el. (2006) The Transcription Factor NFIA Controls the Onset of Gliogenesis in the Developing Spinal Cord; Neuron; Vol. 52; No. 6; 953-968; 10.1016/j.neuron.2006.11.019
• Rebelo, Sandra and Chen, Zhou-Feng, et el. (2006) Involvement of DRG11 in the development of the primary afferent nociceptive system; Molecular and Cellular Neuroscience; Vol. 33; No. 3; 236-246; 10.1016/j.mcn.2006.07.013
• Ligon, Keith L. and Kesari, Santosh, et el. (2006) Development of NG2 neural progenitor cells requires Olig gene function; Proceedings of the National Academy of Sciences of the United States of America; Vol. 103; No. 20; 7853-7858; 10.1073/pnas.0511001103
• Carvalho, Gil B. and Kapahi, Pankaj, et el. (2006) Allocrine Modulation of Feeding Behavior by the Sex Peptide of Drosophila; Current Biology; Vol. 16; No. 7; 692-696; PMCID PMC2745344; 10.1016/j.cub.2006.02.064
• Mukouyama, Yoh-suke and Deneen, Benjamin, et el. (2006) Olig2^+ neuroepithelial motoneuron progenitors are not multipotent stem cells in vivo; Proceedings of the National Academy of Sciences of the United States of America; Vol. 103; No. 5; 1551-1556; PMCID PMC1345718; 10.1073/pnas.0510658103
• Choi, Gloria B. and Anderson, David J. (2005) A Nose by Any Other Name (Should Smell as Sweetly); Cell; Vol. 123; No. 4; 550-553; 10.1016/j.cell.2005.11.004
• Lee, Jiyoun and Zylka, Mark J., et el. (2005) A Steroid-Conjugated Contrast Agent for Magnetic Resonance Imaging of Cell Signaling; Journal of the American Chemical Society; Vol. 127; No. 38; 13164-13166; 10.1021/ja051294x
• Shin, Donghun and Anderson, David J. (2005) Isolation of arterial-specific genes by subtractive hybridization reveals molecular heterogeneity among arterial endothelial cells; Developmental Dynamics; Vol. 233; No. 4; 1589-1604; 10.1002/dvdy.20479
• Choi, Gloria B. and Dong, Hong-Wei, et el. (2005) Lhx6 Delineates a Pathway Mediating Innate Reproductive Behaviors from the Amygdala to the Hypothalamus; Neuron; Vol. 46; No. 4; 647-660; 10.1016/j.neuron.2005.04.011
• Lo, Liching and Dormand, Emma L., et el. (2005) Late-emigrating neural crest cells in the roof plate are restricted to a sensory fate by GDF7; Proceedings of the National Academy of Sciences of the United States of America; Vol. 102; No. 20; 7192-7197; PMCID PMC1091754; 10.1073/pnas.0502581102
• Mukouyama, Yoh-suke and Gerber, Hans-Peter, et el. (2005) Peripheral nerve-derived VEGF promotes arterial differentiation via neuropilin 1-mediated positive feedback; Development; Vol. 132; No. 5; 941-952; 10.1242/dev.01675
• Zylka, Mark J. and Rice, Frank L., et el. (2005) Topographically Distinct Epidermal Nociceptive Circuits Revealed by Axonal Tracers Targeted to Mrgprd; Neuron; Vol. 45; No. 1; 17-25; 10.1016/j.neuron.2004.12.015
• Joseph, Nancy M. and Mukouyama, Yoh-suke, et el. (2004) Neural crest stem cells undergo multilineage differentiation in developing peripheral nerves to generate endoneurial fibroblasts in addition to Schwann cells; Development; Vol. 131; No. 22; 5599-5612; 10.1242/dev.01429
• Suh, Greg S. and Wong, Allan M., et el. (2004) A single population of olfactory sensory neurons mediates an innate avoidance behaviour in Drosophila; Nature; Vol. 431; No. 7010; 854-859; 10.1038/nature02980
• Anderson, D. J. and Lo, L., et el. (2004) The Logic of Neural Cell Lineage Restriction: Neuropoiesis Revisited; ISBN 9783540205586; Stem cells in the nervous system : functional and clinical implications; 25-41; 10.1007/978-3-642-18883-1_2
• Mouritsen, Henrik and Huyvaert, Kathryn P., et el. (2003) Waved albatrosses can navigate with strong magnets attached to their head; Journal of Experimental Biology; Vol. 206; No. 22; 4155-4166; 10.1242/jeb.00650
• Gabay, Limor and Lowell, Sally, et el. (2003) Deregulation of Dorsoventral Patterning by FGF Confers Trilineage Differentiation Capacity on CNS Stem Cells In Vitro; Neuron; Vol. 40; No. 3; 485-499; 10.1016/S0896-6273(03)00637-8
• Han, C. J. and O'Tuathaigh, Colm M., et el. (2003) Trace but not delay fear conditioning requires attention and the anterior cingulate cortex; Proceedings of the National Academy of Sciences of the United States of America; Vol. 100; No. 22; 13087-13092; PMCID PMC240749; 10.1073/pnas.2132313100
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• Stemple, Derek L. and Anderson, David J. (1993) Lineage Diversification of the Neural Crest: In Vitro Investigations; Developmental Biology; Vol. 159; No. 1; 12-23; 10.1006/dbio.1993.1218
• Anderson, David J. (1993) Molecular Control of Cell Fate in the Neural Crest: The Sympathoadrenal Lineage; Annual Review of Neuroscience; Vol. 16; 129-158; 10.1146/annurev.ne.16.030193.001021
• Anderson, David J. (1993) Cell and molecular biology of neural crest cell lineage diversification; Current Opinion in Neurobiology; Vol. 3; No. 1; 8-13; 10.1016/0959-4388(93)90028-W
• Anderson, David J. (1993) Cell fate determination in the peripheral nervous system: The sympathoadrenal progenitor; Journal of Neurobiology; Vol. 24; No. 2; 185-198; 10.1002/neu.480240206
• Stemple, Derek L. and Anderson, David J. (1992) Isolation of a stem cell for neurons and glia from the mammalian neural crest; Cell; Vol. 71; No. 6; 973-985; 10.1016/0092-8674(92)90393-Q
• Anderson, David J. (1992) The highs and lows of an NGF receptor; Current Biology; Vol. 2; No. 9; 461-462; 10.1016/0960-9822(92)90651-P
• Birren, Susan J. and Verdi, Joseph M., et el. (1992) Membrane depolarization induces p140^(trk) and NGF responsiveness, but not p75^(LNGFR), in MAH cells; Science; Vol. 257; No. 5068; 395-397; 10.1126/science.1321502
• Mori, Nozomu and Schoenherr, Christopher, et el. (1992) A common silencer element in the SCG10 and type II Na^+ channel genes binds a factor present in nonneuronal cells but not in neuronal cells; Neuron; Vol. 9; No. 1; 45-54; 10.1016/0896-6273(92)90219-4
• Ip, Nancy Y. and Nye, Steven H., et el. (1992) CNTF and LIF act on neuronal cells via shared signaling pathways that involve the IL-6 signal transducing receptor component gp130; Cell; Vol. 69; No. 7; 1121-1132; 10.1016/0092-8674(92)90634-O
• Johnson, Jane E. and Birren, Susan J., et el. (1992) DNA Binding and Transcriptional Regulatory Activity of Mammalian Achaete-Acute Homologous (MASH) Proteins Revealed by Interaction with a Muscle-Specific Enhancer; Proceedings of the National Academy of Sciences of the United States of America; Vol. 89; No. 8; 3596-3600; PMCID PMC48915; 10.1073/pnas.89.8.3596
• Michelsohn, Arie M. and Anderson, David J. (1992) Changes in Competence Determine the Timing of Two Sequential Glucocorticoid Effects on Sympathoadrenal Progenitors; Neuron; Vol. 8; No. 3; 589-604; 10.1016/0896-6273(92)90285-L
• Johnson, Jane E. and Zimmerman, Kathryn, et el. (1992) Induction and repression of mammalian achaete-scute homologue (MASH) gene expression during neuronal differentiation of P19 embryonal carcinoma cells; Development; Vol. 114; No. 1; 75-87
• Anderson, David J. (1992) Molecular Control of Neural Development; ISBN 9780878933075; An Introduction to Molecular Neurobiology; 355-387
• Anderson, D. J. (1992) The Sympathoadrenal Progenitor of the Neural Crest: Basic Biology and Therapeutic Potential; ISBN 9783540558897; Gene transfer and therapy in the nervous system; 40-58; 10.1007/978-3-642-84842-1_5
• Carnahan, Josette F. and Anderson, David J., et el. (1991) Evidence That Enteric Neurons May Derive from the Sympathoadrenal Lineage; Developmental Biology; Vol. 148; No. 2; 552-561; 10.1016/0012-1606(91)90273-6
• Vandenbergh, David J. and Mori, Nozomu, et el. (1991) Co-expression of multiple neurotransmitter enzyme genes in normal and immortalized sympathoadrenal progenitor cells; Developmental Biology; Vol. 148; No. 1; 10-22; 10.1016/0012-1606(91)90313-R
• Anderson, David J. and Carnahan, Josette F., et el. (1991) Antibody Markers Identify a Common Progenitor to Sympathetic Neurons and Chromaffin Cells in vivo and Reveal the Timing of Commitment to Neuronal Differentiation in the Sympathoadrenal Lineage; Journal of Neuroscience; Vol. 11; No. 11; 3507-3519; PMCID PMC6575531; 10.1523/JNEUROSCI.11-11-03507.1991
• Lo, Li-Ching and Johnson, Jane E., et el. (1991) Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells; Genes and Development; Vol. 5; No. 9; 1524-1537; 10.1101/gad.5.9.1524
• Lo, L.-C. and Birren, S. J., et el. (1991) V-myc immortalization of early rat neural crest cells yields a clonal cell line which generates both glial and adrenergic progenitor cells; Developmental Biology; Vol. 145; No. 1; 139-153; 10.1016/0012-1606(91)90220-W
• Stemple, Derek L. and Anderson, David J. (1991) A Schwann cell antigen recognized by monoclonal antibody 217c is the rat low-affinity nerve growth factor receptor; Neuroscience Letters; Vol. 124; No. 1; 57-60; 10.1016/0304-3940(91)90821-A
• Johnson, Jane E. and Birren, Susan J., et el. (1990) Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors; Nature; Vol. 346; No. 6287; 858-861; 10.1038/346858a0
• Wuenschell, Carol W. and Mori, Nozomu, et el. (1990) Analysis of SCG10 Gene Expression in Transgenic Mice Reveals That Neural Specificity Is Achieved through Selective Derepression; Neuron; Vol. 4; No. 4; 595-602; 10.1016/0896-6273(90)90117-X
• Mori, Nozomu and Stein, Reuven, et el. (1990) A Cell Type-Preferred Silencer Element That Controls the Neural-Specific Expression of the SCG10 Gene; Neuron; Vol. 4; No. 4; 583-594; 10.1016/0896-6273(90)90116-W
• Anderson, David J. (1990) Career Choices for Developing Neurons; Engineering and Science; Vol. 53; No. 3; 14-23
• Sigmund, Orit and Naort, Zvi, et el. (1990) Effect of nerve growth factor and fibroblast growth factor on SCG10 and c-fos expression and neurite outgrowth in protein kinase C-depleted PC12 cells; Journal of Biological Chemistry; Vol. 265; No. 4; 2257-2261
• Birren, Susan J. and Anderson, David J. (1990) A v-myc-Immortalized Sympathoadrenal Progenitor Cell Line in Which Neuronal Differentiation Is Initiated by FGF but Not NGF; Neuron; Vol. 4; No. 2; 189-201; 10.1016/0896-6273(90)90094-V
• Anderson, David J. (1990) Development and plasticity in the sympathoadrenal lineage of the neural crest; Discussions in Neurosciences; Vol. 7; No. 2-3; 26-32
• Mori, N. and Birren, S. J., et el. (1990) Contributions of Cell-extrinsic and Cell-intrinsic Factors to the Differentiation of a Neural-crest-derived Neuroendocrine Progenitor Cell; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 55; 255-264; 10.1101/SQB.1990.055.01.028
• Vandenbergh, David J. and Wuenschell, Carol W., et el. (1989) Chromatin structure as a molecular marker of cell lineage and developmental potential in neural crest-derived chromaffin cells; Neuron; Vol. 3; No. 4; 507-518; 10.1016/0896-6273(89)90209-2
• Anderson, David J. (1989) The Neural Crest Cell Lineage Problem: Neuropoiesis?; Neuron; Vol. 3; No. 1; 1-12; 10.1016/0896-6273(89)90110-4
• Anderson, David J. (1989) Cellular 'neoteny': a possible developmental basis for chromaffin cell plasticity; Trends in Genetics; Vol. 5; No. 6; 174-184; 10.1016/0168-9525(89)90072-3
• Anderson, David J. (1989) New roles for PDGF and CNTF in controlling the timing of glial cell differentiation in the optic nerve; Trends in Neurosciences; Vol. 12; No. 3; 83-85; 10.1016/0166-2236(89)90160-4
• Anderson, David J. (1989) Development and Plasticity of a Neural Crest-Derived Neuroendocrine Sublineage; ISBN 9780845115084; The Assembly of the Nervous System; 17-36
• Anderson, David J. and Michelsohn, Arie (1989) Role of glucocorticoids in the chromaffin-neuron developmental decision; International Journal of Developmental Neuroscience; Vol. 7; No. 5; 475-487; 10.1016/0736-5748(89)90007-5
• Stein, Reuven and Mori, Nozomu, et el. (1988) The NGF-Inducible SCG10 mRNA Encodes a Novel Membrane-Bound Protein Present in Growth Cones and Abundant in Developing Neurons; Neuron; Vol. 1; No. 6; 463-476; 10.1016/0896-6273(88)90177-8
• Stemple, Derek L. and Mahanthappa, Nagesh K., et el. (1988) Basic FGF Induces Neuronal Differentiation, Cell Division, and NGF Dependence in Chromaffin Cells: A Sequence of Events in Sympathetic Development; Neuron; Vol. 1; No. 6; 517-525; 10.1016/0896-6273(88)90182-1
• Stein, Reuven and Orit, Sigmond, et el. (1988) The induction of a neural-specific gene, SCG10, by nerve growth factor in PC12 cells is transcriptional, protein synthesis dependent, and glucocorticoid inhibitable; Developmental Biology; Vol. 127; No. 2; 316-325; 10.1016/0012-1606(88)90318-1
• Anderson, D. J. (1988) Cell fate and gene expression in the developing neural crest; ISBN 9780387185538; Neural Development and Regeneration; 187-198; 10.1007/978-3-642-73148-8_17
• Anderson, David J. (1987) Molecular Biology of the Acetylcholine Receptor: Structure and Regulation of Biogenesis; ISBN 9780845127254; The Vertebrate Neuromuscular Junction; 285-315
• Anderson, David J. and Axel, Richard (1986) A Bipotential Neuroendocrine Precursor Whose Choice of Cell Fate Is Determined by NGF and Glucocorticoids; Cell; Vol. 47; No. 6; 1079-1090; 10.1016/0092-8674(86)90823-8
• Anderson, David J. and Axel, Richard (1985) Molecular probes for the development and plasticity of neural crest derivatives; Cell; Vol. 42; No. 2; 649-662; 10.1016/0092-8674(85)90122-9
• Anderson, David J. and Stein, R., et el. (1985) Gene Expression in Differentiating and Transdifferentiating Neural Crest Cells; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 50; 855-863; 10.1101/SQB.1985.050.01.103
• Anderson, David J. and Mostov, Keith E., et el. (1983) Mechanisms of integration of de novo-synthesized polypeptides into membranes: Signal-recognition particle is required for integration into microsomal membranes of calcium ATPase and of lens MP26 but not of cytochrome b_5; Proceedings of the National Academy of Sciences of the United States of America; Vol. 80; No. 23; 7249-7253; PMCID PMC390032; 10.1073/pnas.80.23.7249
• Anderson, David J. and Blobel, Günter (1983) Biosynthesis of Acetylcholine Receptor in Vitro; ISBN 978-0-12-181996-5; Biomembranes Part J: Membrane Biogenesis: Assembly and Targeting; 367-378; 10.1016/S0076-6879(83)96033-0
• Anderson, David J. and Blobel, Günter (1983) Immunoprecipitation of Proteins from Cell-Free Translations; ISBN 978-0-12-181996-5; Biomembranes, Part J: Membrane Biogenesis: Assemby and Targeting (General Methods: Eukaryotes), 96; 111-120; 10.1016/S0076-6879(83)96012-3
• Anderson, David J. and Blobel, Günter, et el. (1983) Transmembrane orientation of an early biosynthetic form of acetylcholine receptor delta subunit determined by proteolytic dissection in conjunction with monoclonal antibodies; Journal of Neuroscience; Vol. 3; No. 9; 1773-1784; PMCID PMC6564464; 10.1523/jneurosci.03-09-01773.1983
• Anderson, David J. and Blobel, Günter (1983) Identification of homo-oligomers as potential intermediates in acetylcholine receptor subunit assembly; Proceedings of the National Academy of Sciences of the United States of America; Vol. 80; No. 14; 4359-4363; PMCID PMC384037; 10.1073/pnas.80.14.4359
• Buck, L. and Stein, R., et el. (1983) Gene Expression and the Diversity of Identified Neurons; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 48; 485-492; 10.1101/SQB.1983.048.01.053
• Anderson, D. J. and Blobel, G. (1983) Molecular Events in the Synthesis and Assembly of a Nicotinic Acetylcholine Receptor; Cold Spring Harbor Symposia on Quantitative Biology; Vol. 48; 125-134; 10.1101/SQB.1983.048.01.015
• Anderson, David J. and Blobel, Günter (1983) In Vitro Biosynthesis of the Subunits of Acetylcholine Receptor; ISBN 9780444804327; Proceedings of the 9th Meeting of the International Neurobiology Society; 95-106; 10.1016/S0079-6123(08)60010-2
• Anderson, David J. (1983) Acetylcholine receptor biosynthesis: from kinetics to molecular mechanism; Trends in Neurosciences; Vol. 6; No. 5; 169-171; 10.1016/0166-2236(83)90079-6
• Anderson, David J. and Walter, Peter, et el. (1982) Signal recognition protein is required for the integration of acetylcholine receptor delta subunit, a transmembrane glycoprotein, into the endoplasmic reticulum membrane; Journal of Cell Biology; Vol. 93; No. 2; 501-506; PMCID PMC2112847; 10.1083/jcb.93.2.501
• Hertzberg, Elliot L. and Anderson, David J., et el. (1982) Comparative Analysis of the Major Polypeptides from Liver Gap Junctions and Lens Fiber Junctions; Journal of Cell Biology; Vol. 92; No. 1; 53-59; PMCID PMC2112018; 10.1083/jcb.92.1.53
• Anderson, David J. and Walter, Peter, et el. (1982) Early Translational Events in the Synthesis of Acetylcholine Receptor; ISBN 9780890047446; Molecular Genetic Neuroscience; 373-385
• Anderson, David J. and Blobel, Gunter (1981) In vitro synthesis, glycosylation, and membrane insertion of the four subunits of Torpedo acetylcholine receptor; Proceedings of the National Academy of Sciences of the United States of America; Vol. 78; No. 9; 5598-5602; 10.1073/pnas.78.9.5598