14 publications found.
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Ugur B, Bao H, Stawarski M, Duraine LR, Zuo Z, Lin YQ, Neely GG, Macleod GT, Chapman ER, Bellen HJ (2017). The Krebs cycle enzyme Isocitrate Dehydrogenase 3A couples mitochondrial metabolism to synaptic transmission. Cell Reports 21:3794-3806 Abstract
Kanca O, Bellen HJ, Schnorrer F (2017). Gene tagging strategies to assess protein expression, localization, and function in Drosophila. Genetics 207:389-412 Abstract
Chao HT, Liu L, Bellen HJ (2017). Building dialogues between clinical and biomedical research through cross-species collaborations. Seminars in Cell & Developmental Biology 70:49-57 Abstract
Liu L, MacKenzie KR, Putluri N, Maletić-Savatić M, Bellen HJ (2017). The glia-neuron lactate shuttle and elevated ROS promote lipid synthesis in neurons and lipid droplet accumulation in glia via APOE/D. Cell Metabolism 26:719-737 Abstract Cell Metabolism 26:701-2, Preview. Science Translational Medicine 9(412):eaap8170, Editor's Choice.
Wangler MF, Yamamoto S, Chao HT, Posey JE, Westerfield M, Postlethwait J, Members of the Undiagnosed Diseases Network (UDN), Hieter P, Boycott KM, Campeau PM, Bellen HJ (2017). Model organisms facilitate rare disease diagnosis and therapeutic research. Genetics 207:9-27 Abstract
Luo X, Rosenfeld JA, Yamamoto S, Harel T, Zuo Z, Hall M, Wierenga KJ, Pastore MT, Bartholomew D, Delgado MR, Rotenberg J, Lewis RA, Emrick L, Bacino CA, Eldomery MK, Coban Akdemir Z, Xia F, Yang Y, Lalani SR, Lotze T, Lupski JR, Lee B, Bellen HJ, Wangler MF; Members of the UDN (2017). Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS Genetics 13:e1006905 Abstract
Wangler MF, Chao YH, Bayat V, Giagtzoglou N, Shinde AB, Putluri N, Coarfa C, Donti T, Graham BH, Faust JE, McNew JA, Moser A, Sardiello M, Baes M, Bellen HJ (2017). Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. PLoS Genetics 13:e1006825 Abstract
Wong CO, Gregory S, Hu H, Chao Y, Sepúlveda VE, He Y, Li-Kroeger D, Goldman WE, Bellen HJ, Venkatachalam K (2017). Lysosomal degradation is required for sustained phagocytosis of bacteria by macrophages. Cell Host Microbe 21:719-730 Abstract Cell Host Microbe 21:657-9, Preview.
Wang J, Al-Ouran R, Hu Y, Kim SY, Wan YW, Wangler MF, Yamamoto S, Chao HT, Comjean A, Mohr SE, UDN, Perrimon N, Liu Z*, Bellen HJ* (2017). MARRVEL: integration of human and model organism genetic resources to facilitate functional annotation of the human genome. The American Journal of Human Genetics 100:843-853 Abstract Selected among Best of AJHG 2016-2017. *co-corresponding author
Nagarkar-Jaiswal S, Manivannan SN, Zuo Z, Bellen HJ (2017). A cell cycle-independent, conditional gene inactivation strategy for differentially tagging wild-type and mutant cells. eLife 31:e26420 Abstract
Malmanche N, Dourlen P, Gistelinck M, Demiautte F, Link N, Dupont C, Vanden Broeck L, Werkmeister E, Amouyel P, Bongiovanni A, Bauderlique H, Moechars D, Royou A, Bellen HJ, Lafont F, Callaerts P, Lambert JC, Dermaut B (2017). Developmental expression of 4-Repeat-Tau induces neuronal aneuploidy in Drosophila tauopathy models. Scientific Reports 7:40764 Abstract
Chao HT, Davids M, Burke E, Pappas JG, Rosenfeld JA, McCarty AJ, Davis T, Wolfe L, Toro C, Tifft C, Xia F, Stong N, Johnson TK, Warr CG, Undiagnosed Diseases Network, Yamamoto S, Adams DR, Markello TC, Gahl WA, Bellen HJ, Wangler MF, Malicdan MC (2017). A syndromic neurodevelopmental disorder caused by de novo variants in EBF3. The American Journal of Human Genetics 100:128-137 Abstract
Yoon WH, Sandoval H, Nagarkar-Jaiswal S, Jaiswal M, Yamamoto S, HaeltermanNA, Putluri N, Putluri V, Sreekumar A, Tos T, Aksoy A, Donti T, Graham BH, OhnoM, Nishi E, Hunter J, Muzny DM, Carmichael J, Shen J, Arboleda VA, Nelson SF,Wangler MF, Karaca E, Lupski JR, Bellen HJ (2017). Loss of Nardilysin, a mitochondrial co-chaperone for α-ketoglutarate dehydrogenase, promotes mTORC1 activation and neurodegeneration. Neuron 93:115-131 Abstract
Lin G, Mao D, Bellen HJ (2017). Amyotrophic Lateral Sclerosis pathogenesis converges on defects in protein homeostasis associated with TDP-43 mislocalization and proteasome-mediated degradation overload. Current Topics in Developmental Biology 121:111-171 Abstract