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Ranasinghe KG, Gill JS, Kothare H, Beagle AJ, Mizuiri D, Honma SM, Gorno-Tempini MLuisa, Miller BL, Vossel KA, Nagarajan SS et al..  2017.  Abnormal vocal behavior predicts executive and memory deficits in Alzheimer's disease.. Neurobiol Aging. 52:71-80.
Tracy TE, Gan L.  2017.  Acetylated tau in Alzheimer's disease: An instigator of synaptic dysfunction underlying memory loss: Increased levels of acetylated tau blocks the postsynaptic signaling required for plasticity and promotes memory deficits associated with tauopathy.. Bioessays. 39(4)
Carlomagno Y, Chung D-EChloe, Yue M, Castanedes-Casey M, Madden BJ, Dunmore J, Tong J, DeTure M, Dickson DW, Petrucelli L et al..  2017.  An acetylation-phosphorylation switch that regulates tau aggregation propensity and function.. J Biol Chem. 292(37):15277-15286.
Lobingier BT, Hüttenhain R, Eichel K, Miller KB, Ting AY, von Zastrow M, Krogan NJ.  2017.  An Approach to Spatiotemporally Resolve Protein Interaction Networks in Living Cells.. Cell. 169(2):350-360.e12.
Alegro M, Theofilas P, Nguy A, Castruita PA, Seeley W, Heinsen H, Ushizima DM, Grinberg LT.  2017.  Automating cell detection and classification in human brain fluorescent microscopy images using dictionary learning and sparse coding.. J Neurosci Methods. 282:20-33.
Perry DC, Brown JA, Possin KL, Datta S, Trujillo A, Radke A, Karydas A, Kornak J, Sias AC, Rabinovici GD et al..  2017.  Clinicopathological correlations in behavioural variant frontotemporal dementia.. Brain. 140(12):3329-3345.
Jost M, Chen Y, Gilbert LA, Horlbeck MA, Krenning L, Menchon G, Rai A, Cho MY, Stern JJ, Prota AE et al..  2017.  Combined CRISPRi/a-Based Chemical Genetic Screens Reveal that Rigosertib Is a Microtubule-Destabilizing Agent.. Mol Cell. 68(1):210-223.e6.
Kampmann M.  2017.  A CRISPR Approach to Neurodegenerative Diseases.. Trends Mol Med. 23(6):483-485.
Nagy T, Kampmann M.  2017.  CRISPulator: a discrete simulation tool for pooled genetic screens.. BMC Bioinformatics. 18(1):347.
Possin KL, Merrilees J, Bonasera SJ, Bernstein A, Chiong W, Lee K, Wilson L, Hooper SM, Dulaney S, Braley T et al..  2017.  Development of an adaptive, personalized, and scalable dementia care program: Early findings from the Care Ecosystem.. PLoS Med. 14(3):e1002260.
Possin KL, Kim H, Geschwind MD, Moskowitz T, Johnson ET, Sha SJ, Apple A, Xu D, Miller BL, Finkbeiner S et al..  2017.  Egocentric and allocentric visuospatial working memory in premotor Huntington's disease: A double dissociation with caudate and hippocampal volumes.. Neuropsychologia. 101:57-64.
Kampmann M.  2017.  Elucidating drug targets and mechanisms of action by genetic screens in mammalian cells.. Chem Commun (Camb). 53(53):7162-7167.
Sigg MAbedin, Menchen T, Lee C, Johnson J, Jungnickel MK, Choksi SP, Garcia G, Busengdal H, Dougherty GW, Pennekamp P et al..  2017.  Evolutionary Proteomics Uncovers Ancient Associations of Cilia with Signaling Pathways.. Dev Cell. 43(6):744-762.e11.
Olney NT, Spina S, Miller BL.  2017.  Frontotemporal Dementia.. Neurol Clin. 35(2):339-374.
Spina S, Schonhaut DR, Boeve BF, Seeley WW, Ossenkoppele R, O'Neil JP, Lazaris A, Rosen HJ, Boxer AL, Perry DC et al..  2017.  Frontotemporal dementia with the V337M mutation: Tau-PET and pathology correlations.. Neurology. 88(8):758-766.
Tsvetanova NG, Trester-Zedlitz M, Newton BW, Riordan DP, Sundaram AB, Johnson JR, Krogan NJ, von Zastrow M.  2017.  G Protein-Coupled Receptor Endocytosis Confers Uniformity in Responses to Chemically Distinct Ligands.. Mol Pharmacol. 91(2):145-156.
Chen J, Yu J-T, Wojta K, Wang H-F, Zetterberg H, Blennow K, Yokoyama JS, Weiner MW, Kramer JH, Rosen H et al..  2017.  Genome-wide association study identifies locus influencing human plasma tau levels.. Neurology. 88(7):669-676.
Park RJ, Wang T, Koundakjian D, Hultquist JF, Lamothe-Molina P, Monel B, Schumann K, Yu H, Krupzcak KM, Garcia-Beltran W et al..  2017.  A genome-wide CRISPR screen identifies a restricted set of HIV host dependency factors.. Nat Genet. 49(2):193-203.
Ward ME, Chen R, Huang H-Y, Ludwig C, Telpoukhovskaia M, Taubes A, Boudin H, Minami SS, Reichert M, Albrecht P et al..  2017.  Individuals with progranulin haploinsufficiency exhibit features of neuronal ceroid lipofuscinosis.. Sci Transl Med. 9(385)
Rauch BJ, Silvis MR, Hultquist JF, Waters CS, McGregor MJ, Krogan NJ, Bondy-Denomy J.  2017.  Inhibition of CRISPR-Cas9 with Bacteriophage Proteins.. Cell. 168(1-2):150-158.e10.
Olney NT, Alquezar C, Ramos EMarisa, Nana AL, Fong JC, Karydas AM, Taylor JB, Stephens ML, Argouarch AR, Van Berlo VA et al..  2017.  Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia.. Acta Neuropathol. 134(5):813-816.
Theofilas P, Ehrenberg AJ, Dunlop S, Alho ATDi Loren, Nguy A, Leite RElaine Par, Rodriguez RDiehl, Mejia MB, Suemoto CK, Ferretti-Rebustini REloah De L et al..  2017.  Locus coeruleus volume and cell population changes during Alzheimer's disease progression: A stereological study in human postmortem brains with potential implication for early-stage biomarker discovery.. Alzheimers Dement. 13(3):236-246.
Krabbe G, S Minami S, Etchegaray JI, Taneja P, Djukic B, Davalos D, Le D, Lo I, Zhan L, Reichert MC et al..  2017.  Microglial NFκB-TNFα hyperactivation induces obsessive-compulsive behavior in mouse models of progranulin-deficient frontotemporal dementia.. Proc Natl Acad Sci U S A. 114(19):5029-5034.
Sun G, Guzman E, Balasanyan V, Conner CM, Wong K, Zhou HRobin, Kosik KS, Montell DJ.  2017.  A molecular signature for anastasis, recovery from the brink of apoptotic cell death.. J Cell Biol. 216(10):3355-3368.
Goetzl EJ, Miller BL.  2017.  Multicellular hypothesis for the pathogenesis of Alzheimer's disease.. FASEB J. 31(5):1792-1795.
Pressman PS, Simpson M, Gola K, Shdo SM, Spinelli EG, Miller BL, Gorno-Tempini MLuisa, Rankin K, Levenson RW.  2017.  Observing conversational laughter in frontotemporal dementia.. J Neurol Neurosurg Psychiatry. 88(5):418-424.
Huang AY, Yu D, Davis LK, Sul JHoon, Tsetsos F, Ramensky V, Zelaya I, Ramos EMarisa, Osiecki L, Chen JA et al..  2017.  Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.. Neuron. 94(6):1101-1111.e7.
Wang C, Ward ME, Chen R, Liu K, Tracy TE, Chen X, Xie M, Sohn PDongmin, Ludwig C, Meyer-Franke A et al..  2017.  Scalable Production of iPSC-Derived Human Neurons to Identify Tau-Lowering Compounds by High-Content Screening.. Stem Cell Reports. 9(4):1221-1233.
Watanabe M, Buth JE, Vishlaghi N, de la Torre-Ubieta L, Taxidis J, Khakh BS, Coppola G, Pearson CA, Yamauchi K, Gong D et al..  2017.  Self-Organized Cerebral Organoids with Human-Specific Features Predict Effective Drugs to Combat Zika Virus Infection.. Cell Rep. 21(2):517-532.
Yokoyama JS, Karch CM, Fan CC, Bonham LW, Kouri N, Ross OA, Rademakers R, Kim J, Wang Y, Höglinger GU et al..  2017.  Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.. Acta Neuropathol. 133(5):825-837.
Boehm D, Jeng M, Camus G, Gramatica A, Schwarzer R, Johnson JR, Hull PA, Montano M, Sakane N, Pagans S et al..  2017.  SMYD2-Mediated Histone Methylation Contributes to HIV-1 Latency.. Cell Host Microbe. 21(5):569-579.e6.
Maus M, Cuk M, Patel B, Lian J, Ouimet M, Kaufmann U, Yang J, Horvath R, Hornig-Do H-T, Chrzanowska-Lightowlers ZM et al..  2017.  Store-Operated Ca Entry Controls Induction of Lipolysis and the Transcriptional Reprogramming to Lipid Metabolism.. Cell Metab. 25(3):698-712.
Kruth KA, Fang M, Shelton DN, Abu-Halawa O, Mahling R, Yang H, Weissman JS, Loh ML, Müschen M, Tasian SK et al..  2017.  Suppression of B-cell development genes is key to glucocorticoid efficacy in treatment of acute lymphoblastic leukemia.. Blood. 129(22):3000-3008.
Yokoyama JS, Marx G, Brown JA, Bonham LW, Wang D, Coppola G, Seeley WW, Rosen HJ, Miller BL, Kramer JH et al..  2017.  Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging.. Brain Imaging Behav. 11(2):391-400.
Vitte J, Gao F, Coppola G, Judkins AR, Giovannini M.  2017.  Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development.. Nat Commun. 8(1):300.
Beckerman P, Bi-Karchin J, Park ASeo Deok, Qiu C, Dummer PD, Soomro I, Boustany-Kari CM, Pullen SS, Miner JH, Hu C-AA et al..  2017.  Transgenic expression of human APOL1 risk variants in podocytes induces kidney disease in mice.. Nat Med. 23(4):429-438.
Liu CY, Ohki Y, Tomita T, Osawa S, Reed BR, Jagust W, Van Berlo V, Jin L-W, Chui HC, Coppola G et al..  2017.  Two Novel Mutations in the First Transmembrane Domain of Presenilin1 Cause Young-Onset Alzheimer's Disease.. J Alzheimers Dis. 58(4):1035-1041.