applebyb's genetics [90 articles] Export

Recent papers added to applebyb's library classified by the tag genetics. You can also see everyone's genetics.

	Influence of the Pro12Ala polymorphism of PPAR-gamma on age at onset and sRAGE levels in Alzheimer's disease. [My Copy] Brain research, Vol. 1291 (29 September 2009), pp. 133-139. by Lifen Yao, Keshen Li, Liming Zhang, Songpo Yao, Zhongyuan Piao, Lin Song posted to srage ppar-gamma polymorphism genetics biomarkers alzheimers_disease age by applebyb on 2009-11-06 12:48:07 as
	The heritability and genetics of frontotemporal lobar degeneration. [My Copy] Neurology, Vol. 73, No. 18. (3 November 2009), pp. 1451-1456. by J. D. Rohrer, R. Guerreiro, J. Vandrovcova, et al.J. Uphill, D. Reiman, J. Beck, A. M. Isaacs, A. Authier, R. Ferrari, N. C. Fox, I. R. Mackenzie, J. D. Warren, R. de Silva, J. Holton, T. Revesz, J. Hardy, S. Mead, M. N. Rossor posted to tau pgrn mapt genetics frontotemporal_lobar_degeneration frontotemporal_dementia by applebyb on 2009-11-04 22:52:28 as along with 2 people daforerog giovanni
	Prion-induced Activation of Cholesterogenic Gene Expression by Srebp2 in Neuronal Cells [My Copy] Journal of Biological Chemistry, Vol. 284, No. 45. (6 November 2009), pp. 31260-31269. by Christian Bach, Sabine Gilch, Romina Rost, et al.Alex D. Greenwood, Marion Horsch, Glaucia N. M. Hajj, Susanne Brodesser, Axel Facius, Sandra SchÃ¤dler, Konrad Sandhoff, Johannes Beckers, Christine Leib-MÃ¶sch, Hermann M. SchÃ¤tzl, Ina Vorberg posted to prion neurons genetics genes cholesterol_synthesis cholesterol_biosynthesis cholesterol by applebyb on 2009-11-01 11:06:39 as
	Spontaneous Generation of Prion Infectivity in Fatal Familial Insomnia Knockin Mice [My Copy] Vol. 63, No. 4. (27 August 2009), pp. 438-450. by Walker S. Jackson, Andrew W. Borkowski, Henryk Faas, et al.Andrew D. Steele, Oliver D. King, Nicki Watson, Alan Jasanoff, Susan Lindquist posted to genetics ffi by applebyb on 2009-08-28 12:25:32 as
	MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels. [My Copy] Journal of Alzheimer's disease : JAD, Vol. 17, No. 1. (May 2009), pp. 125-133. by Daniela Galimberti, Eliana Venturelli, Chiara Villa, et al.Chiara Fenoglio, Francesca Clerici, Alessandra Marcone, Luisa Benussi, Francesca Cortini, Diego Scalabrini, Luca Perini, Ilaria Restelli, Giuliano Binetti, Stefano Cappa, Claudio Mariani, Nereo Bresolin, Elio Scarpini posted to risk pathogenesis genetics ftd by applebyb on 2009-08-14 13:07:15 as
	How young people find out about their family history of Huntington's disease. [My Copy] Social science & medicine (1982), Vol. 68, No. 10. (May 2009), pp. 1892-1900. by Karen Forrest Keenan, Edwin van Teijlingen, Lorna McKee, Zosia Miedzybrodzka, Sheila A. Simpson posted to yod genetics by applebyb on 2009-08-14 13:00:41 as
	Stress: a dilemma concerning healthy CJD mutation carriers. [My Copy] The Israel Medical Association journal : IMAJ, Vol. 11, No. 3. (March 2009) by A. Gigi posted to cjd gcjd genetics risk by applebyb on 2009-07-17 22:59:59 as
	The consequences of pathogenic mutations to the human prion protein [My Copy] Protein Engineering, Design and Selection, Vol. 22, No. 8. (1 August 2009), pp. 461-468. by Marc W. van der Kamp, Valerie Daggett posted to genetics pathogenesis prion by applebyb on 2009-07-17 01:59:46 as along with 1 person carlosjavierna
	Amyloids Go Genomic: Insights Regarding the Sequence Determinants of Prion Formation from Genome-Wide Studies. [My Copy] Chembiochem : a European journal of chemical biology (13 July 2009) by Hilal A. Lashuel, Rohit V. Pappu posted to genetics prion by applebyb on 2009-07-16 01:20:19 as
	Creutzfeldt-Jakob disease with E200K PRNP mutation: a case report and revision of the literature. [My Copy] Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology (14 July 2009) by Michelangelo Mancuso, Gabriele Siciliano, Sabina Capellari, et al.Daniele Orsucci, Policarpo Moretti, Giuseppe D. Fede, Silvia Suardi, Rosaria Strammiello, Piero Parchi, Fabrizio Tagliavini, Luigi Murri posted to cjd genetics phenotype by applebyb on 2009-07-16 01:19:32 as
	Phosphorylation of Prion Protein at Serine 43 Induces Prion Protein Conformational Change [My Copy] J. Neurosci., Vol. 29, No. 27. (8 July 2009), pp. 8743-8751. by Paresa N. Giannopoulos, Catherine Robertson, Julie Jodoin, Hemant Paudel, Stephanie A. Booth, Andrea C. Leblanc posted to genetics pathogenesis prion by applebyb on 2009-07-09 17:49:04 as
	Genetic screen identifies serpin5 as a regulator of the toll pathway and CHMP2B toxicity associated with frontotemporal dementia. [My Copy] Proceedings of the National Academy of Sciences of the United States of America (6 July 2009) by S. Tariq Ahmad, Sean T. Sweeney, Jin-A A. Lee, Neal T. Sweeney, Fen-Biao B. Gao posted to ftd genetics by applebyb on 2009-07-09 17:42:52 as
	Cathepsin D (C224T) Polymorphism in Sporadic and Genetic Creutzfeldt-Jakob Disease. [My Copy] Alzheimer disease and associated disorders (30 June 2009) by Gabor G. Kovacs, Pascual Sanchez-Juan, Thomas Ströbel, et al.Maaike Schuur, Anna Poleggi, Sara Nocentini, Claudia Giannattasio, Girma Belay, Matthew Bishop, Sabina Capellari, Piero Parchi, Ellen Gelpi, Aniko Gal, Agnes Bakos, Maria J. Molnar, Uta Heinemann, Inga Zerr, Richard S. Knight, Eva Mitrova, Cornelia van Duijn, Herbert Budka posted to cjd genetics phenotype polymorphism by applebyb on 2009-07-05 15:59:35 as
	A Case of Dementia With PRNP D178Ncis-129M and No Insomnia. [My Copy] Alzheimer disease and associated disorders (30 June 2009) by Rita J. Guerreiro, Tina Vaskov, Cynthia Crews, Andrew Singleton, John Hardy posted to ffi genetics phenotype by applebyb on 2009-07-05 15:55:21 as
	Genomic and post-genomic analyses of human prion diseases. [My Copy] Genome medicine, Vol. 1, No. 6. (22 June 2009) by Maurizio Pocchiari, Anna Poleggi, Serena Principe, Silvia Graziano, Franco Cardone posted to cjd genetics by applebyb on 2009-07-05 15:46:24 as
	Increased frequency of positive family history of dementia in sporadic CJD [My Copy] Neurobiology of Aging, Vol. 30, No. 4. (April 2009), pp. 615-621. by Anna Krasnianski, Nicolas von Ahsen, Uta Heinemann, et al.Bettina Meissner, Walter J. Schulz-Schaeffer, Hans A. Kretzschmar, Victor W. Armstrong, Inga Zerr posted to cjd genetics risk scjd by applebyb on 2009-06-26 11:59:31 as
	Attitudes and knowledge about genetic testing before and after finding the disease-causing mutation among individuals at high risk for familial, early-onset Alzheimer's disease. [My Copy] Genetic testing and molecular biomarkers, Vol. 13, No. 1. (February 2009), pp. 121-125. by B. Marcheco-Teruel, E. Fuentes-Smith posted to ad genetics yod by applebyb on 2009-06-19 12:21:08 as
	Global distribution of fatal familial insomnia: founder or recurrent mutations. [My Copy] Neurogenetics, Vol. 9, No. 4. (October 2008) by H. S. Lee, L. G. Goldfarb posted to ffi genetics by applebyb on 2009-06-19 12:20:29 as
	p53-Dependent transcriptional control of cellular prion by presenilins. [My Copy] The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 29, No. 20. (20 May 2009), pp. 6752-6760. by B. Vincent, C. Sunyach, H. D. Orzechowski, P. St George-Hyslop, F. Checler posted to alzheimers_disease biology genetics prion by applebyb on 2009-05-25 21:31:20 as
	Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN [My Copy] Neurology, Vol. 72, No. 9. (3 March 2009), pp. 813-820. by J. L. Whitwell, C. R. Jack, B. F. Boeve, et al.M. L. Senjem, M. Baker, R. Rademakers, R. J. Ivnik, D. S. Knopman, Z. K. Wszolek, R. C. Petersen, K. A. Josephs posted to ftld genetics mapt mri neuroimaging pgrn by applebyb on 2009-03-04 00:44:45 as
	Presymptomatic Signs in Healthy CJD Mutation Carriers [My Copy] posted to cjd gcjd genetics phenotype presentation by applebyb on 2009-01-28 21:11:56 as
	Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members. [My Copy] Brain : a journal of neurology (21 January 2009) by Nicole Finch, Matt Baker, Richard Crook, et al.Katie Swanson, Karen Kuntz, Rebecca Surtees, Gina Bisceglio, Anne Rovelet-Lecrux, Bradley Boeve, Ronald C C. Petersen, Dennis W W. Dickson, Steven G G. Younkin, Vincent Deramecourt, Julia Crook, Neill R R. Graff-Radford, Rosa Rademakers posted to diagnosis ftld genetics pgrn by applebyb on 2009-01-25 18:39:35 as
	MRI and clinical syndrome in dura materrelated Creutzfeldt-Jakob disease. [My Copy] Journal of neurology (23 January 2009) by B Meissner, K Kallenberg, P Sanchez-Juan, et al.S Ramljak, A Krasnianski, U Heinemann, S Eigenbrod, E Gelpi, B Barsic, H A. Kretzschmar, W J. Schulz-Schaeffer, M Knauth, I Zerr posted to cjd codon129 genetics icjd mri neuroimaging prion by applebyb on 2009-01-25 18:36:42 as
	'Agrypnia excitata' in a case of sporadic Creutzfeldt-Jakob disease VV2 [My Copy] J Neurol Neurosurg Psychiatry, Vol. 80, No. 2. (1 February 2009), pp. 244-246. by C. La Morgia, P. Parchi, S. Capellari, et al.R. Lodi, C. Tonon, R. Rinaldi, S. Mondini, F. Cirignotta posted to genetics phenotype prion scjd by applebyb on 2009-01-17 01:10:48 as
	Novel exon 1 progranulin gene variant in Alzheimers disease [My Copy] European Journal of Neurology, Vol. 15, No. 10. (October 2008), pp. 1111-1117. by Cortini, F., Fenoglio, et al. C., Guidi, I., Venturelli, E., Pomati, S., Marcone, A., Scalabrini, D., Villa, C., Clerici, F., Dalla Valle, E., Mariani, C., Cappa, S., Bresolin, N., Scarpini, E., Galimberti, D. posted to alzheimers_disease ftld genetics pgrn by applebyb on 2009-01-09 15:37:10 as
	A Patient With Creutzfeldt-Jakob Disease With an Insertion of 7 Octa-Repeats in the PRNP Gene: Molecular Characteristics and Clinical Features. [My Copy] The American journal of the medical sciences, Vol. 336, No. 6. (December 2008), pp. 519-523. by Yan-Jun J. Guo, Xiao-Fan F. Wang, Jun Han, et al.Bao-Yun Y. Zhang, Wei-Qin Q. Zhao, Qi Shi, Yan-Zhen Z. Wan, Chen Gao, Ji-Mei M. Li, DE-Xin X. Wang, Xiao-Ping P. Dong posted to cjd genetics phenotype prion prnp by applebyb on 2009-01-02 14:39:13 as
	Role of MAPT mutations and haplotype in frontotemporal lobar degeneration in Northern Finland [My Copy] BMC Neurology, Vol. 8 (17 December 2008), 48. by Anna-Lotta, Anne M. Remes posted to ftld genetics mapt tau by applebyb on 2009-01-02 14:37:25 as
	Phenotypic heterogeneity and genetic modifiers in prion disease caused by a Pro102Leu mutation in the PRNP gene. [My Copy] Nature clinical practice. Neurology (17 December 2008) by Manuela Neumann posted to gcjd genetics phenotype prion prnp by applebyb on 2009-01-02 14:36:48 as
	Early-Onset Familial Lewy Body Dementia With Extensive Tauopathy: A Clinical, Genetic, and Neuropathological Study. [My Copy] Journal of neuropathology and experimental neurology (19 December 2008) by Jordi Clarimón, Laura Molina-Porcel, Teresa Gómez-Isla, et al.Rafael Blesa, Cristina Guardia-Laguarta, Anna González-Neira, Montserrat Estorch, Josep M Grau, Lluís Barraquer, Carles Roig, Isidre Ferrer, Alberto Lleó posted to genetics lbd neuropathology symptoms tau yod by applebyb on 2009-01-02 14:34:38 as
	Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide. [My Copy] Neurobiology of disease (6 December 2008) by Luisa Benussi, Roberta Ghidoni, Eleonora Pegoiani, Davide V V. Moretti, Orazio Zanetti, Giuliano Binetti posted to cbd ftld genetics pgrn by applebyb on 2008-12-25 00:43:55 as
	A novel presenilin 1 mutation (V261L) associated with presenile Alzheimers disease and spastic paraparesis [My Copy] European Journal of Neurology, Vol. 15, No. 9. (September 2008), pp. 991-994. by Jimenez Caballero, P. E., De D. Boguna, et al. C., Martin Correa, E., Servia Candela, M., Marsal Alonso, C. posted to ad genetics phenotype ps-1 by applebyb on 2008-12-25 00:41:32 as
	The role of stress and anxiety in the onset of familial Creutzfeldt-Jakob Disease (CJD): Review. [My Copy] Stress (Amsterdam, Netherlands) (2 December 2008) by Ariela Gigi posted to gcjd genetics prion risk by applebyb on 2008-12-06 11:16:08 as
	Atypical frontotemporal dementia as a new clinical phenotype of Gerstmann-Straussler-Scheinker disease with the PrP-P102L mutation. Description of a previously unreported Italian family [My Copy] Neurological Sciences by Anna Giovagnoli, Giuseppe Di Fede, Anna Aresi, Fabiola Reati, Giacomina Rossi, Fabrizio Tagliavini posted to ftd genetics gss phenotype prion by applebyb on 2008-11-27 14:59:46 as
	Impact of apolipoprotein E (ApoE) polymorphism on brain ApoE levels. [My Copy] The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 28, No. 45. (5 November 2008), pp. 11445-11453. by D. R. Riddell, H. Zhou, K. Atchison, et al.H. K. Warwick, P. J. Atkinson, J. Jefferson, L. Xu, S. Aschmies, Y. Kirksey, Y. Hu, E. Wagner, A. Parratt, J. Xu, Z. Li, M. M. Zaleska, J. S. Jacobsen, M. N. Pangalos, P. H. Reinhart posted to ad amyloid apoe genetics polymorphism by applebyb on 2008-11-23 15:57:42 as along with 1 person daforerog
	Comparing test-specific distress of susceptibility versus deterministic genetic testing for Alzheimer's disease [My Copy] Alzheimer's and Dementia, Vol. 4, No. 6. (November 2008), pp. 406-413. by M. Cassidy, J. Roberts, T. Bird, et al.E. Steinbart, L. Cupples, C. Chen, E. Linnenbringer, R. Green posted to ad apoe app gad genetics ps-1 ps-2 by applebyb on 2008-11-22 20:03:52 as
	Familial Creutzfeldt-Jakob disease presenting as epilepsia partialis continua. [My Copy] Epileptic disorders : international epilepsy journal with videotape, Vol. 10, No. 4. (18 November 2008), pp. 271-275. by Max R R. Lowden, Kevin Scott, Milind J J. Kothari posted to cjd diagnosis gcjd genetics phenotype prion_disease by applebyb on 2008-11-21 14:45:47 as
	A novel insertional mutation in the prion protein gene: clinical and bio-molecular findings. [My Copy] Journal of neurology, neurosurgery, and psychiatry, Vol. 79, No. 12. (December 2008), pp. 1395-1398. by C. Mauro, G. Giaccone, G. Piscosquito, et al.A. Lavorgna, M. Nigro, G. Di Fede, A. Leonardi, C. Coppola, S. Formisano, F. Tagliavini, R. Cotrufo, G. Puoti posted to genetics prion_disease prnp by applebyb on 2008-11-21 14:38:55 as
	Association between HFE 187 C>G (H63D) mutation and early-onset familial Alzheimer's disease PSEN-1 839A>C (E280A) mutation. [My Copy] Annals of hematology, Vol. 87, No. 8. (August 2008), pp. 671-673. by I. C. Avila-Gomez, M. Jiménez-Del-Rio, F. Lopera-Restrepo, C. Velez-Pardo posted to ad genetics ps-1 yod by applebyb on 2008-11-21 14:19:33 as
	Presenilin 1 Polymorphism Associated with Alzheimer’s Disease in Apolipoprotein E4Carriers [My Copy] posted to ad apoe genetics polymorphism ps1 risk by applebyb on 2008-10-29 00:03:44 as
	A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation [My Copy] Neurology, Vol. 71, No. 18. (28 October 2008), pp. 1431-1438. by E. Tunnell, R. Wollman, S. Mallik, C. J. Cortes, S. J. Dearmond, J. A. Mastrianni posted to genetics gss prion prpsc by applebyb on 2008-10-28 00:37:31 as
	Immune-Directed Gene Therapeutic Development for Alzheimer's, Prion, and Parkinson's Diseases. [My Copy] Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology (18 October 2008) by Kathleen A. Maguire-Zeiss, Howard J. Federoff posted to ad genetics pd prion therapy by applebyb on 2008-10-25 01:30:34 as
	Review. The neuropathology of kuru and variant Creutzfeldt-Jakob disease. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3685-3687. by C. A. McLean posted to cjd codon129 genetics incubation kuru phenotype prion vcjd by applebyb on 2008-10-20 00:07:40 as
	A clinical study of kuru patients with long incubation periods at the end of the epidemic in Papua New Guinea. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3725-3739. by J. Collinge, J. Whitfield, E. McKintosh, et al.A. Frosh, S. Mead, A. F. Hill, S. Brandner, D. Thomas, M. P. Alpers posted to age genetics incubation kuru phenotype prion risk by applebyb on 2008-10-20 00:01:37 as
	Genetic susceptibility, evolution and the kuru epidemic. [My Copy] Philosophical transactions of the Royal Society of London. Series B, Biological sciences, Vol. 363, No. 1510. (27 November 2008), pp. 3741-3746. by S. Mead, J. Whitfield, M. Poulter, et al.P. Shah, J. Uphill, J. Beck, T. Campbell, H. Al-Dujaily, H. Hummerich, M. P. Alpers, J. Collinge posted to anthropology codon129 genetics kuru prion risk by applebyb on 2008-10-19 23:59:39 as
	Gene expression changes in the course of normal brain aging are sexually dimorphic [My Copy] Proceedings of the National Academy of Sciences, Vol. 105, No. 40. (7 October 2008), pp. 15605-15610. by Nicole C. Berchtold, David H. Cribbs, Paul D. Coleman, et al.Joseph Rogers, Elizabeth Head, Ronald Kim, Tom Beach, Carol Miller, Juan Troncoso, John Q. Trojanowski, Ronald H. Zielke, Carl W. Cotman posted to age genetics neurodegeneration by applebyb on 2008-10-15 02:02:23 as along with 1 person psique
	Arch Neurol -- Download Directly to Citation Manager [My Copy] posted to ad dementia ftld genetics gsk-3 neurodegeneration tau by applebyb on 2008-10-15 01:39:35 as
	Apolipoprotein E Polymorphism and Brain Morphology in Mild Cognitive Impairment [My Copy] posted to apoe cognition genetics by applebyb on 2008-10-13 00:03:43 as
	Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease. [My Copy] Neurology (18 June 2008) by N Brouwers, K Sleegers, S Engelborghs, et al.S Maurer-Stroh, I Gijselinck, J van der Zee, B A A. Pickut, M Van den Broeck, M Mattheijssens, K Peeters, J Schymkowitz, F Rousseau, J-J J. Martin, M Cruts, P P P. De Deyn, C Van Broeckhoven posted to ad genetics prgn risk by applebyb on 2008-10-03 14:39:28 as along with 1 person giovanni
	Update on recent molecular and genetic advances in frontotemporal lobar degeneration. [My Copy] Journal of neuropathology and experimental neurology, Vol. 67, No. 7. (July 2008), pp. 635-648. by E. H. Bigio posted to ftld genetics review by applebyb on 2008-09-26 01:13:11 as
	The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles. [My Copy] Biological psychiatry, Vol. 41, No. 2. (15 January 1997), pp. 191-195. by D. Tsuang, M. A. Raskind, J. Leverenz, E. R. Peskind, G. Schellenberg, T. D. Bird posted to genetics sd-ftd tau by applebyb on 2008-09-13 02:16:32 as

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prion	267
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hemineglect	1
hgh	1
hiv	1
hpa	1
hsp	1
hypersexuality	1
hypothesis	1
iatrogenic	1
impulse	1
infection	1
inflammation	1
initial_treatment	1
intelligence	1
jakob	1
korsakoff	1
kufs_disease	1
lactoferrin	1
leukoencephalopathy	1
limibic_encephalitis	1
lipid	1
lipid_rafts	1
liposomes	1
logopenia	1
lymphoreticular	1
major_depression	1
major_depressive_disorder	1
management	1
manganese	1
medication_regimens	1
medication_trials	1
medicine	1
mentoring	1
metadata	1
metal	1
mice	1
misdiagnosis	1
misfolding	1
mixed_dementia	1
mm1	1
mmse	1
mood	1
motor_neuron_disease	1
mrna	1
msa	1
muscle	1
network_structure	1
neural_circuits	1
neuroanatomy	1
neuroimagin	1
neurology	1
neurons	1
neuropath	1
neuroradiology	1
neurostimulation	1
neurotoxicity	1
nms	1
npi	1
nucleation	1
nucleic_acid	1
nucleus_accumbens	1
onset	1
oppenheimer_brownell	1
p102l	1
palliative_care	1
paraneoplastic_syndrome	1
parity	1
parkinsonism	1
peptides	1
ph	1
pharmacology	1
physiology	1
pib	1
plaques	1
plasminogen	1
polymorphisms	1
posterior_cortical_atrophy	1
ppar-gamma	1
preclinical	1
pregnancy	1
presenilin	1
prevalence	1
primary	1
progressive_supranuclear_palsy	1
prusiner	1
ps2	1
ps-2	1
pseudodementia	1
psychiatriy	1
psychosocial	1
psychotherapy	1
psychotropics	1
ptau	1
public_health	1
randomized_trials	1
rapidly_progressive_dementia	1
redox	1
remission_rates	1
right	1
role	1
rpd	1
rtms	1
sd-ftd	1
sd-nft	1
serotonin	1
simvastatin	1
snps	1
sod-1	1
sporadic	1
sporadic_fatal_insomnia	1
srage	1
stard	1
statistics	1
stem_cells	1
steroids	1
stimulant	1
stimulants	1
stimulation	1
strains	1
stroke	1
suicidal_ideation	1
surveillance	1
synapse	1
tardive_dyskinesia	1
tbi	1
telomeres	1
thalamus	1
theory	1
therapeutic_response	1
tissue	1
transient_global_amnesia	1
traumatic_brain_injury	1
trea	1
treamtent	1
treatment_alternatives	1
treatment_outcome	1
trisomy_21	1
ttau	1
ubiquitination	1
ultrasound	1
vad	1
variant	1
verbal_fluency	1
vpa	1
vv1	1
weight	1
wernicke_encephalopathy	1
wilsons_disease	1

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