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giovanni's library [774 articles]

最近录入 giovanni's 文献库.
  • Retromer deficiency observed in Alzheimer's disease causes hippocampal dysfunction, neurodegeneration, and Abeta accumulation
    Proceedings of the National Academy of Sciences (14 May 2008), 0802545105.
    by Alim Muhammad, Ingrid Flores, Hong Zhang, Rui Yu, Agnieszka Staniszewski, Emmanuel Planel, Mathieu Herman, Lingling Ho, Robert Kreber, Lawrence S Honig, Barry Ganetzky, Karen Duff, Ottavio Arancio, Scott A Small
    posted to retromer by giovanni on 2008-05-15 16:14:12 as **
  • A map of human protein interactions derived from co-expression of human mRNAs and their orthologs
    Mol Syst Biol, Vol. 4 (15 April 2008)
    by Arun K Ramani, Zhihua Li, Traver G Hart, Mark W Carlson, Daniel R Boutz, Edward M Marcotte
    posted to network by giovanni on 2008-05-06 19:04:09 as ** along with 4 people and 1 group ardalby tmmurali biomcgary phoenixzxl OPIG
  • Mapping the Genetic Architecture of Gene Expression in Human Liver
    PLoS Biology, Vol. 6, No. 5. (1 May 2008), e107.
    by Eric E Schadt, Cliona Molony, Eugene Chudin, Ke Hao, Xia Yang, Pek Y Lum, Andrew Kasarskis, Bin Zhang, Susanna Wang, Christine Suver, Jun Zhu, Joshua Millstein, Solveig Sieberts, John Lamb, Debraj Guhathakurta, Jonathan Derry, John D Storey, Iliana Avila-Campillo, Mark J Kruger, Jason M Johnson, Carol A Rohl, Atila van Nas, Margarete Mehrabian, Thomas A Drake, Aldons J Lusis, Ryan C Smith, Peter F Guengerich, Stephen C Strom, Erin Schuetz, Thomas H Rushmore, Roger Ulrich
    posted to genetics_genomics by giovanni on 2008-05-06 18:50:19 as **
  • Therapeutic potential of resveratrol: the in vivo evidence
    Nature Reviews Drug Discovery, Vol. 5, No. 6. (26 May 2006), pp. 493-506.
    by Joseph A Baur, David A Sinclair
    posted to resveratrol by giovanni on 2008-05-04 17:19:57 as ** along with 3 people askrajiv johncumbers chenlc03
  • The genetics of frontotemporal lobar degeneration
    Current Neurology and Neuroscience Reports, Vol. 7, No. 5. (2007), pp. 434-442.
    by Rosa Rademakers, Mike Hutton
    posted to review ftd by giovanni on 2008-04-27 15:10:03 as **
  • The orphan nuclear receptor, RORalpha , regulates gene expression that controls lipid metabolism: staggerer (sg/sg) mice are resistant to diet induced obesity
    J. Biol. Chem. (25 April 2008), M710526200.
    by Patrick Lau, Rebecca Fitzsimmons, Suryaprakash Raichur, Shu-Ching M Wang, Adriane Lechtken, George E Muscat
    posted to pgc1-alpha by giovanni on 2008-04-26 02:52:54 as **
  • Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia
    Science (27 March 2008), 1155174.
    by Tom Walsh, Jon M Mcclellan, Shane E Mccarthy, Anjene M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abishek Bhandari, Sunday M Stray, Caitlin F Rippey, Patricia Roccanova, Vlad Makarov, B Lakshmi, Robert L Findling, Linmarie Sikich, Thomas Stromberg, Barry Merriman, Nitin Gogtay, Philip Butler, Kristen Eckstrand, Laila Noory, Peter Gochman, Robert Long, Zugen Chen, Sean Davis, Carl Baker, Evan E Eichler, Paul S Meltzer, Stanley F Nelson, Andrew B Singleton, Ming K Lee, Judith L Rapoport, Mary-Claire King, Jonathan Sebat
    posted to schizophrenia copy_number by giovanni on 2008-04-25 14:44:13 as ** along with 7 people and 1 group renatomilani lisa1 djkt sekulerlab GustavoLacerda MWagner applebyb VisionLab
  • Hippocampal expression analyses reveal selective association of immediate-early, neuroenergetic, and myelinogenic pathways with cognitive impairment in aged rats.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 27, No. 12. (21 March 2007), pp. 3098-3110.
    by WB Rowe, EM Blalock, KC Chen, I Kadish, D Wang, JE Barrett, O Thibault, NM Porter, GM Rose, PW Landfield
    posted to aging by giovanni on 2008-04-25 01:49:25 as **
  • Iron-dependent regulation of frataxin expression: implications for treatment of Friedreich ataxia
    Hum. Mol. Genet. (17 April 2008), ddn127.
    by Kuanyu Li, Edward K Besse, Dung Ha, Gennadiy Kovtunovych, Tracey A Rouault
    posted to frda iron by giovanni on 2008-04-20 02:01:42 as **
  • Shared Genetic Causes of Cardiac Hypertrophy in Children and Adults
    N Engl J Med (9 April 2008), NEJMoa075463.
    by Hiroyuki Morita, Heidi L Rehm, Andres Menesses, Barbara Mcdonough, Amy E Roberts, Raju Kucherlapati, Jeffrey A Towbin, JG Seidman, Christine E Seidman
    posted to cardiomyopathy heart by giovanni on 2008-04-10 01:00:40 as **
  • TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
    Lancet neurology (4 April 2008)
    by Vivianna M M Van Deerlin, James B B Leverenz, Lynn M M Bekris, Thomas D D Bird, Wuxing Yuan, Lauren B B Elman, Dana Clay, Elisabeth McCarty M Wood, Alice S S Chen-Plotkin, Maria Martinez-Lage, Ellen Steinbart, Leo McCluskey, Murray Grossman, Manuela Neumann, I-Lin L Wu, Wei-Shiung S Yang, Robert Kalb, Douglas R R Galasko, Thomas J J Montine, John Q Q Trojanowski, Virginia M-Y M Lee, Gerard D D Schellenberg, Chang-En E Yu
    posted to tdp43 by giovanni on 2008-04-09 20:57:19 as **
  • Altered Histone Monoubiquitylation Mediated by Mutant Huntingtin Induces Transcriptional Dysregulation
    J. Neurosci., Vol. 28, No. 15. (9 April 2008), pp. 3947-3957.
    by Mee-Ohk Kim, Prianka Chawla, Ryan P Overland, Eva Xia, Ghazaleh Sadri-Vakili, Jang-Ho J Cha
    posted to huntington by giovanni on 2008-04-09 17:42:17 as **
  • Discovering microRNAs from deep sequencing data using miRDeep
    Nature Biotechnology, Vol. 26, No. 4., pp. 407-415.
    by Marc R Friedländer, Wei Chen, Catherine Adamidi, Jonas Maaskola, Ralf Einspanier, Signe Knespel, Nikolaus Rajewsky
    posted to mirna by giovanni on 2008-04-08 21:23:14 as ** along with 2 people and 1 group stajich tmmurali Berkeley Mycology
  • Gene regulation and DNA damage in the ageing human brain
    Nature, Vol. 429, No. 6994. (24 June 2004), pp. 883-891.
    by Tao Lu, Ying Pan, Shyan-Yuan Kao, Cheng Li, Isaac Kohane, Jennifer Chan, Bruce A Yankner
    posted to aging by giovanni on 2008-04-05 15:33:28 as ** along with 2 people and 1 group tabu jeremymiller GeschwindLab
  • Base-calling of automated sequencer traces using phred. II. Error probabilities.
    Genome Res, Vol. 8, No. 3. (March 1998), pp. 186-194.
    by B Ewing, P Green
    posted to phred by giovanni on 2008-04-03 23:37:16 as ** along with 2 people and 2 groups balajis indigoviolet Bioinformatics EisenLab
  • Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
    Genome Res, Vol. 8, No. 3. (March 1998), pp. 175-185.
    by B Ewing, L Hillier, MC Wendl, P Green
    posted to phred by giovanni on 2008-04-03 23:36:38 as ** along with 1 person and 1 group balajis Bioinformatics
  • Gene expression study on peripheral blood identifies progranulin mutations
    Annals of Neurology (in press)
    by G Coppola, A Karydas, R Rademakers, Q Wang, M Baker, M Hutton, BL Miller, DH Geschwind
    posted to blood progranulin by giovanni on 2008-04-03 23:28:46 as **
  • Genetic Investigation in Frontotemporal Dementia and Alzheimer's Disease: the GIFT Study
    Annals of Neurology, Vol. 62, No. Suppl 11, S52. (2007)
    by G Coppola, B Miller, H Chui, A Varpetian, A Levey, C Cotman, C Decarli, G Bartzokis, W Kukull, T Foroud, D Geschwind
    posted to ftd gift resequencing by giovanni on 2008-04-03 23:26:46 as **
  • TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis.
    Nature genetics (30 March 2008)
    by Edor Kabashi, Paul N N Valdmanis, Patrick Dion, Dan Spiegelman, Brendan J J McConkey, Christine Vande V Velde, Jean-Pierre P Bouchard, Lucette Lacomblez, Ksenia Pochigaeva, Francois Salachas, Pierre-Francois F Pradat, William Camu, Vincent Meininger, Nicolas Dupre, Guy A A Rouleau
    posted to als tdp43 by giovanni on 2008-04-03 23:09:19 as **
  • <I>TDP-43</I> A315T mutation in familial motor neuron disease
    Annals of Neurology, Vol. 9999, No. 9999. (2008), NA.
    by Michael A Gitcho, Robert H Baloh, Sumi Chakraverty, Kevin Mayo, Joanne B Norton, Denise Levitch, Kimmo J Hatanpaa, Charles L White, Eileen H Bigio, Richard Caselli, Matt Baker, Muhammad T Al-Lozi, John C Morris, Alan Pestronk, Rosa Rademakers, Alison M Goate, Nigel J Cairns
    posted to tdp43 by giovanni on 2008-04-03 23:06:29 as ** along with 1 person applebyb
  • Association of GSK3B with Alzheimer's Disease and Frontotemporal Dementia
    Archives of Neurology (in press)
    by B Schaffer, L Bertram, BL Miller, K Mullin, S Weintraub, N Johnson, EH Bigio, M Mesulam, M Wiedau-Pazos, GR Jackson, JL Cummings, RM Cantor, AI Levey, RE Tanzi, DH Geschwind
    posted to alzheimer ftd gsk3b by giovanni on 2008-04-03 22:57:26 as **
  • Presenilin mutations in Alzheimer's disease.
    Human mutation, Vol. 11, No. 3. (1998), pp. 183-190.
    by M Cruts, C Van Broeckhoven
    posted to presenilin by giovanni on 2008-04-03 22:10:05 as **
  • Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation.
    Neurobiol Aging (22 September 2007)
    by Anna Bersano, Roberto Del Bo, Costanza Lamperti, Serena Ghezzi, Gigliola Fagiolari, Francesco Fortunato, Elena Ballabio, Maurizio Moggio, Livia Candelise, Daniela Galimberti, Roberta Virgilio, Silvia Lanfranconi, Yvan Torrente, Marinella Carpo, Nereo Bresolin, Giacomo P P Comi, Stefania Corti
    posted to vcp by giovanni on 2008-04-03 22:07:49 as ** along with 1 person Oyinlola
  • Mutations and polymorphisms in the prion protein gene.
    Human mutation, Vol. 2, No. 3. (1993), pp. 168-173.
    by MS Palmer, J Collinge
    posted to prion by giovanni on 2008-04-03 22:02:23 as **
  • New developments in high-throughput resequencing and variation detection using high density microarrays.
    Human mutation, Vol. 19, No. 4. (April 2002), pp. 402-409.
    by JA Warrington, NA Shah, X Chen, M Janis, C Liu, S Kondapalli, V Reyes, MP Savage, Z Zhang, R Watts, M DeGuzman, A Berno, J Snyder, J Baid
    posted to resequencing by giovanni on 2008-04-03 19:06:59 as **
  • Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip
    European Journal of Human Genetics, Vol. aop, No. current.
    by Marianne Lévêque, Sandrine Marlin, Laurence Jonard, Vincent Procaccio, Pascal Reynier, Patrizia Amati-Bonneau, Sylvain Baulande, Denis Pierron, Didier Lacombe, Françoise Duriez, Christine Francannet, Thierry Mom, Hubert Journel, Hélène Catros, Valérie Drouin-Garraud, Marie-Françoise Obstoy, Hélène Dollfus, Marie-Madeleine Eliot, Laurence Faivre, Christian Duvillard, Remy Couderc, Eréa-Noël Garabedian, Christine Petit, Delphine Feldmann, Françoise Denoyelle
    posted to resequencing by giovanni on 2008-04-03 19:02:22 as **
  • Molecular Characterization of Neisseria meningitidis Isolates Using a Resequencing DNA Microarray.
    The Journal of molecular diagnostics : JMD (27 March 2008)
    by Caroline E E Corless, Edward Kaczmarski, Ray Borrow, Malcolm Guiver
    posted to resequencing by giovanni on 2008-04-03 19:00:59 as **
  • Catechol-o-methyltransferase, cognition, and psychosis: Val158Met and beyond.
    Biological psychiatry, Vol. 60, No. 2. (15 July 2006), pp. 141-151.
    by EM Tunbridge, PJ Harrison, DR Weinberger
    posted to comt ftd by giovanni on 2008-04-03 18:38:15 as **
  • The serotonin transporter gene-linked polymorphism and negative emotionality: placing single gene effects in the context of genetic background and environment.
    Genes, brain, and behavior, Vol. 2, No. 6. (December 2003), pp. 332-335.
    by A Holmes, AR Hariri
    posted to ftd serotonin by giovanni on 2008-04-03 18:37:09 as **
  • Quantifying age-related myelin breakdown with MRI: novel therapeutic targets for preventing cognitive decline and Alzheimer's disease.
    Journal of Alzheimer's disease : JAD, Vol. 6, No. 6 Suppl. (December 2004)
    by G Bartzokis, PH Lu, J Mintz
    posted to alzheimer by giovanni on 2008-04-03 18:20:02 as **
  • Apolipoprotein E genotype and age-related myelin breakdown in healthy individuals: implications for cognitive decline and dementia.
    Archives of general psychiatry, Vol. 63, No. 1. (January 2006), pp. 63-72.
    by G Bartzokis, PH Lu, DH Geschwind, N Edwards, J Mintz, JL Cummings
    posted to alz by giovanni on 2008-04-03 18:17:48 as **
  • Apolipoprotein E affects both myelin breakdown and cognition: implications for age-related trajectories of decline into dementia.
    Biol Psychiatry, Vol. 62, No. 12. (15 December 2007), pp. 1380-1387.
    by G Bartzokis, PH Lu, DH Geschwind, K Tingus, D Huang, MF Mendez, N Edwards, J Mintz
    posted to alzheimer by giovanni on 2008-04-03 18:17:38 as ** along with 1 person applebyb
  • A Century of Alzheimer's Disease
    Science, Vol. 314, No. 5800. (3 November 2006), pp. 777-781.
    by Michel Goedert, Maria G Spillantini
    posted to alzheimer review by giovanni on 2008-04-03 15:55:51 as **
  • Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival
    J. Cell Biol. (31 March 2008), jcb.200712039.
    by Philip Van Damme, Annelies Van Hoecke, Diether Lambrechts, Peter Vanacker, Elke Bogaert, John van Swieten, Peter Carmeliet, Ludo Van Den Bosch, Wim Robberecht
    posted to progranulin by giovanni on 2008-04-01 17:06:13 as ** along with 1 person applebyb
  • Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.
    J Neurol Sci (18 March 2008)
    by Carles Gaig, Mario Ezquerra, Maria José J Martí, Francesc Valldeoriola, Esteban Muñoz, Albert Lladó, Maria Jesús J Rey, Adriana Cardozo, José Luis L Molinuevo, Eduardo Tolosa
    posted to ftd lrrk2 by giovanni on 2008-03-21 20:54:18 as **
  • Cellular and Mitochondrial Remodeling upon Defects in Iron-Sulfur Protein Biogenesis
    J. Biol. Chem., Vol. 283, No. 13. (28 March 2008), pp. 8318-8330.
    by Anja Hausmann, Birgit Samans, Roland Lill, Ulrich Muhlenhoff
    posted to iron iron-sulfur mitochondria by giovanni on 2008-03-21 17:57:12 as **
  • TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
    Science, Vol. 319, No. 5870. (21 March 2008), pp. 1668-1672.
    by Jemeen Sreedharan, Ian P Blair, Vineeta B Tripathi, Xun Hu, Caroline Vance, Boris Rogelj, Steven Ackerley, Jennifer C Durnall, Kelly L Williams, Emanuele Buratti, Francisco Baralle, Jacqueline de Belleroche, Douglas J Mitchell, Nigel P Leigh, Ammar Al-Chalabi, Christopher C Miller, Garth Nicholson, Christopher E Shaw
    posted to als tdp43 by giovanni on 2008-03-21 17:39:07 as ** along with 1 person davidlott
  • Gene expression-based screening identifies microtubule inhibitors as inducers of PGC-1alpha and oxidative phosphorylation
    Proceedings of the National Academy of Sciences (17 March 2008), 0800979105.
    by Zoltan Arany, Bridget K Wagner, Yanhong Ma, Jessica Chinsomboon, Dina Laznik, Bruce M Spiegelman
    posted to pgc1-alpha by giovanni on 2008-03-17 23:10:45 as ** along with 1 person jyuh
  • Proteomic analysis of hearts from frataxin knockout mice: Marked rearrangement of energy metabolism, a response to cellular stress and altered expression of proteins involved in cell structure, motility and metabolism
    PROTEOMICS, Vol. 9999, No. 9999. (2008), NA.
    by Robert Sutak, Xiangcong Xu, Megan Whitnall, Mohammed A Kashem, Daniel Vyoral, Des R Richardson
    posted to frda heart by giovanni on 2008-03-16 00:03:08 as **
  • Parvalbumin gene delivery improves diastolic function in the aged myocardium in vivo.
    Mol Ther, Vol. 10, No. 2. (August 2004), pp. 399-403.
    by DE Michele, ML Szatkowski, FP Albayya, JM Metzger
    posted to heart by giovanni on 2008-03-12 19:21:57 as **
  • Array-Based Gene Discovery with Three Unrelated Subjects Shows SCARB2/LIMP-2 Deficiency Causes Myoclonus Epilepsy and Glomerulosclerosis.
    Am J Hum Genet, Vol. 82, No. 3. (3 March 2008), pp. 673-684.
    by Samuel F F Berkovic, Leanne M M Dibbens, Alicia Oshlack, Jeremy D D Silver, Marina Katerelos, Danya F F Vears, Renate Lüllmann-Rauch, Judith Blanz, Ke Wei W Zhang, Jim Stankovich, Renate M M Kalnins, John P P Dowling, Eva Andermann, Frederick Andermann, Enrico Faldini, Rudi D'Hooge, Lata Vadlamudi, Richard A A Macdonell, Bree L L Hodgson, Marta A A Bayly, Judy Savige, John C C Mulley, Gordon K K Smyth, David A A Power, Paul Saftig, Melanie Bahlo
    posted to mapping snp_ibd by giovanni on 2008-03-07 00:45:09 as **
  • Peroxisome proliferator activator receptor gamma coactivator-1 expression is reduced in obesity: potential pathogenic role of saturated fatty acids and p38 mitogen-activated protein kinase activation.
    J Biol Chem, Vol. 282, No. 21. (25 May 2007), pp. 15439-15450.
    by S Crunkhorn, F Dearie, C Mantzoros, H Gami, WS da Silva, D Espinoza, R Faucette, K Barry, AC Bianco, ME Patti
    posted to pgc1-alpha by giovanni on 2008-03-06 02:18:59 as ** along with 1 person jyuh
  • Aluminum triggers decreased aconitase activity via Fe-S cluster disruption and the overexpression of isocitrate dehydrogenase and isocitrate lyase: a metabolic network mediating cellular survival.
    J Biol Chem, Vol. 280, No. 5. (4 February 2005), pp. 3159-3165.
    by J Middaugh, R Hamel, G Jean-Baptiste, R Beriault, D Chenier, VD Appanna
    posted to aluminum by giovanni on 2008-03-06 02:14:17 as **
  • Aluminum-induced mitochondrial dysfunction leads to lipid accumulation in human hepatocytes: a link to obesity.
    Cell Physiol Biochem, Vol. 20, No. 5. (2007), pp. 627-638.
    by R Mailloux, J Lemire, V Appanna
    posted to lipogenesis mitochondria ox_stress by giovanni on 2008-03-05 20:45:34 as **
  • Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humans.
    Diabetes, Vol. 49, No. 9. (September 2000), pp. 1604-1607.
    by J Hebinck, C Hardt, L Schöls, M Vorgerd, L Briedigkeit, CR Kahn, M Ristow
    posted to diabetes frda insulin_r by giovanni on 2008-03-05 20:16:29 as **
  • An association between NIDDM and a GAA trinucleotide repeat polymorphism in the X25/frataxin (Friedreich's ataxia) gene.
    Diabetes, Vol. 47, No. 5. (May 1998), pp. 851-854.
    by M Ristow, E Giannakidou, J Hebinck, K Busch, M Vorgerd, J Kotzka, B Knebel, J Mueller-Berghaus, C Epplen, A Pfeiffer, CR Kahn, A Doria, W Krone, D Mueller-Wieland
    posted to diabetes frda by giovanni on 2008-03-05 19:55:46 as **
  • No association between the Friedreich's ataxia gene and NIDDM in the French population.
    Diabetes, Vol. 47, No. 10. (October 1998), pp. 1654-1656.
    by S Dupont, D Dubois, N Vionnet, C Boitard, S Caillat-Zucman, J Timsit, P Froguel
    posted to diabetes frda by giovanni on 2008-03-05 19:52:49 as **
  • Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia.
    Neurobiol Aging (29 February 2008)
    by Livia Bernardi, Carmine Tomaino, Maria Anfossi, Maura Gallo, Silvana Geracitano, Angela Costanzo, Rosanna Colao, Gianfranco Puccio, Francesca Frangipane, Sabrina A M A Curcio, Maria Mirabelli, Nicoletta Smirne, David Iapaolo, Raffaele Giovanni G Maletta, Amalia C C Bruni
    posted to presenilin progranulin by giovanni on 2008-03-04 21:01:47 as ** along with 1 person applebyb
  • Disturbance of nuclear and cytoplasmic Tar DNA binding protein (TDP-43) induces disease-like redistribution, sequestration and aggregate formation.
    J Biol Chem (27 February 2008)
    by Matthew J J Winton, Lionel M M Igaz, Margaret M M Wong, Linda K K Kwong, John Q Q Trojanowski, Virginia M-Y M Lee
    posted to tdp43 by giovanni on 2008-02-29 20:57:07 as **
  • Myopathy with lactic acidosis is linked to chromosome 12q23.3-24.11 and caused by an intron mutation in the ISCU gene resulting in a splicing defect
    Hum. Mol. Genet. (23 February 2008), ddn057.
    by Angelica Olsson, Lisbet Lind, Lars-Eric Thornell, Monica Holmberg
    posted to isu by giovanni on 2008-02-23 15:22:46 as **
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