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mgaldzics library [70 articles]

Neue Artikel in mgaldzics Bibliothek.
  • Assessing the validity of blood-based gene expression profiles for the classification of schizophrenia and bipolar disorder: a preliminary report.
    Am J Med Genet B Neuropsychiatr Genet, Vol. 133, No. 1. (5 February 2005), pp. 1-5.
    by MT Tsuang, N Nossova, T Yager, MM Tsuang, SC Guo, KG Shyu, SJ Glatt, CC Liew
    posted to blood brain expression by mgaldzic on 2007-05-22 19:52:36 as ** along with 1 group CHIP
  • Evaluating the comparability of gene expression in blood and brain.
    Am J Med Genet B Neuropsychiatr Genet, Vol. 141, No. 3. (5 April 2006), pp. 261-268.
    by PF Sullivan, C Fan, CM Perou
  • Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome.
    Ann Neurol, Vol. 56, No. 6. (December 2004), pp. 808-814.
    by Y Tang, MB Schapiro, DN Franz, BJ Patterson, FJ Hickey, EK Schorry, RJ Hopkin, M Wylie, T Narayan, TA Glauser, DL Gilbert, AD Hershey, FR Sharp
  • Universal Reference RNA as a standard for microarray experiments.
    BMC Genomics, Vol. 5, No. 1. (9 March 2004)
  • High throughput analysis of gene expression in the human brain.
    J Neurosci Res, Vol. 59, No. 1. (1 January 2000), pp. 1-10.
  • Gene expression profiling in postmortem Rett Syndrome brain: differential gene expression and patient classification.
    Neurobiol Dis, Vol. 8, No. 5. (October 2001), pp. 847-865.
  • Genetic inheritance of gene expression in human cell lines.
    Am J Hum Genet, Vol. 75, No. 6. (December 2004), pp. 1094-1105.
  • Computational inference of neural information flow networks.
    PLoS Comput Biol, Vol. 2, No. 11. (24 November 2006)
    by VA Smith, J Yu, TV Smulders, AJ Hartemink, ED Jarvis
  • Ancient and Recent Positive Selection Transformed Opioid cis-Regulation in Humans.
    PLoS Biol, Vol. 3, No. 12. (15 November 2005)
    by Matthew V V Rockman, Matthew W W Hahn, Nicole Soranzo, Fritz Zimprich, David B B Goldstein, Gregory A A Wray
  • Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome.
    Nat Genet (4 February 2007)
    by Nathaniel D D Heintzman, Rhona K K Stuart, Gary Hon, Yutao Fu, Christina W W Ching, R David D Hawkins, Leah O O Barrera, Sara Van Calcar, Chunxu Qu, Keith A A Ching, Wei Wang, Zhiping Weng, Roland D D Green, Gregory E E Crawford, Bing Ren
  • An integrated genomic-based approach to individualized treatment of patients with advanced-stage ovarian cancer.
    J Clin Oncol, Vol. 25, No. 5. (10 February 2007), pp. 517-525.
    by HK Dressman, A Berchuck, G Chan, J Zhai, A Bild, R Sayer, J Cragun, J Clarke, RS Whitaker, L Li, J Gray, J Marks, GS Ginsburg, A Potti, M West, JR Nevins, JM Lancaster
  • Genomic signatures to guide the use of chemotherapeutics.
    Nat Med (22 October 2006)
    by Anil Potti, Holly K K Dressman, Andrea Bild, Richard F F Riedel, Gina Chan, Robyn Sayer, Janiel Cragun, Hope Cottrill, Michael J J Kelley, Rebecca Petersen, David Harpole, Jeffrey Marks, Andrew Berchuck, Geoffrey S S Ginsburg, Phillip Febbo, Johnathan Lancaster, Joseph R R Nevins
  • Genomic sweeping for hypermethylated genes
    Bioinformatics, Vol. 23, No. 3. (1 February 2007), pp. 281-288.
    by Liang Goh, Susan K Murphy, Sayan Muhkerjee, Terrence S Furey
  • Integration of New Neurons into Functional Neural Networks.
    J Neurosci, Vol. 26, No. 47. (22 November 2006), pp. 12237-12241.
    by Victor Ramirez-Amaya, Diano F F Marrone, Fred H H Gage, Paul F F Worley, Carol A A Barnes
  • The role of stem cells in Parkinson's disease.
    Neurosurg Clin N Am, Vol. 18, No. 1. (January 2007), pp. 129-142.
    by A Gupta, TM Dawson
    posted to stem parkinson cells by mgaldzic on 2007-02-05 22:19:06 as ** along with 1 group CHIP
  • Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
    Clin Genet, Vol. 57, No. 2. (February 2000), pp. 103-109.
    by C Prasad, AN Prasad, BN Chodirker, C Lee, AK Dawson, LJ Jocelyn, AE Chudley
  • Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.
    Pediatrics, Vol. 114, No. 2. (August 2004), pp. 451-457.
    by MA Manning, SB Cassidy, C Clericuzio, AM Cherry, S Schwartz, L Hudgins, GM Enns, HE Hoyme
    posted to speech language deletion autism 22q by mgaldzic on 2007-02-02 06:01:35 as ** along with 1 group CHIP
  • A case of autism with an interstitial deletion on 4q leading to hemizygosity for genes encoding for glutamine and glycine neurotransmitter receptor sub-units (AMPA 2, GLRA3, GLRB) and neuropeptide receptors NPY1R, NPY5R.
    BMC Med Genet, Vol. 5 (16 April 2004)
  • Social timing, clock genes and autism: a new hypothesis.
    J Intellect Disabil Res, Vol. 46, No. Pt 4. (May 2002), pp. 352-358.
    by D Wimpory, B Nicholas, S Nash
    posted to timing social hypothesis clock autism by mgaldzic on 2007-02-02 05:55:58 as ** along with 1 group CHIP
  • Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.
    Am J Hum Genet, Vol. 77, No. 3. (September 2005), pp. 377-388.
    by DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, MD Ritchie, GR Delong, RK Abramson, HH Wright, ML Cuccaro, JP Hussman, JR Gilbert, MA Pericak-Vance
    posted to receptor gene gaba autism association by mgaldzic on 2007-02-02 05:54:54 as ** along with 1 group CHIP
  • Association of Per1 and Npas2 with autistic disorder: support for the clock genes/social timing hypothesis
    Molecular Psychiatry, Vol. aop, No. current.
    by B Nicholas, V Rudrasingham, S Nash, G Kirov, MJ Owen, DC Wimpory,
  • Genome-wide atlas of gene expression in the adult mouse brain
    Nature
    by Ed S Lein, Michael J Hawrylycz, Nancy Ao, Mikael Ayres, Amy Bensinger, Amy Bernard, Andrew F Boe, Mark S Boguski, Kevin S Brockway, Emi J Byrnes, Lin Chen, Li Chen, Tsuey-Ming Chen, Mei C Chin, Jimmy Chong, Brian E Crook, Aneta Czaplinska, Chinh N Dang, Suvro Datta, Nick R Dee, Aimee L Desaki, Tsega Desta, Ellen Diep, Tim A Dolbeare, Matthew J Donelan, Hong-Wei Dong, Jennifer G Dougherty, Ben J Duncan, Amanda J Ebbert, Gregor Eichele, Lili K Estin, Casey Faber, Benjamin A Facer, Rick Fields, Shanna R Fischer, Tim P Fliss, Cliff Frensley, Sabrina N Gates, Katie J Glattfelder, Kevin R Halverson, Matthew R Hart, John G Hohmann, Maureen P Howell, Darren P Jeung, Rebecca A Johnson, Patrick T Karr, Reena Kawal, Jolene M Kidney, Rachel H Knapik, Chihchau L Kuan, James H Lake, Annabel R Laramee, Kirk D Larsen, Christopher Lau, Tracy A Lemon, Agnes J Liang, Ying Liu, Lon T Luong, Jesse Michaels, Judith J Morgan, Rebecca J Morgan, Marty T Mortrud, Nerick F Mosqueda, Lydia L Ng, Randy Ng, Geralyn J Orta, Caroline C Overly, Tu H Pak, Sheana E Parry, Sayan D Pathak, Owen C Pearson, Ralph B Puchalski, Zackery L Riley, Hannah R Rockett, Stephen A Rowland, Joshua J Royall, Marcos J Ruiz, Nadia R Sarno, Katherine Schaffnit, Nadiya V Shapovalova, Taz Sivisay, Clifford R Slaughterbeck, Simon C Smith, Kimberly A Smith, Bryan I Smith, Andy J Sodt, Nick N Stewart, Kenda-Ruth Stumpf, Susan M Sunkin, Madhavi Sutram, Angelene Tam, Carey D Teemer, Christina Thaller, Carol L Thompson, Lee R Varnam, Axel Visel, Ray M Whitlock, Paul E Wohnoutka, Crissa K Wolkey, Victoria Y Wong, Matthew Wood, Murat B Yaylaoglu, Rob C Young, Brian L Youngstrom, Xu F Yuan, Bin Zhang, Theresa A Zwingman, Allan R Jones
  • Heritable clustering and pathway discovery in breast cancer integrating epigenetic and phenotypic data
    BMC Bioinformatics, Vol. 8, No. 1. (2007)
    by Zailong Wang, Pearlly Yan, Dustin Potter, Charis Eng, Tim Huang, Shili Lin
  • Computational RNA secondary structure design: empirical complexity and improved methods
    BMC Bioinformatics, Vol. 8, No. 1. (2007)
    by Rosalia A Hernandez, Holger Hoos, Anne Condon
  • A new algorithm for RNA secondary structure design.
    J Mol Biol, Vol. 336, No. 3. (20 February 2004), pp. 607-624.
    by M Andronescu, AP Fejes, F Hutter, HH Hoos, A Condon
  • RNAsoft: A suite of RNA secondary structure prediction and design software tools.
    Nucleic Acids Res, Vol. 31, No. 13. (1 July 2003), pp. 3416-3422.
  • MicroRNA gene expression during retinoic acid-induced differentiation of human acute promyelocytic leukemia
    Oncogene, Vol. aop, No. current.
    by R Garzon, F Pichiorri, T Palumbo, M Visentini, R Aqeilan, A Cimmino, H Wang, H Sun, S Volinia, H Alder, GA Calin, CG Liu, M Andreeff, CM Croce,
  • Mutant huntingtin: nuclear translocation and cytotoxicity mediated by GAPDH.
    Proc Natl Acad Sci U S A, Vol. 103, No. 9. (28 February 2006), pp. 3405-3409.
    by BI Bae, MR Hara, MB Cascio, CL Wellington, MR Hayden, CA Ross, HC Ha, XJ Li, SH Snyder, A Sawa
  • Huntingtin phosphorylation sites mapped by mass spectrometry. Modulation of cleavage and toxicity.
    J Biol Chem, Vol. 281, No. 33. (18 August 2006), pp. 23686-23697.
  • Intercellular miscommunication in polyglutamine pathogenesis
    Nature Neuroscience, Vol. 9, No. 10., pp. 1205-1206.
    by Christopher A Ross, Don W Cleveland
  • Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport.
    Nat Neurosci (27 August 2006)
    by Sara K K Custer, Gwenn A A Garden, Nishi Gill, Udo Rueb, Randell T T Libby, Christian Schultz, Stephan J J Guyenet, Thomas Deller, Lesnick E E Westrum, Bryce L L Sopher, Albert R R La Spada
  • Transcription meets metabolism in neurodegeneration
    Nature Medicine, Vol. 12, No. 11., pp. 1239-1241.
    by Christopher A Ross, Leslie M Thompson
  • Primate disrupted-in-schizophrenia-1 (DISC1): high divergence of a gene for major mental illnesses in recent evolutionary history.
    Neurosci Res, Vol. 56, No. 3. (November 2006), pp. 286-293.
    by L Bord, J Wheeler, M Paek, M Saleh, A Lyons-Warren, CA Ross, N Sawamura, A Sawa
  • Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling.
    Hum Mol Genet, Vol. 15, No. 20. (15 October 2006), pp. 3024-3033.
  • DISC1-NDEL1/NUDEL protein interaction, an essential component for neurite outgrowth, is modulated by genetic variations of DISC1.
    Hum Mol Genet, Vol. 15, No. 22. (15 November 2006), pp. 3313-3323.
  • Disrupted-in-schizophrenia-1 (DISC1): a key susceptibility factor for major mental illnesses.
    Ann N Y Acad Sci, Vol. 1086 (November 2006), pp. 126-133.
    by N Sawamura, A Sawa
  • A novel trinucleotide repeat expansion at chromosome 3q26.2 identified by a CAG/CTG repeat expansion detection array
    Human Genetics, Vol. 120, No. 2. (September 2006), pp. 193-200.
  • The association of CAG repeat length with clinical progression in Huntington disease.
    Neurology, Vol. 66, No. 7. (11 April 2006), pp. 1016-1020.
    by A Rosenblatt, KY Liang, H Zhou, MH Abbott, LM Gourley, RL Margolis, J Brandt, CA Ross
    posted to repeat length huntington cag by mgaldzic on 2007-01-31 20:57:27 as ** along with 1 group CHIP
  • Genome-wide significance for a modifier of age at neurological onset in Huntington's Disease at 6q23-24: the HD MAPS study
    BMC Medical Genetics, Vol. 7 (17 August 2006), 71.
    by Jian-Liang Li, Michael R Hayden, Simon C Warby, Alexandra Durr, Patrick J Morrison, Martha Nance, Christopher A Ross, Russell L Margolis, Adam Rosenblatt, Ferdinando Squitieri, Luigi Frati, Estrella Gomez-Tortosa, Carmen A Garcia, Oksana Suchowersky, Mary L Klimek, Ronald JA Trent, Elizabeth Mccusker, Andrea Novelletto, Marina Frontali, Jane S Paulsen, Randi Jones, Tetsuo Ashizawa, Alice Lazzarini, Vanessa C Wheeler, Ranjana Prakash, Gang Xu, Luc Djousse, Jayalakshmi S Mysore, Tammy Gillis, Michael Hakky
    posted to modifier maps huntington hd genome age 6q23-24 by mgaldzic on 2007-01-31 20:53:26 as ** along with 1 group CHIP
  • Neurobiology of schizophrenia.
    Neuron, Vol. 52, No. 1. (5 October 2006), pp. 139-153.
    by CA Ross, RL Margolis, SA Reading, M Pletnikov, JT Coyle
  • A computational model for functional mapping of genes that regulate intracellular circadian rhythms
    Theoretical Biology and Medical Modelling, Vol. 4, No. 1. (2007)
    by Tian Liu, Xueli Liu, Yunmei Chen, Rongling Wu
    posted to rythm qtl model expression circadian by mgaldzic on 2007-01-30 13:34:34 as ** along with 1 group CHIP
  • notes Stimulus fading and differential reinforcement for the treatment of needle phobia in a youth with autism.
    J Appl Behav Anal, Vol. 39, No. 4. (2006), pp. 449-452.
    by DB Shabani, WW Fisher
    posted to treatment phobia needle blood autism by mgaldzic on 2007-01-25 06:12:36 as * along with 1 group CHIP
  • Structure of the Autism Symptom Phenotype: A Proposed Multidimensional Model.
    J Am Acad Child Adolesc Psychiatry, Vol. 46, No. 2. (February 2007), pp. 188-196.
    by Stelios Georgiades, Peter Szatmari, Lonnie Zwaigenbaum, Eric Duku, Susan Bryson, Wendy Roberts, Jeremy Goldberg, William Mahoney
    posted to phenotype autism by mgaldzic on 2007-01-25 06:10:18 as ** along with 1 group CHIP
  • A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence.
    Int J Dev Neurosci (20 December 2006)
    by Mao Sheng S Yang, Michael Gill
  • The ENCODE Project at UC Santa Cruz
    Nucleic Acids Research, Vol. 35, No. Supplement 1., D663.
    by Thomas Dj, Rosenbloom Kr, H Clawson, Hinrichs As, H Trumbower, Raney Bj, D Karolchik, Barber Gp, Harte Ra, J Hillman-Jackson, Kuhn Rm, Rhead Bl, Smith Ke, A Thakkapallayil, Zweig As, D Haussler, Kent Wj
    posted to epigenetics encode by mgaldzic on 2007-01-24 16:17:57 as ** along with 1 group CHIP
  • Association of adenomatous polyposis coli (APC) gene polymorphisms with autism spectrum disorder (ASD).
    Am J Med Genet B Neuropsychiatr Genet (12 January 2007)
    by Xiao-Lei L Zhou, Maibritt Giacobini, Britt-Marie M Anderlid, Henrik Anckarsäter, Davood Omrani, Christopher Gillberg, Magnus Nordenskjöld, Annika Lindblom
    posted to utr snp polymorphism haplotype gene autism apc by mgaldzic on 2007-01-17 20:04:56 as ** along with 1 group CHIP
  • Application of genome-wide expression analysis to human health and disease.
    Proc Natl Acad Sci U S A (21 March 2005)
    by J Perren P Cobb, Michael N N Mindrinos, Carol Miller-Graziano, Steve E E Calvano, Henry V V Baker, Wenzhong Xiao, Krzysztof Laudanski, Bernard H H Brownstein, Constance M M Elson, Douglas L L Hayden, David N N Herndon, Stephen F F Lowry, Ronald V V Maier, David A A Schoenfeld, Lyle L L Moldawer, Ronald W W Davis, Ronald G G Tompkins, Henry V V Baker, Paul Bankey, Timothy Billiar, Bernard H H Brownstein, Steve E E Calvano, David Camp, Irshad Chaudry, J Perren P Cobb, Ronald W W Davis, Constance M M Elson, Bradley Freeman, Richard Gamelli, Nicole Gibran, Brian Harbrecht, Douglas L L Hayden, Wyrta Heagy, David Heimbach, David N N Herndon, Jureta Horton, John Hunt, Krzysztof Laudanski, James Lederer, Stephen F F Lowry, Ronald V V Maier, John Mannick, Bruce McKinley, Carol Miller-Graziano, Michael N N Mindrinos, Joseph Minei, Lyle L L Moldawer, Ernest Moore, Frederick Moore, Robert Munford, Avery Nathens, Grant O'keefe, Gary Purdue, Laurence Rahme, Daniel Remick, Matthew Sailors, David A A Schoenfeld, Michael Shapiro, Geoffrey Silver, Richard Smith, Gregory Stephanopoulos, Gary Stormo, Ronald G G Tompkins, Mehmet Toner, Shaw Warren, Michael West, Steven Wolfe, Wenzhong Xiao, Vernon Young
  • A highly standardized, robust, and cost-effective method for genome-wide transcriptome analysis of peripheral blood applicable to large-scale clinical trials.
    Genomics, Vol. 87, No. 5. (May 2006), pp. 653-664.
    by S Debey, T Zander, B Brors, A Popov, R Eils, JL Schultze
  • Common genetic variants account for differences in gene expression among ethnic groups.
    Nat Genet (7 January 2007)
    by Richard S S Spielman, Laurel A A Bastone, Joshua T T <