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Taggat som: deletion [69 articles]

Senaste hänvisningarna som insorterats under taggen deletion.
  • Construction of consecutive deletions of the Escherichia coli chromosome
    Mol Syst Biol, Vol. 3 (2007)
    by Jun-Ichi Kato, Masayuki Hashimoto
    posted to bacterial chromosome deletion ecoli by zwang on 2007-08-15 03:07:11 as *
  • Yeast life span extension by depletion of 60s ribosomal subunits is mediated by Gcn4.
    Cell, Vol. 133, No. 2. (18 April 2008), pp. 292-302.
    by KK Steffen, VL MacKay, EO Kerr, M Tsuchiya, D Hu, LA Fox, N Dang, ED Johnston, JA Oakes, BN Tchao, DN Pak, S Fields, BK Kennedy, M Kaeberlein
    posted to yeast gene deletion complex cellcycle by zwang on 2008-07-10 09:28:01 as **
  • Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism.
    J Med Genet, Vol. 37, No. 10. (October 2000), pp. 752-758.
    by P Blanco, M Shlumukova, CA Sargent, MA Jobling, N Affara, ME Hurles
    posted to 11 cited deletion herv te by yoanjacquemin on 2008-02-08 12:57:27 as **
  • Systematic pathway analysis using high-resolution fitness profiling of combinatorial gene deletions
    Nature Genetics, Vol. 39, No. 2. (07 January 2007), pp. 199-206.
    by Robert P St Onge, Ramamurthy Mani, Julia Oh, Michael Proctor, Eula Fung, Ronald W Davis, Corey Nislow, Frederick P Roth, Guri Giaever
  • Isolation and behavior of Escherichia coli deletion mutants lacking chemotaxis functions.
    J. Bacteriol., Vol. 151, No. 1. (1 July 1982), pp. 106-113.
    by JS Parkinson, SE Houts
    posted to chemotaxis coli deletion mutants by vladimirov on 2008-03-14 12:43:49 as **
  • Mitochondrial DNA damage and the aging process: facts and imaginations.
    Free Radic Res, Vol. 40, No. 12. (December 2006), pp. 1284-1294.
    by RJ Wiesner, G Zsurka, WS Kunz
  • Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.
    Am J Hum Genet, Vol. 71, No. 4. (October 2002), pp. 906-922.
  • notes GTF2I hemizygosity implicated in mental retardation in Williams syndrome: Genotype-phenotype analysis of five families with deletions in the Williams syndrome region
    American Journal of Medical Genetics Part A, Vol. 123A, No. 1. (17 September 2003), pp. 45-59.
    by Colleen A Morris, Carolyn B Mervis, Holly H Hobart, Ronald G Gregg, Jacquelyn Bertrand, Gregory J Ensing, Annemarie Sommer, Cynthia A Moore, Robert J Hopkin, Patricia A Spallone, Mark T Keating, Lucy Osborne, Kendra W Kimberley, Dean D Stock
  • Spatiotemporal boundary formation: boundary, form, and motion perception from transformations of surface elements.
    Journal of experimental psychology. General, Vol. 123, No. 1. (March 1994), pp. 3-20.
    by TF Shipley, PJ Kellman
  • Spatio-temporal boundary formation: the role of local motion signals in boundary perception
    Vision Research, Vol. 37, No. 10. (14 April 1997), pp. 1281-1293.
    by Thomas F Shipley, Philip J Kellman
    posted to psychophysics motion deletion boundary accretion by timotay on 2008-06-04 18:11:25 as **
  • High intrinsic rate of DNA loss in Drosophila.
    Nature, Vol. 384, No. 6607. (28 November 1996), pp. 346-349.
    by DA Petrov, ER Lozovskaya, DL Hartl
  • High rate of DNA loss in the Drosophila melanogaster and Drosophila virilis species groups.
    Mol Biol Evol, Vol. 15, No. 3. (March 1998), pp. 293-302.
    by DA Petrov, DL Hartl
  • Pseudogene evolution in Drosophila suggests a high rate of DNA loss.
    Mol Biol Evol, Vol. 15, No. 11. (November 1998), pp. 1562-1567.
    by DA Petrov, YC Chao, EC Stephenson, DL Hartl
  • Evolution of complexity in signaling pathways.
    Proc Natl Acad Sci U S A (23 October 2006)
    by Orkun S S Soyer, Sebastian Bonhoeffer
  • Differential oocyte-specific expression of Cre recombinase activity in GDF-9-iCre, Zp3cre, and Msx2Cre transgenic mice.
    Biol Reprod, Vol. 71, No. 5. (November 2004), pp. 1469-1474.
    by ZJ Lan, X Xu, AJ Cooney
    posted to cre deletion gdf-9 msx2 mutagenesis oocyte zp3 by sebastien_vigneau on 2007-10-10 13:33:06 as **
  • A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene.
    Proc Natl Acad Sci U S A, Vol. 93, No. 9. (30 April 1996), pp. 3937-3941.
    by M Stoffel, MM Le Beau, R Espinosa, SF Bohlander, D Le Paslier, D Cohen, KS Xiang, NJ Cox, SS Fajans, GI Bell
    posted to blcap cancer chr20 deletion human leukemia by rschulz on 2008-03-17 17:14:49 as **
  • Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.
    Blood, Vol. 82, No. 11. (1 December 1993), pp. 3424-3429.
    by D Roulston, R Espinosa, M Stoffel, GI Bell, MM Le Beau
    posted to blcap cancer chr20 deletion human leukemia by rschulz on 2008-03-17 17:12:17 as **
  • Association between Microdeletion and Microduplication at 16p11.2 and Autism.
    N Engl J Med (9 January 2008)
    by Lauren A A Weiss, Yiping Shen, Joshua M M Korn, Dan E E Arking, David T T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R A Ferreira, Todd Green, Orah S S Platt, Douglas M M Ruderfer, Christopher A A Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E E Tanzi, Kari Stefansson, Susan L L Santangelo, James F F Gusella, Pamela Sklar, Bai-Lin L Wu, Mark J J Daly,
  • Genomic profiling of drug sensitivities via induced haploinsufficiency
    Nature Genetics, Vol. 21, No. 3. (March 1999), pp. 278-283.
    by G Giaever, DD Shoemaker, TW Jones, H Liang, EA Winzeler, A Astromoff, RW Davis
  • Discovering Modes of Action for Therapeutic Compounds Using a Genome-Wide Screen of Yeast Heterozygotes
    Cell, Vol. 116, No. 1. (9 January 2004), pp. 121-137.
    by Pek Y Lum, Christopher D Armour, Sergey B Stepaniants, Guy Cavet, Maria K Wolf, Scott J Butler, Jerald C Hinshaw, Philippe Garnier, Glenn D Prestwich, Amy Leonardson
  • Re-analysis of data and its integration
    FEBS Letters, Vol. 579, No. 8. (21 March 2005), pp. 1802-1807.
    by Lars J Jensen, Lars M Steinmetz
  • Linking functionally related genes by sensitive and quantitative characterization of genetic interaction profiles
    Proceedings of the National Academy of Sciences, Vol. 105, No. 15. (15 April 2008), pp. 5821-5826.
    by Laurence Decourty, Cosmin Saveanu, Kenza Zemam, Florence Hantraye, Emmanuel Frachon, Jean-Claude Rousselle, Micheline Fromont-Racine, Alain Jacquier
  • An integrated platform of genomic assays reveals small-molecule bioactivities
    Nat Chem Biol, Vol. 4, No. 8. (2008), pp. 498-506.
    by Shawn Hoon, Smith, Iain M Wallace, Sundari Suresh, Molly Miranda, Eula Fung, Michael Proctor, Kevan M Shokat, Chao Zhang, Ronald W Davis, Guri Giaever, Robert P St Onge, Corey Nislow
  • The Chemical Genomic Portrait of Yeast: Uncovering a Phenotype for All Genes
    Science, Vol. 320, No. 5874. (18 April 2008), pp. 362-365.
    by Maureen E Hillenmeyer, Eula Fung, Jan Wildenhain, Sarah E Pierce, Shawn Hoon, William Lee, Michael Proctor, St, Mike Tyers, Daphne Koller, Russ B Altman, Ronald W Davis, Corey Nislow, Guri Giaever
  • High-throughput classification of yeast mutants for functional genomics using metabolic footprinting.
    Nat Biotechnol, Vol. 21, No. 6. (June 2003), pp. 692-696.
    by J Allen, HM Davey, D Broadhurst, JK Heald, JJ Rowland, SG Oliver, DB Kell
  • A functional genomics strategy that uses metabolome data to reveal the phenotype of silent mutations.
    Nat Biotechnol, Vol. 19, No. 1. (January 2001), pp. 45-50.
    by LM Raamsdonk, B Teusink, D Broadhurst, N Zhang, A Hayes, MC Walsh, JA Berden, KM Brindle, DB Kell, JJ Rowland, HV Westerhoff, K van Dam, SG Oliver
  • Evaluation of predicted network modules in yeast metabolism using NMR-based metabolite profiling.
    Genome Res, Vol. 17, No. 4. (April 2007), pp. 510-519.
    by JG Bundy, B Papp, R Harmston, RA Browne, EM Clayson, N Burton, RJ Reece, SG Oliver, KM Brindle
  • Metabolic flux balance analysis and the in silico analysis of Escherichia coli K-12 gene deletions.
    BMC Bioinformatics, Vol. 1 (2000)
    by JS Edwards, BO Palsson
  • Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae.
    Mol Biol Cell, Vol. 13, No. 3. (March 2002), pp. 847-853.
  • What causes mitochondrial DNA deletions in human cells?
    Nature Genetics, Vol. 40, No. 3. (27 February 2008), pp. 275-279.
    by Kim J Krishnan, Amy K Reeve, David C Samuels, Patrick F Chinnery, John K Blackwood, Robert W Taylor, Sjoerd Wanrooij, Johannes N Spelbrink, Robert N Lightowlers, Doug M Turnbull
  • Superoxide dismutase activity is essential for stationary phase survival in Saccharomyces cerevisiae. Mitochondrial production of toxic oxygen species in vivo.
    J Biol Chem, Vol. 271, No. 21. (24 May 1996), pp. 12275-12280.
    by VD Longo, EB Gralla, JS Valentine
  • Integrated genomic and proteomic analyses of a systematically perturbed metabolic network.
    Science, Vol. 292, No. 5518. (4 May 2001), pp. 929-934.
  • Yeast cells lacking the mitochondrial gene encoding the ATP synthase subunit 6 exhibit a selective loss of complex IV and unusual mitochondrial morphology.
    J Biol Chem, Vol. 282, No. 15. (13 April 2007), pp. 10853-10864.
  • Global Mapping of the Yeast Genetic Interaction Network
    Science, Vol. 303, No. 5659. (06 February 2004), pp. 808-813.
    by Amy HY Tong, Guillaume Lesage, Gary D Bader, Huiming Ding, Hong Xu, Xiaofeng Xin, James Young, Gabriel F Berriz, Renee L Brost, Michael Chang, Yiqun Chen, Xin Cheng, Gordon Chua, Helena Friesen, Debra S Goldberg, Jennifer Haynes, Christine Humphries, Grace He, Shamiza Hussein, Lizhu Ke, Nevan Krogan, Zhijian Li, Joshua N Levinson, Hong Lu, Patrice Menard, Christella Munyana, Ainslie B Parsons, Owen Ryan, Raffi Tonikian, Tania Roberts, Anne-Marie Sdicu, Jesse Shapiro, Bilal Sheikh, Bernhard Suter, Sharyl L Wong, Lan V Zhang, Hongwei Zhu, Christopher G Burd, Sean Munro, Chris Sander, Jasper Rine, Jack Greenblatt, Matthias Peter, Anthony Bretscher, Graham Bell, Frederick P Roth, Grant W Brown, Brenda Andrews, Howard Bussey, Charles Boone
  • Integrative analysis of the mitochondrial proteome in yeast.
    PLoS Biol, Vol. 2, No. 6. (June 2004)
    by H Prokisch, C Scharfe, DG Camp, W Xiao, L David, C Andreoli, ME Monroe, RJ Moore, MA Gritsenko, C Kozany, KK Hixson, HM Mottaz, H Zischka, M Ueffing, ZS Herman, RW Davis, T Meitinger, PJ Oefner, RD Smith, LM Steinmetz
  • Functional profiling of the Saccharomyces cerevisiae genome.
    Nature, Vol. 418, No. 6896. (25 July 2002), pp. 387-391.
  • A unique and universal molecular barcode array
    Nature Methods, Vol. 3, No. 8. (21 July 2006), pp. 601-603.
    by Sarah E Pierce, Eula L Fung, Daniel F Jaramillo, Angela M Chu, Ronald W Davis, Corey Nislow, Guri Giaever
  • Exon 19 deletion mutations of epidermal growth factor receptor are associated with prolonged survival in non-small cell lung cancer patients treated with gefitinib or erlotinib.
    Clin Cancer Res, Vol. 12, No. 13. (1 July 2006), pp. 3908-3914.
    by DM Jackman, BY Yeap, LV Sequist, N Lindeman, AJ Holmes, VA Joshi, DW Bell, MS Huberman, B Halmos, MS Rabin, DA Haber, TJ Lynch, M Meyerson, BE Johnson, PA Jänne
    posted to deletion iressa mutation nsclc by pjasper on 2007-04-25 21:23:34 as **
  • Dimerization and the signal transduction pathway of a small in-frame deletion in the epidermal growth factor receptor.
    FASEB J, Vol. 20, No. 2. (February 2006), pp. 311-313.
    posted to deletion mutation by pjasper on 2007-04-25 15:56:23 as **
  • In-frame deletion in the EGF receptor alters kinase inhibition by gefitinib.
    Biochem J, Vol. 397, No. 3. (1 August 2006), pp. 537-543.
    posted to deletion iressa mutant by pjasper on 2007-04-25 16:46:50 as **
  • Gene size reduction in the bacterial aphid endosymbiont, Buchnera.
    Molecular Biology and Evolution, Vol. 16, No. 12. (December 1999), pp. 1820-1822.
    posted to pressure mutations evolution deletion by mjoach on 2008-05-15 23:51:26 as *
  • 96 haploid yeast strains with individual disruptions of ORFs between YOR097C and YOR192C, constructed for the Saccharomyces Genome Deletion Project, have an additional mutation in the mismatch repair gene MSH3.
    Genetics (18 October 2007)
    by Kevin R R Lehner, Megan M M Stone, Rosann A A Farber, Thomas D D Petes
    posted to collection deletion yeast by mimulus_99 on 2007-10-25 19:23:58 as ***
  • 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
  • Insertion, Deletion Codes With Feature-Based Embedding: A New Paradigm for Watermark Synchronization With Applications to Speech Watermarking
    IEEE Transactions on Information Forensics and Security, Vol. 3, No. 2. (June 2008), pp. 153-165.
    by David J Coumou, Gaurav Sharma
  • Sequence Context affects the rate of short insertions and deletions in flies and primates
    Genome Biology, Vol. 9 (21 February 2008), R37.
    by Amos Tanay, Eric D Siggia
  • Similarities in Transthyretin Gene Expression and Differences in Transcription Factors: Liver and Yolk Sac Compared to Choroid Plexus
    Proceedings of the National Academy of Sciences of the United States of America, Vol. 87, No. 17. (1990), pp. 6589-6593.
    by Robert H Costa, Terry A Van Dyke, Chen Yan, Frank Kuo, James E Darnell
    posted to 5 analysis deletion by leelisax on 2007-10-12 15:41:57 as **
  • Promoter and Upstream Regulatory Activities of the Mouse Cellular Retinoic Acid-binding Protein-I Gene
    J. Biol. Chem., Vol. 271, No. 9. (1 March 1996), pp. 5073-5078.
    by Li-Na Wei, Liming Chang
    posted to 5 analysis deletion by leelisax on 2007-10-12 17:19:37 as **
  • Detection of APC gene deletion by double competitive polymerase chain reaction in patients with familial adenomatous polyposis.
    Int J Oncol, Vol. 29, No. 2. (August 2006), pp. 413-421.
    posted to carcinogenesis deletion repeat by jlangdon on 2008-01-18 14:08:38 as **
  • Recurrent reciprocal deletions and duplications of 16p13.11: The deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant.
    Journal of medical genetics (11 June 2008)
    by Femke D D Hannes, Andrew J J Sharp, Heather C C Mefford, Thomy de Ravel, Claudia A A Ruivenkamp, Martijn H H Breuning, Jean-Pierre P Fryns, Koen Devriendt, Griet Van Buggenhout, Annick Vogels, Helen H H Stewart, Raoul C C Hennekam, Gregory M M Cooper, Regina Regan, Samantha Jl J Knight, Evan E E Eichler, Joris R R Vermeesch
    posted to nahr duplication deletion by jlangdon on 2008-06-23 11:33:50 as **
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