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de dchughes mir [220 articles]

Recent papers added to de dchughes library classified by the tag mir. You can also see everyone's mir.
  • Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7).
    Genomics, Vol. 81, No. 3. (March 2003), pp. 304-314.
    by S Johnson, S Halford, AG Morris, RJ Patel, SE Wilkie, AJ Hardcastle, AT Moore, K Zhang, DM Hunt
    posted to rim1 retinal-dystrophy retina mir by dchughes on 2008-07-10 13:01:15 as **
  • The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a.
    Human molecular genetics, Vol. 9, No. 5. (22 March 2000), pp. 821-828.
    by JM Jones, JD Huang, V Mermall, BA Hamilton, MS Mooseker, A Escayg, NG Copeland, NA Jenkins, MH Meisler
    posted to neuron myo5a mir dendritic-mrna dendritic-compartment by dchughes on 2008-07-10 12:52:52 as **
  • Regulation of rod phototransduction machinery by ciliary neurotrophic factor.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 26, No. 52. (27 December 2006), pp. 13523-13530.
    by R Wen, Y Song, S Kjellstrom, A Tanikawa, Y Liu, Y Li, L Zhao, RA Bush, AM Laties, PA Sieving
    posted to rhodopsin retina mir cntf by dchughes on 2008-07-07 16:22:35 as **
  • Target mRNAs are repressed as efficiently by microRNA-binding sites in the 5' UTR as in the 3' UTR.
    Proc Natl Acad Sci U S A (29 May 2007)
    by J Robin R Lytle, Therese A A Yario, Joan A A Steitz
    posted to rnai mirna mir by dchughes on 2008-07-04 12:34:19 as ** along with 6 people and 1 group jyuh tardigrade andersbj heliopais oelemento maralena microRNA
  • Endosomal trafficking of Src tyrosine kinase
    Trends in Cell Biology, Vol. 18, No. 7. (July 2008), pp. 322-329.
    by Emma Sandilands, Margaret C Frame
    posted to vesicles src mir by dchughes on 2008-07-03 15:00:25 as **
  • Growth arrest specific protein 6/Axl signaling in human inflammatory renal diseases.
    American journal of kidney diseases : the official journal of the National Kidney Foundation, Vol. 43, No. 2. (February 2004), pp. 286-295.
    by A Fiebeler, JK Park, DN Muller, C Lindschau, M Mengel, S Merkel, B Banas, FC Luft, H Haller
    posted to mir kidney axl by dchughes on 2008-07-03 14:10:45 as **
  • RPGR is mutated in patients with a complex X linked phenotype combining primary ciliary dyskinesia and retinitis pigmentosa.
    Journal of medical genetics, Vol. 43, No. 4. (April 2006), pp. 326-333.
    by A Moore, E Escudier, G Roger, A Tamalet, B Pelosse, S Marlin, A Clément, M Geremek, B Delaisi, AM Bridoux, A Coste, M Witt, B Duriez, S Amselem
    posted to rpgr retinitis-pigmentosa mir cilia by dchughes on 2008-07-01 13:43:06 as **
  • Overexpression of RPGR Leads to Male Infertility in Mice Due to Defects in Flagellar Assembly.
    Biology of reproduction (25 June 2008)
    by Sandra Brunner, Dvora Colman, Alexander J J Travis, Ulrich F O F Luhmann, Wei Shi, Silke Feil, Coni Imsand, Jacquelyn Nelson, Christian Grimm, Thomas Rülicke, Reinald Fundele, John Neidhardt, Wolfgang Berger
    posted to sperm rpgr mir male-fertility by dchughes on 2008-07-01 13:42:09 as **
  • Proliferating Cells Express mRNAs with Shortened 3' Untranslated Regions and Fewer MicroRNA Target Sites
    Science, Vol. 320, No. 5883. (20 June 2008), pp. 1643-1647.
    by Rickard Sandberg, Joel R Neilson, Arup Sarma, Phillip A Sharp, Christopher B Burge
    posted to utr mrna mirna mir by dchughes on 2008-07-01 11:55:45 as ** along with 5 people faion emptyhb bootsy lisa1 djkt
  • CELL BIOLOGY: Arrestin' Movement in Cilia.
    Science (New York, N.Y.), Vol. 320, No. 5884. (27 June 2008), pp. 1726-1727.
    by R Rohatgi, MP Scott
    posted to polarity mir cilia arrestin-1 by dchughes on 2008-07-01 11:53:34 as **
  • A novel gene that encodes a protein with a putative src homology 3 domain is a candidate gene for familial juvenile nephronophthisis.
    Human molecular genetics, Vol. 6, No. 13. (December 1997), pp. 2317-2323.
    by S Saunier, J Calado, R Heilig, F Silbermann, F Benessy, G Morin, M Konrad, M Broyer, MC Gubler, J Weissenbach, C Antignac
    posted to nphp1 mir jouberts-syndrome by dchughes on 2008-07-01 11:49:54 as **
  • A novel gene encoding an SH3 domain protein is mutated in nephronophthisis type 1.
    Nature genetics, Vol. 17, No. 2. (October 1997), pp. 149-153.
    by F Hildebrandt, E Otto, C Rensing, HG Nothwang, M Vollmer, J Adolphs, H Hanusch, M Brandis
    posted to nphp1 mir jouberts-syndrome by dchughes on 2008-07-01 11:25:15 as **
  • Polymorphisms in the CNTF and CNTF receptor genes are associated with muscle strength in men and women.
    Journal of applied physiology (Bethesda, Md. : 1985), Vol. 102, No. 5. (May 2007), pp. 1824-1831.
    by G De Mars, A Windelinckx, G Beunen, C Delecluse, J Lefevre, MA Thomis
    posted to sports-genetics mir cntf by dchughes on 2008-06-30 16:00:09 as **
  • Structural and functional abnormalities of retinal ribbon synapses due to Cacna2d4 mutation.
    Investigative ophthalmology & visual science, Vol. 47, No. 8. (August 2006), pp. 3523-3530.
    by KA Wycisk, B Budde, S Feil, S Skosyrski, F Buzzi, J Neidhardt, E Glaus, P Nürnberg, K Ruether, W Berger
    posted to retinitis-pigmentosa retinal-dystrophy mir cacna2d4 by dchughes on 2008-06-30 15:57:13 as **
  • The human retinitis pigmentosa GTPase regulator gene variant database.
    Human mutation, Vol. 29, No. 5. (May 2008), pp. 605-608.
    by X Shu, E McDowall, AF Brown, AF Wright
    posted to rpgr retinitis-pigmentosa mir by dchughes on 2008-06-27 11:00:59 as **
  • Mutations in the gene coding for guanylate cyclase-activating protein 2 (GUCA1B gene) in patients with autosomal dominant retinal dystrophies.
    Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie, Vol. 243, No. 3. (March 2005), pp. 235-242.
    by M Sato, M Nakazawa, T Usui, N Tanimoto, H Abe, H Ohguro
    posted to retinal-dystrophy retina mir guca1b by dchughes on 2008-06-26 14:24:59 as **
  • Mutation in the auxiliary calcium-channel subunit CACNA2D4 causes autosomal recessive cone dystrophy.
    American journal of human genetics, Vol. 79, No. 5. (November 2006), pp. 973-977.
    by KA Wycisk, C Zeitz, S Feil, M Wittmer, U Forster, J Neidhardt, B Wissinger, E Zrenner, R Wilke, S Kohl, W Berger
    posted to retinal-dystrophy retina mir cacna2d4 by dchughes on 2008-06-26 14:15:07 as **
  • Vasopressin V2 receptor expression along rat, mouse, and human renal epithelia with focus on TAL.
    American journal of physiology. Renal physiology, Vol. 293, No. 4. (October 2007)
    by K Mutig, A Paliege, T Kahl, T Jöns, W Müller-Esterl, S Bachmann
    posted to mir kidney avpr2 by dchughes on 2008-06-25 15:49:34 as **
  • Identification of novel mutations in X-linked retinitis pigmentosa families and implications for diagnostic testing.
    Molecular vision, Vol. 14 (2008), pp. 1081-1093.
    by J Neidhardt, E Glaus, B Lorenz, C Netzer, Y Li, M Schambeck, M Wittmer, S Feil, R Kirschner-Schwabe, T Rosenberg, FP Cremers, AA Bergen, D Barthelmes, H Baraki, F Schmid, G Tanner, J Fleischhauer, U Orth, C Becker, E Wegscheider, G Nürnberg, P Nürnberg, HJ Bolz, A Gal, W Berger
    posted to rpgr retinitis-pigmentosa mir by dchughes on 2008-06-24 16:41:16 as **
  • Species-specific subcellular localization of RPGR and RPGRIP isoforms: implications for the phenotypic variability of congenital retinopathies among species.
    Human molecular genetics, Vol. 11, No. 16. (1 August 2002), pp. 1899-1907.
    by TA Mavlyutov, H Zhao, PA Ferreira
    posted to rpgr retinitis-pigmentosa mir by dchughes on 2008-06-20 16:26:45 as **
  • Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.
    Journal of medical genetics, Vol. 42, No. 11. (November 2005)
    by JC Booij, RJ Florijn, JB ten Brink, W Loves, F Meire, MJ van Schooneveld, PT de Jong, AA Bergen
    posted to rpgr retinitis-pigmentosa mir aipl1 by dchughes on 2008-06-20 16:17:35 as **
  • A retinitis pigmentosa GTPase regulator (RPGR)- deficient mouse model for X-linked retinitis pigmentosa (RP3)
    Proceedings of the National Academy of Sciences, Vol. 97, No. 7. (28 March 2000), pp. 3649-3654.
    by Dong-Hyun Hong, Basil S Pawlyk, Jingzi Shang, Michael A Sandberg, Eliot L Berson, Tiansen Li
    posted to rpgr retinitis-pigmentosa mir by dchughes on 2008-06-20 14:18:22 as **
  • Identification and characterization of a novel RPGR isoform in human retina.
    Human mutation, Vol. 28, No. 8. (August 2007), pp. 797-807.
    by J Neidhardt, E Glaus, D Barthelmes, C Zeitz, J Fleischhauer, W Berger
    posted to smc1 rpgr retinitis-pigmentosa mir by dchughes on 2008-06-17 11:34:03 as **
  • RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa.
    Human molecular genetics, Vol. 8, No. 8. (August 1999), pp. 1571-1578.
    by R Kirschner, T Rosenberg, R Schultz-Heienbrok, S Lenzner, S Feil, R Roepman, FP Cremers, HH Ropers, W Berger
    posted to smc rpgr retinitis-pigmentosa mir by dchughes on 2008-06-17 11:30:34 as **
  • Negative regulation of multifunctional Ca2+//calmodulin-dependent protein kinases: physiological and pharmacological significance of protein phosphatases
    Br J Pharmacol, Vol. 154, No. 4. (5 May 2008), pp. 729-740.
    by A Ishida, N Sueyoshi, Y Shigeri, I Kameshita
    posted to phosphatase mir camkii by dchughes on 2008-06-10 17:07:44 as ** along with 1 person renatomilani
  • A photoreceptor-specific cadherin is essential for the structural integrity of the outer segment and for photoreceptor survival.
    Neuron, Vol. 32, No. 5. (6 December 2001), pp. 775-786.
    by A Rattner, PM Smallwood, J Williams, C Cooke, A Savchenko, A Lyubarsky, EN Pugh, J Nathans
    posted to retinitis-pigmentosa pcdh12 mir by dchughes on 2008-06-10 15:11:35 as **
  • Incidence and clinical features of X-linked Cornelia de Lange syndrome due to SMC1L1 mutations.
    Human mutation, Vol. 28, No. 2. (February 2007), pp. 205-206.
    by G Borck, M Zarhrate, JP Bonnefont, A Munnich, V Cormier-Daire, L Colleaux
    posted to smc1 smc mir mental-retardation cornelia-de-lange-syndrome by dchughes on 2008-06-10 11:05:03 as **
  • Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of cornelia de Lange syndrome with predominant mental retardation.
    American journal of human genetics, Vol. 80, No. 3. (March 2007), pp. 485-494.
    by MA Deardorff, M Kaur, D Yaeger, A Rampuria, S Korolev, J Pie, C Gil-Rodríguez, M Arnedo, B Loeys, AD Kline, M Wilson, K Lillquist, V Siu, FJ Ramos, A Musio, LS Jackson, D Dorsett, ID Krantz
    posted to smc1 smc mir mental-retardation by dchughes on 2008-06-10 10:52:42 as **
  • Synaptic Protein Degradation Underlies Destabilization of Retrieved Fear Memory.
    Science (7 February 2008)
    by Sue-Hyun H Lee, Jun-Hyeok H Choi, Nuribalhae Lee, Hye-Ryeon R Lee, Jae-Ick I Kim, Nam-Kyung K Yu, Sun-Lim L Choi, Seung-Hee H Lee, Hyoung Kim, Bong-Kiun K Kaang
    posted to ubiquitin synaptic-plasticity protein-degradation mirs mir by dchughes on 2008-05-07 11:25:29 as ** along with 1 person davidlott
  • Proteasome inhibition enhances the induction and impairs the maintenance of late-phase long-term potentiation
    Learn. Mem., Vol. 15, No. 5. (25 April 2008), pp. 335-347.
    by Chenghai Dong, Sudarshan C Upadhya, Lan Ding, Thuy K Smith, Ashok N Hegde
    posted to ubiquitin synaptic-plasticity proteosome protein-degradation mir by dchughes on 2008-05-01 16:44:18 as ** along with 1 person zibdum
  • Mutations in String/CDC25 inhibit cell cycle re-entry and neurodegeneration in a Drosophila model of Ataxia telangiectasia
    Genes Dev. (11 April 2008), gad.1639608.
    by Stacey A Rimkus, Rebeccah J Katzenberger, Anthony T Trinh, Gerald E Dodson, Randal S Tibbetts, David A Wassarman
    posted to neuron mir atm by dchughes on 2008-05-01 16:40:14 as **
  • Cloning, physical mapping and expression analysis of the human 5-HT3 serotonin receptor-like genes HTR3C, HTR3D and HTR3E.
    Gene, Vol. 310 (22 May 2003), pp. 101-111.
    by B Niesler, B Frank, J Kapeller, GA Rappold
    posted to serotonin mir htr3e by dchughes on 2008-04-24 11:21:37 as **
  • The 5-hydroxytryptamine type 3 (5-HT3) receptor reveals a novel determinant of single-channel conductance.
    Biochemical Society transactions, Vol. 32, No. Pt3. (June 2004), pp. 547-552.
    by JA Peters, SP Kelley, JI Dunlop, EF Kirkness, TG Hales, JJ Lambert
    posted to 5-ht htr3e mir serotonin by dchughes on 2008-04-18 12:06:11 as **
  • A cluster of novel serotonin receptor 3-like genes on human chromosome 3.
    Gene, Vol. 319 (13 November 2003), pp. 137-148.
    by AM Karnovsky, LF Gotow, DD McKinley, JL Piechan, CL Ruble, CJ Mills, KA Schellin, JL Slightom, LR Fitzgerald, CW Benjamin, SL Roberds
    posted to htr3e mir serotonin by dchughes on 2008-04-18 12:03:25 as **
  • Expressed sequence tag analysis of human retina for the NEIBank Project: retbindin, an abundant, novel retinal cDNA and alternative splicing of other retina-preferred gene transcripts.
    Molecular vision, Vol. 8 (15 June 2002), pp. 196-204.
    by G Wistow, SL Bernstein, MK Wyatt, S Ray, A Behal, JW Touchman, G Bouffard, D Smith, K Peterson
    posted to mir nrl by dchughes on 2008-04-16 13:18:59 as **
  • Multiple Phosphorylated Isoforms of NRL Are Expressed in Rod Photoreceptors
    J. Biol. Chem., Vol. 276, No. 39. (21 September 2001), pp. 36824-36830.
    by Prabodha K Swain, David Hicks, Alan J Mears, Ingrid J Apel, Julie E Smith, Sinoj K John, Anita Hendrickson, Ann H Milam, Anand Swaroop
    posted to mir nrl by dchughes on 2008-04-16 13:18:29 as **
  • ARF6 in the nervous system
    European Journal of Cell Biology, Vol. 86, No. 9. (14 September 2007), pp. 513-524.
    by Jacek Jaworski
    posted to arf6 mir neuroscience by dchughes on 2008-04-01 11:52:38 as ** along with 1 person FMoncini
  • Regulation of actin cytoskeleton dynamics by Arf-family GTPases
    Trends in Cell Biology, Vol. 18, No. 4. (April 2008), pp. 184-192.
    by Kenneth R Myers, James E Casanova
    posted to actin-reorganisation arf6 mir by dchughes on 2008-04-01 11:50:07 as **
  • A conserved C-terminal domain of EFA6-family ARF6-guanine nucleotide exchange factors induces lengthening of microvilli-like membrane protrusions.
    J Cell Sci, Vol. 115, No. Pt 14. (15 July 2002), pp. 2867-2879.
    by V Derrien, C Couillault, M Franco, S Martineau, P Montcourrier, R Houlgatte, P Chavrier
    posted to arf6 efa6a mir psd4 by dchughes on 2008-03-06 12:28:10 as ** along with 1 person FMoncini
  • GEP100 links epidermal growth factor receptor signalling to Arf6 activation to induce breast cancer invasion
    Nature Cell Biology, Vol. 10, No. 1. (16 December 2007), pp. 85-92.
    by Masaki Morishige, Shigeru Hashimoto, Eiji Ogawa, Yoshinobu Toda, Hirokazu Kotani, Mayumi Hirose, Shumei Wei, Ari Hashimoto, Atsuko Yamada, Hajime Yano, Yuichi Mazaki, Hiroshi Kodama, Yoshinori Nio, Toshiaki Manabe, Hiromi Wada, Hidenori Kobayashi, Hisataka Sabe
    posted to arf6 efa6a mir psd4 by dchughes on 2008-03-06 12:27:15 as ** along with 1 person laurabailey
  • Leptin as a neuroprotective agent
    Biochemical and Biophysical Research Communications, Vol. 368, No. 2. (4 April 2008), pp. 181-185.
    by Bor L Tang
    posted to leptin mir neuroscience by dchughes on 2008-02-27 15:51:06 as ** along with 1 person cchand
  • The discoidin domain receptor 1 as a novel susceptibility gene for schizophrenia
    Molecular Psychiatry, Vol. aop, No. current.
    by B Roig, C Virgos, N Franco, L Martorell, J Valero, J Costas, A Carracedo, A Labad, E Vilella
    posted to discoidin-domain-receptor-1 mir schizophrenia by dchughes on 2008-02-21 17:23:04 as **
  • Regional and developmental regulation of syntaphilin expression in the brain: a candidate molecular element of synaptic functional differentiation
    Molecular Brain Research, Vol. 116, No. 1-2. (19 August 2003), pp. 38-49.
    by Sunit Das, Judit Boczan, Claudia Gerwin, Philip B Zald, Zu-Hang Sheng
    posted to mir synapse syntaphilin by dchughes on 2008-02-20 11:51:16 as **
  • Regional and developmental regulation of syntaphilin expression in the brain: a candidate molecular element of synaptic functional differentiation.
    Brain Res Mol Brain Res, Vol. 116, No. 1-2. (19 August 2003), pp. 38-49.
    by S Das, J Boczan, C Gerwin, PB Zald, ZH Sheng
    posted to mir synapse synaptic-plasticity syntaphilin by dchughes on 2008-02-20 11:18:29 as **
  • Docking of axonal mitochondria by syntaphilin controls their mobility and affects short-term facilitation.
    Cell, Vol. 132, No. 1. (11 January 2008), pp. 137-148.
    by JS Kang, JH Tian, PY Pan, P Zald, C Li, C Deng, ZH Sheng
    posted to axon mir mitochondria syntaphilin by dchughes on 2008-02-20 11:11:46 as **
  • Loss of X-Linked Mental Retardation Gene Oligophrenin1 in Mice Impairs Spatial Memory and Leads to Ventricular Enlargement and Dendritic Spine Immaturity
    J. Neurosci., Vol. 27, No. 35. (29 August 2007), pp. 9439-9450.
    by Malik Khelfaoui, Cecile Denis, Elly van Galen, Frederic de Bock, Alain Schmitt, Christophe Houbron, Elise Morice, Bruno Giros, Ger Ramakers, Laurent Fagni, Jamel Chelly, Marika Nosten-Bertrand, Pierre Billuart
    posted to mental-retardation mir ophn1 by dchughes on 2008-02-12 12:42:44 as ** along with 1 person fluomouse
  • Src in synaptic transmission and plasticity.
    Oncogene, Vol. 23, No. 48. (18 October 2004), pp. 8007-8016.
    by LV Kalia, JR Gingrich, MW Salter
    posted to mir src synaptic-plasticity by dchughes on 2008-02-01 14:59:51 as **
  • How has DISC1 enabled drug discovery
    Molecular and Cellular Neuroscience, Vol. 37, No. 2. (February 2008), pp. 187-195.
    by Qi Wang, Hanna Jaaro-Peled, Akira Sawa, Nicholas J Brandon
    posted to disc1 mir schizophrenia by dchughes on 2008-02-01 09:33:31 as **
  • Essential roles in synaptic plasticity for synaptogyrin I and synaptophysin I.
    Neuron, Vol. 24, No. 3. (November 1999), pp. 687-700.
    by R Janz, TC Südhof, RE Hammer, V Unni, SA Siegelbaum, VY Bolshakov
    posted to mir schizophrenia synaptic-plasticity synaptogyrin by dchughes on 2008-01-23 12:42:51 as **
  • SYNGR1 is associated with schizophrenia and bipolar disorder in southern India.
    J Hum Genet, Vol. 50, No. 12. (2005), pp. 635-640.
    by R Verma, S Kubendran, SK Das, S Jain, SK Brahmachari
    posted to mir schizophrenia synaptogyrin by dchughes on 2008-01-23 12:41:03 as ** along with 1 person N0131826
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