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    Results: 1 to 50 of 1518

    1.

    Let the locals lead.

    Smith RJ, Veríssimo D, Leader-Williams N, Cowling RM, Knight AT.

    Nature. 2009 Nov 19;462(7271):280-1. No abstract available. PMID: 19924192 [PubMed - in process]Related articles

    2.

    Unilateral vocal fold paralysis in premature infants after ligation of patent ductus arteriosus: vascular clip versus suture ligature.

    Spanos WC, Brookes JT, Smith MC, Burkhart HM, Bell EF, Smith RJ.

    Ann Otol Rhinol Laryngol. 2009 Oct;118(10):750-3.PMID: 19894404 [PubMed - in process]Related articles

    3.

    Baker et al overlook Memphis' Dr Myles, v. Lynk, NMA pioneer.

    Smith RJ.

    J Natl Med Assoc. 2009 Oct;101(10):1071; author reply 1071. No abstract available. PMID: 19860311 [PubMed - in process]Related articles

    4.

    Effect of plyometric training on swimming block start performance in adolescents.

    Bishop DC, Smith RJ, Smith MF, Rigby HE.

    J Strength Cond Res. 2009 Oct;23(7):2137-43.PMID: 19855343 [PubMed - in process]Related articles

    5.

    Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

    Schrauwen I, Ealy M, Fransen E, Vanderstraeten K, Thys M, Meyer NC, Cosgarea M, Huber A, Mazzoli M, Pfister M, Smith RJ, Van Camp G.

    Hum Genet. 2009 Oct 22. [Epub ahead of print]PMID: 19847460 [PubMed - as supplied by publisher]Related articles

    6.

    Lateral hypothalamic orexin/hypocretin neurons: A role in reward-seeking and addiction.

    Aston-Jones G, Smith RJ, Sartor GC, Moorman DE, Massi L, Tahsili-Fahadan P, Richardson KA.

    Brain Res. 2009 Oct 6. [Epub ahead of print]PMID: 19815001 [PubMed - as supplied by publisher]Related articles

    7.

    The c.-103T>C variant in the 5'-UTR of SLC26A4 gene: a pathogenic mutation or coincidental polymorphism?

    Yang T, Smith RJ.

    Hum Mutat. 2009 Oct;30(10):1469-70; author reply 1471. No abstract available. PMID: 19787632 [PubMed - in process]Related articles

    8.

    A contemporary review of AudioGene audioprofiling: a machine-based candidate gene prediction tool for autosomal dominant nonsyndromic hearing loss.

    Hildebrand MS, DeLuca AP, Taylor KR, Hoskinson DP, Hur IA, Tack D, McMordie SJ, Huygen PL, Casavant TL, Smith RJ.

    Laryngoscope. 2009 Nov;119(11):2211-5. No abstract available. PMID: 19780026 [PubMed - in process]Related articles

    9.

    GIGYF2 gene disruption in mice results in neurodegeneration and altered insulin-like growth factor signaling.

    Giovannone B, Tsiaras WG, de la Monte S, Klysik J, Lautier C, Karashchuk G, Goldwurm S, Smith RJ.

    Hum Mol Genet. 2009 Dec 1;18(23):4629-39. Epub 2009 Sep 10.PMID: 19744960 [PubMed - in process]Related articlesFree article

    10.

    Developmental aspects of the upper airway: report from an NHLBI Workshop, March 5-6, 2009.

    Marcus CL, Smith RJ, Mankarious LA, Arens R, Mitchell GS, Elluru RG, Forte V, Goudy S, Jabs EW, Kane AA, Katz E, Paydarfar D, Pereira K, Reeves RH, Richtsmeier JT, Ruiz RL, Thach BT, Tunkel DE, Whitsett JA, Wootton D, Blaisdell CJ.

    Proc Am Thorac Soc. 2009 Sep 15;6(6):513-20.PMID: 19741259 [PubMed - in process]Related articlesFree article

    11.

    Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.

    Grillet N, Schwander M, Hildebrand MS, Sczaniecka A, Kolatkar A, Velasco J, Webster JA, Kahrizi K, Najmabadi H, Kimberling WJ, Stephan D, Bahlo M, Wiltshire T, Tarantino LM, Kuhn P, Smith RJ, Müller U.

    Am J Hum Genet. 2009 Sep;85(3):328-37.PMID: 19732867 [PubMed - indexed for MEDLINE]Related articles

    12.

    Commentary on "Dysplasia in adults with recurrent respiratory papillomatosis: incidence and risk factors".

    Robinson RA, Gupta H, Karnell LH, Smith RJ, Hoffman HT.

    Ann Otol Rhinol Laryngol. 2009 Jul;118(7):486-7. No abstract available. PMID: 19708486 [PubMed - indexed for MEDLINE]Related articles

    13.

    A claudin-9-based ion permeability barrier is essential for hearing.

    Nakano Y, Kim SH, Kim HM, Sanneman JD, Zhang Y, Smith RJ, Marcus DC, Wangemann P, Nessler RA, Bánfi B.

    PLoS Genet. 2009 Aug;5(8):e1000610. Epub 2009 Aug 21.PMID: 19696885 [PubMed - in process]Related articlesFree article

    14.

    In vitro efficiency and mechanistic role of indocyanine green as photodynamic therapy agent for human melanoma.

    Mamoon AM, Gamal-Eldeen AM, Ruppel ME, Smith RJ, Tsang T, Miller LM.

    Photodiagnosis Photodyn Ther. 2009 Jun;6(2):105-16.PMID: 19683211 [PubMed - in process]Related articles

    15.

    Orexin/hypocretin signaling at the orexin 1 receptor regulates cue-elicited cocaine-seeking.

    Smith RJ, See RE, Aston-Jones G.

    Eur J Neurosci. 2009 Aug;30(3):493-503. Epub 2009 Jul 28.PMID: 19656173 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Inactivating the activated: identifying functions of specific neural networks.

    Smith RJ, Aston-Jones G.

    Nat Neurosci. 2009 Aug;12(8):965-6. No abstract available. PMID: 19636350 [PubMed - indexed for MEDLINE]Related articles

    17.

    The Genetics of otosclerosis.

    Ealy M, Smith RJ.

    Hear Res. 2009 Jul 14. [Epub ahead of print]PMID: 19607896 [PubMed - as supplied by publisher]Related articles

    18.

    Function and expression pattern of nonsyndromic deafness genes.

    Hilgert N, Smith RJ, Van Camp G.

    Curr Mol Med. 2009 Jun;9(5):546-64.PMID: 19601806 [PubMed - in process]Related articles

    19.

    Alexithymia, absorption, and cognitive failures in depersonalization disorder: a comparison to posttraumatic stress disorder and healthy volunteers.

    Simeon D, Giesbrecht T, Knutelska M, Smith RJ, Smith LM.

    J Nerv Ment Dis. 2009 Jul;197(7):492-8.PMID: 19597356 [PubMed - indexed for MEDLINE]Related articles

    20.

    Orexin/hypocretin is necessary for context-driven cocaine-seeking.

    Smith RJ, Tahsili-Fahadan P, Aston-Jones G.

    Neuropharmacology. 2010 Jan;58(1):179-84. Epub 2009 Jul 8.PMID: 19591850 [PubMed - in process]Related articles

    21.

    Sexual intercourse involving giant sperm in Cretaceous ostracode.

    Matzke-Karasz R, Smith RJ, Symonova R, Miller CG, Tafforeau P.

    Science. 2009 Jun 19;324(5934):1535.PMID: 19541990 [PubMed - indexed for MEDLINE]Related articles

    22.

    No Evidence for Association Between the Renin-Angiotensin-Aldosterone System and Otosclerosis in a Large Belgian-Dutch Population.

    Schrauwen I, Thys M, Vanderstraeten K, Fransen E, Ealy M, Cremers CW, Dhooge I, Van de Heyning P, Offeciers E, Smith RJ, Van Camp G.

    Otol Neurotol. 2009 Dec;30(8):1079-1083.PMID: 19503013 [PubMed - as supplied by publisher]Related articles

    23.

    Therapeutic regulation of gene expression in the inner ear using RNA interference.

    Maeda Y, Sheffield AM, Smith RJ.

    Adv Otorhinolaryngol. 2009;66:13-36. Epub 2009 Jun 2. Review.PMID: 19494570 [PubMed - indexed for MEDLINE]Related articles

    24.

    Col11a2 deletion reveals the molecular basis for tectorial membrane mechanical anisotropy.

    Masaki K, Gu JW, Ghaffari R, Chan G, Smith RJ, Freeman DM, Aranyosi AJ.

    Biophys J. 2009 Jun 3;96(11):4717-24.PMID: 19486694 [PubMed - indexed for MEDLINE]Related articles

    25.

    The rare third branchial cleft cyst.

    Joshi MJ, Provenzano MJ, Smith RJ, Sato Y, Smoker WR.

    AJNR Am J Neuroradiol. 2009 Oct;30(9):1804-6. Epub 2009 May 27.PMID: 19474121 [PubMed - in process]Related articles

    26.

    Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.

    Yang T, Gurrola JG 2nd, Wu H, Chiu SM, Wangemann P, Snyder PM, Smith RJ.

    Am J Hum Genet. 2009 May;84(5):651-7. Epub 2009 May 7.PMID: 19426954 [PubMed - indexed for MEDLINE]Related articlesFree article

    27.

    Use and misuse of the reduced major axis for line-fitting.

    Smith RJ.

    Am J Phys Anthropol. 2009 Nov;140(3):476-86.PMID: 19425097 [PubMed - in process]Related articles

    28.

    Contributions of dust exposure and cigarette smoking to emphysema severity in coal miners in the United States.

    Kuempel ED, Wheeler MW, Smith RJ, Vallyathan V, Green FH.

    Am J Respir Crit Care Med. 2009 Aug 1;180(3):257-64. Epub 2009 May 7.PMID: 19423717 [PubMed - indexed for MEDLINE]Related articles

    29.

    A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family.

    Hilgert N, Kahrizi K, Dieltjens N, Bazazzadegan N, Najmabadi H, Smith RJ, Van Camp G.

    J Med Genet. 2009 Apr;46(4):272-6.PMID: 19357116 [PubMed - indexed for MEDLINE]Related articles

    30.

    Human male infertility caused by mutations in the CATSPER1 channel protein.

    Avenarius MR, Hildebrand MS, Zhang Y, Meyer NC, Smith LL, Kahrizi K, Najmabadi H, Smith RJ.

    Am J Hum Genet. 2009 Apr;84(4):505-10. Epub 2009 Apr 2.PMID: 19344877 [PubMed - indexed for MEDLINE]Related articlesFree article

    31.

    Middle ear adenoma with neuroendocrine differentiation (MEA-ND) in the pediatric population.

    Dogru S, Wilkinson EP, Robinson RA, Smith RJ.

    Int J Pediatr Otorhinolaryngol. 2009 Jun;73(6):895-8. Epub 2009 Mar 19.PMID: 19303146 [PubMed - indexed for MEDLINE]Related articles

    32.

    Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss.

    Shearer AE, Hildebrand MS, Webster JA, Kahrizi K, Meyer NC, Jalalvand K, Arzhanginy S, Kimberling WJ, Stephan D, Bahlo M, Smith RJ, Najmabadi H.

    Laryngoscope. 2009 Apr;119(4):727-33.PMID: 19274735 [PubMed - indexed for MEDLINE]Related articles

    33.

    A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.

    Schrauwen I, Ealy M, Huentelman MJ, Thys M, Homer N, Vanderstraeten K, Fransen E, Corneveaux JJ, Craig DW, Claustres M, Cremers CW, Dhooge I, Van de Heyning P, Vincent R, Offeciers E, Smith RJ, Van Camp G.

    Am J Hum Genet. 2009 Mar;84(3):328-38. Epub 2009 Feb 19.PMID: 19230858 [PubMed - indexed for MEDLINE]Related articlesFree article

    34.

    Liquid phase production of graphene by exfoliation of graphite in surfactant/water solutions.

    Lotya M, Hernandez Y, King PJ, Smith RJ, Nicolosi V, Karlsson LS, Blighe FM, De S, Wang Z, McGovern IT, Duesberg GS, Coleman JN.

    J Am Chem Soc. 2009 Mar 18;131(10):3611-20.PMID: 19227978 [PubMed]Related articles

    35.

    A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family.

    Shearer AE, Hildebrand MS, Bromhead CJ, Kahrizi K, Webster JA, Azadeh B, Kimberling WJ, Anousheh A, Nazeri A, Stephan D, Najmabadi H, Smith RJ, Bahlo M.

    Am J Med Genet A. 2009 Mar;149A(3):555-8. No abstract available. PMID: 19215054 [PubMed - indexed for MEDLINE]Related articles

    36.

    Familial transmission of oculoauriculovertebral spectrum (Goldenhar syndrome) is not due to mutations in either EYA1 or SALL1.

    Goodin K, Prucka S, Woolley AL, Kohlhase J, Smith RJ, Grant J, Robin NH.

    Am J Med Genet A. 2009 Mar;149A(3):535-8. No abstract available. PMID: 19213029 [PubMed - indexed for MEDLINE]Related articles

    37.

    Glomeruli of Dense Deposit Disease contain components of the alternative and terminal complement pathway.

    Sethi S, Gamez JD, Vrana JA, Theis JD, Bergen HR 3rd, Zipfel PF, Dogan A, Smith RJ.

    Kidney Int. 2009 May;75(9):952-60. Epub 2009 Jan 28.PMID: 19177158 [PubMed - indexed for MEDLINE]Related articlesFree article

    38.

    Can the viral reservoir of latently infected CD4(+) T cells be eradicated with antiretroviral HIV drugs?

    Smith RJ, Aggarwala BD.

    J Math Biol. 2009 Nov;59(5):697-715. Epub 2009 Jan 23.PMID: 19165438 [PubMed - in process]Related articles

    39.

    Continuous decoding of finger position from surface EMG signals for the control of powered prostheses.

    Smith RJ, Tenore F, Huberdeau D, Etienne-Cummings R, Thakor NV.

    Conf Proc IEEE Eng Med Biol Soc. 2008;2008:197-200.PMID: 19162627 [PubMed - indexed for MEDLINE]Related articles

    40.

    Mutation in the COCH gene is associated with superior semicircular canal dehiscence.

    Hildebrand MS, Tack D, Deluca A, Hur IA, Van Rybroek JM, McMordie SJ, Muilenburg A, Hoskinson DP, Van Camp G, Pensak ML, Storper IS, Huygen PL, Casavant TL, Smith RJ.

    Am J Med Genet A. 2009 Feb;149A(2):280-5. No abstract available. PMID: 19161137 [PubMed - indexed for MEDLINE]Related articles

    41.

    Efficacy and safety of OK-432 immunotherapy of lymphatic malformations.

    Smith MC, Zimmerman MB, Burke DK, Bauman NM, Sato Y, Smith RJ; OK-432 Collaborative Study Group.

    Laryngoscope. 2009 Jan;119(1):107-15.PMID: 19117316 [PubMed - indexed for MEDLINE]Related articles

    42.

    Monitoring stress levels in postgraduate medical training.

    Hill JD, Smith RJ.

    Laryngoscope. 2009 Jan;119(1):75-8.PMID: 19117300 [PubMed - indexed for MEDLINE]Related articles

    43.

    Molecular phylogenetics of Haemodoraceae in the Greater Cape and Southwest Australian Floristic Regions.

    Hopper SD, Smith RJ, Fay MF, Manning JC, Chase MW.

    Mol Phylogenet Evol. 2009 Apr;51(1):19-30. Epub 2008 Dec 3.PMID: 19063982 [PubMed - indexed for MEDLINE]Related articles

    44.

    Factor I and factor H deficiency in renal diseases: similar defects in the fluid phase have a different outcome at the surface of the glomerular basement membrane.

    Zipfel PF, Smith RJ, Skerka C.

    Nephrol Dial Transplant. 2009 Feb;24(2):385-7. Epub 2008 Dec 4. Review. No abstract available. PMID: 19056782 [PubMed - indexed for MEDLINE]Related articles

    45.

    Nonperturbative measurement of the local magnetic field using pulsed polarimetry for fusion reactor conditions (invited).

    Smith RJ.

    Rev Sci Instrum. 2008 Oct;79(10):10E703.PMID: 19044521 [PubMed]Related articles

    46.

    Somatoform dissociation in depersonalization disorder.

    Simeon D, Smith RJ, Knutelska M, Smith LM.

    J Trauma Dissociation. 2008;9(3):335-48.PMID: 19042782 [PubMed - indexed for MEDLINE]Related articles

    47.

    Production of high titre disabled infectious single cycle (DISC) HSV from a microcarrier culture.

    Zecchini TA, Smith RJ.

    Cytotechnology. 1999 Jul;30(1-3):203-10.PMID: 19003370 [PubMed - in process]Related articles

    48.

    Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.

    Hilgert N, Huentelman MJ, Thorburn AQ, Fransen E, Dieltjens N, Mueller-Malesinska M, Pollak A, Skorka A, Waligora J, Ploski R, Castorina P, Primignani P, Ambrosetti U, Murgia A, Orzan E, Pandya A, Arnos K, Norris V, Seeman P, Janousek P, Feldmann D, Marlin S, Denoyelle F, Nishimura CJ, Janecke A, Nekahm-Heis D, Martini A, Mennucci E, Tóth T, Sziklai I, Del Castillo I, Moreno F, Petersen MB, Iliadou V, Tekin M, Incesulu A, Nowakowska E, Bal J, Van de Heyning P, Roux AF, Blanchet C, Goizet C, Lancelot G, Fialho G, Caria H, Liu XZ, Xiaomei O, Govaerts P, Grønskov K, Hostmark K, Frei K, Dhooge I, Vlaeminck S, Kunstmann E, Van Laer L, Smith RJ, Van Camp G.

    Eur J Hum Genet. 2009 Apr;17(4):517-24. Epub 2008 Nov 5.PMID: 18985073 [PubMed - indexed for MEDLINE]Related articles

    49.

    Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.

    Hildebrand MS, Tack D, McMordie SJ, DeLuca A, Hur IA, Nishimura C, Huygen P, Casavant TL, Smith RJ.

    Genet Med. 2008 Nov;10(11):797-804.PMID: 18941426 [PubMed - indexed for MEDLINE]Related articles

    50.

    Ecology and genetic diversity of the dense-flowered orchid, Neotinea maculata, at the centre and edge of its range.

    Duffy KJ, Scopece G, Cozzolino S, Fay MF, Smith RJ, Stout JC.

    Ann Bot. 2009 Aug;104(3):507-16. Epub 2008 Oct 21.PMID: 18940852 [PubMed - indexed for MEDLINE]Related articles

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