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Items: 1 to 50 of 119

1.

CHD4 regulates the DNA damage response and RAD51 expression in glioblastoma.

McKenzie LD, LeClair JW, Miller KN, Strong AD, Chan HL, Oates EL, Ligon KL, Brennan CW, Chheda MG.

Sci Rep. 2019 Mar 14;9(1):4444. doi: 10.1038/s41598-019-40327-w.

2.

New atrial fibrillation diagnosed by 30-day rhythm monitoring.

Farris GR, Smith BG, Oates ET, Colon C, Doppalapudi H.

Am Heart J. 2019 Mar;209:29-35. doi: 10.1016/j.ahj.2018.11.003. Epub 2018 Nov 12.

PMID:
30639611
3.

Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures.

Böhm J, Malfatti E, Oates E, Jones K, Brochier G, Boland A, Deleuze JF, Romero NB, Laporte J.

J Med Genet. 2018 Oct 16. pii: jmedgenet-2018-105390. doi: 10.1136/jmedgenet-2018-105390. [Epub ahead of print]

PMID:
30327447
4.

Congenital Titinopathy: Comprehensive characterization and pathogenic insights.

Oates EC, Jones KJ, Donkervoort S, Charlton A, Brammah S, Smith JE 3rd, Ware JS, Yau KS, Swanson LC, Whiffin N, Peduto AJ, Bournazos A, Waddell LB, Farrar MA, Sampaio HA, Teoh HL, Lamont PJ, Mowat D, Fitzsimons RB, Corbett AJ, Ryan MM, O'Grady GL, Sandaradura SA, Ghaoui R, Joshi H, Marshall JL, Nolan MA, Kaur S, Punetha J, Töpf A, Harris E, Bakshi M, Genetti CA, Marttila M, Werlauff U, Streichenberger N, Pestronk A, Mazanti I, Pinner JR, Vuillerot C, Grosmann C, Camacho A, Mohassel P, Leach ME, Foley AR, Bharucha-Goebel D, Collins J, Connolly AM, Gilbreath HR, Iannaccone ST, Castro D, Cummings BB, Webster RI, Lazaro L, Vissing J, Coppens S, Deconinck N, Luk HM, Thomas NH, Foulds NC, Illingworth MA, Ellard S, McLean CA, Phadke R, Ravenscroft G, Witting N, Hackman P, Richard I, Cooper ST, Kamsteeg EJ, Hoffman EP, Bushby K, Straub V, Udd B, Ferreiro A, North KN, Clarke NF, Lek M, Beggs AH, Bönnemann CG, MacArthur DG, Granzier H, Davis MR, Laing NG.

Ann Neurol. 2018 Jun;83(6):1105-1124. doi: 10.1002/ana.25241.

PMID:
29691892
5.

Tales of diversity: Genomic and morphological characteristics of forty-six Arthrobacter phages.

Klyczek KK, Bonilla JA, Jacobs-Sera D, Adair TL, Afram P, Allen KG, Archambault ML, Aziz RM, Bagnasco FG, Ball SL, Barrett NA, Benjamin RC, Blasi CJ, Borst K, Braun MA, Broomell H, Brown CB, Brynell ZS, Bue AB, Burke SO, Casazza W, Cautela JA, Chen K, Chimalakonda NS, Chudoff D, Connor JA, Cross TS, Curtis KN, Dahlke JA, Deaton BM, Degroote SJ, DeNigris DM, DeRuff KC, Dolan M, Dunbar D, Egan MS, Evans DR, Fahnestock AK, Farooq A, Finn G, Fratus CR, Gaffney BL, Garlena RA, Garrigan KE, Gibbon BC, Goedde MA, Guerrero Bustamante CA, Harrison M, Hartwell MC, Heckman EL, Huang J, Hughes LE, Hyduchak KM, Jacob AE, Kaku M, Karstens AW, Kenna MA, Khetarpal S, King RA, Kobokovich AL, Kolev H, Konde SA, Kriese E, Lamey ME, Lantz CN, Lapin JS, Lawson TO, Lee IY, Lee SM, Lee-Soety JY, Lehmann EM, London SC, Lopez AJ, Lynch KC, Mageeney CM, Martynyuk T, Mathew KJ, Mavrich TN, McDaniel CM, McDonald H, McManus CJ, Medrano JE, Mele FE, Menninger JE, Miller SN, Minick JE, Nabua CT, Napoli CK, Nkangabwa M, Oates EA, Ott CT, Pellerino SK, Pinamont WJ, Pirnie RT, Pizzorno MC, Plautz EJ, Pope WH, Pruett KM, Rickstrew G, Rimple PA, Rinehart CA, Robinson KM, Rose VA, Russell DA, Schick AM, Schlossman J, Schneider VM, Sells CA, Sieker JW, Silva MP, Silvi MM, Simon SE, Staples AK, Steed IL, Stowe EL, Stueven NA, Swartz PT, Sweet EA, Sweetman AT, Tender C, Terry K, Thomas C, Thomas DS, Thompson AR, Vanderveen L, Varma R, Vaught HL, Vo QD, Vonberg ZT, Ware VC, Warrad YM, Wathen KE, Weinstein JL, Wyper JF, Yankauskas JR, Zhang C, Hatfull GF.

PLoS One. 2017 Jul 17;12(7):e0180517. doi: 10.1371/journal.pone.0180517. eCollection 2017.

6.

Usefulness of three-dimensional echocardiography in the assessment of valvular involvement in Loeffler endocarditis.

Hernandez CM, Arisha MJ, Ahmad A, Oates E, Nanda NC, Nanda A, Wasan A, Caleti BE, Bernal CLP, Gallardo SM.

Echocardiography. 2017 Jul;34(7):1050-1056. doi: 10.1111/echo.13575. Epub 2017 Jun 9.

PMID:
28600838
7.

Improving genetic diagnosis in Mendelian disease with transcriptome sequencing.

Cummings BB, Marshall JL, Tukiainen T, Lek M, Donkervoort S, Foley AR, Bolduc V, Waddell LB, Sandaradura SA, O'Grady GL, Estrella E, Reddy HM, Zhao F, Weisburd B, Karczewski KJ, O'Donnell-Luria AH, Birnbaum D, Sarkozy A, Hu Y, Gonorazky H, Claeys K, Joshi H, Bournazos A, Oates EC, Ghaoui R, Davis MR, Laing NG, Topf A; Genotype-Tissue Expression Consortium, Kang PB, Beggs AH, North KN, Straub V, Dowling JJ, Muntoni F, Clarke NF, Cooper ST, Bönnemann CG, MacArthur DG.

Sci Transl Med. 2017 Apr 19;9(386). pii: eaal5209. doi: 10.1126/scitranslmed.aal5209.

8.

Descending septal branch of right coronary artery: Rare, but important in hypertrophic cardiomyopathy.

Chatterjee A, Oates ET, Leesar MA, Alli OO.

Cardiovasc Revasc Med. 2017 Sep;18(6S1):23-25. doi: 10.1016/j.carrev.2017.03.026. Epub 2017 Mar 25.

PMID:
28365416
9.

Targeted Re-Sequencing Emulsion PCR Panel for Myopathies: Results in 94 Cases.

Punetha J, Kesari A, Uapinyoying P, Giri M, Clarke NF, Waddell LB, North KN, Ghaoui R, O'Grady GL, Oates EC, Sandaradura SA, Bönnemann CG, Donkervoort S, Plotz PH, Smith EC, Tesi-Rocha C, Bertorini TE, Tarnopolsky MA, Reitter B, Hausmanowa-Petrusewicz I, Hoffman EP.

J Neuromuscul Dis. 2016 May 27;3(2):209-225.

PMID:
27854218
10.

Diagnosis and etiology of congenital muscular dystrophy: We are halfway there.

O'Grady GL, Lek M, Lamande SR, Waddell L, Oates EC, Punetha J, Ghaoui R, Sandaradura SA, Best H, Kaur S, Davis M, Laing NG, Muntoni F, Hoffman E, MacArthur DG, Clarke NF, Cooper S, North K.

Ann Neurol. 2016 Jul;80(1):101-11. doi: 10.1002/ana.24687. Epub 2016 May 25.

PMID:
27159402
11.

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.

Zaharieva IT, Thor MG, Oates EC, van Karnebeek C, Hendson G, Blom E, Witting N, Rasmussen M, Gabbett MT, Ravenscroft G, Sframeli M, Suetterlin K, Sarkozy A, D'Argenzio L, Hartley L, Matthews E, Pitt M, Vissing J, Ballegaard M, Krarup C, Slørdahl A, Halvorsen H, Ye XC, Zhang LH, Løkken N, Werlauff U, Abdelsayed M, Davis MR, Feng L, Phadke R, Sewry CA, Morgan JE, Laing NG, Vallance H, Ruben P, Hanna MG, Lewis S, Kamsteeg EJ, Männikkö R, Muntoni F.

Brain. 2016 Mar;139(Pt 3):674-91. doi: 10.1093/brain/awv352. Epub 2015 Dec 22.

12.

Reply: The p.Ser107Leu in BICD2 is a mutation 'hot spot' causing distal spinal muscular atrophy.

Rossor AM, Oates EC, Salter HK, Liu Y, Murphy SM, Schule R, Gonzales MA, Scoto M, Phadke R, Sewry CA, Houlden H, Jordanova A, Tournev I, Chamova T, Litvinenko I, Zuchner S, Herrmann DN, Blake J, Sowden JE, Acsadi G, Rodriguez ML, Menezes MP, Clarke NF, Auer Grumbach M, Bullock SL, Muntoni F, Reilly MM, North KN.

Brain. 2015 Nov;138(Pt 11):e392. doi: 10.1093/brain/awv160. Epub 2015 Jun 10. No abstract available.

13.

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2.

Rossor AM, Oates EC, Salter HK, Liu Y, Murphy SM, Schule R, Gonzalez MA, Scoto M, Phadke R, Sewry CA, Houlden H, Jordanova A, Tournev I, Chamova T, Litvinenko I, Zuchner S, Herrmann DN, Blake J, Sowden JE, Acsadi G, Rodriguez ML, Menezes MP, Clarke NF, Auer Grumbach M, Bullock SL, Muntoni F, Reilly MM, North KN.

Brain. 2015 Feb;138(Pt 2):293-310. doi: 10.1093/brain/awu356. Epub 2014 Dec 14.

14.

Recessive ACTA1 variant causes congenital muscular dystrophy with rigid spine.

O'Grady GL, Best HA, Oates EC, Kaur S, Charlton A, Brammah S, Punetha J, Kesari A, North KN, Ilkovski B, Hoffman EP, Clarke NF.

Eur J Hum Genet. 2015 Jun;23(6):883-6. doi: 10.1038/ejhg.2014.169. Epub 2014 Sep 3.

15.

Longitudinal assessment of cognition and T2-hyperintensities in NF1: an 18-year study.

Payne JM, Pickering T, Porter M, Oates EC, Walia N, Prelog K, North KN.

Am J Med Genet A. 2014 Mar;164A(3):661-5. doi: 10.1002/ajmg.a.36338. Epub 2013 Dec 19.

PMID:
24357578
16.

Stability of cervical specimens in SurePath medium for human papillomavirus testing with the Roche cobas 4800 assay.

Gilbert L, Oates E, Ratnam S.

J Clin Microbiol. 2013 Oct;51(10):3412-4. doi: 10.1128/JCM.01391-13. Epub 2013 Jul 31.

17.

Pre-operative staging of the axilla in primary breast cancer. By redefining the abnormal appearing node can we reduce investigations without affecting overall treatment?

Amonkar SJ, Oates E, McLean L, Nicholson S.

Breast. 2013 Dec;22(6):1114-8. doi: 10.1016/j.breast.2013.06.004. Epub 2013 Jul 11.

PMID:
23849874
18.

Evolution of the human gastrokine locus and confounding factors regarding the pseudogenicity of GKN3.

Geahlen JH, Lapid C, Thorell K, Nikolskiy I, Huh WJ, Oates EL, Lennerz JK, Tian X, Weis VG, Khurana SS, Lundin SB, Templeton AR, Mills JC.

Physiol Genomics. 2013 Aug 1;45(15):667-83. doi: 10.1152/physiolgenomics.00169.2012. Epub 2013 May 28.

19.

Mutations in BICD2 cause dominant congenital spinal muscular atrophy and hereditary spastic paraplegia.

Oates EC, Rossor AM, Hafezparast M, Gonzalez M, Speziani F, MacArthur DG, Lek M, Cottenie E, Scoto M, Foley AR, Hurles M, Houlden H, Greensmith L, Auer-Grumbach M, Pieber TR, Strom TM, Schule R, Herrmann DN, Sowden JE, Acsadi G, Menezes MP, Clarke NF, Züchner S; UK10K, Muntoni F, North KN, Reilly MM.

Am J Hum Genet. 2013 Jun 6;92(6):965-73. doi: 10.1016/j.ajhg.2013.04.018. Epub 2013 May 9.

20.

Young Australian adults with NF1 have poor access to health care, high complication rates, and limited disease knowledge.

Oates EC, Payne JM, Foster SL, Clarke NF, North KN.

Am J Med Genet A. 2013 Apr;161A(4):659-66. doi: 10.1002/ajmg.a.35840. Epub 2013 Feb 20.

PMID:
23427176
21.

Neuromuscular junction abnormalities in DNM2-related centronuclear myopathy.

Gibbs EM, Clarke NF, Rose K, Oates EC, Webster R, Feldman EL, Dowling JJ.

J Mol Med (Berl). 2013 Jun;91(6):727-37. doi: 10.1007/s00109-013-0994-4. Epub 2013 Jan 22.

PMID:
23338057
22.

Autosomal dominant congenital spinal muscular atrophy: a true form of spinal muscular atrophy caused by early loss of anterior horn cells.

Oates EC, Reddel S, Rodriguez ML, Gandolfo LC, Bahlo M, Hawke SH, Lamandé SR, Clarke NF, North KN.

Brain. 2012 Jun;135(Pt 6):1714-23. doi: 10.1093/brain/aws108.

PMID:
22628388
23.

Interaction between enfuvirtide, an injectable fusion inhibitor, and niacin in an HIV-infected patient.

Oates E, Dzintars K.

Ann Pharmacother. 2010 Dec;44(12):2014-7. doi: 10.1345/aph.1P346. Epub 2010 Nov 2.

PMID:
21045170
24.

Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.

Kouwenhoven EN, van Heeringen SJ, Tena JJ, Oti M, Dutilh BE, Alonso ME, de la Calle-Mustienes E, Smeenk L, Rinne T, Parsaulian L, Bolat E, Jurgelenaite R, Huynen MA, Hoischen A, Veltman JA, Brunner HG, Roscioli T, Oates E, Wilson M, Manzanares M, Gómez-Skarmeta JL, Stunnenberg HG, Lohrum M, van Bokhoven H, Zhou H.

PLoS Genet. 2010 Aug 19;6(8):e1001065. doi: 10.1371/journal.pgen.1001065.

25.

The transcription factor MIST1 is a novel human gastric chief cell marker whose expression is lost in metaplasia, dysplasia, and carcinoma.

Lennerz JK, Kim SH, Oates EL, Huh WJ, Doherty JM, Tian X, Bredemeyer AJ, Goldenring JR, Lauwers GY, Shin YK, Mills JC.

Am J Pathol. 2010 Sep;177(3):1514-33. doi: 10.2353/ajpath.2010.100328. Epub 2010 Aug 13.

26.

RAB26 and RAB3D are direct transcriptional targets of MIST1 that regulate exocrine granule maturation.

Tian X, Jin RU, Bredemeyer AJ, Oates EJ, Błazewska KM, McKenna CE, Mills JC.

Mol Cell Biol. 2010 Mar;30(5):1269-84. doi: 10.1128/MCB.01328-09. Epub 2009 Dec 28.

27.

A necessary and sufficient determinant for protein-selective glycosylation in vivo.

Miller E, Fiete D, Blake NM, Beranek M, Oates EL, Mi Y, Roseman DS, Baenziger JU.

J Biol Chem. 2008 Jan 25;283(4):1985-91. Epub 2007 Nov 29.

28.

Scintigraphic evaluation of intrathecal infusion systems: selection of patients for surgical or medical management.

Stinchon JF, Shah NP, Ordia J, Oates E.

Clin Nucl Med. 2006 Jan;31(1):1-4.

PMID:
16374111
29.

Excision of a mediastinal parathyroid adenoma after coronary artery bypass surgery.

Lazar HL, Oates E, Beazley RM.

Ann Thorac Surg. 2005 Sep;80(3):1105-6.

PMID:
16122500
30.

Radionuclide imaging of the thyroid gland: patterns, pearls, and pitfalls.

Smith JR, Oates E.

Clin Nucl Med. 2004 Mar;29(3):181-93. Review.

PMID:
15162989
31.

Metal-directed self-assembly of bimetallic dithiocarbamate transition metal cryptands and their binding capabilities.

Beer PD, Berry NG, Cowley AR, Hayes EJ, Oates EC, Wong WW.

Chem Commun (Camb). 2003 Oct 7;(19):2408-9.

PMID:
14587705
32.

Rhabdomyolysis of bilateral teres major muscles.

Oza UD, Oates E.

Clin Nucl Med. 2003 Feb;28(2):126-7. No abstract available.

PMID:
12544131
33.

Normal gallbladder ejection fraction after morphine augmentation.

Achong DM, Oates E.

Clin Nucl Med. 1999 Nov;24(11):837-41.

PMID:
10551461
34.

Risperidone as an adjunct therapy for post-traumatic stress disorder.

Krashin D, Oates EW.

Mil Med. 1999 Aug;164(8):605-6.

PMID:
10459276
35.

Testes exhibit elevated expression of calcitonin gene-related peptide receptor component protein.

Balkan W, Oates EL, Howard GA, Roos BA.

Endocrinology. 1999 Mar;140(3):1459-69.

PMID:
10067875
36.

Does local irradiation affect gastric emptying in humans?

Makrauer FL, Oates E, Becker J, Abrams R, O'Connor T, McCallum R, Shumaker J.

Am J Med Sci. 1999 Jan;317(1):33-7.

PMID:
9892269
37.

Post-therapy iodine-131 localization in unsuspected large renal cyst: possible mechanisms.

Wen C, Iuanow E, Oates E, Lee SL, Perrone R.

J Nucl Med. 1998 Dec;39(12):2158-61.

38.

Thoracic uptake of technetium-99m-HDP.

Kim KS, Oates E.

J Nucl Med. 1998 Nov;39(11):2014. No abstract available.

39.

Unusual appearance of lingual thyroid in congenital hypothyroidism.

Strain J, Oates E, Sadeghi-Nejad A.

Clin Nucl Med. 1998 Jul;23(7):460. No abstract available.

PMID:
9676951
40.

In-111 DTPA to evaluate the patency of an implanted intrathecal infusion pump.

Schmidt E, Oates E.

Clin Nucl Med. 1997 Nov;22(11):768-70.

PMID:
9363387
41.

Effect of multiple coil closure of patent ductus arteriosus on blood flow to the left lung as determined by lung perfusion scans.

Evangelista JK, Hijazi ZM, Geggel RL, Oates E, Fulton DR.

Am J Cardiol. 1997 Jul 15;80(2):242-4.

PMID:
9230177
42.
44.

Early cardioverter defibrillator infection: value of indium-111 leukocyte imaging.

Bhadelia RA, Oates E.

Ann Thorac Surg. 1997 Jan;63(1):236-8.

PMID:
8993278
45.

Immunity against measles in school-aged children: implications for measles revaccination strategies.

Ratnam S, West R, Gadag V, Williams B, Oates E.

Can J Public Health. 1996 Nov-Dec;87(6):407-10.

PMID:
9009400
46.

Gastric emptying and first-pass metabolism of ethanol in elderly subjects with and without atrophic gastritis.

Pedrosa MC, Russell RM, Saltzman JR, Golner BB, Dallal GE, Sepe TE, Oates E, Egerer G, Seitz HK.

Scand J Gastroenterol. 1996 Jul;31(7):671-7.

PMID:
8819216
47.
48.
49.

Enhanced hepatic uptake of thallium-201 in patients with severe narrowing of the right coronary artery.

Chuttani K, Metherall J, Griffith J, Oates E, Konstam MA, Pauker SG, Salem DN, Udelson JE.

Am J Cardiol. 1995 Nov 15;76(14):1020-4.

PMID:
7484854
50.

Technetium-99m-sulfur colloid SPECT imaging in infants with suspected heterotaxy syndrome.

Oates E, Austin JM, Becker JL.

J Nucl Med. 1995 Aug;36(8):1368-71.

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