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Items: 1 to 50 of 141

2.

Hispanic Men and Women's Knowledge, Beliefs, Perceived Susceptibility, and Barriers to Clinical Breast Examination and Mammography Practices in South Texas Colonias.

Bolton CD, Sunil TS, Hurd T, Guerra H.

J Community Health. 2019 Jun 3. doi: 10.1007/s10900-019-00682-1. [Epub ahead of print]

PMID:
31161398
3.

Mitochondrial fragmentation drives selective removal of deleterious mtDNA in the germline.

Lieber T, Jeedigunta SP, Palozzi JM, Lehmann R, Hurd TR.

Nature. 2019 Jun;570(7761):380-384. doi: 10.1038/s41586-019-1213-4. Epub 2019 May 15.

PMID:
31092924
4.

Photoreceptor actin dysregulation in syndromic and non-syndromic retinitis pigmentosa.

Megaw R, Hurd TW.

Biochem Soc Trans. 2018 Dec 17;46(6):1463-1473. doi: 10.1042/BST20180138. Epub 2018 Nov 21. Review.

PMID:
30464047
5.

Mitochondrial DNA Purifying Selection in Mammals and Invertebrates.

Palozzi JM, Jeedigunta SP, Hurd TR.

J Mol Biol. 2018 Dec 7;430(24):4834-4848. doi: 10.1016/j.jmb.2018.10.019. Epub 2018 Oct 30. Review.

PMID:
30385240
6.

Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells.

Kistler KE, Trcek T, Hurd TR, Chen R, Liang FX, Sall J, Kato M, Lehmann R.

Elife. 2018 Sep 27;7. pii: e37949. doi: 10.7554/eLife.37949.

7.

Ambivalence: A Key to Clinical Trial Participation?

Chilton JA, Rasmus ML, Lytton J, Kaplan CD, Jones LA, Hurd TC.

Front Oncol. 2018 Aug 10;8:300. doi: 10.3389/fonc.2018.00300. eCollection 2018. Review.

8.

Intermediate frequency of aversive conditioning best restores wariness in habituated elk (Cervus canadensis).

Found R, Kloppers EL, Hurd TE, St Clair CC.

PLoS One. 2018 Jun 25;13(6):e0199216. doi: 10.1371/journal.pone.0199216. eCollection 2018.

9.

Characterization of a novel RP2-OSTF1 interaction and its implication for actin remodelling.

Lyraki R, Lokaj M, Soares DC, Little A, Vermeren M, Marsh JA, Wittinghofer A, Hurd T.

J Cell Sci. 2018 Feb 20;131(4). pii: jcs211748. doi: 10.1242/jcs.211748.

10.

A fluorescent activatable probe for imaging intracellular Mg2+ .

Treadwell R, de Moliner F, Subiros-Funosas R, Hurd T, Knox K, Vendrell M.

Org Biomol Chem. 2018 Jan 3;16(2):239-244. doi: 10.1039/c7ob02965a.

11.

Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes.

Corre T, Arjona FJ, Hayward C, Youhanna S, de Baaij JHF, Belge H, Nägele N, Debaix H, Blanchard MG, Traglia M, Harris SE, Ulivi S, Rueedi R, Lamparter D, Macé A, Sala C, Lenarduzzi S, Ponte B, Pruijm M, Ackermann D, Ehret G, Baptista D, Polasek O, Rudan I, Hurd TW, Hastie ND, Vitart V, Waeber G, Kutalik Z, Bergmann S, Vargas-Poussou R, Konrad M, Gasparini P, Deary IJ, Starr JM, Toniolo D, Vollenweider P, Hoenderop JGJ, Bindels RJM, Bochud M, Devuyst O.

J Am Soc Nephrol. 2018 Jan;29(1):335-348. doi: 10.1681/ASN.2017030267. Epub 2017 Nov 1.

12.

Osteoclast stimulation factor 1 (Ostf1) KNOCKOUT increases trabecular bone mass in mice.

Vermeren M, Lyraki R, Wani S, Airik R, Albagha O, Mort R, Hildebrandt F, Hurd T.

Mamm Genome. 2017 Dec;28(11-12):498-514. doi: 10.1007/s00335-017-9718-3. Epub 2017 Sep 21.

13.

A framework for analyzing contagion in assortative banking networks.

Hurd TR, Gleeson JP, Melnik S.

PLoS One. 2017 Feb 23;12(2):e0170579. doi: 10.1371/journal.pone.0170579. eCollection 2017.

14.

Building trust and diversity in patient-centered oncology clinical trials: An integrated model.

Hurd TC, Kaplan CD, Cook ED, Chilton JA, Lytton JS, Hawk ET, Jones LA.

Clin Trials. 2017 Apr;14(2):170-179. doi: 10.1177/1740774516688860. Epub 2017 Feb 7. Review.

PMID:
28166647
15.

A Retrospective Comparison of the Performance of Two Negative Pressure Wound Therapy Systems in the Management of Wounds of Mixed Etiology.

Hurd T, Rossington A, Trueman P, Smith J.

Adv Wound Care (New Rochelle). 2017 Jan 1;6(1):33-37. doi: 10.1089/wound.2015.0679.

16.

Long Oskar Controls Mitochondrial Inheritance in Drosophila melanogaster.

Hurd TR, Herrmann B, Sauerwald J, Sanny J, Grosch M, Lehmann R.

Dev Cell. 2016 Dec 5;39(5):560-571. doi: 10.1016/j.devcel.2016.11.004.

17.

Disease mechanisms of X-linked retinitis pigmentosa due to RP2 and RPGR mutations.

Lyraki R, Megaw R, Hurd T.

Biochem Soc Trans. 2016 Oct 15;44(5):1235-1244. Review.

PMID:
27911705
18.

Correction: Curly Encodes Dual Oxidase, Which Acts with Heme Peroxidase Curly Su to Shape the Adult Drosophila Wing.

Hurd TR, Liang FX, Lehmann R.

PLoS Genet. 2016 Aug 26;12(8):e1006285. doi: 10.1371/journal.pgen.1006285. eCollection 2016 Aug.

19.

SDCCAG8 Interacts with RAB Effector Proteins RABEP2 and ERC1 and Is Required for Hedgehog Signaling.

Airik R, Schueler M, Airik M, Cho J, Ulanowicz KA, Porath JD, Hurd TW, Bekker-Jensen S, Schrøder JM, Andersen JS, Hildebrandt F.

PLoS One. 2016 May 25;11(5):e0156081. doi: 10.1371/journal.pone.0156081. eCollection 2016.

20.

Curly Encodes Dual Oxidase, Which Acts with Heme Peroxidase Curly Su to Shape the Adult Drosophila Wing.

Hurd TR, Liang FX, Lehmann R.

PLoS Genet. 2015 Nov 20;11(11):e1005625. doi: 10.1371/journal.pgen.1005625. eCollection 2015 Nov. Erratum in: PLoS Genet. 2016 Aug;12(8):e1006285.

21.

Optineurin Negatively Regulates Osteoclast Differentiation by Modulating NF-κB and Interferon Signaling: Implications for Paget's Disease.

Obaid R, Wani SE, Azfer A, Hurd T, Jones R, Cohen P, Ralston SH, Albagha OME.

Cell Rep. 2015 Nov 10;13(6):1096-1102. doi: 10.1016/j.celrep.2015.09.071. Epub 2015 Oct 29.

22.

Loss of retinitis pigmentosa 2 (RP2) protein affects cone photoreceptor sensory cilium elongation in mice.

Li L, Rao KN, Zheng-Le Y, Hurd TW, Lillo C, Khanna H.

Cytoskeleton (Hoboken). 2015 Sep;72(9):447-54. doi: 10.1002/cm.21255. Epub 2015 Oct 14.

23.

Ultrastructural Analysis of Drosophila Ovaries by Electron Microscopy.

Hurd TR, Sanchez CG, Teixeira FK, Petzold C, Dancel-Manning K, Wang JY, Lehmann R, Liang FX.

Methods Mol Biol. 2015;1328:151-62. doi: 10.1007/978-1-4939-2851-4_11.

24.

Sizing Individual Au Nanoparticles in Solution with Sub-Nanometer Resolution.

German SR, Hurd TS, White HS, Mega TL.

ACS Nano. 2015 Jul 28;9(7):7186-94. doi: 10.1021/acsnano.5b01963. Epub 2015 Jun 23.

PMID:
26083098
25.

ATP synthase promotes germ cell differentiation independent of oxidative phosphorylation.

Teixeira FK, Sanchez CG, Hurd TR, Seifert JR, Czech B, Preall JB, Hannon GJ, Lehmann R.

Nat Cell Biol. 2015 May;17(5):689-96. doi: 10.1038/ncb3165. Epub 2015 Apr 27.

26.

Evaluation of the stage IB designation of the American Joint Committee on Cancer staging system in breast cancer.

Mittendorf EA, Ballman KV, McCall LM, Yi M, Sahin AA, Bedrosian I, Hansen N, Gabram S, Hurd T, Giuliano AE, Hunt KK.

J Clin Oncol. 2015 Apr 1;33(10):1119-27. doi: 10.1200/JCO.2014.57.2958. Epub 2014 Dec 8.

27.

Mutations in EMP2 cause childhood-onset nephrotic syndrome.

Gee HY, Ashraf S, Wan X, Vega-Warner V, Esteve-Rudd J, Lovric S, Fang H, Hurd TW, Sadowski CE, Allen SJ, Otto EA, Korkmaz E, Washburn J, Levy S, Williams DS, Bakkaloglu SA, Zolotnitskaya A, Ozaltin F, Zhou W, Hildebrandt F.

Am J Hum Genet. 2014 Jun 5;94(6):884-90. doi: 10.1016/j.ajhg.2014.04.010. Epub 2014 May 8.

28.

Renal-retinal ciliopathy gene Sdccag8 regulates DNA damage response signaling.

Airik R, Slaats GG, Guo Z, Weiss AC, Khan N, Ghosh A, Hurd TW, Bekker-Jensen S, Schrøder JM, Elledge SJ, Andersen JS, Kispert A, Castelli M, Boletta A, Giles RH, Hildebrandt F.

J Am Soc Nephrol. 2014 Nov;25(11):2573-83. doi: 10.1681/ASN.2013050565. Epub 2014 Apr 10.

29.

Five National Cancer Institute-designated cancer centers' data collection on racial/ethnic minority participation in therapeutic trials: a current view and opportunities for improvement.

Hawk ET, Habermann EB, Ford JG, Wenzel JA, Brahmer JR, Chen MS Jr, Jones LA, Hurd TC, Rogers LM, Nguyen LH, Ahluwalia JS, Fouad M, Vickers SM.

Cancer. 2014 Apr 1;120 Suppl 7:1113-21. doi: 10.1002/cncr.28571.

30.
31.
32.

Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.

Knowles MR, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD, Rosenfeld M, Ferkol TW, Dell SD, Milla CE, Randell SH, Yin W, Sannuti A, Metjian HM, Noone PG, Noone PJ, Olson CA, Patrone MV, Dang H, Lee HS, Hurd TW, Gee HY, Otto EA, Halbritter J, Kohl S, Kircher M, Krischer J, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Zariwala MA.

Am J Respir Crit Care Med. 2014 Mar 15;189(6):707-17. doi: 10.1164/rccm.201311-2047OC.

33.

Towards a unified taxonomy of health indicators: academic health centers and communities working together to improve population health.

Aguilar-Gaxiola S, Ahmed S, Franco Z, Kissack A, Gabriel D, Hurd T, Ziegahn L, Bates NJ, Calhoun K, Carter-Edwards L, Corbie-Smith G, Eder MM, Ferrans C, Hacker K, Rumala BB, Strelnick AH, Wallerstein N.

Acad Med. 2014 Apr;89(4):564-72. doi: 10.1097/ACM.0000000000000198. Review.

34.

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.

Gee HY, Otto EA, Hurd TW, Ashraf S, Chaki M, Cluckey A, Vega-Warner V, Saisawat P, Diaz KA, Fang H, Kohl S, Allen SJ, Airik R, Zhou W, Ramaswami G, Janssen S, Fu C, Innis JL, Weber S, Vester U, Davis EE, Katsanis N, Fathy HM, Jeck N, Klaus G, Nayir A, Rahim KA, Al Attrach I, Al Hassoun I, Ozturk S, Drozdz D, Helmchen U, O'Toole JF, Attanasio M, Lewis RA, Nürnberg G, Nürnberg P, Washburn J, MacDonald J, Innis JW, Levy S, Hildebrandt F.

Kidney Int. 2014 Apr;85(4):880-7. doi: 10.1038/ki.2013.450. Epub 2013 Nov 20.

35.

Costs and outcomes evaluation of patient navigation after abnormal cancer screening: evidence from the Patient Navigation Research Program.

Bensink ME, Ramsey SD, Battaglia T, Fiscella K, Hurd TC, McKoy JM, Patierno SR, Raich PC, Seiber EE, Warren-Mears V, Whitley E, Paskett ED, Mandelblatt S; Patient Navigation Research Program.

Cancer. 2014 Feb 15;120(4):570-8. doi: 10.1002/cncr.28438. Epub 2013 Oct 25.

36.

Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.

Halbritter J, Bizet AA, Schmidts M, Porath JD, Braun DA, Gee HY, McInerney-Leo AM, Krug P, Filhol E, Davis EE, Airik R, Czarnecki PG, Lehman AM, Trnka P, Nitschké P, Bole-Feysot C, Schueler M, Knebelmann B, Burtey S, Szabó AJ, Tory K, Leo PJ, Gardiner B, McKenzie FA, Zankl A, Brown MA, Hartley JL, Maher ER, Li C, Leroux MR, Scambler PJ, Zhan SH, Jones SJ, Kayserili H, Tuysuz B, Moorani KN, Constantinescu A, Krantz ID, Kaplan BS, Shah JV; UK10K Consortium, Hurd TW, Doherty D, Katsanis N, Duncan EL, Otto EA, Beales PL, Mitchison HM, Saunier S, Hildebrandt F.

Am J Hum Genet. 2013 Nov 7;93(5):915-25. doi: 10.1016/j.ajhg.2013.09.012. Epub 2013 Oct 17.

37.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D, Bower R, O'Toole E, Porath JD, Hurd TW, Chaki M, Diaz KA, Kohl S, Lovric S, Hwang DY, Braun DA, Schueler M, Airik R, Otto EA, Leigh MW, Noone PG, Carson JL, Davis SD, Pittman JE, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Dell SD, Rosenfeld M, Milla CE, Loges NT, Omran H, Porter ME, King SM, Knowles MR, Drummond IA, Hildebrandt F.

Am J Hum Genet. 2013 Oct 3;93(4):672-86. doi: 10.1016/j.ajhg.2013.08.015.

38.

Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.

Knowles MR, Ostrowski LE, Loges NT, Hurd T, Leigh MW, Huang L, Wolf WE, Carson JL, Hazucha MJ, Yin W, Davis SD, Dell SD, Ferkol TW, Sagel SD, Olivier KN, Jahnke C, Olbrich H, Werner C, Raidt J, Wallmeier J, Pennekamp P, Dougherty GW, Hjeij R, Gee HY, Otto EA, Halbritter J, Chaki M, Diaz KA, Braun DA, Porath JD, Schueler M, Baktai G, Griese M, Turner EH, Lewis AP, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Omran H, Zariwala MA.

Am J Hum Genet. 2013 Oct 3;93(4):711-20. doi: 10.1016/j.ajhg.2013.07.025. Epub 2013 Sep 19.

39.

Breast cancer knowledge, attitude and screening behaviors among Hispanics in South Texas colonias.

Sunil TS, Hurd T, Deem C, Nevarez L, Guidry J, Rios R, Guerra H, Ortiz J, Jones L.

J Community Health. 2014 Feb;39(1):60-71. doi: 10.1007/s10900-013-9740-7.

PMID:
23903907
40.

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.

Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, Diaz KA, Olbrich H, Wolf WE, Sheridan E, Batten TF, Halbritter J, Porath JD, Kohl S, Lovric S, Hwang DY, Pittman JE, Burns KA, Ferkol TW, Sagel SD, Olivier KN, Morgan LC, Werner C, Raidt J, Pennekamp P, Sun Z, Zhou W, Airik R, Natarajan S, Allen SJ, Amirav I, Wieczorek D, Landwehr K, Nielsen K, Schwerk N, Sertic J, Köhler G, Washburn J, Levy S, Fan S, Koerner-Rettberg C, Amselem S, Williams DS, Mitchell BJ, Drummond IA, Otto EA, Omran H, Knowles MR, Hildebrandt F.

Am J Hum Genet. 2013 Aug 8;93(2):336-45. doi: 10.1016/j.ajhg.2013.06.007. Epub 2013 Jul 25.

41.

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

Gee HY, Saisawat P, Ashraf S, Hurd TW, Vega-Warner V, Fang H, Beck BB, Gribouval O, Zhou W, Diaz KA, Natarajan S, Wiggins RC, Lovric S, Chernin G, Schoeb DS, Ovunc B, Frishberg Y, Soliman NA, Fathy HM, Goebel H, Hoefele J, Weber LT, Innis JW, Faul C, Han Z, Washburn J, Antignac C, Levy S, Otto EA, Hildebrandt F.

J Clin Invest. 2013 Aug;123(8):3243-53. doi: 10.1172/JCI69134. Epub 2013 Jul 8.

42.

Genetic modifier screens to identify components of a redox-regulated cell adhesion and migration pathway.

Hurd TR, Leblanc MG, Jones LN, DeGennaro M, Lehmann R.

Methods Enzymol. 2013;528:197-215. doi: 10.1016/B978-0-12-405881-1.00012-4.

43.

A logic model for community engagement within the Clinical and Translational Science Awards consortium: can we measure what we model?

Eder MM, Carter-Edwards L, Hurd TC, Rumala BB, Wallerstein N.

Acad Med. 2013 Oct;88(10):1430-6. doi: 10.1097/ACM.0b013e31829b54ae.

44.

Ablation of the X-linked retinitis pigmentosa 2 (Rp2) gene in mice results in opsin mislocalization and photoreceptor degeneration.

Li L, Khan N, Hurd T, Ghosh AK, Cheng C, Molday R, Heckenlively JR, Swaroop A, Khanna H.

Invest Ophthalmol Vis Sci. 2013 Jul 2;54(7):4503-11. doi: 10.1167/iovs.13-12140.

45.

Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype.

Hurd TW, Otto EA, Mishima E, Gee HY, Inoue H, Inazu M, Yamada H, Halbritter J, Seki G, Konishi M, Zhou W, Yamane T, Murakami S, Caridi G, Ghiggeri G, Abe T, Hildebrandt F.

J Am Soc Nephrol. 2013 May;24(6):967-77. doi: 10.1681/ASN.2012101034. Epub 2013 May 9.

46.
47.

Inactivation of pyruvate dehydrogenase kinase 2 by mitochondrial reactive oxygen species.

Hurd TR, Collins Y, Abakumova I, Chouchani ET, Baranowski B, Fearnley IM, Prime TA, Murphy MP, James AM.

J Biol Chem. 2012 Oct 12;287(42):35153-60. doi: 10.1074/jbc.M112.400002. Epub 2012 Aug 21.

48.

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling.

Chaki M, Airik R, Ghosh AK, Giles RH, Chen R, Slaats GG, Wang H, Hurd TW, Zhou W, Cluckey A, Gee HY, Ramaswami G, Hong CJ, Hamilton BA, Cervenka I, Ganji RS, Bryja V, Arts HH, van Reeuwijk J, Oud MM, Letteboer SJ, Roepman R, Husson H, Ibraghimov-Beskrovnaya O, Yasunaga T, Walz G, Eley L, Sayer JA, Schermer B, Liebau MC, Benzing T, Le Corre S, Drummond I, Janssen S, Allen SJ, Natarajan S, O'Toole JF, Attanasio M, Saunier S, Antignac C, Koenekoop RK, Ren H, Lopez I, Nayir A, Stoetzel C, Dollfus H, Massoudi R, Gleeson JG, Andreoli SP, Doherty DG, Lindstrad A, Golzio C, Katsanis N, Pape L, Abboud EB, Al-Rajhi AA, Lewis RA, Omran H, Lee EY, Wang S, Sekiguchi JM, Saunders R, Johnson CA, Garner E, Vanselow K, Andersen JS, Shlomai J, Nurnberg G, Nurnberg P, Levy S, Smogorzewska A, Otto EA, Hildebrandt F.

Cell. 2012 Aug 3;150(3):533-48. doi: 10.1016/j.cell.2012.06.028.

49.

3D spheroid defects in NPHP knockdown cells are rescued by the somatostatin receptor agonist octreotide.

Ghosh AK, Hurd T, Hildebrandt F.

Am J Physiol Renal Physiol. 2012 Oct 15;303(8):F1225-9. doi: 10.1152/ajprenal.00135.2012. Epub 2012 Jul 25.

50.

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair.

Zhou W, Otto EA, Cluckey A, Airik R, Hurd TW, Chaki M, Diaz K, Lach FP, Bennett GR, Gee HY, Ghosh AK, Natarajan S, Thongthip S, Veturi U, Allen SJ, Janssen S, Ramaswami G, Dixon J, Burkhalter F, Spoendlin M, Moch H, Mihatsch MJ, Verine J, Reade R, Soliman H, Godin M, Kiss D, Monga G, Mazzucco G, Amann K, Artunc F, Newland RC, Wiech T, Zschiedrich S, Huber TB, Friedl A, Slaats GG, Joles JA, Goldschmeding R, Washburn J, Giles RH, Levy S, Smogorzewska A, Hildebrandt F.

Nat Genet. 2012 Jul 8;44(8):910-5. doi: 10.1038/ng.2347.

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