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Items: 1 to 20 of 40

1.

foxc1 is required for embryonic head vascular smooth muscle differentiation in zebrafish.

Whitesell TR, Chrystal PW, Ryu JR, Munsie N, Grosse A, French CR, Workentine ML, Li R, Zhu LJ, Waskiewicz A, Lehmann OJ, Lawson ND, Childs SJ.

Dev Biol. 2019 Sep 1;453(1):34-47. doi: 10.1016/j.ydbio.2019.06.005. Epub 2019 Jun 11.

PMID:
31199900
2.

Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer.

Umali J, Hawkey-Noble A, French CR.

Vision Res. 2019 Mar;156:66-72. doi: 10.1016/j.visres.2019.01.008. Epub 2019 Feb 2.

PMID:
30684501
3.

Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting.

Chauhan G, Adams HHH, Satizabal CL, Bis JC, Teumer A, Sargurupremraj M, Hofer E, Trompet S, Hilal S, Smith AV, Jian X, Malik R, Traylor M, Pulit SL, Amouyel P, Mazoyer B, Zhu YC, Kaffashian S, Schilling S, Beecham GW, Montine TJ, Schellenberg GD, Kjartansson O, Guðnason V, Knopman DS, Griswold ME, Windham BG, Gottesman RF, Mosley TH, Schmidt R, Saba Y, Schmidt H, Takeuchi F, Yamaguchi S, Nabika T, Kato N, Rajan KB, Aggarwal NT, De Jager PL, Evans DA, Psaty BM, Rotter JI, Rice K, Lopez OL, Liao J, Chen C, Cheng CY, Wong TY, Ikram MK, van der Lee SJ, Amin N, Chouraki V, DeStefano AL, Aparicio HJ, Romero JR, Maillard P, DeCarli C, Wardlaw JM, Hernández MDCV, Luciano M, Liewald D, Deary IJ, Starr JM, Bastin ME, Muñoz Maniega S, Slagboom PE, Beekman M, Deelen J, Uh HW, Lemmens R, Brodaty H, Wright MJ, Ames D, Boncoraglio GB, Hopewell JC, Beecham AH, Blanton SH, Wright CB, Sacco RL, Wen W, Thalamuthu A, Armstrong NJ, Chong E, Schofield PR, Kwok JB, van der Grond J, Stott DJ, Ford I, Jukema JW, Vernooij MW, Hofman A, Uitterlinden AG, van der Lugt A, Wittfeld K, Grabe HJ, Hosten N, von Sarnowski B, Völker U, Levi C, Jimenez-Conde J, Sharma P, Sudlow CLM, Rosand J, Woo D, Cole JW, Meschia JF, Slowik A, Thijs V, Lindgren A, Melander O, Grewal RP, Rundek T, Rexrode K, Rothwell PM, Arnett DK, Jern C, Johnson JA, Benavente OR, Wasssertheil-Smoller S, Lee JM, Wong Q, Mitchell BD, Rich SS, McArdle PF, Geerlings MI, van der Graaf Y, de Bakker PIW, Asselbergs FW, Srikanth V, Thomson R, McWhirter R, Moran C, Callisaya M, Phan T, Rutten-Jacobs LCA, Bevan S, Tzourio C, Mather KA, Sachdev PS, van Duijn CM, Worrall BB, Dichgans M, Kittner SJ, Markus HS, Ikram MA, Fornage M, Launer LJ, Seshadri S, Longstreth WT Jr, Debette S; Stroke Genetics Network (SiGN), the International Stroke Genetics Consortium (ISGC), METASTROKE, Alzheimer's Disease Genetics Consortium (ADGC), and the Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium.

Neurology. 2019 Jan 16. pii: 10.1212/WNL.0000000000006851. doi: 10.1212/WNL.0000000000006851. [Epub ahead of print]

4.

Anti-Epileptic Drug Combination Efficacy in an In Vitro Seizure Model - Phenytoin and Valproate, Lamotrigine and Valproate.

Taing KD, O'Brien TJ, Williams DA, French CR.

PLoS One. 2017 Jan 11;12(1):e0169974. doi: 10.1371/journal.pone.0169974. eCollection 2017.

5.

Effect of phenytoin on sodium conductances in rat hippocampal CA1 pyramidal neurons.

Zeng Z, Hill-Yardin EL, Williams D, O'Brien T, Serelis A, French CR.

J Neurophysiol. 2016 Oct 1;116(4):1924-1936. doi: 10.1152/jn.01060.2015. Epub 2016 Aug 3.

6.

The antiepileptic medications carbamazepine and phenytoin inhibit native sodium currents in murine osteoblasts.

Petty SJ, Milligan CJ, Todaro M, Richards KL, Kularathna PK, Pagel CN, French CR, Hill-Yardin EL, O'Brien TJ, Wark JD, Mackie EJ, Petrou S.

Epilepsia. 2016 Sep;57(9):1398-405. doi: 10.1111/epi.13474. Epub 2016 Jul 21.

7.

Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.

Neurology Working Group of the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium, the Stroke Genetics Network (SiGN), and the International Stroke Genetics Consortium (ISGC).

Lancet Neurol. 2016 Jun;15(7):695-707. doi: 10.1016/S1474-4422(16)00102-2. Epub 2016 Apr 7.

8.

Minimally invasive endovascular stent-electrode array for high-fidelity, chronic recordings of cortical neural activity.

Oxley TJ, Opie NL, John SE, Rind GS, Ronayne SM, Wheeler TL, Judy JW, McDonald AJ, Dornom A, Lovell TJ, Steward C, Garrett DJ, Moffat BA, Lui EH, Yassi N, Campbell BC, Wong YT, Fox KE, Nurse ES, Bennett IE, Bauquier SH, Liyanage KA, van der Nagel NR, Perucca P, Ahnood A, Gill KP, Yan B, Churilov L, French CR, Desmond PM, Horne MK, Kiers L, Prawer S, Davis SM, Burkitt AN, Mitchell PJ, Grayden DB, May CN, O'Brien TJ.

Nat Biotechnol. 2016 Mar;34(3):320-7. doi: 10.1038/nbt.3428. Epub 2016 Feb 8.

PMID:
26854476
9.

Properties of an intermediate-duration inactivation process of the voltage-gated sodium conductance in rat hippocampal CA1 neurons.

French CR, Zeng Z, Williams DA, Hill-Yardin EL, O'Brien TJ.

J Neurophysiol. 2016 Feb 1;115(2):790-802. doi: 10.1152/jn.01000.2014. Epub 2015 Nov 4.

10.

Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease.

French CR, Seshadri S, Destefano AL, Fornage M, Arnold CR, Gage PJ, Skarie JM, Dobyns WB, Millen KJ, Liu T, Dietz W, Kume T, Hofker M, Emery DJ, Childs SJ, Waskiewicz AJ, Lehmann OJ.

J Clin Invest. 2014 Nov;124(11):4877-81. doi: 10.1172/JCI75109. Epub 2014 Sep 24.

11.

An in vivo technique for investigating electrophysiological effects of centrally administered drugs on single neurons and network behaviour.

Gandrathi A, Zheng T, O'Brien P, Ali I, O'Brien TJ, French CR.

J Neurosci Methods. 2013 Oct 15;219(2):197-204. doi: 10.1016/j.jneumeth.2013.06.010. Epub 2013 Jul 17.

PMID:
23872526
12.

Molecular mechanisms regulating ocular apoptosis in zebrafish gdf6a mutants.

Pant SD, March LD, Famulski JK, French CR, Lehmann OJ, Waskiewicz AJ.

Invest Ophthalmol Vis Sci. 2013 Aug 28;54(8):5871-9. doi: 10.1167/iovs.12-11315.

PMID:
23847306
13.

Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model.

French CR, Stach TR, March LD, Lehmann OJ, Waskiewicz AJ.

Invest Ophthalmol Vis Sci. 2013 Jul 10;54(7):4636-47. doi: 10.1167/iovs.13-11674.

PMID:
23737474
14.

Routine polysomnography in an epilepsy monitoring unit.

Phillips MC, Costello CA, White EJ, Smit M, Carino J, Strawhorn A, Jackson B, Kwan P, French CR, Yerra SR, Tan KM, O'Brien TJ, Goldin J.

Epilepsy Res. 2013 Aug;105(3):401-4. doi: 10.1016/j.eplepsyres.2013.02.015. Epub 2013 Mar 25.

PMID:
23535035
15.

Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies.

Asai-Coakwell M, March L, Dai XH, Duval M, Lopez I, French CR, Famulski J, De Baere E, Francis PJ, Sundaresan P, Sauvé Y, Koenekoop RK, Berry FB, Allison WT, Waskiewicz AJ, Lehmann OJ.

Hum Mol Genet. 2013 Apr 1;22(7):1432-42. doi: 10.1093/hmg/dds560. Epub 2013 Jan 9.

PMID:
23307924
16.

Aberrant forebrain signaling during early development underlies the generation of holoprosencephaly and coloboma.

Gongal PA, French CR, Waskiewicz AJ.

Biochim Biophys Acta. 2011 Mar;1812(3):390-401. doi: 10.1016/j.bbadis.2010.09.005. Epub 2010 Sep 16. Review.

17.

Meis1 specifies positional information in the retina and tectum to organize the zebrafish visual system.

Erickson T, French CR, Waskiewicz AJ.

Neural Dev. 2010 Sep 1;5:22. doi: 10.1186/1749-8104-5-22.

18.

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.

Ye M, Berry-Wynne KM, Asai-Coakwell M, Sundaresan P, Footz T, French CR, Abitbol M, Fleisch VC, Corbett N, Allison WT, Drummond G, Walter MA, Underhill TM, Waskiewicz AJ, Lehmann OJ.

Hum Mol Genet. 2010 Jan 15;19(2):287-98. doi: 10.1093/hmg/ddp496. Epub 2009 Oct 28.

PMID:
19864492
19.

Gdf6a is required for the initiation of dorsal-ventral retinal patterning and lens development.

French CR, Erickson T, French DV, Pilgrim DB, Waskiewicz AJ.

Dev Biol. 2009 Sep 1;333(1):37-47. doi: 10.1016/j.ydbio.2009.06.018. Epub 2009 Jun 21.

20.

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.

Asai-Coakwell M, French CR, Ye M, Garcha K, Bigot K, Perera AG, Staehling-Hampton K, Mema SC, Chanda B, Mushegian A, Bamforth S, Doschak MR, Li G, Dobbs MB, Giampietro PF, Brooks BP, Vijayalakshmi P, Sauvé Y, Abitbol M, Sundaresan P, van Heyningen V, Pourquié O, Underhill TM, Waskiewicz AJ, Lehmann OJ.

Hum Mol Genet. 2009 Mar 15;18(6):1110-21. doi: 10.1093/hmg/ddp008. Epub 2009 Jan 6.

PMID:
19129173

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