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Items: 27

1.

Orosensory Detection of Dietary Fatty Acids Is Altered in CB₁R-/- Mice.

Brissard L, Leemput J, Hichami A, Passilly-Degrace P, Maquart G, Demizieux L, Degrace P, Khan NA.

Nutrients. 2018 Sep 21;10(10). pii: E1347. doi: 10.3390/nu10101347.

2.

Zizyphin modulates calcium signalling in human taste bud cells and fat taste perception in the mouse.

Murtaza B, Berrichi M, Bennamar C, Tordjmann T, Djeziri FZ, Hichami A, Leemput J, Belarbi M, Ozdener H, Khan NA.

Fundam Clin Pharmacol. 2017 Oct;31(5):486-494. doi: 10.1111/fcp.12289. Epub 2017 May 24.

PMID:
28370265
3.

Predictors of current functioning and functional decline in schizophrenia.

Joseph J, Kremen WS, Franz CE, Glatt SJ, van de Leemput J, Chandler SD, Tsuang MT, Twamley EW.

Schizophr Res. 2017 Oct;188:158-164. doi: 10.1016/j.schres.2017.01.038. Epub 2017 Jan 28.

4.

Genetics of Schizophrenia: Historical Insights and Prevailing Evidence.

van de Leemput J, Hess JL, Glatt SJ, Tsuang MT.

Adv Genet. 2016;96:99-141. doi: 10.1016/bs.adgen.2016.08.001. Epub 2016 Sep 27. Review.

PMID:
27968732
5.

The potential of genetic and gene expression analysis in the diagnosis of neuropsychiatric disorders.

van de Leemput J, Glatt SJ, Tsuang MT.

Expert Rev Mol Diagn. 2016 Jun;16(6):677-95. doi: 10.1586/14737159.2016.1171714. Epub 2016 Apr 26. Review.

PMID:
27017833
6.

A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.

Johnson JO, Stevanin G, van de Leemput J, Hernandez DG, Arepalli S, Forlani S, Zonozi R, Gibbs JR, Brice A, Durr A, Singleton AB.

Mov Disord. 2015 Feb;30(2):262-6. doi: 10.1002/mds.26059. Epub 2014 Dec 27.

7.

Mice engineered for an obligatory Mdm4 exon skipping express higher levels of the Mdm4-S isoform but exhibit increased p53 activity.

Bardot B, Bouarich-Bourimi R, Leemput J, Lejour V, Hamon A, Plancke L, Jochemsen AG, Simeonova I, Fang M, Toledo F.

Oncogene. 2015 May 28;34(22):2943-8. doi: 10.1038/onc.2014.230. Epub 2014 Aug 4.

PMID:
25088193
8.

CORTECON: a temporal transcriptome analysis of in vitro human cerebral cortex development from human embryonic stem cells.

van de Leemput J, Boles NC, Kiehl TR, Corneo B, Lederman P, Menon V, Lee C, Martinez RA, Levi BP, Thompson CL, Yao S, Kaykas A, Temple S, Fasano CA.

Neuron. 2014 Jul 2;83(1):51-68. doi: 10.1016/j.neuron.2014.05.013.

9.

Canine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24.

Agler C, Nielsen DM, Urkasemsin G, Singleton A, Tonomura N, Sigurdsson S, Tang R, Linder K, Arepalli S, Hernandez D, Lindblad-Toh K, van de Leemput J, Motsinger-Reif A, O'Brien DP, Bell J, Harris T, Steinberg S, Olby NJ.

PLoS Genet. 2014 Feb 6;10(2):e1003991. doi: 10.1371/journal.pgen.1003991. eCollection 2014 Feb.

10.

Invasive pulmonary aspergillosis due to a multi-azole resistant Aspergillus fumigatus.

Jeurissen A, Cooreman S, Van Kerckhoven W, Van Leemput J, Vanhove P, Lagrou K, Heytens L.

Acta Clin Belg. 2012 Jan-Feb;67(1):46-8.

PMID:
22480040
11.

SCA15 due to large ITPR1 deletions in a cohort of 333 white families with dominant ataxia.

Marelli C, van de Leemput J, Johnson JO, Tison F, Thauvin-Robinet C, Picard F, Tranchant C, Hernandez DG, Huttin B, Boulliat J, Sangla I, Marescaux C, Brique S, Dollfus H, Arepalli S, Benatru I, Ollagnon E, Forlani S, Hardy J, Stevanin G, Dürr A, Singleton A, Brice A.

Arch Neurol. 2011 May;68(5):637-43. doi: 10.1001/archneurol.2011.81.

12.

Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series.

van de Leemput J, Wavrant-De Vrièze F, Rafferty I, Bras JM, Giunti P, Fisher EM, Hardy JA, Singleton AB, Houlden H.

Mov Disord. 2010 Apr 30;25(6):771-3. doi: 10.1002/mds.22970.

13.

Human ataxias: a genetic dissection of inositol triphosphate receptor (ITPR1)-dependent signaling.

Schorge S, van de Leemput J, Singleton A, Houlden H, Hardy J.

Trends Neurosci. 2010 May;33(5):211-9. doi: 10.1016/j.tins.2010.02.005. Epub 2010 Mar 11.

14.

Spontaneous hepatic rupture in a normotensive monoamniotic twin pregnancy: case report and review of the literature.

DeKoninck PL, Loquet P, Leyman P, Van Leemput J, d'Archambeau O, Van Wiemeersch J, Devlieger R.

Gynecol Obstet Invest. 2010;70(1):69-72. doi: 10.1159/000290063. Epub 2010 Mar 4. Review.

PMID:
20203522
15.

Expression of 8-oxoguanine DNA glycosylase (Ogg1) in mouse retina.

Bigot K, Leemput J, Vacher M, Campalans A, Radicella JP, Lacassagne E, Provost A, Masson C, Menasche M, Abitbol M.

Mol Vis. 2009 Jun 5;15:1139-52.

16.

Sirt1 involvement in rd10 mouse retinal degeneration.

Jaliffa C, Ameqrane I, Dansault A, Leemput J, Vieira V, Lacassagne E, Provost A, Bigot K, Masson C, Menasche M, Abitbol M.

Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3562-72. doi: 10.1167/iovs.08-2817. Epub 2009 Apr 30.

PMID:
19407027
17.

CX3CR1+ CD115+ CD135+ common macrophage/DC precursors and the role of CX3CR1 in their response to inflammation.

Auffray C, Fogg DK, Narni-Mancinelli E, Senechal B, Trouillet C, Saederup N, Leemput J, Bigot K, Campisi L, Abitbol M, Molina T, Charo I, Hume DA, Cumano A, Lauvau G, Geissmann F.

J Exp Med. 2009 Mar 16;206(3):595-606. doi: 10.1084/jem.20081385. Epub 2009 Mar 9.

18.

ATM localization and gene expression in the adult mouse eye.

Leemput J, Masson C, Bigot K, Errachid A, Dansault A, Provost A, Gadin S, Aoufouchi S, Menasche M, Abitbol M.

Mol Vis. 2009;15:393-416. Epub 2009 Feb 20.

19.

Pelvic inflammatory disease due to Streptococcus pneumoniae: a usual pathogen at an unusual place.

Lemoyne S, Van Leemput J, Smet D, Desmedt E, Devos H, Van Schaeren J, Jeurissen A.

Acta Clin Belg. 2008 Nov-Dec;63(6):398-401.

PMID:
19170357
20.

A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20.

Knight MA, Hernandez D, Diede SJ, Dauwerse HG, Rafferty I, van de Leemput J, Forrest SM, Gardner RJ, Storey E, van Ommen GJ, Tapscott SJ, Fischbeck KH, Singleton AB.

Hum Mol Genet. 2008 Dec 15;17(24):3847-53. doi: 10.1093/hmg/ddn283. Epub 2008 Sep 18.

21.

A genome-wide association study identifies protein quantitative trait loci (pQTLs).

Melzer D, Perry JR, Hernandez D, Corsi AM, Stevens K, Rafferty I, Lauretani F, Murray A, Gibbs JR, Paolisso G, Rafiq S, Simon-Sanchez J, Lango H, Scholz S, Weedon MN, Arepalli S, Rice N, Washecka N, Hurst A, Britton A, Henley W, van de Leemput J, Li R, Newman AB, Tranah G, Harris T, Panicker V, Dayan C, Bennett A, McCarthy MI, Ruokonen A, Jarvelin MR, Guralnik J, Bandinelli S, Frayling TM, Singleton A, Ferrucci L.

PLoS Genet. 2008 May 9;4(5):e1000072. doi: 10.1371/journal.pgen.1000072.

22.

Genotype, haplotype and copy-number variation in worldwide human populations.

Jakobsson M, Scholz SW, Scheet P, Gibbs JR, VanLiere JM, Fung HC, Szpiech ZA, Degnan JH, Wang K, Guerreiro R, Bras JM, Schymick JC, Hernandez DG, Traynor BJ, Simon-Sanchez J, Matarin M, Britton A, van de Leemput J, Rafferty I, Bucan M, Cann HM, Hardy JA, Rosenberg NA, Singleton AB.

Nature. 2008 Feb 21;451(7181):998-1003. doi: 10.1038/nature06742.

23.

Novel mouse model of monocular amaurosis fugax.

Lelong DC, Bieche I, Perez E, Bigot K, Leemput J, Laurendeau I, Vidaud M, Jais JP, Menasche M, Abitbol M.

Stroke. 2007 Dec;38(12):3237-44. Epub 2007 Nov 1.

PMID:
17975099
24.

The RNA-binding protein Musashi-1 is produced in the developing and adult mouse eye.

Raji B, Dansault A, Leemput J, de la Houssaye G, Vieira V, Kobetz A, Arbogast L, Masson C, Menasche M, Abitbol M.

Mol Vis. 2007 Aug 10;13:1412-27.

PMID:
17768378
25.

Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humans.

van de Leemput J, Chandran J, Knight MA, Holtzclaw LA, Scholz S, Cookson MR, Houlden H, Gwinn-Hardy K, Fung HC, Lin X, Hernandez D, Simon-Sanchez J, Wood NW, Giunti P, Rafferty I, Hardy J, Storey E, Gardner RJ, Forrest SM, Fisher EM, Russell JT, Cai H, Singleton AB.

PLoS Genet. 2007 Jun;3(6):e108. Epub 2007 May 16.

26.

Diagnosis and outcome from suspected mesenteric ischaemia following cardiac surgery.

Edwards M, Sidebotham D, Smith M, Leemput JV, Anderson B.

Anaesth Intensive Care. 2005 Apr;33(2):210-7.

27.

Profiling gene expression in whole blood samples following an in-vitro challenge.

Spijker S, van de Leemput JC, Hoekstra C, Boomsma DI, Smit AB.

Twin Res. 2004 Dec;7(6):564-70.

PMID:
15607006

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