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439 results

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A small-molecule screen for enhanced homing of systemically infused cells.
Levy O, Mortensen LJ, Boquet G, Tong Z, Perrault C, Benhamou B, Zhang J, Stratton T, Han E, Safaee H, Musabeyezu J, Yang Z, Multon MC, Rothblatt J, Deleuze JF, Lin CP, Karp JM. Levy O, et al. Among authors: deleuze jf. Cell Rep. 2015 Mar 3;10(8):1261-1268. doi: 10.1016/j.celrep.2015.01.057. Epub 2015 Feb 26. Cell Rep. 2015. PMID: 25732817 Free PMC article.
Association study in three different populations between the GPR88 gene and major psychoses.
Del Zompo M, Deleuze JF, Chillotti C, Cousin E, Niehaus D, Ebstein RP, Ardau R, Macé S, Warnich L, Mujahed M, Severino G, Dib C, Jordaan E, Murad I, Soubigou S, Koen L, Bannoura I, Rocher C, Laurent C, Derock M, Faucon Biguet N, Mallet J, Meloni R. Del Zompo M, et al. Among authors: deleuze jf. Mol Genet Genomic Med. 2014 Mar;2(2):152-9. doi: 10.1002/mgg3.54. Epub 2013 Dec 12. Mol Genet Genomic Med. 2014. PMID: 24689078 Free PMC article.
ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease.
Macé S, Cousin E, Ricard S, Génin E, Spanakis E, Lafargue-Soubigou C, Génin B, Fournel R, Roche S, Haussy G, Massey F, Soubigou S, Bréfort G, Benoit P, Brice A, Campion D, Hollis M, Pradier L, Benavides J, Deleuze JF. Macé S, et al. Among authors: deleuze jf. Neurobiol Dis. 2005 Feb;18(1):119-25. doi: 10.1016/j.nbd.2004.09.011. Neurobiol Dis. 2005. PMID: 15649702
iPSCs derived from infertile men carrying complex genetic abnormalities can generate primordial germ-like cells.
Mouka A, Arkoun B, Moison P, Drévillon L, Jarray R, Brisset S, Mayeur A, Bouligand J, Boland-Auge A, Deleuze JF, Yates F, Lemonnier T, Callier P, Duffourd Y, Nitschke P, Ollivier E, Bourdin A, De Vos J, Livera G, Tachdjian G, Maouche-Chrétien L, Tosca L. Mouka A, et al. Among authors: deleuze jf. Sci Rep. 2022 Aug 22;12(1):14302. doi: 10.1038/s41598-022-17337-2. Sci Rep. 2022. PMID: 35995809 Free PMC article.
Genome-scan for bipolar disorder with sib-pair families in the Sardinian population: a new susceptibility locus on chromosome 1p22-p21?
Del Zompo M, Severino G, Ardau R, Chillotti C, Piccardi M, Dib C, Muzard G, Soubigou S, Derock M, Fournel R, Vaubien Y, Roche S, Bowen-Squires L, Génin E, Cousin E, Deleuze JF, Biguet NF, Mallet J, Meloni R. Del Zompo M, et al. Among authors: deleuze jf. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1200-8. doi: 10.1002/ajmg.b.31092. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468074
Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.
Esteves T, Durr A, Mundwiller E, Loureiro JL, Boutry M, Gonzalez MA, Gauthier J, El-Hachimi KH, Depienne C, Muriel MP, Acosta Lebrigio RF, Gaussen M, Noreau A, Speziani F, Dionne-Laporte A, Deleuze JF, Dion P, Coutinho P, Rouleau GA, Zuchner S, Brice A, Stevanin G, Darios F. Esteves T, et al. Among authors: deleuze jf. Am J Hum Genet. 2014 Feb 6;94(2):268-77. doi: 10.1016/j.ajhg.2013.12.005. Epub 2014 Jan 2. Am J Hum Genet. 2014. PMID: 24388663 Free PMC article.
GRID2 mutations span from congenital to mild adult-onset cerebellar ataxia.
Coutelier M, Burglen L, Mundwiller E, Abada-Bendib M, Rodriguez D, Chantot-Bastaraud S, Rougeot C, Cournelle MA, Milh M, Toutain A, Bacq D, Meyer V, Afenjar A, Deleuze JF, Brice A, Héron D, Stevanin G, Durr A. Coutelier M, et al. Among authors: deleuze jf. Neurology. 2015 Apr 28;84(17):1751-9. doi: 10.1212/WNL.0000000000001524. Epub 2015 Apr 3. Neurology. 2015. PMID: 25841024
439 results