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Items: 1 to 50 of 228

1.

Mobilization of CD4+ T lymphocytes in inflamed mucosa reduces pain in colitis mice: toward a vaccinal strategy to alleviate inflammatory visceral pain.

Basso L, Boué J, Augé C, Deraison C, Blanpied C, Cenac N, Lluel P, Vergnolle N, Dietrich G.

Pain. 2018 Feb;159(2):331-341. doi: 10.1097/j.pain.0000000000001103.

PMID:
29140925
2.

T-lymphocyte-derived enkephalins reduce Th1/Th17 colitis and associated pain in mice.

Basso L, Garnier L, Bessac A, Boué J, Blanpied C, Cenac N, Laffont S, Dietrich G.

J Gastroenterol. 2018 Feb;53(2):215-226. doi: 10.1007/s00535-017-1341-2. Epub 2017 Apr 19.

PMID:
28424989
3.

Mu and delta opioid receptor knockout mice show increased colonic sensitivity.

Reiss D, Ceredig RA, Secher T, Boué J, Barreau F, Dietrich G, Gavériaux-Ruff C.

Eur J Pain. 2017 Apr;21(4):623-634. doi: 10.1002/ejp.965. Epub 2016 Oct 17.

PMID:
27748566
4.

Endogenous analgesia mediated by CD4(+) T lymphocytes is dependent on enkephalins in mice.

Basso L, Boué J, Mahiddine K, Blanpied C, Robiou-du-Pont S, Vergnolle N, Deraison C, Dietrich G.

J Neuroinflammation. 2016 Jun 1;13(1):132. doi: 10.1186/s12974-016-0591-x.

5.

Protective effects of n-6 fatty acids-enriched diet on intestinal ischaemia/reperfusion injury involve lipoxin A4 and its receptor.

Gobbetti T, Ducheix S, le Faouder P, Perez T, Riols F, Boue J, Bertrand-Michel J, Dubourdeau M, Guillou H, Perretti M, Vergnolle N, Cenac N.

Br J Pharmacol. 2015 Feb;172(3):910-23. doi: 10.1111/bph.12957. Epub 2014 Dec 15.

6.

Endogenous regulation of inflammatory pain by T-cell-derived opioids: when friend turns to foe.

Basso L, Boué J, Bourreille A, Dietrich G.

Inflamm Bowel Dis. 2014 Oct;20(10):1870-7. doi: 10.1097/MIB.0000000000000073. Review.

PMID:
24846722
7.

Endogenous regulation of visceral pain via production of opioids by colitogenic CD4(+) T cells in mice.

Boué J, Basso L, Cenac N, Blanpied C, Rolli-Derkinderen M, Neunlist M, Vergnolle N, Dietrich G.

Gastroenterology. 2014 Jan;146(1):166-75. doi: 10.1053/j.gastro.2013.09.020. Epub 2013 Sep 18.

PMID:
24055279
8.

Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions. 1975.

Boué J, Boué A, Lazar P.

Birth Defects Res A Clin Mol Teratol. 2013 Jul;97(7):471-86. doi: 10.1002/bdra.23174. No abstract available.

PMID:
23873813
9.

Essential fatty acids deficiency promotes lipogenic gene expression and hepatic steatosis through the liver X receptor.

Ducheix S, Montagner A, Polizzi A, Lasserre F, Marmugi A, Bertrand-Michel J, Podechard N, Al Saati T, Chétiveaux M, Baron S, Boué J, Dietrich G, Mselli-Lakhal L, Costet P, Lobaccaro JM, Pineau T, Theodorou V, Postic C, Martin PG, Guillou H.

J Hepatol. 2013 May;58(5):984-92. doi: 10.1016/j.jhep.2013.01.006. Epub 2013 Jan 16.

PMID:
23333450
10.

Food-grade bacteria expressing elafin protect against inflammation and restore colon homeostasis.

Motta JP, Bermúdez-Humarán LG, Deraison C, Martin L, Rolland C, Rousset P, Boue J, Dietrich G, Chapman K, Kharrat P, Vinel JP, Alric L, Mas E, Sallenave JM, Langella P, Vergnolle N.

Sci Transl Med. 2012 Oct 31;4(158):158ra144. doi: 10.1126/scitranslmed.3004212.

11.

Denatured G-protein coupled receptors as immunogens to generate highly specific antibodies.

Talmont F, Moulédous L, Boué J, Mollereau C, Dietrich G.

PLoS One. 2012;7(9):e46348. doi: 10.1371/journal.pone.0046348. Epub 2012 Sep 27.

12.

Potential association of paraoxonase-1, type 2 diabetes mellitus, and periodontitis.

Noack B, Aslanhan Z, Boué J, Petig C, Teige M, Schaper F, Hoffmann T, Hannig C.

J Periodontol. 2013 May;84(5):614-23. doi: 10.1902/jop.2012.120062. Epub 2012 Jul 6.

PMID:
22769439
13.

Immune conditions associated with CD4+ T effector-induced opioid release and analgesia.

Boué J, Blanpied C, Djata-Cabral M, Pelletier L, Vergnolle N, Dietrich G.

Pain. 2012 Feb;153(2):485-93. doi: 10.1016/j.pain.2011.11.013. Epub 2011 Dec 19.

PMID:
22188867
14.

Endogenous opioid-mediated analgesia is dependent on adaptive T cell response in mice.

Boué J, Blanpied C, Brousset P, Vergnolle N, Dietrich G.

J Immunol. 2011 May 1;186(9):5078-84. doi: 10.4049/jimmunol.1003335. Epub 2011 Mar 21.

15.

mu-Opioid receptor is induced by IL-13 within lymph nodes from patients with Sézary syndrome.

Bénard A, Cavaillès P, Boué J, Chapey E, Bayry J, Blanpied C, Meyer N, Lamant L, Kaveri SV, Brousset P, Dietrich G.

J Invest Dermatol. 2010 May;130(5):1337-44. doi: 10.1038/jid.2009.433. Epub 2010 Jan 28.

16.

Thrombin receptor: An endogenous inhibitor of inflammatory pain, activating opioid pathways.

Martin L, Augé C, Boué J, Buresi MC, Chapman K, Asfaha S, Andrade-Gordon P, Steinhoff M, Cenac N, Dietrich G, Vergnolle N.

Pain. 2009 Nov;146(1-2):121-9. doi: 10.1016/j.pain.2009.07.016. Epub 2009 Aug 11.

PMID:
19674841
17.

Delta opioid receptors mediate chemotaxis in bone marrow-derived dendritic cells.

Bénard A, Boué J, Chapey E, Jaume M, Gomes B, Dietrich G.

J Neuroimmunol. 2008 Jun 15;197(1):21-8. doi: 10.1016/j.jneuroim.2008.03.020. Epub 2008 May 16.

PMID:
18486241
18.

Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation.

Bienvenu T, des Portes V, McDonell N, Carrié A, Zemni R, Couvert P, Ropers HH, Moraine C, van Bokhoven H, Fryns JP, Allen K, Walsh CA, Boué J, Kahn A, Chelly J, Beldjord C.

Am J Med Genet. 2000 Aug 14;93(4):294-8.

PMID:
10946356
19.

Novel and recurrent tyrosine aminotransferase gene mutations in tyrosinemia type II.

Hühn R, Stoermer H, Klingele B, Bausch E, Fois A, Farnetani M, Di Rocco M, Boué J, Kirk JM, Coleman R, Scherer G.

Hum Genet. 1998 Mar;102(3):305-13.

PMID:
9544843
20.

Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24.

des Portes V, Soufir N, Carrié A, Billuart P, Bienvenu T, Vinet MC, Beldjord C, Ponsot G, Kahn A, Boué J, Chelly J.

Am J Med Genet. 1997 Oct 31;72(3):324-8.

PMID:
9332663
21.

A gene for dominant nonspecific X-linked mental retardation is located in Xq28.

des Portes V, Billuart P, Carrié A, Bachner L, Bienvenu T, Vinet MC, Beldjord C, Ponsot G, Kahn A, Boué J, Chelly J.

Am J Hum Genet. 1997 Apr;60(4):903-9.

22.

[Genetics of Fragile X syndrome and its prevention].

Boué J, Simon-Bouy B.

J Gynecol Obstet Biol Reprod (Paris). 1997;26(3):273-9. Review. French.

PMID:
9265049
23.

Parental origin and mechanisms of formation of three cases of 12p tetrasomy.

Turleau C, Simon-Bouy B, Austruy E, Grisard MC, Lemaire F, Molina-Gomes D, Siffroi JP, Boué J.

Clin Genet. 1996 Jul;50(1):41-6.

PMID:
8891385
24.

Screening of CYP21 gene mutations in 129 French patients affected by steroid 21-hydroxylase deficiency.

Barbat B, Bogyo A, Raux-Demay MC, Kuttenn F, Boué J, Simon-Bouy B, Serre JL, Mornet E.

Hum Mutat. 1995;5(2):126-30.

PMID:
7749410
25.

Transition from normal to premutated alleles in fragile X syndrome results from a multistep process.

Montagnon M, Bogyo A, Deluchat C, Jokic M, Chateau C, Taillandier A, Thomas F, Simon-Bouy B, Boué J, Serre JL, et al.

Eur J Hum Genet. 1994;2(2):125-31.

PMID:
8044657
26.

Molecular analysis of a ring chromosome X in a family with fragile X syndrome.

Mornet E, Bogyo A, Deluchat C, Simon-Bouy B, Mathieu M, Thépot F, Grisard MC, Leguern E, Boué J, Boué A.

Hum Genet. 1993 Oct;92(4):373-8.

PMID:
8225318
27.

Affected sibs with fragile X syndrome exhibit an age-dependent decrease in the size of the fragile X full mutation.

Mornet E, Jokic M, Bogyo A, Tejada I, Deluchat C, Boué J, Boué A.

Clin Genet. 1993 Mar;43(3):157-9.

PMID:
8098999
28.

Linkage disequilibrium between the fragile X mutation and two closely linked CA repeats suggests that fragile X chromosomes are derived from a small number of founder chromosomes.

Oudet C, Mornet E, Serre JL, Thomas F, Lentes-Zengerling S, Kretz C, Deluchat C, Tejada I, Boué J, Boué A, et al.

Am J Hum Genet. 1993 Feb;52(2):297-304.

29.

Prenatal diagnosis of cystic fibrosis: ultrasonography of the gallbladder at 17-19 weeks of gestation.

Duchatel F, Muller F, Oury JF, Mennesson B, Boue J, Boue A.

Fetal Diagn Ther. 1993 Jan-Feb;8(1):28-36.

PMID:
8452646
30.

Collaborative study of the molecular epidemiology of Tay-Sachs disease in Europe.

Akli S, Boue J, Sandhoff K, Kleijer W, Vamos E, Young E, Gatti R, Di Natale P, Motte J, Vanier MT, et al.

Eur J Hum Genet. 1993;1(3):229-38.

PMID:
8044648
31.
32.

[Accidental ultrasonographic disclosure of isolated intra-abdominal fetal hyperechogenicity. Apropos of a series of 87 cases].

Muller F, Simon-Bouy B, Aubry MC, Duchatel F, Bessis R, Boué J.

J Radiol. 1992 Dec;73(12):699-704. French.

PMID:
1301444
33.

Prenatal diagnosis of Niemann-Pick type C disease: current strategy from an experience of 37 pregnancies at risk.

Vanier MT, Rodriguez-Lafrasse C, Rousson R, Mandon G, Boué J, Choiset A, Peyrat MF, Dumontel C, Juge MC, Pentchev PG, et al.

Am J Hum Genet. 1992 Jul;51(1):111-22.

34.

Three families with high expression of a fragile site at Xq27.3, lack of anomalies at the FMR-1 CpG island, and no clear phenotypic association.

Oberlé I, Boué J, Croquette MF, Voelckel MA, Mattei MG, Mandel JL.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):224-31.

PMID:
1605195
35.

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development.

Devys D, Biancalana V, Rousseau F, Boué J, Mandel JL, Oberlé I.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):208-16.

PMID:
1605193
36.

Direct DNA analysis of fragile X syndrome in Spanish pedigrees.

Tejada I, Mornet E, Biancalana V, Oberlé I, Boué J, Mandel JL, Boué A.

Am J Med Genet. 1992 Apr 15-May 1;43(1-2):282-90.

PMID:
1351363
37.

Carrier detection and prenatal diagnosis of cystic fibrosis using an intragenic TA-repeat polymorphism.

Mornet E, Chateau C, Simon-Bouy B, Boue J, Zielenski J, Tsui LC, Boue A.

Hum Genet. 1992 Feb;88(4):479-81.

PMID:
1371264
38.

[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].

Mornet E, Boué J, Crète P, Raux-Demay MC, Kutten F, Boué A.

Arch Fr Pediatr. 1992 Jan;49(1):57-62. French. No abstract available.

PMID:
1550455
39.

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.

Rousseau F, Heitz D, Biancalana V, Blumenfeld S, Kretz C, Boué J, Tommerup N, Van Der Hagen C, DeLozier-Blanchet C, Croquette MF, et al.

N Engl J Med. 1991 Dec 12;325(24):1673-81.

40.
41.

First-trimester diagnosis of hypophosphatasia. Importance of gestational age and purity of CV samples.

Muller F, Oury JF, Bussière P, Lewin F, Boué J.

Prenat Diagn. 1991 Sep;11(9):725-30.

PMID:
1788179
42.

Nine mutations in the cystic fibrosis (CF) gene account for 80% of the CF chromosomes in French patients.

Simon-Bouy B, Mornet E, Serre JL, Taillandier A, Boué J, Boué A.

Clin Genet. 1991 Sep;40(3):218-24.

PMID:
1723032
43.

Pelizaeus-Merzbacher disease: a valine to phenylalanine point mutation in a putative extracellular loop of myelin proteolipid.

Pham-Dinh D, Popot JL, Boespflug-Tanguy O, Landrieu P, Deleuze JF, Boué J, Jollès P, Dautigny A.

Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7562-6.

44.

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Oberlé I, Rousseau F, Heitz D, Kretz C, Devys D, Hanauer A, Boué J, Bertheas MF, Mandel JL.

Science. 1991 May 24;252(5009):1097-102.

PMID:
2031184
45.

The delta F508 mutation in mild adult forms of cystic fibrosis (CF).

Simon-Bouy B, Mornet E, Taillandier A, Serre JL, Boue J, Boue A.

Clin Genet. 1991 Apr;39(4):304-5.

PMID:
1712680
46.

Consequences of prenatal diagnosis of cystic fibrosis on the reproductive attitudes of parents of affected children.

Boué J, Muller F, Simon-Bouy B, Faure C, Boué A.

Prenat Diagn. 1991 Apr;11(4):209-14.

PMID:
1680231
47.

Amniotic fluid GGT and congenital extrahepatic biliary damage.

Muller F, Gauthier F, Laurent J, Schmitt M, Boué J.

Lancet. 1991 Jan 26;337(8735):232-3. No abstract available.

PMID:
1670856
48.

Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency.

Mornet E, Crété P, Kuttenn F, Raux-Demay MC, Boué J, White PC, Boué A.

Am J Hum Genet. 1991 Jan;48(1):79-88.

49.

[Fortuitous discovery in echography of an isolated fetal intra-abdominal hyperechogenic mass. 87 cases].

Muller F, Simon-Bouy B, Aubry MC, Duchatel F, Bessis R, Boué J.

J Gynecol Obstet Biol Reprod (Paris). 1991;20(8):1115-21. French.

PMID:
1687411
50.

The cystic fibrosis delta F508 mutation in the French population.

Simon-Bouy B, Mornet E, Serre JL, Taillandier A, Boué J, Boué A.

Hum Genet. 1990 Sep;85(4):431-2.

PMID:
2210765

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