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Items: 1 to 50 of 79

1.

A Logic for Checking the Probabilistic Steady-State Properties of Reaction Networks.

Picard V, Siegel A, Bourdon J.

J Comput Biol. 2017 Aug;24(8):734-745. doi: 10.1089/cmb.2017.0099. Epub 2017 Jul 7.

PMID:
28686462
2.

Red blood cell Gardos channel (KCNN4): the essential determinant of erythrocyte dehydration in hereditary xerocytosis.

Rapetti-Mauss R, Picard V, Guitton C, Ghazal K, Proulle V, Badens C, Soriani O, Garçon L, Guizouarn H.

Haematologica. 2017 Oct;102(10):e415-e418. doi: 10.3324/haematol.2017.171389. Epub 2017 Jun 15. No abstract available.

3.

A Prostate Cancer "Nimbosus": Genomic Instability and SChLAP1 Dysregulation Underpin Aggression of Intraductal and Cribriform Subpathologies.

Chua MLK, Lo W, Pintilie M, Murgic J, Lalonde E, Bhandari V, Mahamud O, Gopalan A, Kweldam CF, van Leenders GJLH, Verhoef EI, Hoogland AM, Livingstone J, Berlin A, Dal Pra A, Meng A, Zhang J, Orain M, Picard V, Hovington H, Bergeron A, Lacombe L, Fradet Y, Têtu B, Reuter VE, Fleshner N, Fraser M, Boutros PC, van der Kwast TH, Bristow RG.

Eur Urol. 2017 Nov;72(5):665-674. doi: 10.1016/j.eururo.2017.04.034. Epub 2017 May 13.

PMID:
28511883
4.

Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia.

Astuti D, Sabir A, Fulton P, Zatyka M, Williams D, Hardy C, Milan G, Favaretto F, Yu-Wai-Man P, Rohayem J, López de Heredia M, Hershey T, Tranebjaerg L, Chen JH, Chaussenot A, Nunes V, Marshall B, McAfferty S, Tillmann V, Maffei P, Paquis-Flucklinger V, Geberhiwot T, Mlynarski W, Parkinson K, Picard V, Bueno GE, Dias R, Arnold A, Richens C, Paisey R, Urano F, Semple R, Sinnott R, Barrett TG.

Hum Mutat. 2017 Jul;38(7):764-777. doi: 10.1002/humu.23233. Epub 2017 Jun 1.

5.

A somatic mosaicism in the G6PD gene inducing a late onset chronic non-spherocytic hemolytic anemia.

Couronné L, Tertian G, Boutron A, Picard V, Ouled-Haddou H, Hughes P, Hermine O, Préhu C, Tchernia G, Garçon L.

Am J Hematol. 2017 Aug;92(8):E153-E155. doi: 10.1002/ajh.24760. Epub 2017 Jun 1. No abstract available.

PMID:
28395132
6.

Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency.

Alhenc-Gelas M, Plu-Bureau G, Hugon-Rodin J, Picard V, Horellou MH; GFHT study group on Genetic Thrombophilia.

Thromb Haemost. 2017 Jun 2;117(6):1040-1051. doi: 10.1160/TH16-08-0635. Epub 2017 Mar 16.

PMID:
28300866
7.

Genomic hallmarks of localized, non-indolent prostate cancer.

Fraser M, Sabelnykova VY, Yamaguchi TN, Heisler LE, Livingstone J, Huang V, Shiah YJ, Yousif F, Lin X, Masella AP, Fox NS, Xie M, Prokopec SD, Berlin A, Lalonde E, Ahmed M, Trudel D, Luo X, Beck TA, Meng A, Zhang J, D'Costa A, Denroche RE, Kong H, Espiritu SM, Chua ML, Wong A, Chong T, Sam M, Johns J, Timms L, Buchner NB, Orain M, Picard V, Hovington H, Murison A, Kron K, Harding NJ, P'ng C, Houlahan KE, Chu KC, Lo B, Nguyen F, Li CH, Sun RX, de Borja R, Cooper CI, Hopkins JF, Govind SK, Fung C, Waggott D, Green J, Haider S, Chan-Seng-Yue MA, Jung E, Wang Z, Bergeron A, Dal Pra A, Lacombe L, Collins CC, Sahinalp C, Lupien M, Fleshner NE, He HH, Fradet Y, Tetu B, van der Kwast T, McPherson JD, Bristow RG, Boutros PC.

Nature. 2017 Jan 19;541(7637):359-364. doi: 10.1038/nature20788. Epub 2017 Jan 9.

PMID:
28068672
8.

Translating a Prognostic DNA Genomic Classifier into the Clinic: Retrospective Validation in 563 Localized Prostate Tumors.

Lalonde E, Alkallas R, Chua MLK, Fraser M, Haider S, Meng A, Zheng J, Yao CQ, Picard V, Orain M, Hovington H, Murgic J, Berlin A, Lacombe L, Bergeron A, Fradet Y, Têtu B, Lindberg J, Egevad L, Grönberg H, Ross-Adams H, Lamb AD, Halim S, Dunning MJ, Neal DE, Pintilie M, van der Kwast T, Bristow RG, Boutros PC.

Eur Urol. 2017 Jul;72(1):22-31. doi: 10.1016/j.eururo.2016.10.013. Epub 2016 Nov 1.

PMID:
27815082
9.

Model of the delayed translation of cyclin B maternal mRNA after sea urchin fertilization.

Picard V, Mulner-Lorillon O, Bourdon J, Morales J, Cormier P, Siegel A, Bellé R.

Mol Reprod Dev. 2016 Dec;83(12):1070-1082. doi: 10.1002/mrd.22746. Epub 2016 Oct 23.

PMID:
27699901
10.

Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study.

Pincez T, Guitton C, Gauthier F, de Lambert G, Picard V, Fénéant-Thibault M, Turhan A, Mohandas N, Tchernia G, Garçon L.

Blood. 2016 Mar 24;127(12):1616-8. doi: 10.1182/blood-2015-11-679357. Epub 2016 Jan 15. No abstract available.

11.

Non-immune Hemolysis: Diagnostic Considerations.

Beris P, Picard V.

Semin Hematol. 2015 Oct;52(4):287-303. doi: 10.1053/j.seminhematol.2015.07.005. Epub 2015 Jul 21. Review.

PMID:
26404441
12.

Infantile pyknocytosis, a rare cause of hemolytic anemia in newborns: report of two cases in twin girls and literature overview.

El Nabouch M, Rakotoharinandrasana I, Ndayikeza A, Picard V, Kayemba-Kay's S.

Clin Case Rep. 2015 Jul;3(7):535-8. doi: 10.1002/ccr3.288. Epub 2015 May 8.

13.

A mutation in the Gardos channel is associated with hereditary xerocytosis.

Rapetti-Mauss R, Lacoste C, Picard V, Guitton C, Lombard E, Loosveld M, Nivaggioni V, Dasilva N, Salgado D, Desvignes JP, Béroud C, Viout P, Bernard M, Soriani O, Vinti H, Lacroze V, Feneant-Thibault M, Thuret I, Guizouarn H, Badens C.

Blood. 2015 Sep 10;126(11):1273-80. doi: 10.1182/blood-2015-04-642496. Epub 2015 Jul 6.

14.

Myelodysplastic syndrome with clonal cytogenetic abnormalities followed by fatal erythroid leukemia after 14 years of exposure to hydroxyurea for sickle cell anemia.

Aumont C, Driss F, Lazure T, Picard V, Creidy R, De Botton S, Saada V, Lambotte O, Bilhou-Nabera C, Tertian G, Michot JM.

Am J Hematol. 2015 Jul;90(7):E131-2. doi: 10.1002/ajh.24010. No abstract available.

15.

ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

King MJ, Garçon L, Hoyer JD, Iolascon A, Picard V, Stewart G, Bianchi P, Lee SH, Zanella A; International Council for Standardization in Haematology.

Int J Lab Hematol. 2015 Jun;37(3):304-25. doi: 10.1111/ijlh.12335. Epub 2015 Mar 18.

PMID:
25790109
16.

Early-onset chronic axonal neuropathy, strokes, and hemolysis: inherited CD59 deficiency.

Haliloglu G, Maluenda J, Sayinbatur B, Aumont C, Temucin C, Tavil B, Cetin M, Oguz KK, Gut I, Picard V, Melki J, Topaloglu H.

Neurology. 2015 Mar 24;84(12):1220-4. doi: 10.1212/WNL.0000000000001391. Epub 2015 Feb 25.

PMID:
25716358
17.

Clinical and laboratory characteristics of paediatric and adolescent index cases with venous thromboembolism and antithrombin deficiency. An observational multicentre cohort study.

Limperger V, Franke A, Kenet G, Holzhauer S, Picard V, Junker R, Heller C, Gille C, Manner D, Kurnik K, Knoefler R, Mesters R, Halimeh S, Nowak-Göttl U.

Thromb Haemost. 2014 Sep 2;112(3):478-85. doi: 10.1160/TH14-02-0149. Epub 2014 Jun 26.

PMID:
24966143
18.

Attitudes of family physicians towards adolescent cannabis users: a qualitative study in France.

Vorilhon P, Picard V, Marty L, Vaillant Roussel H, Llorca PM, Laporte C.

Fam Pract. 2014 Oct;31(5):585-91. doi: 10.1093/fampra/cmu030. Epub 2014 Jun 17.

PMID:
24939655
19.

Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis.

Picard V, Proust A, Eveillard M, Flatt JF, Couec ML, Caillaux G, Fénéant-Thibault M, Finkelstein A, Raphaël M, Delaunay J, Bruce LJ, Pissard S, Thomas C.

Blood. 2014 Mar 20;123(12):1963-5. doi: 10.1182/blood-2014-01-548149. No abstract available.

20.

Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels.

Albuisson J, Murthy SE, Bandell M, Coste B, Louis-Dit-Picard H, Mathur J, Fénéant-Thibault M, Tertian G, de Jaureguiberry JP, Syfuss PY, Cahalan S, Garçon L, Toutain F, Simon Rohrlich P, Delaunay J, Picard V, Jeunemaitre X, Patapoutian A.

Nat Commun. 2013;4:1884. doi: 10.1038/ncomms2899. Erratum in: Nat Commun. 2013;4:2440.

21.

Recurrent mutation in the PIEZO1 gene in two families of hereditary xerocytosis with fetal hydrops.

Beneteau C, Thierry G, Blesson S, Le Vaillant C, Picard V, Béné MC, Eveillard M, Le Caignec C.

Clin Genet. 2014 Mar;85(3):293-5. doi: 10.1111/cge.12147. Epub 2013 Apr 14. No abstract available.

PMID:
23581886
22.

A chemically-modified inactive antithrombin as a potent antagonist of fondaparinux and heparin anticoagulant activity.

Fazavana J, Bianchini EP, Saller F, Smadja C, Picard V, Taverna M, Borgel D.

J Thromb Haemost. 2013 Jun;11(6):1128-36. doi: 10.1111/jth.12249.

23.

In vitro generated Rh(null) red cells recapitulate the in vivo deficiency: a model for rare blood group phenotypes and erythroid membrane disorders.

Cambot M, Mazurier C, Canoui-Poitrine F, Hebert N, Picot J, Clay D, Picard V, Ripoche P, Douay L, Dubart-Kupperschmitt A, Cartron JP.

Am J Hematol. 2013 May;88(5):343-9. doi: 10.1002/ajh.23414. Epub 2013 Mar 15.

24.

Testing for hereditary spherocytosis: a French experience.

Mayeur-Rousse C, Gentil M, Botton J, Thibaut MF, Guitton C, Picard V.

Haematologica. 2012 Dec;97(12):e48-9; author reply e52. doi: 10.3324/haematol.2012.074070. No abstract available.

25.

Vertical Deviations Secondary to Supranuclear Origins.

Picard V.

Am Orthopt J. 2011;61:23-7. Review.

PMID:
22069847
26.

Ultra-resistant schizophrenia is not associated with the multidrug-resistant transporter 1 (MDR1) gene rs1045642 variant.

Mouaffak F, Kebir O, Picard V, Bonhomme-Faivre L, Millet B, Olié JP, Reynaud M, Krebs MO, Benyamina A.

J Clin Psychopharmacol. 2011 Apr;31(2):236-8. doi: 10.1097/JCP.0b013e31820f9152. No abstract available.

PMID:
21364332
27.

Development of a recombinant antithrombin variant as a potent antidote to fondaparinux and other heparin derivatives.

Bianchini EP, Fazavana J, Picard V, Borgel D.

Blood. 2011 Feb 10;117(6):2054-60. doi: 10.1182/blood-2010-06-288522. Epub 2010 Nov 3.

28.

Influence of natural SERPINC1 mutations on ex vivo thrombin generation.

Alhenc-Gelas M, Canonico M, Picard V.

J Thromb Haemost. 2010 Apr;8(4):845-8. doi: 10.1111/j.1538-7836.2010.03750.x. Epub 2010 Jan 17. No abstract available.

29.

MDR1 polymorphism role in patients treated with cetuximab and irinotecan in irinotecan refractory colorectal cancer.

Paule B, Castagne V, Picard V, Saffroy R, Adam R, Guettier C, Farinotti R, Bonhomme-Faivre L.

Med Oncol. 2010 Dec;27(4):1066-72. doi: 10.1007/s12032-009-9336-3. Epub 2009 Oct 28.

PMID:
19862647
30.

Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.

Picard V, Chen JM, Tardy B, Aillaud MF, Boiteux-Vergnes C, Dreyfus M, Emmerich J, Lavenu-Bombled C, Nowak-Göttl U, Trillot N, Aiach M, Alhenc-Gelas M.

Hum Genet. 2010 Jan;127(1):45-53. doi: 10.1007/s00439-009-0742-6. Epub 2009 Sep 17.

PMID:
19760264
31.

Effect of the ABCB1 3435C>T polymorphism on tacrolimus concentrations and dosage requirements in liver transplant recipients.

Bonhomme-Faivre L, Picard V, Saliba F, Abbara C, Fodil M, Chaunoy M, Farinotti R.

Am J Health Syst Pharm. 2009 Sep 15;66(18):1645-51. doi: 10.2146/ajhp080396.

PMID:
19729569
32.

Structure-activity relationship of isoform selective inhibitors of Rac1/1b GTPase nucleotide binding.

Beausoleil E, Chauvignac C, Taverne T, Lacombe S, Pognante L, Leblond B, Pallares D, Oliveira CD, Bachelot F, Carton R, Peillon H, Coutadeur S, Picard V, Lambeng N, Désiré L, Schweighoffer F.

Bioorg Med Chem Lett. 2009 Oct 1;19(19):5594-8. doi: 10.1016/j.bmcl.2009.08.037. Epub 2009 Aug 13.

PMID:
19716293
33.

Association between ABCB1 C3435T polymorphism and increased risk of cannabis dependence.

Benyamina A, Bonhomme-Faivre L, Picard V, Sabbagh A, Richard D, Blecha L, Rahioui H, Karila L, Lukasiewicz M, Farinotti R, Picard V, Marill C, Reynaud M.

Prog Neuropsychopharmacol Biol Psychiatry. 2009 Oct 1;33(7):1270-4. doi: 10.1016/j.pnpbp.2009.07.016. Epub 2009 Jul 20.

PMID:
19625010
34.

High frequency of MAGE-A4 and MAGE-A9 expression in high-risk bladder cancer.

Bergeron A, Picard V, LaRue H, Harel F, Hovington H, Lacombe L, Fradet Y.

Int J Cancer. 2009 Sep 15;125(6):1365-71. doi: 10.1002/ijc.24503.

35.

Characterization of EHT 1864, a novel small molecule inhibitor of Rac family small GTPases.

Onesto C, Shutes A, Picard V, Schweighoffer F, Der CJ.

Methods Enzymol. 2008;439:111-29. doi: 10.1016/S0076-6879(07)00409-0.

PMID:
18374160
36.

Specificity and mechanism of action of EHT 1864, a novel small molecule inhibitor of Rac family small GTPases.

Shutes A, Onesto C, Picard V, Leblond B, Schweighoffer F, Der CJ.

J Biol Chem. 2007 Dec 7;282(49):35666-78. Epub 2007 Oct 11.

37.

Comprehensive characterization of the photodissociation pathways of protonated tryptophan.

Lepère V, Lucas B, Barat M, Fayeton JA, Picard VJ, Jouvet C, Carçabal P, Nielsen I, Dedonder-Lardeux C, Grégoire G, Fujii A.

J Chem Phys. 2007 Oct 7;127(13):134313.

PMID:
17919030
38.

Antithrombin Cambridge II (A384S): prevalence in patients of the Paris Thrombosis Study (PATHROS).

Picard V, Présot I, Scarabin PY, Aiach M, Emmerich J, Alhenc-Gelas M.

Blood. 2007 Oct 1;110(7):2777-8. No abstract available.

39.

MAGE-A9 mRNA and protein expression in bladder cancer.

Picard V, Bergeron A, Larue H, Fradet Y.

Int J Cancer. 2007 May 15;120(10):2170-7.

40.

[Coagulation factor mutations and thrombosis].

Aiach M, Alhenc-Gelas M, Borgel D, Emmerich J, Gandrille S, Picard V.

Med Sci (Paris). 2006 Nov;22(11):985-9. Review. French.

41.

Cancer-testis antigen expression in bladder cancer.

Fradet Y, Picard V, Bergeron A, LaRue H.

Prog Urol. 2006 Sep;16(4):421-8. No abstract available.

PMID:
17069033
42.

Identification of a tyrosine-based motif (YGSI) in the amino terminus of Nramp1 (Slc11a1) that is important for lysosomal targeting.

Lam-Yuk-Tseung S, Picard V, Gros P.

J Biol Chem. 2006 Oct 20;281(42):31677-88. Epub 2006 Aug 12.

43.

Cancer-testis antigen expression in bladder cancer.

Fradet Y, Picard V, Bergeron A, LaRue H.

Prog Urol. 2005 Dec;15(6 Suppl 1):1303-13.

PMID:
16734221
44.

Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.

Picard V, Nowak-Göttl U, Biron-Andreani C, Fouassier M, Frere C, Goualt-Heilman M, de Maistre E, Regina S, Rugeri L, Ternisien C, Trichet C, Vergnes C, Aiach M, Alhenc-Gelas M.

Hum Mutat. 2006 Jun;27(6):600. Erratum in: Hum Mutat. 2006 Nov;27(11):1160.

PMID:
16705712
45.

Interactions between the dopamine agonist, bromocriptine and the efflux protein, P-glycoprotein at the blood-brain barrier in the mouse.

Vautier S, Lacomblez L, Chacun H, Picard V, Gimenez F, Farinotti R, Fernandez C.

Eur J Pharm Sci. 2006 Feb;27(2-3):167-74. Epub 2005 Nov 2.

PMID:
16263252
46.

RAC1 inhibition targets amyloid precursor protein processing by gamma-secretase and decreases Abeta production in vitro and in vivo.

Désiré L, Bourdin J, Loiseau N, Peillon H, Picard V, De Oliveira C, Bachelot F, Leblond B, Taverne T, Beausoleil E, Lacombe S, Drouin D, Schweighoffer F.

J Biol Chem. 2005 Nov 11;280(45):37516-25. Epub 2005 Sep 8.

47.

Conformational Asn187Asp/Lys antithrombin variants and thrombosis. Clinical and biological features in 13 new heterozygotes.

Picard V, Bauters A, Khairy M, Ochat N, Jude B, Aiach M, Alhenc-Gelas M.

Thromb Haemost. 2005 Jan;93(1):57-62.

PMID:
15630491
48.

MDR-1 C3435T polymorphism influences cyclosporine a dose requirement in liver-transplant recipients.

Bonhomme-Faivre L, Devocelle A, Saliba F, Chatled S, Maccario J, Farinotti R, Picard V.

Transplantation. 2004 Jul 15;78(1):21-5.

PMID:
15257034
49.

Two new antithrombin variants support a role for K114 and R13 in heparin binding.

Picard V, Susen S, Bellucci S, Aiach M, Alhenc-Gelas M.

J Thromb Haemost. 2003 Feb;1(2):386-7. No abstract available.

50.

Antithrombin Phe229Leu: a new homozygous variant leading to spontaneous antithrombin polymerization in vivo associated with severe childhood thrombosis.

Picard V, Dautzenberg MD, Villoutreix BO, Orliaguet G, Alhenc-Gelas M, Aiach M.

Blood. 2003 Aug 1;102(3):919-25. Epub 2003 Feb 20.

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