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Items: 1 to 50 of 85

1.

Random walk with restart on multiplex and heterogeneous biological networks.

Valdeolivas A, Tichit L, Navarro C, Perrin S, Odelin G, Levy N, Cau P, Remy E, Baudot A.

Bioinformatics. 2019 Feb 1;35(3):497-505. doi: 10.1093/bioinformatics/bty637.

PMID:
30020411
2.

Low lamin A expression in lung adenocarcinoma cells from pleural effusions is a pejorative factor associated with high number of metastatic sites and poor Performance status.

Kaspi E, Frankel D, Guinde J, Perrin S, Laroumagne S, Robaglia-Schlupp A, Ostacolo K, Harhouri K, Tazi-Mezalek R, Micallef J, Dutau H, Tomasini P, De Sandre-Giovannoli A, Lévy N, Cau P, Astoul P, Roll P.

PLoS One. 2017 Aug 14;12(8):e0183136. doi: 10.1371/journal.pone.0183136. eCollection 2017.

3.

MG132-induced progerin clearance is mediated by autophagy activation and splicing regulation.

Harhouri K, Navarro C, Depetris D, Mattei MG, Nissan X, Cau P, De Sandre-Giovannoli A, Lévy N.

EMBO Mol Med. 2017 Sep;9(9):1294-1313. doi: 10.15252/emmm.201607315.

4.

Identification of CD146 as a novel molecular actor involved in systemic sclerosis.

Kaspi E, Heim X, Granel B, Guillet B, Stalin J, Nollet M, Bertaud-Foucault A, Robaglia-Schlupp A, Roll P, Cau P, Leroyer A, Bachelier R, Benyamine A, Dignat-George F, Blot-Chabaud M, Bardin N.

J Allergy Clin Immunol. 2017 Nov;140(5):1448-1451.e6. doi: 10.1016/j.jaci.2017.04.046. Epub 2017 Jun 9. No abstract available.

PMID:
28606586
5.

Erratum to: Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice.

Roubertoux PL, Baril N, Cau P, Scajola C, Ghata A, Bartoli C, Bourgeois P, di Christofaro J, Tordjman S, Carlier M.

Behav Genet. 2017 May;47(3):323. doi: 10.1007/s10519-017-9845-3. No abstract available.

PMID:
28337630
6.

Differential Brain, Cognitive and Motor Profiles Associated with Partial Trisomy. Modeling Down Syndrome in Mice.

Roubertoux PL, Baril N, Cau P, Scajola C, Ghata A, Bartoli C, Bourgeois P, Christofaro JD, Tordjman S, Carlier M.

Behav Genet. 2017 May;47(3):305-322. doi: 10.1007/s10519-017-9835-5. Epub 2017 Feb 15. Erratum in: Behav Genet. 2017 May;47(3):323.

PMID:
28204906
7.
8.

WITHDRAWN: Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Cau P, Navarro C, Harhouri K, Roll P, Sigaudy S, Kaspi E, Perrin S, De Sandre-Giovannoli A, Lévy N.

Semin Cell Dev Biol. 2014 Mar 28. pii: S1084-9521(14)00058-5. doi: 10.1016/j.semcdb.2014.03.022. [Epub ahead of print]

PMID:
24685615
9.

Nuclear matrix, nuclear envelope and premature aging syndromes in a translational research perspective.

Cau P, Navarro C, Harhouri K, Roll P, Sigaudy S, Kaspi E, Perrin S, De Sandre-Giovannoli A, Lévy N.

Semin Cell Dev Biol. 2014 May;29:125-47. doi: 10.1016/j.semcdb.2014.03.021. Epub 2014 Mar 22. Review.

PMID:
24662892
10.

New ZMPSTE24 (FACE1) mutations in patients affected with restrictive dermopathy or related progeroid syndromes and mutation update.

Navarro CL, Esteves-Vieira V, Courrier S, Boyer A, Duong Nguyen T, Huong le TT, Meinke P, Schröder W, Cormier-Daire V, Sznajer Y, Amor DJ, Lagerstedt K, Biervliet M, van den Akker PC, Cau P, Roll P, Lévy N, Badens C, Wehnert M, De Sandre-Giovannoli A.

Eur J Hum Genet. 2014 Aug;22(8):1002-11. doi: 10.1038/ejhg.2013.258. Epub 2013 Oct 30.

11.

Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatus.

Cacciagli P, Sutera-Sardo J, Borges-Correia A, Roux JC, Dorboz I, Desvignes JP, Badens C, Delepine M, Lathrop M, Cau P, Lévy N, Girard N, Sarda P, Boespflug-Tanguy O, Villard L.

Am J Hum Genet. 2013 Sep 5;93(3):579-86. doi: 10.1016/j.ajhg.2013.07.023.

12.

HIV protease inhibitors do not cause the accumulation of prelamin A in PBMCs from patients receiving first line therapy: the ANRS EP45 "aging" study.

Perrin S, Cremer J, Faucher O, Reynes J, Dellamonica P, Micallef J, Solas C, Lacarelle B, Stretti C, Kaspi E, Robaglia-Schlupp A, Nicolino-Brunet C, Tamalet C, Lévy N, Poizot-Martin I, Cau P, Roll P.

PLoS One. 2012;7(12):e53035. doi: 10.1371/journal.pone.0053035. Epub 2012 Dec 28. Erratum in: PLoS One. 2013;8(8). doi:10.1371/annotation/f02cdfd3-b271-46fd-a78f-5a030f0b416d. Tamalet, Corine Nicolino-Brunet Catherine [corrected to Nicolino-Brunet, Corinne]; [ corrected to Tamalet, Catherine].

13.

HIV-1 infection and first line ART induced differential responses in mitochondria from blood lymphocytes and monocytes: the ANRS EP45 "Aging" study.

Perrin S, Cremer J, Roll P, Faucher O, Ménard A, Reynes J, Dellamonica P, Naqvi A, Micallef J, Jouve E, Tamalet C, Solas C, Pissier C, Arnoux I, Nicolino-Brunet C, Espinosa L, Lévy N, Kaspi E, Robaglia-Schlupp A, Poizot-Martin I, Cau P.

PLoS One. 2012;7(7):e41129. doi: 10.1371/journal.pone.0041129. Epub 2012 Jul 19.

14.

UMD-DYSF, a novel locus specific database for the compilation and interactive analysis of mutations in the dysferlin gene.

Blandin G, Beroud C, Labelle V, Nguyen K, Wein N, Hamroun D, Williams B, Monnier N, Rufibach LE, Urtizberea JA, Cau P, Bartoli M, Lévy N, Krahn M.

Hum Mutat. 2012 Mar;33(3):E2317-31. doi: 10.1002/humu.22015. Epub 2011 Dec 29.

PMID:
22213072
15.

High prevalence of laminopathies among patients with metabolic syndrome.

Dutour A, Roll P, Gaborit B, Courrier S, Alessi MC, Tregouet DA, Angelis F, Robaglia-Schlupp A, Lesavre N, Cau P, Lévy N, Badens C, Morange PE.

Hum Mol Genet. 2011 Oct 1;20(19):3779-86. doi: 10.1093/hmg/ddr294. Epub 2011 Jun 30.

PMID:
21724554
16.

A naturally occurring human minidysferlin protein repairs sarcolemmal lesions in a mouse model of dysferlinopathy.

Krahn M, Wein N, Bartoli M, Lostal W, Courrier S, Bourg-Alibert N, Nguyen K, Vial C, Streichenberger N, Labelle V, DePetris D, Pécheux C, Leturcq F, Cau P, Richard I, Lévy N.

Sci Transl Med. 2010 Sep 22;2(50):50ra69. doi: 10.1126/scitranslmed.3000951.

17.

LBR mutation and nuclear envelope defects in a patient affected with Reynolds syndrome.

Gaudy-Marqueste C, Roll P, Esteves-Vieira V, Weiller PJ, Grob JJ, Cau P, Lévy N, De Sandre-Giovannoli A.

J Med Genet. 2010 Jun;47(6):361-70. doi: 10.1136/jmg.2009.071696.

PMID:
20522425
18.

Immunolabelling and flow cytometry as new tools to explore dysferlinopathies.

Wein N, Krahn M, Courrier S, Bartoli M, Salort-Campana E, Nguyen K, Fernandez C, Pouget J, Fossat C, Depetris D, Leturcq F, Cau P, Levy N.

Neuromuscul Disord. 2010 Jan;20(1):57-60. doi: 10.1016/j.nmd.2009.08.004. Epub 2009 Oct 23.

PMID:
19854055
19.

Epileptic and developmental disorders of the speech cortex: ligand/receptor interaction of wild-type and mutant SRPX2 with the plasminogen activator receptor uPAR.

Royer-Zemmour B, Ponsole-Lenfant M, Gara H, Roll P, Lévêque C, Massacrier A, Ferracci G, Cillario J, Robaglia-Schlupp A, Vincentelli R, Cau P, Szepetowski P.

Hum Mol Genet. 2008 Dec 1;17(23):3617-30. doi: 10.1093/hmg/ddn256. Epub 2008 Aug 21.

PMID:
18718938
20.

Nuclear localization of a novel human syntaxin 1B isoform.

Pereira S, Massacrier A, Roll P, Vérine A, Etienne-Grimaldi MC, Poitelon Y, Robaglia-Schlupp A, Jamali S, Roeckel-Trevisiol N, Royer B, Pontarotti P, Lévêque C, Seagar M, Lévy N, Cau P, Szepetowski P.

Gene. 2008 Nov 1;423(2):160-71. doi: 10.1016/j.gene.2008.07.010. Epub 2008 Jul 17.

PMID:
18691641
21.

Combined treatment with statins and aminobisphosphonates extends longevity in a mouse model of human premature aging.

Varela I, Pereira S, Ugalde AP, Navarro CL, Suárez MF, Cau P, Cadiñanos J, Osorio FG, Foray N, Cobo J, de Carlos F, Lévy N, Freije JM, López-Otín C.

Nat Med. 2008 Jul;14(7):767-72. doi: 10.1038/nm1786. Epub 2008 Jun 29.

PMID:
18587406
22.

HGPS and related premature aging disorders: from genomic identification to the first therapeutic approaches.

Pereira S, Bourgeois P, Navarro C, Esteves-Vieira V, Cau P, De Sandre-Giovannoli A, Lévy N.

Mech Ageing Dev. 2008 Jul-Aug;129(7-8):449-59. doi: 10.1016/j.mad.2008.04.003. Epub 2008 Apr 12. Review.

PMID:
18513784
23.

Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas.

Royer B, Soares DC, Barlow PN, Bontrop RE, Roll P, Robaglia-Schlupp A, Blancher A, Levasseur A, Cau P, Pontarotti P, Szepetowski P.

BMC Genet. 2007 Oct 18;8:72.

24.

[Role of DNA microarrays in the diagnosis of pleural exudates: a feasibility study].

Greillier L, Roll P, Barlesi F, Robaglia-Schlupp A, Fraticelli A, Cau P, Astoul P.

Rev Mal Respir. 2007 Sep;24(7):859-67. French.

PMID:
17925668
25.

Determinants and evolution of squamous intraepithelial lesions in HIV-infected women, 1991-2004.

Drogoul-Vey MP, Marimoutou C, Robaglia-Schlupp A, Beerli M, Gastaut JA, Cau P, Poizot-Martin I.

AIDS Care. 2007 Sep;19(8):1052-7.

PMID:
17852004
26.

Molecular bases of progeroid syndromes.

Navarro CL, Cau P, Lévy N.

Hum Mol Genet. 2006 Oct 15;15 Spec No 2:R151-61. Review.

PMID:
16987878
27.

Epilepsy and deletions at chromosome 2q24.

Pereira S, Vieira JP, Cau P, Genton P, Szepetowski P.

Am J Med Genet A. 2006 Jun 15;140(12):1354-5. No abstract available.

PMID:
16700054
28.

SRPX2 mutations in disorders of language cortex and cognition.

Roll P, Rudolf G, Pereira S, Royer B, Scheffer IE, Massacrier A, Valenti MP, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz MN, Lemainque A, Delepine M, Caloustian C, de Saint Martin A, Bruneau N, Depétris D, Mattéi MG, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer BA, Ravid R, Marescaux C, Berkovic SF, Hirsch E, Lathrop M, Cau P, Szepetowski P.

Hum Mol Genet. 2006 Apr 1;15(7):1195-207. Epub 2006 Feb 23.

PMID:
16497722
29.

Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex.

Jamali S, Bartolomei F, Robaglia-Schlupp A, Massacrier A, Peragut JC, Régis J, Dufour H, Ravid R, Roll P, Pereira S, Royer B, Roeckel-Trevisiol N, Fontaine M, Guye M, Boucraut J, Chauvel P, Cau P, Szepetowski P.

Brain. 2006 Mar;129(Pt 3):625-41. Epub 2006 Jan 6.

PMID:
16399808
30.

Loss of ZMPSTE24 (FACE-1) causes autosomal recessive restrictive dermopathy and accumulation of Lamin A precursors.

Navarro CL, Cadiñanos J, De Sandre-Giovannoli A, Bernard R, Courrier S, Boccaccio I, Boyer A, Kleijer WJ, Wagner A, Giuliano F, Beemer FA, Freije JM, Cau P, Hennekam RC, López-Otín C, Badens C, Lévy N.

Hum Mol Genet. 2005 Jun 1;14(11):1503-13. Epub 2005 Apr 20.

PMID:
15843403
31.

Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy.

Navarro CL, De Sandre-Giovannoli A, Bernard R, Boccaccio I, Boyer A, Geneviève D, Hadj-Rabia S, Gaudy-Marqueste C, Smitt HS, Vabres P, Faivre L, Verloes A, Van Essen T, Flori E, Hennekam R, Beemer FA, Laurent N, Le Merrer M, Cau P, Lévy N.

Hum Mol Genet. 2004 Oct 15;13(20):2493-503. Epub 2004 Aug 18.

PMID:
15317753
32.

Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A.

Pereira S, Vieira JP, Barroca F, Roll P, Carvalhas R, Cau P, Sequeira S, Genton P, Szepetowski P.

Neurology. 2004 Jul 13;63(1):191-2. No abstract available.

PMID:
15249644
33.
34.

[An experimental study on the systemic distribution of calibrated talc after intra-pleural injection].

Fraticelli A, Robaglia A, Gimenez C, Cau P, Monjanel-Mouterde S, Astoul P.

Rev Mal Respir. 2003 Dec;20(6 Pt 1):881-8. French.

PMID:
14743089
35.

[Skin stem cells].

Hautier A, Krahn M, Magalon G, Robaglia-Schlupp A, Cau P.

Ann Dermatol Venereol. 2003 Nov;130(11):1072-9. Review. French. No abstract available.

PMID:
14724548
36.

[Are we sectioning the cochlear efferent system during vestibular neurotomy?].

Chays A, Maison S, Robaglia-Schlupp A, Cau P, Broder L, Magnan J.

Rev Laryngol Otol Rhinol (Bord). 2003;124(1):53-8. French.

PMID:
12934443
37.

Lamin a truncation in Hutchinson-Gilford progeria.

De Sandre-Giovannoli A, Bernard R, Cau P, Navarro C, Amiel J, Boccaccio I, Lyonnet S, Stewart CL, Munnich A, Le Merrer M, Lévy N.

Science. 2003 Jun 27;300(5628):2055. Epub 2003 Apr 17. No abstract available.

38.

Distribution of calibrated talc after intrapleural administration: an experimental study in rats.

Fraticelli A, Robaglia-Schlupp A, Riera H, Monjanel-Mouterde S, Cau P, Astoul P.

Chest. 2002 Nov;122(5):1737-41.

PMID:
12426279
39.

PMP22 overexpression causes dysmyelination in mice.

Robaglia-Schlupp A, Pizant J, Norreel JC, Passage E, Sabéran-Djoneidi D, Ansaldi JL, Vinay L, Figarella-Branger D, Lévy N, Clarac F, Cau P, Pellissier JF, Fontés M.

Brain. 2002 Oct;125(Pt 10):2213-21.

PMID:
12244079
40.

The alpha(1A) subunits of rat brain calcium channels are developmentally regulated by alternative RNA splicing.

Vigues S, Gastaldi M, Massacrier A, Cau P, Valmier J.

Neuroscience. 2002;113(3):509-17.

PMID:
12150771
41.

IMHS clinical experience in the treatment of peritrochanteric fractures. The results of a multicentric Italian study of 981 cases.

Rebuzzi E, Pannone A, Schiavetti S, Santoriello P, de Nicola U, Fancellu G, Cau P, Gulli S, Dordolin P, Maniscalco P, Morici F, Commessatti M, Pozzi-Mucelli M, Maiorana CS, Bassini F.

Injury. 2002 Jun;33(5):407-12.

PMID:
12095720
43.

Clinical utility of bronchoalveolar lavage cell phenotype analyses in the postoperative monitoring of lung transplant recipients.

Reynaud-Gaubert M, Thomas P, Gregoire R, Badier M, Cau P, Sampol J, Giudicelli R, Fuentes P.

Eur J Cardiothorac Surg. 2002 Jan;21(1):60-6.

PMID:
11788258
44.

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

Muscatelli F, Abrous DN, Massacrier A, Boccaccio I, Le Moal M, Cau P, Cremer H.

Hum Mol Genet. 2000 Dec 12;9(20):3101-10.

PMID:
11115855
45.

Absence of hepatitis C genome in semen of infected men by polymerase chain reaction, branched DNA and in situ hybridization.

Debono E, Halfon P, Bourliere M, Gerolami-Santandrea V, Gastaldi M, Castellani P, Cartouzou G, Botta-Fridlund D, Cau P, Gauthier A.

Liver. 2000 Jun;20(3):257-61.

PMID:
10902978
46.

Early detection of airway involvement in obliterative bronchiolitis after lung transplantation. Functional and bronchoalveolar lavage cell findings.

Reynaud-Gaubert M, Thomas P, Badier M, Cau P, Giudicelli R, Fuentes P.

Am J Respir Crit Care Med. 2000 Jun;161(6):1924-9.

PMID:
10852768
47.

ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells.

Jay P, Bergé-Lefranc JL, Massacrier A, Roessler E, Wallis D, Muenke M, Gastaldi M, Taviaux S, Cau P, Berta P.

Eur J Biochem. 2000 May;267(10):2921-8.

48.

Regulation of calcium channel alpha(1A) subunit splice variant mRNAs in kainate-induced temporal lobe epilepsy.

Vigues S, Gastaldi M, Chabret C, Massacrier A, Cau P, Valmier J.

Neurobiol Dis. 1999 Aug;6(4):288-301.

PMID:
10448056
49.

Two Nkx-3-related genes are expressed in the adult and regenerating central nervous system of the urodele Pleurodeles waltl.

Nicolas S, Caubit X, Massacrier A, Cau P, Le Parco Y.

Dev Genet. 1999;24(3-4):319-28.

PMID:
10322640
50.

Effect of gamma knife radiosurgery on rat brain sodium channel subunit mRNA expression.

Bartolomei F, Massacrier A, Rey M, Viale M, Régis J, Gastaldi M, Cau P.

Stereotact Funct Neurosurg. 1998 Oct;70 Suppl 1:237-42.

PMID:
9782256

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