Publications

Bannière-U676-Y

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Physiopathologie et neuroprotection des lésions cérébrales périnatales

Publications

Equipe 1. Publications (2005 - 2004) - (2003 - 2002) - (2001 - 2000) - (1999)
1. Publications originales

2001

  1. Attia-Sobol J, Encha-Razavi F, Hermier M, Vitrey D, Verloes A, Plauchu H. Lissencephaly type III, stippled epiphyses and loose, thick skin: A new recessively inherited syndrome. Am J Med Genet 2001, 99:14-20
     
  2. Bahi N, Nehlig A, Evrard P, Gressens P. Caffeine does not affect excitotoxic brain lesions in newborn mice. Eur. J. Paediatr. Neurol., 2001, 5 : 161-165.
     
  3. Banrezes B, Maurin M, Verney C. Intrauterine growth retardation does not alter the distribution of tyrosine hydroxylase-immunoreactive neurons of A8, A9 and A10 groups in the rat: a three-dimensional reconstruction study. Dev Brain Res., 2001, 126:13-20.
     
  4. Baud O, Goulet O, Canioni D, Le Deist F, Radford I, Rieu D, Dupuis-Girod S, Cerf-Bensussan N, Cavazzana-Calvo M, Brousse N, Fischer A, Casanova JL. Successful allogenic bone marrow transplantation in immune dysregulation, polyendocrinopathy, enteropathy, X-linked enteropathy (IPEX). N Engl J Med, 2001; 344:1758-62.
     
  5. Baud O, Laudenbach V, Evrard P, Gressens P. Neurotoxic effects of fluorinated glucocorticoid preparations on the developing mouse brain: role of preservatives. Pediatr. Res., 2001, 50 : 706-711.
     
  6. Baud O, Picard V, Durand P, Duchemin J, Proulle V, Alhenc-Gelas M, Devictor D, Dreyfus M. Intracerebral hemorrhage associated with a new antithronbin gene mutation in a neonate. J Pediatr., 2001,139:741-743.
     
  7. Campos-Xavier B, Saraiva JM, Savarirayan R, Verloes A, Feingold J, Faivre L, Munnich A, Le Merrer M, Cormier-Daire V. Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann disease. Hum Genet. 2001;109:653-8.
     
  8. Cantagrel S, Gressens P, Bodard S, Suc AL, Laugier J, Guilloteau D, Chalon S. mRNA d(2) dopaminergic receptor expression after hypoxia-ischemia in rat immature brain. Biol. Neonate, 2001, 80 : 68-73.
     
  9. Castelnau P, Zilbovicius M, Ribeiro MJ, Hertz-Pannier L, Ogier H, Evrard P. Striatal and pontocerebellar hypoperfusion in Hallervorden-Spatz syndrome. Pediatr. Neurol., 2001, 25: 170-174.
     
  10. Couvert P, Bienvenu T, Aquaviva C, Poirier K, Moraine C, Gendrot C, Verloes A, Andres C, Le Fevre AC, Souville I, Steffann J, des Portes V, Ropers HH, Yntema HG, Fryns JP, Briault S, Chelly J, Cherif B. MECP2 is highly mutated in X-linked mental retardation. Hum Mol Genet 2001, 10:941-946
     
  11. Crisponi L, Deiana M, Loi A, Chiappe F, Uda M, Amati P, Bisceglia L, Zelante L, Nagaraja R, Porcu S, Serafina Ristaldi M, Marzella R, Rocchi M, Nicolino M, Lienhardt-Roussie A, Nivelon A, Verloes A, Schlessinger D, Gasparini P, Bonneau D, Cao A, Pilia G. (). The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome. Nat Genet 2001, 27:159-166
     
  12. Dauger S, Aizenfisz S, Renolleau S, Durand E, Vardon G, Gaultier C, Gallego J. Arousal response to hypoxia in newborn mice. Respir Physiol 2001;128:235-40.
     
  13. Dauger S, Guimiot F, Renolleau S, Levacher B, Boda B, Mas C, Simonneau M, Gaultier C, Gallego J. MASH-1/RET pathway involvement in development of brain stem control of respiratory frequency in newborn mice. Physiol Genomics 2001;7:149-57.
     
  14. De Baere E, Dixon MJ, Small KW, Jabs EW, Leroy BP, Devriendt K, Gillerot Y, Mortier G, Meire F, Van Maldergem L, Courtens W, Hjalgrim H, Huang S, Liebaers I, Van Regemorter N, Touraine P, Praphanphoj V, Verloes A, Udar N, Yellore V, Chalukya M, Yelchits S, De Paepe A, Kuttenn F, Fellous M, Veitia R, Messiaen L. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation. Hum Mol Genet. 2001;10:1591-600.
     
  15. Dicou E, Attouf S, Gressens P. Neuroprotective effects of leptin in vivo and in vitro. Neuroreport, 2001, 12 : 3947-3951.
     
  16. Garel C, Chantrel E, Brisse H, Elmaleh D, Luton D, Oury JF, Sebag G, Hassan M. Fetal cerebral cortex : normal gestational landmarks using prenatal MR imaging. AJNR, 2001 ; 22 : 184-189
     
  17. Gerard-Blanluet M, Elbez A, Bazin A, Danan C, Verloes A, Janaud JC. Mosaic trisomy 15 and hemihypertrophy.Ann Genet. 2001; 44:143-8.
     
  18. Gray F, Adle-Biassette H, Chretien F, Lorin De La Grandmaison G, Force G, Keohane C. Neuropathology and neurodegeneration in human immunodeficiency virus infection. Pathogenesis of HIV-induced lesions of the brain, correlations with HIV-associated disorders and modifications according to treatments. Clin Neuropathol. 2001; 20:146-55.
     
  19. Hu Z, Lelièvre V, Rodriguez WI, Tam J, Cheng JW, Cohen-Cory S, Waschek JA. Embryonic expression of pituitary adenylate cyclase activating polypeptide (PACAP) and of its selective type I receptor in the frog Xenopus laevis brain: Potential role in patterning. J. Comp. Neurol. 2001, 441: 266-275.
     
  20. Lang-Lazdunski L, Heurteaux C, Dupont H, Rouelle D, Widmann C, Mantz J : The effects of FK506 on neurologic and histopathologic outcome after transient spinal cord ischemia induced by aortic cross-clamping in rats. Anesth Analg 2001; 92: 237-44.
     
  21. Largeron M, Mesplès B, Gressens P, Cecchelli R, Spedding M, Le Ridant A, Fleury MB. The neuroprotective activity of 8-alkylamino-1,4-benzoxazine antioxidants. Eur J Pharmacol, 2001, 424 : 189-194.
     
  22. Laudenbach V, Calo G, Guerrini R, Lamboley G, Benoist JF, Evrard P, Gressens P. Nocicieptin/orphanin FQ exacerbates excitotoxic white matter lesions in the murine neonatal brain. J. Clin. Invest., 2001, 107: 457-466.
     
  23. Lee M, Lelièvre V, Doshi S, Rodriguez WI, Torres M, de Vellis J, Waschek JA. Pitiutary adenylyl cyclase activating peptide stimulates proliferation but delays maturation in oligodendrocytes J. Neurosci., 2001, 21: 3849-3859.
     
  24. Lelièvre V, Pineau N, Hu Z, Ioffe Y, A Chao, Muller JM, Waschek JA. Proliferative actions of natriuretic peptides on neuroblastoma cells: Involvement of guanylyl cyclase and non-guanylyl cyclase pathways. J. Biol. Chem. 2001, 276: 43668-43676
     
  25. Liu D, Krajniak K, Chun D, Sena M, Casillas R, Lelièvre V, Nguyen T, Bravo D, Colburn S, Waschek JA. VIP gene transcription is regulated by far upstream ap-1/ets enhancer and repressor elements. Biochem. Biophys. Res. Comm., 2001, 284: 211-218.
     
  26. Magre J, Delepine M, Khallouf E, Gedde-Dahl T Jr, Van Maldergem L, Sobel E, Papp J, Meier M, Megarbane A, Bachy A, Verloes A, d'Abronzo FH, Seemanova E, Assan R, Baudic N, Bourut C, Czernichow P, Huet F, Grigorescu F, de Kerdanet M, Lacombe D, Labrune P, Lanza M, Loret H, Matsuda F, Navarro J, Nivelon-Chevalier A, Polak M, Robert JJ, Tric P, Tubiana-Rufi N, Vigouroux C, Weissenbach J, Savasta S, Maassen JA, Trygstad O, Bogalho P, Freitas P, Medina JL, Bonnicci F, Joffe BI, Loyson G, Panz VR, Raal FJ, O'Rahilly S, Stephenson T, Kahn CR, Lathrop M, Capeau J. Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. Nat Genet. 2001;28:365-70.
     
  27. Ossthuyse B, Moons L, Storkebaum E, Beck H, Nuyens D, Brusselmans K, Van Dorpe J, Gorselink M, Heymans S, Theilmeier G, Dewerchin M, Laudenbach V, Vermylen P, Raat H, Acker T, Vleminckx V, Van den Bosch L, Xashman N, Fujisawa H, Drost MR, Sciot R, Bruyninckx F, Hicklin D, Ince C, Gressens P, Lupu F, Plate KH, Robberecht W, Herbert JM, Collen D, Carmeliet P. Deletion of the hypoxia-response element in vascular endothelial growth factor promotor causes motor neuron degeneration. Nat. Genet., 2001, 28 : 131-138.
     
  28. Patkai J, Mesplès B, Dommergues MA, Fromont G, Thornton EM, Renauld JC, Evrard P, Gressens P. Deleterious effects of IL-9-activated mast cells and neuroprotection by antihistamine drugs. Pediatr. Res., 2001, 50 : 222-230.
     
  29. Peyclit A, Keita H, Juvin P, Jardinaud F , Desmonts JM, Girault JA, Mantz J : Effects of riluzole on N-methyl-D-aspartate–induced tyrosine phosphorylation in the rat hippocampus. Brain Res 2001 ; 903 : 222-5.
     
  30. Pineau N, Lelièvre V, Hilairet S, Janet T, Waschek J, Muller JM. Characterization of PHM-preferring GTP-insensitive VIP receptor. – A structural and pharmacological study, Neuropeptides, 2001, 35 : 117-126.
     
  31. Plauchu H, Encha-Razavi F, Hermier M, Attia-Sobol J, Vitrey D, Verloes A. Lissencephaly type III, stippled epiphyses and loose, thick skin: a new recessively inherited syndrome. Am J Med Genet. 2001 ; 99 :14-20
     
  32. Renolleau S, Dauger S, Autret F, Vardon G, Gaultier C, Gallego J. Maturation of baseline breathing and of hypercapnic and hypoxic ventilatory responses in newborn mice. Am J Physiol Regul Integr Comp Physiol 2001;281:R1746-53.
     
  33. Renolleau S, Dauger S, Vardon G, Levacher B, Simonneau M, Yanagisawa M, Gaultier C, Gallego J. Impaired ventilatory responses to hypoxia in mice deficient in endothelin-converting-enzyme-1. Pediatr Res 2001;49:705-12.
     
  34. Riegel M, Baumer A, Jamar M, Delbecque K, Herens C, Verloes A, Schinzel A. Submicroscopic terminal deletions and duplications in retarded patients with unclassified malformation syndromes. Hum Genet. 2001; 109:286-94
     
  35. Sahir N, Mas C, Bourgeois F, Simonneau M, Evrard P, Gressens P. Caffeine-induced telencephalic vesicle evagination in early postimplantation mouse embryos involves cAMP-dependent protein kinase (PKA) inhibition. Cereb. Cortex, 2001, 11: 343-349.
     
  36. Simon A, Martin-Martinelli E, Savy C., Verney C., Raisman-Vozari R, Nguyen-Legros J. Confirmation of the retinopetal/centrifugal nature of the tyrosine hydroxylase-immunoreactive fibers of the retina and optic nerve in the weaver mouse. Dev Brain Res., 2001, 127: 87-93.
     
  37. Tahraoui SL, Marret S, Bodénant C, Leroux P, Dommergues MA, Evrard P, Gressens P. Central role of microglia in neonatal excitotoxic lesions of the murine periventricular white matter. Brain Pathol., 2001, 11 : 56-71.
     
  38. Terrinoni A, Smith FJ, Didona B, Canzona F, Paradisi M, Huber M, Hohl D, David A, Verloes A, Leigh IM, Munro CS, Melino G, McLean WH. Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita. J Invest Dermatol. 2001 ;117:1391-6.
     
  39. van Bokhoven H, Hamel BC, Bamshad M, Sangiorgi E, Gurrieri F, Duijf PH, Vanmolkot KR, van Beusekom E, van Beersum SE, Celli J, Merkx GF, Tenconi R, Fryns JP, Verloes A, Newbury-Ecob RA, Raas-Rotschild A, Majewski F, Beemer FA, Janecke A, Chitayat D, Crisponi G, Kayserili H, Yates JR, Neri G, Brunner HG. p63 Gene mutations in eec syndrome, limb-mammary syndrome, and isolated split hand-split foot malformation suggest a genotype-phenotype correlation. Am J Hum Genet. 2001 ;69:481-92
     
  40. Verloes A, Dresse MF, Keutgen H, Asplund C, Edvard Smith CI. Microphthalmia, facial anomalies, thumb hypoplasia, and agammaglobulinemia. Am J Med Genet. 2001, 99 :209-12
     
  41. Verloes A, Gillerot Y, Maldergem LV, Schoos R, Herens C, Jamar M, Dideberg V, Lesenfants S, Koulischer L.  Major decrease in the incidence of trisomy 21 at birth in south Belgium: mass impact of triple test? Eur J Hum Genet 2001, 9:1-4
     
  42. Verloes A, Jamar M, Dideberg V, Herens C. Episphalosomic syndrome : a MCA syndrome ressembling Fanconi anemia, with increased baseline level of chromosome breaks but no hypersensivity to clastogens. Ann Genet. 2001;44:59-62.
     
  43. Verloes A, Lesenfants S. New syndrome: clavicle hypoplasia, facial dysmorphism, severe myopia, single central incisor and peripheral neuropathy. Clin Dysmorphol 2001, 10: 29-31
     
  44. Verney C, Zecevic N, Ezan P. Expression of calbindin D28K in the dopaminergic mesotelencephalic system in embryonic and fetal human brain. J Comp Neurol., 2001, 429: 45-58.
     
  45. Verney C, Zecevic N, Puelles L. Structure of longitudinal brain zones provide the origin for the substantia nigra and ventral tegmental area in human embryos, as revealed by cytoarchitecture and tyrosine-hydroxylase-, calretinin-, calbindin- and GABA-immunoreaction. J Comp Neurol., 2001, 429 :22-44.
     
  46. Yamamoto A, Morisawa Y, Verloes A, Murakami N, Hirano M, Nonaka I, Nishino I. Infantile autophagic vacuolar myopathy is distinct from Danon disease. Neurology 2001;57:903-5.
     

2000

  1. Baud O, Zupan V, Lacaze-Masmonteil T, Audibert F, Shojaei T, Thebaud B, Ville Y, Frydman R, Dehan M. The relationships between antenatal management, the cause of delivery and neonatal outcome in a large cohort of very preterm singleton infants. Br J Obstet Gynaecol 2000,107:877-884.
     
  2. Debillon T, Gras-Leguen C, Vérielle V, Winer N, Caillon J, Roze JC, Gressens P. Intrauterine infection induces periventricular cell death in rabbits. Pediatr. Res., 2000, 47 : 736-742.
     
  3. Dommergues MA, Patkai J, Renauld JC, Evrard P, Gressens P. Pro-inflammatory cytokines and IL-9 exacerbate excitotoxic lesions of the newborn murine neopallium. Ann. Neurol., 2000, 47 : 54-63.
     
  4. Gerard B, Ginet N, Matthijs G, Evard P, Baumann C, Da Silva F, Gerard-Blanchet M, Mayer M, Grandchamp B, Elion J. Genotype determination at the survival motor neuron locus in a normal population and SMA carriers using competitive PCR and primer extension. Hum Mutat., 2000 16:253-263.
     
  5. Gray F, Adle-Biassette H, Brion F, Ereau T, Le Maner I, Levy V, Corcket G Neuronal apoptosis in human immunodeficiency virus infection. J Neurovirol 2000;6:S38-43
     
  6. Gressens P, Arquié C, Hill JM, Marret S, Sahir N, Robberecht P, Evrard P. VIP and PACAP 38 modulate ibotenate-induced neuronal heterotopias in the newborn hamster neocortex. J. Neuropathol. Exp. Neurol., 2000, 59 : 1051-1062.
     
  7. Gressens P, Baes M, Leroux P, Lombet A, Van Veldhoven P, Janssen A, Vamecq J, Marret S, Evrard P. Neuronal migration in Zellweger mice is secondary to glutamate receptor dysfunction. Ann. Neurol., 2000, 48 : 336-343.
     
  8. Hocini H, Becquart P, Bouhlal H, Adle-Biassette H, Kazatchkine Md, Belec L Secretory leukocyte protease inhibitor inhibits infection of monocytes and lymphocytes with human immunodeficiency virus type 1 but does not interfere with transcytosis of cell-associated virus across tight epithelial barriers. Clin Diagn Lab Immunol 2000;7:515-8
     
  9. Hu Z, Lelièvre V, Chao A, Zhou X, Waschek JA. A Molecular cloning of pituitary adenylate cyclase-activating peptide in frog (Xenopus laevis) : Brain distribution and regulation following castration. Endocrinology, 2000,141, 3366-3376.
     
  10. Hu Z, Lelièvre V, Chao A, Zhou X, Waschek JA. Characterization and mRNA distribution of a cloned pituitary adenylate cyclase-activating polypeptide (PACAP) type I receptor in xenopus brain. Endocrinology, 2000,141 : 657-65.
     
  11. Janssen A, Baes M, Gressens P, Mannaerts GP, Declercq P, Van Veldhoven PP. Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice. Lab. Invest., 2000, 80 : 31-35.
     
  12. Keita H, Lanone S, Samb A, Boszkowski J, Rouelle D, Desmonts JM, Mantz J: Anesthetic concentrations of riluzole inhibit nitric oxide synthase activity, but not expression, in the rat hippocampus. Brain Res 2000; 881: 237-40.
     
  13. Keymolen K, Van-Damme Lombaerts R, Verloes A, Fryns JP Distal limb deficiencies, oral involvement and renal defect : report of a third patient and confirmation of a distinct entity. Am J Med Genet 2000,  93 : 19-21.
     
  14. Lang-Lazdunski L, Heurteaux C, Mignon A, Mantz J, Widmann C, Desmonts JM, Lazdunski M : Ischemic spinal cord injury induced by aortic cross-clamping: prevention by riluzole. Eur J Cardiothorac Surg 2000; 18: 174-81.
     
  15. Lelièvre V, Caigneaux E, Muller JM, Falcon J. Extracellular adenosine deprivation induces epithelial differentiation in HT29 cells: Evidence for a concomitant adenosine A1/A2 receptor balance regulation. Eur. J. Pharmacol., 2000, 391: 21-29.
     
  16. Li A, Bouchaud C, Hénin D, Sanson M, Delattre JY, Pan Y, Anthony D, Duc HT, Evrard P, Trojan J. Expression of insulin-like growth factor-I in rat glioma cells is associated change in both immunogenicity and apoptosis. Neurosci Lett., 2000, 28 : 13-16.
     
  17. Ly A, Bouchaud C, Henin D, Sanson M, Delattre Jy, Pan Y, Anthony D, Duc Ht, Evrard P, Trojan J Expression of insulin-like growth factor-I in rat glioma cells is associated with change in both immunogenicity and apoptosis. Neuroscience Letters 2000 ; 281:1-4
     
  18. Nishino I, Spinazzola A, Papadimitriou A, Hammans S, Steiner I, Hahn C, Connolly AM, Verloes A, Guimarães J, Maillard I, Hamano H, Donati MA, Semrad CE, Russell JA, Andreu AL, Hadjigeorgiou GM, Vu TH, Tadesse S, Nygaard TG, Nonaka I, Hirano I, Bonilla E, Rowland LP, DiMauro S, Hirano M Mitochondrial neurogastrointestinal encephalomyopathy : an autosomal recessive disorder due to thymidine phosphorylase mutations. Ann Neurol 2000,. 47 : 792-800.
     
  19. Picard C, Baud O, Fieschi C, Casanova JL. Diagnosis and management of inheritable disorders of IFN-mediated immunity. Immunol Allergy Clin North Am. 2000, 20:65-76.
     
  20. Sahir N, Bahi N, Evrard P, Gressens P. Caffeine induces in vivo premature appearance of telencephalic vesicles. Dev. Brain Res., 2000, 121 : 213-217.
     
  21. Sfaello I, Castelnau P, Blanc N, Ogier de Baulny H, Evrard P, Arzimanoglou A. Infantile spasms and Menkes disease. Epileptic Disord., 2000, 2:227-230.
     
  22. Simon A., Savy C., Martin-Martinelli E., Douhou A, Frederic F, Verney, C, Nguyen-Legros J, Raisman-Vozari R. Increase of tyrosine hydroxylase-immunoreactive retinopetal fibers in the weaver mouse retinas. Dev Brain Res. 2000, 121:113-117.
     
  23. Verloes A, Lesenfants S, Barr M, Grange DK, Journel H, Lombet J, Mortier G, Roeder E Fronto-Otopalatodigital Osteodysplasia : clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndromes type 1 and 2, and frontometaphyseal dysostosis. Am J Med Genet 2000, 90 : 407-422
     
  24. Verloes A, Lesenfants S, Jamar M, Dideberg V, Herens C. GOMBO syndrome : another “pseudorecessive” disorder due to a cryptic translocation. Am J Med Genet 2000, 95: 185-186.
     
  25. Verloes A, Lesenfants S. Agenesis of the corpus callosum, camptodactyly and obesity. Clin Dysmorphol 2000, 9 : 107-109.
     
  26. Verloes A, Muller C, Philippet P. New dysostosis showing multilevel absence of vertebral pedicles: unique developmental anomaly of vertebral arches? Am J Med Genet 2000, 95 :473-6
     
  27. Verney C, Takahashi T, Bhide PG, Nowakowski RS, Caviness, Jr,VS. Independent controls for neocortical neuron production and histogenetic cell death. Dev Neuroscience, 2000, 22, 125-138.
     
  28. Vitalis T, Cases O, Engelkamp D, Verney C, Price DJ. Defects of tyrosine hydroxylase-immunoreactive neurons in the brain of mice lacking the transcription factor Pax6. J Neurosci., 2000, 20:6501-6516.
     
  29. Zupan V, Nehlig A, Evrard P, Gressens P. Prenatal blockade of vasoactive intestinal peptide alters cell death and synaptic equipment in the murine neocortex. Pediatr. Res., 2000, 47 : 53-63.
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