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Publications depuis 2007

 

 

Articles de synthèse

 

  • Simon M, Pellerin L, Pendaries V, Hsu CY, Mazereeuw-Hautier J, Paul C, Serre G, Jonca N. Le complexe de différenciation épidermique
    Quoi de neuf ?
    Biologie Cutanée - Cobip 2013 , M. Haftek. Editions Matrix, LYON, pp162-189, 2014.

  • Henry J, Leclerc E, Mazereeuw-Hautier J, Serre G, Simon M, Jonca N. L’enveloppe cornée : carapace du cornéocyte.
    Biologie Cutanée M. Haftek. Editions Matrix, LYON, 2012, pp, 2013.

  • Jonca N. Physiologie de la kératinisation.
    La lettre du kératinocyte, n°4, 2013.

  • Huchenq A. Larrigaldie V. Tribune.
    Sciences et Techniques de l’Animal de Laboratoire 39:13, 2013.

  • Danjan F, Huchenq A, Mauny P, Appolinaire S, Chébli K, Marsal D, Magnat W, Larrigaldie V, Texeira M. La crypréservation d’ovaire, une technique plus respectueuse de la règle des 3R.
    Sciences et Techniques de l’Animal de Laboratoire 39:36-42, 2013.

  • Huchenq A. La cryopréservation des lignées de rat.
    Sciences et Techniques de l’Animal de Laboratoire 39:53-58, 2013.

  • Mazereeuw-Hautier J, Dreyfus I, Jonca N. Prise en charge des ichtyoses.
    Nouvelles Dermatologiques 31 (Suppl. 4) :10-15, 2012.

  • Henry J, Toulza E, Hsu C-Y, Pellerin L, Balica S, Mazereeuw-Hautier J, Paul C, Serre G,  Jonca N, Simon M. Update on the Epidermal Differentiation Complex.
    Frontiers in Bioscience 17:1517-1532, 2012.
    article
  • Caubet C, Jonca N, Leclerc EA, Simon M, Guerrin M, Serre G. Cornéodesmosine - aspects fonctionnels.
    In Biologie Cutanée – Peau et Vésicules (dans tous leurs états), M. Haftek. Editions Matrix, LYON, pp117-132, 2011.

  • Jonca N, Leclerc EA, Caubet C, Simon M, Guerrin M, Serre G. Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses.
    Eur J Dermatol 21:35-42, 2011.
    article
  • Jonca N, Caubet C, Guerrin M, Simon M, Serre G. Corneodesmosin: structure, function and involvement in pathophysiology.
    TODJ 4:36-45, 2010.

  • Mazereeuw-Hautier J, Bodemer C. Diagnostic étiologique des ichtyoses.
    Ann Dermatol Vénéréol 136:916-22, 2009.
    article
  • Jonca N, Caubet C, Guerrin M, Simon M, Serre G. Corneodesmosomal proteins.
    In Skin Moisturization 2nd edition, Rawlings AV, Leyden JJ Ed, Informa Healthcare, NEW YORK, pp 99-122, 2009.

  • Mazereeuw-Hautier J, Vabres P, Taïeb A. Bébé collodion et autres anomalies néonatales de la kératinisation.
    In Dermatologie néonatale, Taïeb A, Maloine, 2009.

  • Toulza E, Galliano M-F, Jonca N, Gallinaro H, Serre G, Guerrin M. Transcriptome et différenciation kératinocytaire.
    In Actualité en biologie cutanée, C. Dezutter-Dambuyant, D. Schmitt. Editions Eska, PARIS, pp19-21, 2007.

 

Travaux originaux

 

  • Maier D, Mazereeuw-Hautier J, Tilinca M, Cosgarea R, Jonca N. Novel mutation in NIPAL4 in a Romanian family with autosomal recessive congenital ichthyosis
    Clin Exp Dermatol,in press 2015

  • Valentin F, Oji V, Hausser I, Liebau E, Tarinski T, Metze D, Breitkreutz D, Traupe H, Jonca N, Terheyden P. Increased Expression of Caspase-1 and Interleukin-18 in Peeling Skin Disease, and a Novel Mutation of Corneodesmosin.
    doi: 10.2340/00015555-2142
    Acta Derm Vénéréol in press, 2015.
    article
  • Bergboer JG, Dulak MG, van Vlijmen-Willems IM, Jonca N, van Wijk E, Hendriks WJ, Zeeuwen PL, Schalkwijk J. Analysis of Protein-Protein Interaction Between Late Cornified Envelope Proteins and Corneodesmosin.
    Exp Dermatol 23:769-771, 2014.
    article
  • Leclerc E, Huchenq A, Kezic S, Serre G, Jonca N. Mice deficient for the epidermal dermokine β and ? display transient cornification defects.
    J Cell Sci 120:2862-2872,2014
    article
  • Dreyfus I, Chouquet C, Ezzedine K, Henner S, Chiavérini C, Maza A, Pascal S, Rodriguez L, Vabres P, Martin L, Mallet S, Barbarot S, Dupuis J, Mazereeuw-Hautier J. Prevalence of inherited ichthyosis in France: a study using capture-recapture method.
    Orphanet J Rare Dis 9:1,2014.
    article
  • Dreyfus I, Bourrat E, Maruani A, Bessis D, Chiavérini C, Vabres P, Ezzedine K, Mazereeuw-Hautier J. Factors associated with impaired quality of life in adult patients suffering from Ichthyosis.
    Acta Derm Venereol 94:344-346,2014.
    article
  • Mazereeuw-Hautier J, Chiaverini C, Jonca N, Bieth E, Dreyfus I, Maza A, Cardot-Leccia N, Perrin C, Lacour JP. Lethal form of Keratitis-Ichthyosis-Deafness syndrome caused by the GJB2 mutation p.Ser17Phe.
    Acta Derm Venereol 94:591-592,2014.
    article
  • Mallet A, Kypriotou M, George K, Leclerc E, Rivero D, Mazereeuw-Hautier J, Serre G, Huber M, Jonca N, Hohl D. Identification of the first nonsense CDSN mutation with expression of a truncated protein and causing Peeling skin syndrome type B.
    Br J Dermatol 169: 1322-1325, 2013.
    article
  • Dreyfus I, Taïeb C, Barbarot S, Maza A, Galera I, Bourrat E, Chiaverini C, Ezzedine K, Le Rhun A, Mazereeuw-Hautier J. IQoL-32: A new ichthyosis-specific measure of quality of life. .
    J Am Acad69 :82-87 2013.
    article
  • Mazereeuw-Hautier J, Dreyfus I, Barbarot S, et al. Factors influencing quality of life of inherited ichthyosis: a qualitative study in adult using focus groups.
    Br J Dermatol 223:260-5, 2011.
    article
  • Paul C, Maumus-Robert S, Mazereeuw-Hautier J, Guyen CN, Saudez X, Schmitt AM. Prevalence and risk factors for xerosis in the elderly: a cross-sectional epidemiological study in primary care.
    Dermatology 223:260-5, 2011.
    article
  • Bodemer C, Bourrat E, Mazereeuw-Hautier J, Boralevi F, Barbarot S, Bessis D, Blanchet-Bardon C, Bourdon-Lanoy E, Stalder JF, Ribet V, Guerrero D, Sibaud V. Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis.
    Br J Dermatol 165:1087-1094, 2011.
    article
  • Mazereeuw-Hautier J, Leclerc EA, Simon M, Serre G, Jonca N. A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.
    Br J Dermatol 165:1152-1155, 2011.
    article
  • Leclerc EA, Gazeilles L, Serre G, Guerrin M, Jonca N. The ubiquitous dermokine delta activates Rab5 in the early endocytic pathway.
    PloS One 6:e17816, 2011.
    article
  • Jonca N, Caubet C, Leclerc EA, Guerrin M, Simon M, Serre G. Protease sensitivity of corneodesmosin variants encoded by the six more common CDSN haplotypes.
    J Invest Dermatol 131:1381-1384, 2011.
    article
  • Mattiuzzo N, Toulza E, Jonca N, Serre G, Guerrin M. A large-scale multi-technique approach identifies forty-nine new players of keratinocyte terminal differentiation in human epidermis.
    Exp Dermatol 20:113-118, 2011.
    article
  • Oji V, Tadini G, Akiyama M, Bardon CB, Bodemer C, Bourrat E, Coudiere P, Digiovanna JJ, Elias P, Fischer J, Fleckman P, Gina M, Harper J, Hashimoto T, Hausser I, Hennies HC, Hohl D, Hovnanian A, Ishida-Yamamoto A, Jacyk WK, Leachman S, Leigh I, Mazereeuw-Hautier J, Milstone L, Morice-Picard F, Paller AS, Richard G, Schmuth M, Shimizu H, Sprecher E, Van Steensel M, Taïeb A, Toro JR, Vabres P, Vahlquist A, Williams M, Traupe H. Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009.
    J Am Acad Dermatol 63:607-641,2010.
    article
  • Leclerc EA, Huchenq A, Mattiuzzo NR, Metzger D, Chambon P, Ghyselinck N, Serre G, Jonca N, Guerrin M. Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction.
    J Cell Sci 122:2699-2709, 2009.
    article
  • Todt I, Mazereeuw-Hautier J, Binder B, Willems PJ. Dandy-Walker malformation in patients with KID syndrome associated with a heterozygote mutation (p.Asp50Asn) in the GJB2 gene encoding connexin 26.
    Clin Genet 76:404-408,2009
    article
  • Mazereeuw-Hautier J, Aufenvenne K, Deraison C, Ahvazi B, Oji V, Traupe H, Hovnanian A. Acral self-healing collodion baby: report of a new clinical phenotype caused by a novel TGM1 mutation.
    Br J Dermatol161: 456-63, 2009.
    article
  • Galliano MF, Toulza E, Jonca N, Gonias SL, Serre G, Guerrin M. Binding of alpha2-ML1 to the low density lipoprotein receptor-related protein 1 (LRP1) reveals a new role for LRP1 in the human epidermis.
    PloS ONE 3:e2729, 2008.
    article
  • Simon M, Tazi-Ahnini R, Jonca N, Caubet C, Cork M, Serre G. Alterations in the desquamation-related proteolytic cleavage of corneodesmosin and other corneodesmosomal proteins in psoriatic lesional epidermis.
    Br J Dermatol 159:77-85, 2008.
    article
  • Toulza E, Mattiuzzo N, Galliano M-F, Jonca N, Dossat C, Jacob D, De Daruvar A, Wincker P, Serre G, Guerrin M. Large scale identification of human genes implicated in epidermal barrier function.
    Genome biology 8:R107:1-23, 2007.
    article

 

 

 

 

 

 

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