Irwin McLean (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Irwin McLean" in French language version.

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doi.org

dx.doi.org

  • Palmer, Irvine, Terron-Kwiatkowski et Zhao, « Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis », Nature Genetics, vol. 38, no 4,‎ , p. 441–446 (PMID 16550169, DOI 10.1038/ng1767, S2CID 2500278)
  • Smith, Irvine, Terron-Kwiatkowski et Sandilands, « Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris », Nature Genetics, vol. 38, no 3,‎ , p. 337–342 (PMID 16444271, DOI 10.1038/ng1743, S2CID 21948747)
  • McLean et Irvine, « Heritable filaggrin disorders: The paradigm of atopic dermatitis », The Journal of Investigative Dermatology, vol. 132, no E1,‎ , E20–E21 (PMID 23154627, DOI 10.1038/skinbio.2012.6)
  • Weidinger, Illig, Baurecht et Irvine, « Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations », The Journal of Allergy and Clinical Immunology, vol. 118, no 1,‎ , p. 214–219 (PMID 16815158, DOI 10.1016/j.jaci.2006.05.004)
  • Cristina Has et Cassian Sitaru, Molecular Dermatology: Methods and Protocols, vol. 961, coll. « Methods in Molecular Biology », (ISBN 9781627032261, DOI 10.1007/978-1-62703-227-8, S2CID 21781092)
  • Nomura, Sandilands, Akiyama et Liao, « Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis », The Journal of Allergy and Clinical Immunology, vol. 119, no 2,‎ , p. 434–440 (PMID 17291859, DOI 10.1016/j.jaci.2006.12.646)
  • Basu, Palmer, Lipworth et Irwin Mclean, « Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults », Allergy, vol. 63, no 9,‎ , p. 1211–1217 (PMID 18307574, DOI 10.1111/j.1398-9995.2008.01660.x, S2CID 8105444, lire en ligne)
  • Palmer, Ismail, Lee et Terron-Kwiatkowski, « Filaggrin null mutations are associated with increased asthma severity in children and young adults », The Journal of Allergy and Clinical Immunology, vol. 120, no 1,‎ , p. 64–68 (PMID 17531295, DOI 10.1016/j.jaci.2007.04.001)
  • Henderson, Northstone, Lee et Liao, « The burden of disease associated with filaggrin mutations: A population-based, longitudinal birth cohort study », The Journal of Allergy and Clinical Immunology, vol. 121, no 4,‎ , p. 872–877.e9 (PMID 18325573, DOI 10.1016/j.jaci.2008.01.026)
  • Bisgaard, Simpson, Palmer et Bønnelykke, « Gene-environment interaction in the onset of eczema in infancy: Filaggrin loss-of-function mutations enhanced by neonatal cat exposure », PLOS Medicine, vol. 5, no 6,‎ , e131 (PMID 18578563, PMCID 2504043, DOI 10.1371/journal.pmed.0050131)

dundee.ac.uk

lifesci.dundee.ac.uk

microsoft.com

academic.microsoft.com

nih.gov

ncbi.nlm.nih.gov

  • Palmer, Irvine, Terron-Kwiatkowski et Zhao, « Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis », Nature Genetics, vol. 38, no 4,‎ , p. 441–446 (PMID 16550169, DOI 10.1038/ng1767, S2CID 2500278)
  • Smith, Irvine, Terron-Kwiatkowski et Sandilands, « Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris », Nature Genetics, vol. 38, no 3,‎ , p. 337–342 (PMID 16444271, DOI 10.1038/ng1743, S2CID 21948747)
  • McLean et Irvine, « Heritable filaggrin disorders: The paradigm of atopic dermatitis », The Journal of Investigative Dermatology, vol. 132, no E1,‎ , E20–E21 (PMID 23154627, DOI 10.1038/skinbio.2012.6)
  • Weidinger, Illig, Baurecht et Irvine, « Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations », The Journal of Allergy and Clinical Immunology, vol. 118, no 1,‎ , p. 214–219 (PMID 16815158, DOI 10.1016/j.jaci.2006.05.004)
  • Nomura, Sandilands, Akiyama et Liao, « Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis », The Journal of Allergy and Clinical Immunology, vol. 119, no 2,‎ , p. 434–440 (PMID 17291859, DOI 10.1016/j.jaci.2006.12.646)
  • Basu, Palmer, Lipworth et Irwin Mclean, « Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults », Allergy, vol. 63, no 9,‎ , p. 1211–1217 (PMID 18307574, DOI 10.1111/j.1398-9995.2008.01660.x, S2CID 8105444, lire en ligne)
  • Palmer, Ismail, Lee et Terron-Kwiatkowski, « Filaggrin null mutations are associated with increased asthma severity in children and young adults », The Journal of Allergy and Clinical Immunology, vol. 120, no 1,‎ , p. 64–68 (PMID 17531295, DOI 10.1016/j.jaci.2007.04.001)
  • Henderson, Northstone, Lee et Liao, « The burden of disease associated with filaggrin mutations: A population-based, longitudinal birth cohort study », The Journal of Allergy and Clinical Immunology, vol. 121, no 4,‎ , p. 872–877.e9 (PMID 18325573, DOI 10.1016/j.jaci.2008.01.026)
  • Bisgaard, Simpson, Palmer et Bønnelykke, « Gene-environment interaction in the onset of eczema in infancy: Filaggrin loss-of-function mutations enhanced by neonatal cat exposure », PLOS Medicine, vol. 5, no 6,‎ , e131 (PMID 18578563, PMCID 2504043, DOI 10.1371/journal.pmed.0050131)

rcuk.ac.uk

gtr.rcuk.ac.uk

semanticscholar.org

api.semanticscholar.org

sussex.ac.uk

sro.sussex.ac.uk

wellcome.ac.uk

wikipedia.org

en.wikipedia.org