Sign In

Login

Password

Forgot Password ? Sign Up

Netherton syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Netherton syndrome" in English language version.

refsWebsite
Global rank English rank
7nih.gov
4th place
4th place
6doi.org
2nd place
2nd place
3semanticscholar.org
11th place
8th place

doi.org

  • Chao SC, Richard G, Lee JY (2005). "Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5". Br J Dermatol. 152 (1): 159–165. doi:10.1111/j.1365-2133.2005.06337.x. PMID 15656819. S2CID 22760789.
  • Chavanas S, Bodemer C, Rochat A (June 2000). "Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome". Nat. Genet. 25 (2): 141–142. doi:10.1038/75977. PMID 10835624. S2CID 40421711.
  • Descargues P, Deraison C, Bonnart C, Kreft M, Kishibe M, Ishida-Yamamoto A, Elias P, Barrandon Y, Zambruno G, Sonnenberg A, Hovnanian A (January 2005). "Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity". Nat Genet. 37 (1): 56–65. doi:10.1038/ng1493. PMID 15619623. S2CID 11404025.
  • Renner E, Hartle D, Rylaarsdam S, Young M, Monaco-Shawver L, Kleiner G, Markert ML, Stiehm ER, Belohradsky B, Upton M, Torgerson T, Orange J, Ochs H (August 2009). "Comel-Netherton syndrome defined as primary immunodeficiency". The Journal of Allergy and Clinical Immunology. 124 (3): 536–543. doi:10.1016/j.jaci.2009.06.009. PMC 3685174. PMID 19683336.
  • Ovaere P, Lippens S, Vandenabeele P, Declercq W (August 2009). "The emerging roles of serine protease cascades in the epidermis". Trends Biochem Sci. 34 (9): 453–63. doi:10.1016/j.tibs.2009.08.001. PMID 19726197.
  • Hachem JP, Wagberg F, Schmuth M, Crumrine D, Lissens W, Jayakumar A, Houben E, Mauro TM, Leonardsson G, Brattsand M, Egelrud T, Roseeuw D, Clayman GL, Feingold KR, Williams ML, Elias PM (April 2006). "Serine protease activity and residual LEKTI expression determine phenotype in Netherton syndrome". J Invest Dermatol. 126 (7): 1609–21. doi:10.1038/sj.jid.5700288. PMID 16601670.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Chao SC, Richard G, Lee JY (2005). "Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5". Br J Dermatol. 152 (1): 159–165. doi:10.1111/j.1365-2133.2005.06337.x. PMID 15656819. S2CID 22760789.
  • Chavanas S, Bodemer C, Rochat A (June 2000). "Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome". Nat. Genet. 25 (2): 141–142. doi:10.1038/75977. PMID 10835624. S2CID 40421711.
  • Descargues P, Deraison C, Bonnart C, Kreft M, Kishibe M, Ishida-Yamamoto A, Elias P, Barrandon Y, Zambruno G, Sonnenberg A, Hovnanian A (January 2005). "Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity". Nat Genet. 37 (1): 56–65. doi:10.1038/ng1493. PMID 15619623. S2CID 11404025.
  • Renner E, Hartle D, Rylaarsdam S, Young M, Monaco-Shawver L, Kleiner G, Markert ML, Stiehm ER, Belohradsky B, Upton M, Torgerson T, Orange J, Ochs H (August 2009). "Comel-Netherton syndrome defined as primary immunodeficiency". The Journal of Allergy and Clinical Immunology. 124 (3): 536–543. doi:10.1016/j.jaci.2009.06.009. PMC 3685174. PMID 19683336.
  • Ovaere P, Lippens S, Vandenabeele P, Declercq W (August 2009). "The emerging roles of serine protease cascades in the epidermis". Trends Biochem Sci. 34 (9): 453–63. doi:10.1016/j.tibs.2009.08.001. PMID 19726197.
  • Hachem JP, Wagberg F, Schmuth M, Crumrine D, Lissens W, Jayakumar A, Houben E, Mauro TM, Leonardsson G, Brattsand M, Egelrud T, Roseeuw D, Clayman GL, Feingold KR, Williams ML, Elias PM (April 2006). "Serine protease activity and residual LEKTI expression determine phenotype in Netherton syndrome". J Invest Dermatol. 126 (7): 1609–21. doi:10.1038/sj.jid.5700288. PMID 16601670.

ncbi.nlm.nih.gov

semanticscholar.org

api.semanticscholar.org

  • Chao SC, Richard G, Lee JY (2005). "Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5". Br J Dermatol. 152 (1): 159–165. doi:10.1111/j.1365-2133.2005.06337.x. PMID 15656819. S2CID 22760789.
  • Chavanas S, Bodemer C, Rochat A (June 2000). "Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome". Nat. Genet. 25 (2): 141–142. doi:10.1038/75977. PMID 10835624. S2CID 40421711.
  • Descargues P, Deraison C, Bonnart C, Kreft M, Kishibe M, Ishida-Yamamoto A, Elias P, Barrandon Y, Zambruno G, Sonnenberg A, Hovnanian A (January 2005). "Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity". Nat Genet. 37 (1): 56–65. doi:10.1038/ng1493. PMID 15619623. S2CID 11404025.