These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

235 related items for PubMed ID: 18843291

  • 41. Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation.
    Ding X, Willenborg S, Bloch W, Wickström SA, Wagle P, Brodesser S, Roers A, Jais A, Brüning JC, Hall MN, Rüegg MA, Eming SA.
    J Allergy Clin Immunol; 2020 Jan; 145(1):283-300.e8. PubMed ID: 31401286
    [Abstract] [Full Text] [Related]

  • 42. [Bazex-Dupré-Christol syndrome. Follicular atrophoderma, multiple basal cell carcinomas and hypotrichosis].
    Herges A, Stieler W, Stadler R.
    Hautarzt; 1993 Jun; 44(6):385-91. PubMed ID: 8335462
    [Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 47. The matriptase-prostasin proteolytic cascade in epithelial development and pathology.
    Miller GS, List K.
    Cell Tissue Res; 2013 Feb; 351(2):245-53. PubMed ID: 22350849
    [Abstract] [Full Text] [Related]

  • 48. Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.
    Shimomura Y, Sakamoto F, Kariya N, Matsunaga K, Ito M.
    J Invest Dermatol; 2006 Jun; 126(6):1281-5. PubMed ID: 16439973
    [Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
    Jelani M, Wasif N, Ali G, Chishti M, Ahmad W.
    Clin Genet; 2008 Aug; 74(2):184-8. PubMed ID: 18445047
    [Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 54.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 55. Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.
    Oji V, Hautier JM, Ahvazi B, Hausser I, Aufenvenne K, Walker T, Seller N, Steijlen PM, Küster W, Hovnanian A, Hennies HC, Traupe H.
    Hum Mol Genet; 2006 Nov 01; 15(21):3083-97. PubMed ID: 16968736
    [Abstract] [Full Text] [Related]

  • 56.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 57.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 58.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 59.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 60.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 12.