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

243 related items for PubMed ID: 14705805

  • 1. Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis.
    Akiyama M, Takizawa Y, Sawamura D, Matsuo I, Shimizu H.
    Exp Dermatol; 2003 Oct; 12(5):638-45. PubMed ID: 14705805
    [Abstract] [Full Text] [Related]

  • 2. Altered distribution of keratinization markers in epidermolytic hyperkeratosis.
    Ishida-Yamamoto A, Iizuka H, Manabe M, O'Guin WM, Hohl D, Kartasova T, Kuroki T, Roop DR, Eady RA.
    Arch Dermatol Res; 1995 Oct; 287(8):705-11. PubMed ID: 8554380
    [Abstract] [Full Text] [Related]

  • 3. A case of bullous congenital ichthyosiform erythroderma (BCIE) caused by a mutation in the 1A helix initiation motif of keratin 1.
    Uezato H, Yamamoto Y, Kuwae C, Nonaka K, Oshiro M, Kariya K, Nonaka S.
    J Dermatol; 2005 Oct; 32(10):801-8. PubMed ID: 16361731
    [Abstract] [Full Text] [Related]

  • 4. Abnormalities of basal cell keratin in epidermolysis bullosa simplex do not affect the expression patterns of suprabasal keratins and cornified cell envelope proteins.
    Sasaki Y, Shimizu H, Akiyama M, Yoneda K, Ishida-Yamamoto A, Watanabe S, Hata J, Nishikawa T.
    Arch Dermatol Res; 1998 Nov; 290(11):591-7. PubMed ID: 9860278
    [Abstract] [Full Text] [Related]

  • 5. Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1.
    Sybert VP, Francis JS, Corden LD, Smith LT, Weaver M, Stephens K, McLean WH.
    Am J Hum Genet; 1999 Mar; 64(3):732-8. PubMed ID: 10053007
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma.
    McLean WH, Morley SM, Higgins C, Bowden PE, White M, Leigh IM, Lane EB.
    Exp Dermatol; 1999 Apr; 8(2):120-3. PubMed ID: 10232402
    [Abstract] [Full Text] [Related]

  • 8. A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis.
    Müller FB, Huber M, Kinaciyan T, Hausser I, Schaffrath C, Krieg T, Hohl D, Korge BP, Arin MJ.
    Hum Mol Genet; 2006 Apr 01; 15(7):1133-41. PubMed ID: 16505000
    [Abstract] [Full Text] [Related]

  • 9. A novel substitution in keratin 10 in epidermolytic hyperkeratosis.
    Arin MJ, Longley MA, Anton-Lamprecht I, Kurze G, Huber M, Hohl D, Rothnagel JA, Roop DR.
    J Invest Dermatol; 1999 Apr 01; 112(4):506-8. PubMed ID: 10201536
    [Abstract] [Full Text] [Related]

  • 10. Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation.
    Tsubota A, Akiyama M, Kanitakis J, Sakai K, Nomura T, Claudy A, Shimizu H.
    J Invest Dermatol; 2008 Jul 01; 128(7):1648-52. PubMed ID: 18219278
    [Abstract] [Full Text] [Related]

  • 11. Human keratin diseases: hereditary fragility of specific epithelial tissues.
    Corden LD, McLean WH.
    Exp Dermatol; 1996 Dec 01; 5(6):297-307. PubMed ID: 9028791
    [Abstract] [Full Text] [Related]

  • 12. Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband.
    Nomura K, Umeki K, Hatayama I, Kuronuma T.
    Arch Dermatol; 2001 Sep 01; 137(9):1192-5. PubMed ID: 11559215
    [Abstract] [Full Text] [Related]

  • 13. A keratin 10 gene mutation (Arg156Cys) in a Japanese patient with bullous congenital ichthyosiform erythroderma.
    Saeki H, Hattori N, Mitsui H, Adachi M, Imakado S, Ishibashi Y, Tamaki K.
    J Dermatol; 2002 Mar 01; 29(3):168-71. PubMed ID: 11990254
    [Abstract] [Full Text] [Related]

  • 14. Filaggrin expression in epidermolytic ichthyosis (epidermolytic hyperkeratosis).
    Ishida-Yamamoto A, Eady RA, Underwood RA, Dale BA, Holbrook KA.
    Br J Dermatol; 1994 Dec 01; 131(6):767-79. PubMed ID: 7531997
    [Abstract] [Full Text] [Related]

  • 15. A transgenic mouse model that recapitulates the clinical features of both neonatal and adult forms of the skin disease epidermolytic hyperkeratosis.
    Bickenbach JR, Longley MA, Bundman DS, Dominey AM, Bowden PE, Rothnagel JA, Roop DR.
    Differentiation; 1996 Dec 01; 61(2):129-39. PubMed ID: 8983179
    [Abstract] [Full Text] [Related]

  • 16. New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.
    Whittock NV, Ashton GH, Griffiths WA, Eady RA, McGrath JA.
    Br J Dermatol; 2001 Aug 01; 145(2):330-5. PubMed ID: 11531804
    [Abstract] [Full Text] [Related]

  • 17. A keratin K10 gene mutation in a Japanese patient with epidermolytic hyperkeratosis.
    Nomura K, Meng X, Umeki K, Tamai K, Sawamura D, Hashimoto I, Kikuchi T.
    Jpn J Hum Genet; 1997 Mar 01; 42(1):217-23. PubMed ID: 9184002
    [Abstract] [Full Text] [Related]

  • 18. Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE).
    McLean WH, Eady RA, Dopping-Hepenstal PJ, McMillan JR, Leigh IM, Navsaria HA, Higgins C, Harper JI, Paige DG, Morley SM.
    J Invest Dermatol; 1994 Jan 01; 102(1):24-30. PubMed ID: 7507152
    [Abstract] [Full Text] [Related]

  • 19. Mild recessive epidermolytic hyperkeratosis associated with a novel keratin 10 donor splice-site mutation in a family of Norfolk terrier dogs.
    Credille KM, Barnhart KF, Minor JS, Dunstan RW.
    Br J Dermatol; 2005 Jul 01; 153(1):51-8. PubMed ID: 16029326
    [Abstract] [Full Text] [Related]

  • 20. Ichthyosis bullosa of Siemens--a disease involving keratin 2e.
    McLean WH, Morley SM, Lane EB, Eady RA, Griffiths WA, Paige DG, Harper JI, Higgins C, Leigh IM.
    J Invest Dermatol; 1994 Sep 01; 103(3):277-81. PubMed ID: 7521371
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 13.