메뉴 건너뛰기




Volumn 141, Issue 4, 1999, Pages 748-750

Correspondence

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANNULAR EPIDERMOLYTIC ICHTHYOSIS; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; ELECTRON MICROSCOPY; FEMALE; GENE MUTATION; GENODERMATOSIS; HUMAN; HUMAN TISSUE; ICHTHYOSIS; LETTER; PHENOTYPE; PRIORITY JOURNAL; SKIN BIOPSY; SKIN DISEASE;

EID: 0032716542     PISSN: 00070963     EISSN: 13652133     Source Type: Journal    
DOI: 10.1046/j.1365-2133.1999.03125.x     Document Type: Letter
Times cited : (7)

References (8)
  • 1
    • 0026749966 scopus 로고
    • Annular epidermolytic ichthyosis: A unique phenotype
    • Sahn EE, Weimer CE, Garen PD. Annular epidermolytic ichthyosis: a unique phenotype. J Am Acad Dermatol 1992; 27: 348-55.
    • (1992) J Am Acad Dermatol , vol.27 , pp. 348-355
    • Sahn, E.E.1    Weimer, C.E.2    Garen, P.D.3
  • 2
    • 0014847539 scopus 로고
    • Histopathologic concept of epidermolytic hyperker-atosis
    • Ackerman AB. Histopathologic concept of epidermolytic hyperker-atosis. Arch Dermatol 1970; 102: 253-9.
    • (1970) Arch Dermatol , vol.102 , pp. 253-259
    • Ackerman, A.B.1
  • 3
    • 0031044639 scopus 로고    scopus 로고
    • A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma
    • Joh G-Y, Traupe H, Metze D et al. A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma. J Invest Dermatol 1997; 108: 357-61.
    • (1997) J Invest Dermatol , vol.108 , pp. 357-361
    • Joh, G.-Y.1    Traupe, H.2    Metze, D.3
  • 4
    • 0032465160 scopus 로고    scopus 로고
    • A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma
    • Suga Y, Duncan KO, Heald PW, Roop DR. A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma. J Invest Dermatol 1998; 111: 1220-3.
    • (1998) J Invest Dermatol , vol.111 , pp. 1220-1223
    • Suga, Y.1    Duncan, K.O.2    Heald, P.W.3    Roop, D.R.4
  • 5
    • 0033361793 scopus 로고    scopus 로고
    • Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1
    • Sybert VP, Francis JS, Corden LD et al. Cyclic ichthyosis with epidermolytic hyperkeratosis: a phenotype conferred by mutations in the 2B domain of keratin K1. Am J Hum Genet 1999; 64: 732-8.
    • (1999) Am J Hum Genet , vol.64 , pp. 732-738
    • Sybert, V.P.1    Francis, J.S.2    Corden, L.D.3
  • 6
    • 0030669237 scopus 로고    scopus 로고
    • An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis
    • Yang J-M, Yoneda K, Morita E et al. An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis. J Invest Dermatol 1997; 109: 692-4.
    • (1997) J Invest Dermatol , vol.109 , pp. 692-694
    • Yang, J.-M.1    Yoneda, K.2    Morita, E.3
  • 7
    • 33749357063 scopus 로고
    • Intermediate filament structure: 3. Analysis of sequence homologies
    • Conway JF, Parry DAD. Intermediate filament structure: 3. analysis of sequence homologies. Int J Biol Macromol 1988; 10: 79-98.
    • (1988) Int J Biol Macromol , vol.10 , pp. 79-98
    • Conway, J.F.1    Parry, D.A.D.2
  • 8
    • 0027160195 scopus 로고
    • Keratin intermediate filament structure. Crosslinking studies yield quantitative information on molecular dimensions and mechanism of assembly
    • Steinert PM, Marekov LN, Fraser RBD, Parry DAD. Keratin intermediate filament structure. crosslinking studies yield quantitative information on molecular dimensions and mechanism of assembly. J Mol Biol 1993; 230: 436-52.
    • (1993) J Mol Biol , vol.230 , pp. 436-452
    • Steinert, P.M.1    Marekov, L.N.2    Rbd, F.3    Parry, D.A.D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.