메뉴 건너뛰기




Volumn 64, Issue 6, 2003, Pages 715-720

Familial footpad hyperkeratosis and inheritance of keratin 2, keratin 9, and desmoglein 1 in two pedigrees of Irish Terriers

Author keywords

[No Author keywords available]

Indexed keywords

ACID PROTEIN; BASIC PROTEIN; DESMOGLEIN 1; DNA MARKER; GENOMIC DNA; KERATIN; KERATIN 9; KERATIN TYPE 2; UNCLASSIFIED DRUG;

EID: 0038515045     PISSN: 00029645     EISSN: None     Source Type: Journal    
DOI: 10.2460/ajvr.2003.64.715     Document Type: Article
Times cited : (9)

References (40)
  • 1
    • 0034133213 scopus 로고    scopus 로고
    • Palmoplantar hyperkeratosis in Irish Terriers: Evidence of autosomal recessive inheritance
    • Binder H, Arnold S, Schelling C, et al. Palmoplantar hyperkeratosis in Irish Terriers: evidence of autosomal recessive inheritance. J Small Anim Pract 2000;41:52-55.
    • (2000) J. Small Anim. Pract. , vol.41 , pp. 52-55
    • Binder, H.1    Arnold, S.2    Schelling, C.3
  • 2
    • 84995164775 scopus 로고
    • Footpad hyperkeratosis in a family of Dogue de Bordeaux
    • Paradis M. Footpad hyperkeratosis in a family of Dogue de Bordeaux. Vet Dermatol 1992;3:75-78.
    • (1992) Vet. Dermatol. , vol.3 , pp. 75-78
    • Paradis, M.1
  • 3
    • 0007453261 scopus 로고    scopus 로고
    • Congenital and hereditary defects
    • Scott DW, Miller WH, Griffin CE, eds. 6th ed. Philadelphia: WB Saunders Co
    • Scott DW, Miller WH, Griffin CE. Congenital and hereditary defects. In: Scott DW, Miller WH, Griffin CE, eds. Small animal dermatology. 6th ed. Philadelphia: WB Saunders Co, 2001;913-1003.
    • (2001) Small Animal Dermatology , pp. 913-1003
    • Scott, D.W.1    Miller, W.H.2    Griffin, C.E.3
  • 4
    • 0031583667 scopus 로고    scopus 로고
    • A retrospective clinical study of canine leishmaniasis in 150 dogs naturally infected by leishmania infantum
    • Ciaramella P, Oliva G, Luna RD, et al. A retrospective clinical study of canine leishmaniasis in 150 dogs naturally infected by leishmania infantum. Vet Rec 1997;141:539-543.
    • (1997) Vet. Rec. , vol.141 , pp. 539-543
    • Ciaramella, P.1    Oliva, G.2    Luna, R.D.3
  • 5
    • 0012961917 scopus 로고
    • Zinc-responsive dermatoses in dogs
    • Kirk RW, ed. Philadelphia: WB Saunders Co
    • Kunkle GA. Zinc-responsive dermatoses in dogs. In: Kirk RW, ed. Current veterinary therapy VII. Philadelphia: WB Saunders Co, 1980;472-476.
    • (1980) Current Veterinary Therapy VII , pp. 472-476
    • Kunkle, G.A.1
  • 8
    • 0038260923 scopus 로고
    • Keratinization disorders
    • Kwochka KW, ed. St Louis: Mosby Year Book Inc
    • Kwochka KW. Keratinization disorders. in: Kwochka KW, ed. Current veterinary dermatology. St Louis: Mosby Year Book Inc, 1993;167-190.
    • (1993) Current Veterinary Dermatology , pp. 167-190
    • Kwochka, K.W.1
  • 9
    • 0033020064 scopus 로고    scopus 로고
    • The palmoplantar keratodermas: Much more than palms and soles
    • Kelsell DP, Stevens HP. The palmoplantar keratodermas: much more than palms and soles. Mol Med Today 1999;5:107-113.
    • (1999) Mol. Med. Today , vol.5 , pp. 107-113
    • Kelsell, D.P.1    Stevens, H.P.2
  • 11
    • 0033008259 scopus 로고    scopus 로고
    • Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis
    • Yang JM, Nam K, Kim SW, et al. Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis. J Dermatol Sci 1999;19:126-133.
    • (1999) J. Dermatol. Sci. , vol.19 , pp. 126-133
    • Yang, J.M.1    Nam, K.2    Kim, S.W.3
  • 12
    • 0034075325 scopus 로고    scopus 로고
    • Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene
    • Cserhalmi-Friedmann PB, Squeo R, Gordon D, et al. Epidermolytic hyperkeratosis in a Hispanic family resulting from a mutation in the keratin 1 gene. Clin Exp Dermatol 2000;25:241-243.
    • (2000) Clin. Exp. Dermatol. , vol.25 , pp. 241-243
    • Cserhalmi-Friedmann, P.B.1    Squeo, R.2    Gordon, D.3
  • 13
    • 0027742236 scopus 로고
    • A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis
    • Rothnagel JA, Fisher MP, Axtell SM, et al. A mutational hot spot in keratin 10 (KRT 10) in patients with epidermolytic hyperkeratosis. Hum Mol Genet 1993;12:2147-2150.
    • (1993) Hum. Mol. Genet. , vol.12 , pp. 2147-2150
    • Rothnagel, J.A.1    Fisher, M.P.2    Axtell, S.M.3
  • 14
    • 19244384754 scopus 로고
    • Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis
    • Fuchs E, Coulombe P, Cheng J, et al. Genetic bases of epidermolysis bullosa simplex and epidermolytic hyperkeratosis. J Invest Dermatol 1994;103(suppl):25S-30S.
    • (1994) J. Invest. Dermatol. , vol.103 , Issue.SUPPL.
    • Fuchs, E.1    Coulombe, P.2    Cheng, J.3
  • 15
    • 0032852841 scopus 로고    scopus 로고
    • Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene
    • Moraru R, Cserhalmi-Friedman PB, Grossman ME, et al. Ichthyosis bullosa of Siemens resulting from a novel missense mutation near the helix termination motif of the keratin 2e gene. Clin Exp Dermatol 1999;24:412-415.
    • (1999) Clin. Exp. Dermatol. , vol.24 , pp. 412-415
    • Moraru, R.1    Cserhalmi-Friedman, P.B.2    Grossman, M.E.3
  • 16
    • 0023072758 scopus 로고
    • Distribution of a special subset of keratinocytes characterized by the expression of cytokeratin 9 in adult and foetal human epidermis of various body sites
    • Moll I, Heid H, Franke WW, et al. Distribution of a special subset of keratinocytes characterized by the expression of cytokeratin 9 in adult and foetal human epidermis of various body sites. Differentiation 1987;33:254-265.
    • (1987) Differentiation , vol.33 , pp. 254-265
    • Moll, I.1    Heid, H.2    Franke, W.W.3
  • 17
    • 0034115888 scopus 로고    scopus 로고
    • Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene
    • Warmuth I, Cserhalmi-Friedman PB, Schneiderman P, et al. Epidermolytic palmoplantar keratoderma in a Hispanic kindred resulting from a mutation in the keratin 9 gene. Clin Exp Dermatol 1999;25:244-246.
    • (1999) Clin. Exp. Dermatol. , vol.25 , pp. 244-246
    • Warmuth, I.1    Cserhalmi-Friedman, P.B.2    Schneiderman, P.3
  • 18
    • 0034100522 scopus 로고    scopus 로고
    • Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma
    • Smith FJ, Fisher MP, Healy E, et al. Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma. Exp Dermatol 2000;9:170-177.
    • (2000) Exp. Dermatol. , vol.9 , pp. 170-177
    • Smith, F.J.1    Fisher, M.P.2    Healy, E.3
  • 19
    • 0032970153 scopus 로고    scopus 로고
    • N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma
    • Rickman L, Šimrak D, Stevens HP, et al. N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. Hum Mol Gen 1999;8:971-976.
    • (1999) Hum. Mol. Gen. , vol.8 , pp. 971-976
    • Rickman, L.1    Šimrak, D.2    Stevens, H.P.3
  • 20
    • 0034765318 scopus 로고    scopus 로고
    • Cloning, sequence analysis and radiation hybrid mapping of a mammalian KRT2p gene
    • Miller AB, Lowe JK, Ostrander EA, et al. Cloning, sequence analysis and radiation hybrid mapping of a mammalian KRT2p gene. Funct Integr Genomics 2001;1:305-311.
    • (2001) Funct. Integr. Genomics , vol.1 , pp. 305-311
    • Miller, A.B.1    Lowe, J.K.2    Ostrander, E.A.3
  • 21
    • 0032811518 scopus 로고    scopus 로고
    • Chromosomal localization of acidic and basic keratin genes of the domestic dog
    • Miller AB, Breen M, Murphy KE. Chromosomal localization of acidic and basic keratin genes of the domestic dog. Mamm Genome 1999;10:371-375.
    • (1999) Mamm. Genome , vol.10 , pp. 371-375
    • Miller, A.B.1    Breen, M.2    Murphy, K.E.3
  • 22
    • 0034764308 scopus 로고    scopus 로고
    • Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes
    • Breen M, Jouquand S, Renier C, et al. Chromosome-specific single-locus FISH probes allow anchorage of an 1800-marker integrated radiation-hybrid/linkage map of the domestic dog genome to all chromosomes. Genome Res 2001;11:1784-1795.
    • (2001) Genome Res. , vol.11 , pp. 1784-1795
    • Breen, M.1    Jouquand, S.2    Renier, C.3
  • 23
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
    • (1988) Nucleic Acids Res. , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 24
    • 0033958731 scopus 로고    scopus 로고
    • An integrated linkage-radiation hybrid map of the canine genome
    • Mellersh CS, Hitte C, Richman M, et al. An integrated linkage-radiation hybrid map of the canine genome. Mamm Genome 2000;11:120-130.
    • (2000) Mamm. Genome , vol.11 , pp. 120-130
    • Mellersh, C.S.1    Hitte, C.2    Richman, M.3
  • 25
    • 0034047354 scopus 로고    scopus 로고
    • Refined genetic and comparative physical mapping of the canine copper toxicosis locus
    • Van de Sluis B, Kole S, Van Wolferen M, et al. Refined genetic and comparative physical mapping of the canine copper toxicosis locus. Mamm Genome 2000;11:455-460.
    • (2000) Mamm. Genome , vol.11 , pp. 455-460
    • Van de Sluis, B.1    Kole, S.2    Van Wolferen, M.3
  • 26
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparametric linkage analysis: A unified multipoint approach
    • Kruglyak L, Daly MJ, Reeve-Daly MP, et al. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 1996;58:1347-1363.
    • (1996) Am. J. Hum. Genet. , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3
  • 27
    • 0026879788 scopus 로고
    • Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis
    • Nusgens BV, Verellen-Dumoulin C, Hermanns-Le T, et al. Evidence for a relationship between Ehlers-Danlos type VII C in humans and bovine dermatosparaxis. Nat Genet 1992;1:214-217.
    • (1992) Nat. Genet. , vol.1 , pp. 214-217
    • Nusgens, B.V.1    Verellen-Dumoulin, C.2    Hermanns-Le, T.3
  • 28
    • 0032103707 scopus 로고    scopus 로고
    • Identification and analysis of the dog keratin 9 (KRT 9) gene
    • Lachaume P, Hitte C, Jouquand S, et al. Identification and analysis of the dog keratin 9 (KRT 9) gene. Anim Genet 1998; 29:173-177.
    • (1998) Anim. Genet. , vol.29 , pp. 173-177
    • Lachaume, P.1    Hitte, C.2    Jouquand, S.3
  • 29
    • 0011909528 scopus 로고
    • Desmosomes in differentiation and development
    • Collins JE, Garrod DR, eds. Austin, Tex: RG Landes Co
    • Garrod SR, Collins JE. Desmosomes in differentiation and development. In: Collins JE, Garrod DR, eds. The molecular biology of desmosomes and hemidesmosomes. Austin, Tex: RG Landes Co, 1994;19-33.
    • (1994) The Molecular Biology of Desmosomes and Hemidesmosomes , pp. 19-33
    • Garrod, S.R.1    Collins, J.E.2
  • 30
    • 0038260926 scopus 로고    scopus 로고
    • The International RH Mapping Consortium. A new gene map of the human genome Accessed Aug 20, Accessed at: www.ncbi.nlm.nih.gov/genemap99/loc.cgi?ID=33107
    • The International RH Mapping Consortium. A new gene map of the human genome Accessed Aug 20,2001. Accessed at: www.ncbi.nlm.nih.gov/genemap99/loc.cgi?ID=33107.
    • (2001)
  • 31
    • 0031738330 scopus 로고    scopus 로고
    • Genomic organization and fine maooing of the keratin 2e gene (KRT 2e): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of Siemens
    • Smith F, Maingi C, Covello S et al. Genomic organization and fine maooing of the keratin 2e gene (KRT 2e): K2e V1 domain polymorphism and novel mutations in ichthyosis bullosa of Siemens. J Invest Dermatol 1998;111:810-814.
    • (1998) J. Invest. Dermatol. , vol.111 , pp. 810-814
    • Smith, F.1    Maingi, C.2    Covello, S.3
  • 32
    • 0037923396 scopus 로고    scopus 로고
    • Albert Einstein College of Medicine Human Genome Research Center. Chromosome 12 Map Database. Available at: November
    • Albert Einstein College of Medicine Human Genome Research Center. Chromosome 12 Map Database. Available at: http://sequence.aecom.yu.sdu/chrl2/. November 2001.
    • (2001)
  • 33
    • 0031852396 scopus 로고    scopus 로고
    • Identification of mutations in the canine von Willebrand factor gene associated with type III von Willebrand disease
    • Rieger M, Schwarz HP, Turecek PL, et al. identification of mutations in the canine von Willebrand factor gene associated with type III von Willebrand disease. Thromb Haemost 1998;80:332-337.
    • (1998) Thromb. Haemost. , vol.80 , pp. 332-337
    • Rieger, M.1    Schwarz, H.P.2    Turecek, P.L.3
  • 34
    • 0033631771 scopus 로고    scopus 로고
    • Mutation causing von Willebrand's disease in Scottish Terriers
    • Venta PJ, Yuzbasiyan V, Brewer GJ, et al. Mutation causing von Willebrand's disease in Scottish Terriers. J Vet Intern Med 2000; 14:10-19.
    • (2000) J. Vet. Intern. Med. , vol.14 , pp. 10-19
    • Venta, P.J.1    Yuzbasiyan, V.2    Brewer, G.J.3
  • 35
    • 0037081771 scopus 로고    scopus 로고
    • Identification of a new copper metabolism gene by positional cloning in a purebred dog population
    • Van de Sluis BJ, Rothuizen J, Pearson PL, et al. Identification of a new copper metabolism gene by positional cloning in a purebred dog population. Hum Mol Genet 2002;11:165-173.
    • (2002) Hum. Mol. Genet. , vol.11 , pp. 165-173
    • Van de Sluis, B.J.1    Rothuizen, J.2    Pearson, P.L.3
  • 40
    • 0035487776 scopus 로고    scopus 로고
    • Loricrin keratoderma: A cause of congenital ichthyosiform erythroderma and collodion baby
    • Matsumoto K, Muto M, Seki S, et al. Loricrin keratoderma: a cause of congenital ichthyosiform erythroderma and collodion baby. Br J Dermatol 2000;145:657-660.
    • (2000) Br. J. Dermatol. , vol.145 , pp. 657-660
    • Matsumoto, K.1    Muto, M.2    Seki, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.