메뉴 건너뛰기




Volumn 62, Issue 2, 1998, Pages 386-390

A gene for universal congenital alopecia maps to chromosome 8p21-22

Author keywords

[No Author keywords available]

Indexed keywords

MICROSATELLITE DNA;

EID: 17344370417     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301717     Document Type: Article
Times cited : (54)

References (27)
  • 1
    • 0027241314 scopus 로고
    • Alopecia universalis as a single abnormality in an inbred Pakistani kindred
    • Ahmad M, Abbas H, Haque S (1993) Alopecia universalis as a single abnormality in an inbred Pakistani kindred. Am J Med Genet 46:369-371
    • (1993) Am J Med Genet , vol.46 , pp. 369-371
    • Ahmad, M.1    Abbas, H.2    Haque, S.3
  • 2
    • 0027367333 scopus 로고
    • cDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences
    • Anders DA, Milatovich A, Ozcrlik T, Wenzlau JM, Brown MS, Goldstein JL, Francke U (1993) cDNA cloning of the two subunits of human CAAX farnesyltransferase and chromosomal mapping of FNTA and FNTB loci and related sequences. Genomics 18:105-112
    • (1993) Genomics , vol.18 , pp. 105-112
    • Anders, D.A.1    Milatovich, A.2    Ozcrlik, T.3    Wenzlau, J.M.4    Brown, M.S.5    Goldstein, J.L.6    Francke, U.7
  • 3
    • 0030033174 scopus 로고    scopus 로고
    • X-linked recessive inheritance in a family with isolated congenital alopecia
    • Anzai H, Shimizu H, Nishikawa T (1996) X-linked recessive inheritance in a family with isolated congenital alopecia. Lancet 347:337-338
    • (1996) Lancet , vol.347 , pp. 337-338
    • Anzai, H.1    Shimizu, H.2    Nishikawa, T.3
  • 4
    • 7344254781 scopus 로고
    • Zur Kasuistik der Hypotrichosis congenita familiaris
    • Baer T (1907) Zur Kasuistik der Hypotrichosis congenita familiaris. Arch Dermatol Syph 84:15-18
    • (1907) Arch Dermatol Syph , vol.84 , pp. 15-18
    • Baer, T.1
  • 5
    • 77951392826 scopus 로고
    • Über Atrichia congenita und ihren Erbgang
    • Birke G (1954) Über Atrichia congenita und ihren Erbgang. Arch Dermatol Syph 197:322-343
    • (1954) Arch Dermatol Syph , vol.197 , pp. 322-343
    • Birke, G.1
  • 7
    • 0028587895 scopus 로고
    • Yeast artificial chromosome and radiation hybrid map of loci in chromosome band 8p22, a common region of allelic loss in multiple human cancers
    • Bookstein R, Levy A, MacGrogan D, Lewis TB, Weissenbach J, O'Connell P, Leach AJ (1994) Yeast artificial chromosome and radiation hybrid map of loci in chromosome band 8p22, a common region of allelic loss in multiple human cancers. Genomics 24:317-323
    • (1994) Genomics , vol.24 , pp. 317-323
    • Bookstein, R.1    Levy, A.2    MacGrogan, D.3    Lewis, T.B.4    Weissenbach, J.5    O'Connell, P.6    Leach, A.J.7
  • 10
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Fauré S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, et al (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380:152-154
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Fauré, S.2    Fizames, C.3    Samson, D.4    Drouot, N.5    Vignal, A.6    Millasseau, P.7
  • 11
    • 0023519575 scopus 로고
    • Genetic disorders associated with severe alopecia in children: A report of two unusual cases and a review
    • Feinstein A, Engelberg S, Goodman RM (1987) Genetic disorders associated with severe alopecia in children: a report of two unusual cases and a review. J Craniofac Genet Dev Biol 7:301-310
    • (1987) J Craniofac Genet Dev Biol , vol.7 , pp. 301-310
    • Feinstein, A.1    Engelberg, S.2    Goodman, R.M.3
  • 14
    • 0028063912 scopus 로고
    • Isolated congenital atrichia in an Omani kindred
    • Kenue RK, al-Dhafri KS (1994) Isolated congenital atrichia in an Omani kindred. Dermatology 188:72-75
    • (1994) Dermatology , vol.188 , pp. 72-75
    • Kenue, R.K.1    Al-Dhafri, K.S.2
  • 16
    • 7344224483 scopus 로고
    • Total congenital hereditary alopecia
    • Lundbäck H (1944) Total congenital hereditary alopecia. Acta Dermatol Venereol 25:189-206
    • (1944) Acta Dermatol Venereol , vol.25 , pp. 189-206
    • Lundbäck, H.1
  • 17
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 18
    • 0028784049 scopus 로고
    • Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure
    • Murillas R, Larcher F, Conti CJ, Santos M, Ullrich A, Jorcano JL (1995) Expression of a dominant negative mutant of epidermal growth factor receptor in the epidermis of transgenic mice elicits striking alterations in hair follicle development and skin structure. EMBO J 14:5216-5223
    • (1995) EMBO J , vol.14 , pp. 5216-5223
    • Murillas, R.1    Larcher, F.2    Conti, C.J.3    Santos, M.4    Ullrich, A.5    Jorcano, J.L.6
  • 19
    • 0345712799 scopus 로고
    • Totale familiäre Hypotrichose in 4 Generationen
    • Pajtâs J (1950) Totale familiäre Hypotrichose in 4 Generationen. Dermatologica 101:90-93
    • (1950) Dermatologica , vol.101 , pp. 90-93
    • Pajtâs, J.1
  • 20
    • 0026377699 scopus 로고
    • An in vitro model for the study of human hair growth
    • Philpott MP, Westgate GE, Kealy T (1991) An in vitro model for the study of human hair growth. Ann NY Acad Sci 642: 148-164
    • (1991) Ann NY Acad Sci , vol.642 , pp. 148-164
    • Philpott, M.P.1    Westgate, G.E.2    Kealy, T.3
  • 21
    • 0021912905 scopus 로고
    • Atrichias and hypotrichioses: A brief review with description of a recessive atrichia in two brothers
    • Pinheiro M, Freire-Maia N (1985) Atrichias and hypotrichioses: a brief review with description of a recessive atrichia in two brothers. Hum Hered 35:53-55
    • (1985) Hum Hered , vol.35 , pp. 53-55
    • Pinheiro, M.1    Freire-Maia, N.2
  • 23
    • 0026700010 scopus 로고
    • Heterodimerization of c-erbB2 with different epidermal growth factor receptor mutants elicits stimulatory or inhibitory responses
    • Spivak-Kroizman T, Rotin D, Pinchasi D, Ullrich A, Schlessinger J, Lax I (1992) Heterodimerization of c-erbB2 with different epidermal growth factor receptor mutants elicits stimulatory or inhibitory responses. J Biol Chem 267: 8056-8063
    • (1992) J Biol Chem , vol.267 , pp. 8056-8063
    • Spivak-Kroizman, T.1    Rotin, D.2    Pinchasi, D.3    Ullrich, A.4    Schlessinger, J.5    Lax, I.6
  • 24
    • 0012113973 scopus 로고
    • Alopecia congenita: Report of two families
    • Tillman WG (1952) Alopecia congenita: report of two families. Br Med J 2:428
    • (1952) Br Med J , vol.2 , pp. 428
    • Tillman, W.G.1
  • 25
    • 0024232830 scopus 로고
    • Congenital atrichia with nail dystrophy, abnormal facies, and psychomotor development in two siblings: A new autosomal recessive syndrome?
    • Vogt BR, Traupe H, Hamm H (1988) Congenital atrichia with nail dystrophy, abnormal facies, and psychomotor development in two siblings: a new autosomal recessive syndrome? Pediatr Dermatol 5:236-242
    • (1988) Pediatr Dermatol , vol.5 , pp. 236-242
    • Vogt, B.R.1    Traupe, H.2    Hamm, H.3
  • 26
    • 0029670049 scopus 로고    scopus 로고
    • The p21ras farnesyltransferase alpha subunit in TGF-β and activin signaling
    • Wang T, Danielson PD, Li B, Shah PC, Kim SD, Donahoe PK (1996) The p21ras farnesyltransferase alpha subunit in TGF-β and activin signaling. Science 271:1120-1122
    • (1996) Science , vol.271 , pp. 1120-1122
    • Wang, T.1    Danielson, P.D.2    Li, B.3    Shah, P.C.4    Kim, S.D.5    Donahoe, P.K.6
  • 27
    • 0025292831 scopus 로고
    • Dinucleotide repeat polymorphism at the 3′ end of the LDL receptor gene
    • Zuliani G, Hobbs HH (1990) Dinucleotide repeat polymorphism at the 3′ end of the LDL receptor gene. Nucleic Acids Res 18:4300
    • (1990) Nucleic Acids Res , vol.18 , pp. 4300
    • Zuliani, G.1    Hobbs, H.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.