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Volumn 52, Issue 3, 1999, Pages 510-515

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CHROMOSOME 9P; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE LOCATION; GENETIC LINKAGE; HUMAN; MALE; PEDIGREE; PRIORITY JOURNAL; SENSORY NEUROPATHY; YEAST ARTIFICIAL CHROMOSOME;

EID: 0032980321     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/wnl.52.3.510     Document Type: Article
Times cited : (27)

References (35)
  • 1
    • 0000751211 scopus 로고
    • Hereditary sensory radicular neuropathy
    • Denny-Brown D. Hereditary sensory radicular neuropathy. J Neurol Neurosurg Psychiatry 1951;14:237-252.
    • (1951) J Neurol Neurosurg Psychiatry , vol.14 , pp. 237-252
    • Denny-Brown, D.1
  • 2
    • 50749109971 scopus 로고
    • Hereditary perforating ulcer of the foot
    • Hicks EP. Hereditary perforating ulcer of the foot. Lancet 1922;1:319-321.
    • (1922) Lancet , vol.1 , pp. 319-321
    • Hicks, E.P.1
  • 3
    • 0016203376 scopus 로고
    • Hereditary sensory neuropathy: Association with increased synthesis of immunoglobulin A
    • Whitaker JN, Falchuck ZM, Engel WK, Blaese RM, Strober W. Hereditary sensory neuropathy: association with increased synthesis of immunoglobulin A. Arch Neurol 1974;30:359-371.
    • (1974) Arch Neurol , vol.30 , pp. 359-371
    • Whitaker, J.N.1    Falchuck, Z.M.2    Engel, W.K.3    Blaese, R.M.4    Strober, W.5
  • 4
    • 0000157043 scopus 로고
    • Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons
    • Dyck PJ, Thomas PK, Griffin JW, Low PA, Poduslo JF, eds. Philadelphia: WB Saunders
    • Dyck PJ. Neuronal atrophy and degeneration predominantly affecting peripheral sensory and autonomic neurons. In: Dyck PJ, Thomas PK, Griffin JW, Low PA, Poduslo JF, eds. Peripheral neuropathy. Philadelphia: WB Saunders, 1993:1065-1093.
    • (1993) Peripheral Neuropathy , pp. 1065-1093
    • Dyck, P.J.1
  • 5
    • 3643054286 scopus 로고
    • Perforating ulcers of feet, with osseous atrophy in a family with other evidences of dysgenesis (harelip, cleft palate): An instance of probable myelodysplasia
    • Tocantins LM, Reimann HA. Perforating ulcers of feet, with osseous atrophy in a family with other evidences of dysgenesis (harelip, cleft palate): an instance of probable myelodysplasia. JAMA 1939;112:2251-2255.
    • (1939) JAMA , vol.112 , pp. 2251-2255
    • Tocantins, L.M.1    Reimann, H.A.2
  • 6
    • 0011083928 scopus 로고
    • Hereditary sensory radicular neuropathy and other defects in a large family
    • Reimann HA, McKechnie WG, Stanisavljevic S. Hereditary sensory radicular neuropathy and other defects in a large family. Am J Med 1958;25:573-579.
    • (1958) Am J Med , vol.25 , pp. 573-579
    • Reimann, H.A.1    McKechnie, W.G.2    Stanisavljevic, S.3
  • 7
    • 0030140392 scopus 로고    scopus 로고
    • The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3
    • Nicholson GA, Dawkins JL, Blair IP, et al. The gene for hereditary sensory neuropathy type I (HSN-I) maps to chromosome 9q22.1-q22.3. Nat Genet 1996;13:101-104.
    • (1996) Nat Genet , vol.13 , pp. 101-104
    • Nicholson, G.A.1    Dawkins, J.L.2    Blair, I.P.3
  • 8
    • 0024602536 scopus 로고
    • Estimating the power of a proposed linkage study for a complex genetic trait
    • Ploughman L, Boehnke M. Estimating the power of a proposed linkage study for a complex genetic trait. Am J Hum Genet 1989:543-551.
    • (1989) Am J Hum Genet , pp. 543-551
    • Ploughman, L.1    Boehnke, M.2
  • 9
    • 13344259999 scopus 로고    scopus 로고
    • A comprehensive genetic map of the human genome based on 5,264 microsatellites
    • Dib C, Faure S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996;380:152-154.
    • (1996) Nature , vol.380 , pp. 152-154
    • Dib, C.1    Faure, S.2    Fizames, C.3
  • 12
    • 0021344005 scopus 로고
    • Easy calculations of lod scores and genetic risks on small computers
    • Lathrop GM, Lalouel JM. Easy calculations of lod scores and genetic risks on small computers. Am J Hum Genet 1984;36: 460-465.
    • (1984) Am J Hum Genet , vol.36 , pp. 460-465
    • Lathrop, G.M.1    Lalouel, J.M.2
  • 13
    • 0022646961 scopus 로고
    • Construction of human genetic linkage maps: Likelihood calculations for multilocus linkage analysis
    • Lathrop GM, Lalouel JM, White RL. Construction of human genetic linkage maps: likelihood calculations for multilocus linkage analysis. Genet Epidemiol 1986;3:39-52.
    • (1986) Genet Epidemiol , vol.3 , pp. 39-52
    • Lathrop, G.M.1    Lalouel, J.M.2    White, R.L.3
  • 16
    • 0029946879 scopus 로고    scopus 로고
    • Faster linkage analysis computations for pedigrees with loops or unused alleles
    • Schaffer AA. Faster linkage analysis computations for pedigrees with loops or unused alleles. Hum Hered 1996;46:226-235.
    • (1996) Hum Hered , vol.46 , pp. 226-235
    • Schaffer, A.A.1
  • 17
    • 0029416826 scopus 로고
    • An STS-based map of the human genome
    • with supplementary data from the Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project, Data Release 10 (May 1996)
    • Hudson TJ, Stein LD, Gerety SS, et al. An STS-based map of the human genome. Science 1995;270:1945-1954, with supplementary data from the Whitehead Institute/MIT Center for Genome Research, Human Genetic Mapping Project, Data Release 10 (May 1996).
    • (1995) Science , vol.270 , pp. 1945-1954
    • Hudson, T.J.1    Stein, L.D.2    Gerety, S.S.3
  • 18
    • 0029653653 scopus 로고
    • A YAC contig map of the human genome
    • Chumakov IM, Rigault P, Le Gall I, et al. A YAC contig map of the human genome. Nature 1995;377:175-183.
    • (1995) Nature , vol.377 , pp. 175-183
    • Chumakov, I.M.1    Rigault, P.2    Le Gall, I.3
  • 19
    • 0028049612 scopus 로고
    • A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9
    • Morris DJ, Reis A. A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9. Genomics 1994;23:23-29.
    • (1994) Genomics , vol.23 , pp. 23-29
    • Morris, D.J.1    Reis, A.2
  • 20
    • 0027968936 scopus 로고
    • Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3
    • Farndon PA, Morris DJ, Hardy C, et al. Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6-cM interval and contributes to the fine map of 9q22.3. Genomics 1994;23: 486-489.
    • (1994) Genomics , vol.23 , pp. 486-489
    • Farndon, P.A.1    Morris, D.J.2    Hardy, C.3
  • 21
    • 9044240048 scopus 로고    scopus 로고
    • A radiation hybrid map of the human genome
    • Gyapay G, Schmitt K, Fizames C, et al. A radiation hybrid map of the human genome. Hum Mol Genet 1996;5:339-346.
    • (1996) Hum Mol Genet , vol.5 , pp. 339-346
    • Gyapay, G.1    Schmitt, K.2    Fizames, C.3
  • 22
    • 15844381336 scopus 로고    scopus 로고
    • Human homolog of patched, a candidate gene for the basal cell nevus syndrome
    • Johnson RL, Rothman AL, Xie J, et al. Human homolog of patched, a candidate gene for the basal cell nevus syndrome. Science 1996;272:1668-1671.
    • (1996) Science , vol.272 , pp. 1668-1671
    • Johnson, R.L.1    Rothman, A.L.2    Xie, J.3
  • 23
    • 0025352949 scopus 로고
    • Partial aldolase B gene deletions in hereditary fructose intolerance
    • Cross NC, Cox TM. Partial aldolase B gene deletions in hereditary fructose intolerance. Am J Hum Genet 1990;47:101-106.
    • (1990) Am J Hum Genet , vol.47 , pp. 101-106
    • Cross, N.C.1    Cox, T.M.2
  • 24
    • 0025051338 scopus 로고
    • Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene
    • Kajihara S, Mukai T, Arai Y, Owada M, Kitagawa T, Hori K. Hereditary fructose intolerance caused by a nonsense mutation of the aldolase B gene. Am J Hum Genet 1990;47:562-567.
    • (1990) Am J Hum Genet , vol.47 , pp. 562-567
    • Kajihara, S.1    Mukai, T.2    Arai, Y.3    Owada, M.4    Kitagawa, T.5    Hori, K.6
  • 25
    • 0029089226 scopus 로고
    • A deletion and an insertion in the alleles for the xeroderma pigmentosum (XPA) DNA-binding protein in mildly affected patients
    • Cleaver JE, Charles WC, Thomas GH, McDowell ML. A deletion and an insertion in the alleles for the xeroderma pigmentosum (XPA) DNA-binding protein in mildly affected patients. Hum Mol Genet 1995;4:1685-1687.
    • (1995) Hum Mol Genet , vol.4 , pp. 1685-1687
    • Cleaver, J.E.1    Charles, W.C.2    Thomas, G.H.3    McDowell, M.L.4
  • 26
    • 0029050829 scopus 로고
    • Human fructose-1,6-bisphosphatase gene (FBP1): Exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency
    • el-Maghrabi MR, Lange AJ, Jiang W, et al. Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency. Genomics 1995;27:520-525.
    • (1995) Genomics , vol.27 , pp. 520-525
    • El-Maghrabi, M.R.1    Lange, A.J.2    Jiang, W.3
  • 27
    • 0027410648 scopus 로고
    • The junctional complex of the membrane skeleton
    • Gilligan DM, Bennett V. The junctional complex of the membrane skeleton. Semin Hematol 1993;30:74-83.
    • (1993) Semin Hematol , vol.30 , pp. 74-83
    • Gilligan, D.M.1    Bennett, V.2
  • 28
    • 0029566977 scopus 로고
    • Molecular genetics of androgenic 17 beta-hydroxysteroid dehydrogenases
    • Andersson S. Molecular genetics of androgenic 17 beta-hydroxysteroid dehydrogenases. J Steroid Biochem Mol Biol 1995;55:533-534.
    • (1995) J Steroid Biochem Mol Biol , vol.55 , pp. 533-534
    • Andersson, S.1
  • 29
    • 0030891547 scopus 로고    scopus 로고
    • Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3
    • Chidambaram A, Gailani M, Gerrard B, et al. Characterization of a YAC contig containing the NBCCS locus and a novel Kruppel-type zinc finger sequence on chromosome segment 9q22.3. Genes Chromosomes Cancer 1997;18:212-218.
    • (1997) Genes Chromosomes Cancer , vol.18 , pp. 212-218
    • Chidambaram, A.1    Gailani, M.2    Gerrard, B.3
  • 30
    • 0031149301 scopus 로고    scopus 로고
    • FKHL15, a new human member of the forkhead gene family located on chromosome 9q22
    • Chadwick BP, Obermayr F, Frischauf AM. FKHL15, a new human member of the forkhead gene family located on chromosome 9q22. Genomics 1997;41:390-396.
    • (1997) Genomics , vol.41 , pp. 390-396
    • Chadwick, B.P.1    Obermayr, F.2    Frischauf, A.M.3
  • 31
    • 0028951557 scopus 로고
    • Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2)
    • Nakagawara A, Liu XG, Ikegaki N, et al. Cloning and chromosomal localization of the human TRK-B tyrosine kinase receptor gene (NTRK2). Genomics 1995;25:538-546.
    • (1995) Genomics , vol.25 , pp. 538-546
    • Nakagawara, A.1    Liu, X.G.2    Ikegaki, N.3
  • 32
    • 0000881993 scopus 로고
    • Cathepsin L (CTSL) is located in the chromosome 9q21-q22: A related sequence is located on chromosome 10
    • Fan YS, Byers MG, Eddy RL, et al. Cathepsin L (CTSL) is located in the chromosome 9q21-q22: a related sequence is located on chromosome 10. Cytogenet Cell Genet 1989;51:996.
    • (1989) Cytogenet Cell Genet , vol.51 , pp. 996
    • Fan, Y.S.1    Byers, M.G.2    Eddy, R.L.3
  • 33
    • 0027787542 scopus 로고
    • Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies
    • Evdokiou A, Webb GC, Peters GB, et al. Localization of the human growth arrest-specific gene (GAS1) to chromosome bands 9q21.3-q22, a region frequently deleted in myeloid malignancies. Genomics 1993;18:731-733.
    • (1993) Genomics , vol.18 , pp. 731-733
    • Evdokiou, A.1    Webb, G.C.2    Peters, G.B.3
  • 34
    • 0028809840 scopus 로고
    • Molecular cloning and characterization of NF-IL3A, a transcriptional activator of the human interleukin-3 promoter
    • Zhang W, Zhang J, Kornuc M, Kwan K, Frank R, Nimer SD. Molecular cloning and characterization of NF-IL3A, a transcriptional activator of the human interleukin-3 promoter. Mol Cell Biol 1995;15:6055-6063.
    • (1995) Mol Cell Biol , vol.15 , pp. 6055-6063
    • Zhang, W.1    Zhang, J.2    Kornuc, M.3    Kwan, K.4    Frank, R.5    Nimer, S.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.