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Volumn 129, Issue 3, 2003, Pages 285-289

Genomewide linkage analysis to presbycusis in the Framingham Heart Study

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGE; AGED; ARTICLE; AUDIOMETRY; CHROMOSOME ANALYSIS; CLINICAL STUDY; COHORT ANALYSIS; CONGENITAL DEAFNESS; CONTROLLED STUDY; DISEASE MARKER; EVALUATION; EVIDENCE BASED MEDICINE; FEMALE; GENDER; GENE LOCATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC ORGANIZATION; GENETIC TRAIT; GENOME; HEALTH STATUS; HEARING IMPAIRMENT; HEART; HERITABILITY; HUMAN; MAJOR CLINICAL STUDY; MALE; POPULATION RESEARCH; PRESBYACUSIS; PROMOTER REGION; QUANTITATIVE ANALYSIS;

EID: 0037338594     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.129.3.285     Document Type: Article
Times cited : (74)

References (25)
  • 1
    • 0012266987 scopus 로고    scopus 로고
    • Hyattsville, Md: US Dept of Health and Human Services; 1986. PHS publication
    • National Center for Health Statistics. Prevalence of Selected Chronic Conditions, United States, 1979-1981. Hyattsville, Md: US Dept of Health and Human Services; 1986. PHS publication 86-1583.
    • Prevalence of Selected Chronic Conditions, United States, 1979-1981 , pp. 86-1583
  • 3
    • 0035153199 scopus 로고    scopus 로고
    • Genetic and environmental influences on self-reported reduced hearing in the old and oldest old
    • Christensen K, Frederiksen H, Hoffman HJ. Genetic and environmental influences on self-reported reduced hearing in the old and oldest old. J Am Geriatr Soc. 2001;49:1512-1517.
    • (2001) J Am Geriatr Soc , vol.49 , pp. 1512-1517
    • Christensen, K.1    Frederiksen, H.2    Hoffman, H.J.3
  • 4
    • 0034079619 scopus 로고    scopus 로고
    • Inherited sensorineural low-frequency hearing impairment: Some aspects of phenotype and epidemiology
    • Parving A, Sakihara Y, Christensen B. Inherited sensorineural. low-frequency hearing impairment: some aspects of phenotype and epidemiology. Audiology. 2000; 39:50-60.
    • (2000) Audiology , vol.39 , pp. 50-60
    • Parving, A.1    Sakihara, Y.2    Christensen, B.3
  • 5
    • 0034537965 scopus 로고    scopus 로고
    • A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice
    • Johnson KR, Zheng QY, Erway LC. A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice. Genomics. 2000;70:171-180.
    • (2000) Genomics , vol.70 , pp. 171-180
    • Johnson, K.R.1    Zheng, Q.Y.2    Erway, L.C.3
  • 6
    • 0030849125 scopus 로고    scopus 로고
    • Mitochondrial DNA deletions associated with aging and possibly presbycusis: A human archival temporal bone study
    • Bai U, Seidman MD, Hinojosa R, Quirk WS. Mitochondrial DNA deletions associated with aging and possibly presbycusis: a human archival temporal bone study. Am J Otol. 1997;18:449-453.
    • (1997) Am J Otol , vol.18 , pp. 449-453
    • Bai, U.1    Seidman, M.D.2    Hinojosa, R.3    Quirk, W.S.4
  • 7
    • 0030745117 scopus 로고    scopus 로고
    • Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations
    • Fischel-Ghodsian N, Bykhovskaya Y, Taylor K, et al. Temporal bone analysis of patients with presbycusis reveals high frequency of mitochondrial mutations. Hear Res. 1997;110:147-154.
    • (1997) Hear Res , vol.110 , pp. 147-154
    • Fischel-Ghodsian, N.1    Bykhovskaya, Y.2    Taylor, K.3
  • 8
    • 0034056134 scopus 로고    scopus 로고
    • Biologic activity of mitochondrial metabolites on aging and age-related hearing loss
    • Seidman MD, Khan MJ, Bai U, Shirwany N, Quirk WS. Biologic activity of mitochondrial metabolites on aging and age-related hearing loss. Am J Otol. 2000; 21:161-167.
    • (2000) Am J Otol , vol.21 , pp. 161-167
    • Seidman, M.D.1    Khan, M.J.2    Bai, U.3    Shirwany, N.4    Quirk, W.S.5
  • 10
    • 75949155739 scopus 로고
    • Further observations on the pathology of presbycusis
    • Schuknecht HF. Further observations on the pathology of presbycusis. Arch Otolaryngol. 1964;80:369-382.
    • (1964) Arch Otolaryngol , vol.80 , pp. 369-382
    • Schuknecht, H.F.1
  • 11
    • 0002572171 scopus 로고
    • Epidemiological approaches to heart disease: The Framingham Study
    • Dawber TR, Meadors GF, Moore FEJ. Epidemiological approaches to heart disease: the Framingham Study. Am J Public Health. 1951;41:279-286.
    • (1951) Am J Public Health , vol.41 , pp. 279-286
    • Dawber, T.R.1    Meadors, G.F.2    Moore, F.E.J.3
  • 13
    • 0015834582 scopus 로고
    • Isolation of high-molecular-weight DNA from mammalian cells
    • Gross-Bellard M, Oudet P, Chambon P. Isolation of high-molecular-weight DNA from mammalian cells. Eur J Biochem. 1973;36:32-38.
    • (1973) Eur J Biochem , vol.36 , pp. 32-38
    • Gross-Bellard, M.1    Oudet, P.2    Chambon, P.3
  • 14
    • 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
  • 15
    • 0033358545 scopus 로고    scopus 로고
    • Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure
    • Allison DB, Neale MC, Zannolli R, Schork NJ, Amos CI, Blangero J. Testing the robustness of the likelihood-ratio test in a variance-component quantitative-trait loci-mapping procedure. Am J Hum Genet. 1999;65:531-544.
    • (1999) Am J Hum Genet , vol.65 , pp. 531-544
    • Allison, D.B.1    Neale, M.C.2    Zannolli, R.3    Schork, N.J.4    Amos, C.I.5    Blangero, J.6
  • 16
    • 0031966959 scopus 로고    scopus 로고
    • Multipoint quantitative-trait linkage analysis in general pedigrees
    • Almasy L, Blangero J. Multipoint quantitative-trait linkage analysis in general pedigrees. Am J Hum Genet. 1998;62:1198-1211.
    • (1998) Am J Hum Genet , vol.62 , pp. 1198-1211
    • Almasy, L.1    Blangero, J.2
  • 17
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11:241-247.
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 18
    • 0037086003 scopus 로고    scopus 로고
    • Genetic loci influencing lung function: A genomewide scan in the Framingham study
    • Joost O, Wilk JB, Cupples LA, et al. Genetic loci influencing lung function: a genomewide scan in the Framingham study. Am J Respir Crit Care Med. 2002;165: 495-499.
    • (2002) Am J Respir Crit Care Med , vol.165 , pp. 495-499
    • Joost, O.1    Wilk, J.B.2    Cupples, L.A.3
  • 20
    • 0028815440 scopus 로고
    • Defective myosin VIIA gene responsible for Usher syndrome type 1B
    • Weil D, Blanchard S, Kaplan J, et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature, 1995;374:60-61.
    • (1995) Nature , vol.374 , pp. 60-61
    • Weil, D.1    Blanchard, S.2    Kaplan, J.3
  • 21
    • 0030960855 scopus 로고    scopus 로고
    • Mutations in the myosin VlIA gene cause nonsyndromic recessive deafness
    • Liu XZ, Walsh J, Mburu P, et al. Mutations in the myosin VlIA gene cause nonsyndromic recessive deafness. Nat Genet. 1997;16:188-190.
    • (1997) Nat Genet , vol.16 , pp. 188-190
    • Liu, X.Z.1    Walsh, J.2    Mburu, P.3
  • 22
    • 0030951102 scopus 로고    scopus 로고
    • The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
    • Weil D, Kussel P, Blanchard S, et al. The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene. Nat Genet. 1997;16:191-193.
    • (1997) Nat Genet , vol.16 , pp. 191-193
    • Weil, D.1    Kussel, P.2    Blanchard, S.3
  • 23
    • 0033816925 scopus 로고    scopus 로고
    • A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 10
    • Verpy E, Leibovici M, Zwaenepoel I, et al. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 10. Nat Genet. 2000;26:51-55.
    • (2000) Nat Genet , vol.26 , pp. 51-55
    • Verpy, E.1    Leibovici, M.2    Zwaenepoel, I.3
  • 24
    • 0027058632 scopus 로고
    • A gene for Usher syndrome type I (USH1A) maps to chromosome 14q
    • Kaplan J, Gerber S, Bonneau D, et al. A gene for Usher syndrome type I (USH1A) maps to chromosome 14q. Genomics. 1992;14:979-987.
    • (1992) Genomics , vol.14 , pp. 979-987
    • Kaplan, J.1    Gerber, S.2    Bonneau, D.3
  • 25
    • 0033028072 scopus 로고    scopus 로고
    • DFN820: A novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter
    • , Moynihan L, Houseman M, Newton V, Mueller R, Lench N. DFN820: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter. EurJ Hum Genet. 1999;7:243-246.
    • (1999) Eur J Hum Genet , vol.7 , pp. 243-246
    • Moynihan, L.1    Houseman, M.2    Newton, V.3    Mueller, R.4    Lench, N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.