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Volumn 98, Issue 2, 1996, Pages 236-238

Revised transthyretin Ile 122 allele frequency in African-Americans

Author keywords

[No Author keywords available]

Indexed keywords

DNA; PREALBUMIN;

EID: 0029946836     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050199     Document Type: Article
Times cited : (92)

References (14)
  • 2
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    • Systemic senile amyloidosis - Identification of a new prealbumin (transthyretin) variant in cardiac tissue: Immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy
    • Gorevic PD, Prelli FC. Wright J, Pras M, Frangione B (1989) Systemic senile amyloidosis - identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy. J Clin Invest 83:836-843
    • (1989) J Clin Invest , vol.83 , pp. 836-843
    • Gorevic, P.D.1    Prelli, F.C.2    Wright, J.3    Pras, M.4    Frangione, B.5
  • 4
    • 0026543251 scopus 로고
    • A specific test for transthyretin 122 (Val-lle) based on PCR-primer introduced restriction analysis (PCRPIRA): Confirmation of the gene frequency in blacks
    • Jacobson DR (1992) A specific test for transthyretin 122 (Val-lle) based on PCR-primer introduced restriction analysis (PCRPIRA): confirmation of the gene frequency in blacks. Am J Hum Genet 50:195-198
    • (1992) Am J Hum Genet , vol.50 , pp. 195-198
    • Jacobson, D.R.1
  • 6
    • 0025335359 scopus 로고
    • A homozygous transthyretin variant associated with senile systemic amyloidosis: Evidence for a late-onset disease of genetic etiology
    • Jacobson DR, Gorevic PD, Buxbaum JN (1990) A homozygous transthyretin variant associated with senile systemic amyloidosis: evidence for a late-onset disease of genetic etiology. Am J Hum Genet 47:127-136
    • (1990) Am J Hum Genet , vol.47 , pp. 127-136
    • Jacobson, D.R.1    Gorevic, P.D.2    Buxbaum, J.N.3
  • 7
    • 0025819856 scopus 로고
    • Frequency and genetic background of the position 122 (Val-Ile) transthyretin gene in the black population
    • Jacobson DR, Reveille JD, Buxbaum JN (1991) Frequency and genetic background of the position 122 (Val-Ile) transthyretin gene in the black population. Am J Hum Genet 49:192-198
    • (1991) Am J Hum Genet , vol.49 , pp. 192-198
    • Jacobson, D.R.1    Reveille, J.D.2    Buxbaum, J.N.3
  • 8
    • 0343718029 scopus 로고
    • Genetic analysis of 9 unrelated patients with transthyretin (TTR)-cardiac amyloidosis: Correlation of clinical and genetic findings and description of 2 new TTR variants
    • Kisilevsky R, Benson MD, Frangione B, Gauldie J, Muckle TJ, Young ID (eds) Parthenon Publishing, New York
    • Jacobson DR, Gertz MA, Kane I, Buxbaum JN (1994) Genetic analysis of 9 unrelated patients with transthyretin (TTR)-cardiac amyloidosis: correlation of clinical and genetic findings and description of 2 new TTR variants. In: Kisilevsky R, Benson MD, Frangione B, Gauldie J, Muckle TJ, Young ID (eds) Amyloid and amyloidosis 1993. Parthenon Publishing, New York, pp 474-476
    • (1994) Amyloid and Amyloidosis 1993 , pp. 474-476
    • Jacobson, D.R.1    Gertz, M.A.2    Kane, I.3    Buxbaum, J.N.4
  • 10
    • 44949277138 scopus 로고
    • Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122)
    • Nichols WC, Liepnieks JJ, Snyder EL, Benson MD (1991) Senile cardiac amyloidosis associated with homozygosity for a transthyretin variant (ILE-122). J Lab Clin Med 117:175-180
    • (1991) J Lab Clin Med , vol.117 , pp. 175-180
    • Nichols, W.C.1    Liepnieks, J.J.2    Snyder, E.L.3    Benson, M.D.4
  • 11
    • 0028969996 scopus 로고
    • Transthyretin mutations in health and disease
    • Saraiva MJM (1995) Transthyretin mutations in health and disease. Hum Mutat 5:191-196
    • (1995) Hum Mutat , vol.5 , pp. 191-196
    • Saraiva, M.J.M.1
  • 14
    • 0021572408 scopus 로고
    • Cloning of human prealbumin complementary DNA: Localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy
    • Whitehead AS, Skinner M, Bruns GAP, Costello W, Edge MD, Cohen AS, Sipe JD (1984) Cloning of human prealbumin complementary DNA: localization of the gene to chromosome 18 and detection of a variant prealbumin allele in a family with familial amyloid polyneuropathy. Mol Biol Med 2:411-423
    • (1984) Mol Biol Med , vol.2 , pp. 411-423
    • Whitehead, A.S.1    Skinner, M.2    Bruns, G.A.P.3    Costello, W.4    Edge, M.D.5    Cohen, A.S.6    Sipe, J.D.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.