메뉴 건너뛰기




Volumn 29, Issue 8, 2008, Pages 1007-1016

Mutations and polymorphisms of the gene of the major human blood protein, serum albumin

Author keywords

ALB; Analbuminemia; Bisalbuminemia; Genetic variant; Human; Ligand binding; Serum albumin; Stability

Indexed keywords

LIOTHYRONINE; THYROXINE;

EID: 49149111627     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20754     Document Type: Review
Times cited : (60)

References (106)
  • 1
    • 0019774392 scopus 로고
    • Proalbumin Lille, a new variant of human serum albumin
    • Abdo Y, Rousseaux J, Dautrevaux M. 1981. Proalbumin Lille, a new variant of human serum albumin. FEBS Lett 131:286-288.
    • (1981) FEBS Lett , vol.131 , pp. 286-288
    • Abdo, Y.1    Rousseaux, J.2    Dautrevaux, M.3
  • 2
    • 36649020460 scopus 로고    scopus 로고
    • A receptor-mediated mechanism to support clinical observations of altered albumin variants [Letter]
    • Andersen JT, Sandlie I. 2007. A receptor-mediated mechanism to support clinical observations of altered albumin variants [Letter]. Clin Chem 53:2216.
    • (2007) Clin Chem , vol.53 , pp. 2216
    • Andersen, J.T.1    Sandlie, I.2
  • 4
    • 0041523005 scopus 로고
    • Identical structural changes in inherited albumin variants from different populations
    • Arai K, Ishioka N, Huss K, Madison J, Putnam FW. 1989b. Identical structural changes in inherited albumin variants from different populations. Proc Natl Acad Sci USA 86:434-438.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 434-438
    • Arai, K.1    Ishioka, N.2    Huss, K.3    Madison, J.4    Putnam, F.W.5
  • 7
    • 0000511633 scopus 로고
    • Uber einen Fall von kompletter Analbuminaemie ohne wesentliche klinische Krankheitszichen.
    • Bennhold H, Peters H, Roth E. 1954. Uber einen Fall von kompletter Analbuminaemie ohne wesentliche klinische Krankheitszichen. Verh Dtsch Ges Inn Med 60:630-634.
    • (1954) Verh Dtsch Ges Inn Med , vol.60 , pp. 630-634
    • Bennhold, H.1    Peters, H.2    Roth, E.3
  • 9
    • 0018119379 scopus 로고
    • A circulating variant of human proalbumin
    • Brennan SO, Carrell RW. 1978. A circulating variant of human proalbumin. Nature 274:908-909.
    • (1978) Nature , vol.274 , pp. 908-909
    • Brennan, S.O.1    Carrell, R.W.2
  • 10
    • 0018841041 scopus 로고
    • Functional abnormality of proalbumin Christchurch
    • Brennan SO, Carrell RW 1980. Functional abnormality of proalbumin Christchurch. Biochim Biophys Acta 621:83-88.
    • (1980) Biochim Biophys Acta , vol.621 , pp. 83-88
    • Brennan, S.O.1    Carrell, R.W.2
  • 11
    • 0021797284 scopus 로고
    • The molecular abnormality of albumin Parklands: 365 Asp → His
    • Brennan SO. 1985. The molecular abnormality of albumin Parklands: 365 Asp → His. Biochim Biophys Acta 830:320-324.
    • (1985) Biochim Biophys Acta , vol.830 , pp. 320-324
    • Brennan, S.O.1
  • 12
    • 0023139815 scopus 로고
    • Albumin Canterbury (313 Lys → Asn). A point mutation in the second domain of serum albumin
    • Brennan SO, Herbert P. 1987. Albumin Canterbury (313 Lys → Asn). A point mutation in the second domain of serum albumin. Biochim Biophys Acta 912:191-197.
    • (1987) Biochim Biophys Acta , vol.912 , pp. 191-197
    • Brennan, S.O.1    Herbert, P.2
  • 13
    • 0024455745 scopus 로고
    • Novel human proalbumin variant with intact dibasic sequence facilitates identification of its converting enzyme
    • Brennan SO, Peach RJ, Boswell DR. 1989. Novel human proalbumin variant with intact dibasic sequence facilitates identification of its converting enzyme. Biochim Biophys Acta 993:48-50.
    • (1989) Biochim Biophys Acta , vol.993 , pp. 48-50
    • Brennan, S.O.1    Peach, R.J.2    Boswell, D.R.3
  • 15
    • 0025058468 scopus 로고
    • Albumin Redhill (-1 Arg, 320 Ala → Thr): A glycoprotein variant of human serum albumin whose precursor has an aberrant signal peptidase cleavage site
    • Brennan SO, Myles T, Peach RJ, Donaldson D, George PM. 1990b. Albumin Redhill (-1 Arg, 320 Ala → Thr): a glycoprotein variant of human serum albumin whose precursor has an aberrant signal peptidase cleavage site. Proc Natl Acad Sci USA 87:26-30.
    • (1990) Proc Natl Acad Sci USA , vol.87 , pp. 26-30
    • Brennan, S.O.1    Myles, T.2    Peach, R.J.3    Donaldson, D.4    George, P.M.5
  • 16
    • 0027288476 scopus 로고
    • Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177
    • Brennan SO, Fellowes AR 1993. Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177. Biochim Biophys Acta 1182:46-50.
    • (1993) Biochim Biophys Acta , vol.1182 , pp. 46-50
    • Brennan, S.O.1    Fellowes, A.R.2
  • 17
    • 0032805082 scopus 로고    scopus 로고
    • Albumin Banks Peninsula: A new termination variant characterised by electrospray mass spectrometry
    • Brennan SO, Fellowes AP, George PM. 1999. Albumin Banks Peninsula: a new termination variant characterised by electrospray mass spectrometry. Biochim Biophys Acta 1433:321-326.
    • (1999) Biochim Biophys Acta , vol.1433 , pp. 321-326
    • Brennan, S.O.1    Fellowes, A.P.2    George, P.M.3
  • 25
    • 33745728414 scopus 로고    scopus 로고
    • A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes I: General principles and overview
    • Chen JM, Ferec C, Cooper DN. 2006. A systematic analysis of disease-associated variants in the 3′ regulatory regions of human protein-coding genes I: general principles and overview. Hum Gen 120:303-333.
    • (2006) Hum Gen , vol.120 , pp. 303-333
    • Chen, J.M.1    Ferec, C.2    Cooper, D.N.3
  • 26
    • 0032539531 scopus 로고    scopus 로고
    • Albumin Church Bay: 560 Lys → Glu a new mutation detected by electrospray ionisation mass spectrometry
    • Chua EK, Brennan SO, George PM. 1998. Albumin Church Bay: 560 Lys → Glu a new mutation detected by electrospray ionisation mass spectrometry. Biochim Biophys Acta 1382:305-310.
    • (1998) Biochim Biophys Acta , vol.1382 , pp. 305-310
    • Chua, E.K.1    Brennan, S.O.2    George, P.M.3
  • 27
    • 33645579094 scopus 로고    scopus 로고
    • An intronic mutation within FGB (IVS1 + 2076 a → g) is associated with afibrinogenemia and recurrent transient ischemic attacks
    • Dear A, Daly J, Brennan SO, Tuckfield A, George PM. 2006. An intronic mutation within FGB (IVS1 + 2076 a → g) is associated with afibrinogenemia and recurrent transient ischemic attacks. J Thromb Haemost 4:471-472.
    • (2006) J Thromb Haemost , vol.4 , pp. 471-472
    • Dear, A.1    Daly, J.2    Brennan, S.O.3    Tuckfield, A.4    George, P.M.5
  • 30
    • 0020384678 scopus 로고
    • Characterization of zinc-binding proteins of plasma in familial hyperzincemia
    • Failla ML, van de Veerdonk M, Morgan WT, Smith JC, Jr. 1982. Characterization of zinc-binding proteins of plasma in familial hyperzincemia. J Lab Clin Med 100:943-952.
    • (1982) J Lab Clin Med , vol.100 , pp. 943-952
    • Failla, M.L.1    van de Veerdonk, M.2    Morgan, W.T.3    Smith Jr., J.C.4
  • 39
    • 0029093858 scopus 로고
    • Genetic variants of human serum albumin: Molecular defects and biological stability
    • Galliano M, Rossi A, Porta F, Minchiotti L. 1995. Genetic variants of human serum albumin: molecular defects and biological stability. Int J Clin Pharmacol Res 15:45-55.
    • (1995) Int J Clin Pharmacol Res , vol.15 , pp. 45-55
    • Galliano, M.1    Rossi, A.2    Porta, F.3    Minchiotti, L.4
  • 40
  • 44
    • 0026664548 scopus 로고
    • Atomic structure and chemistry of human serum albumin
    • He XM, Carter DC. 1992. Atomic structure and chemistry of human serum albumin. Nature 358:209-215.
    • (1992) Nature , vol.358 , pp. 209-215
    • He, X.M.1    Carter, D.C.2
  • 46
    • 0022366361 scopus 로고
    • The N-terminal sequence of albumin Redhill, a variant of human serum albumin
    • Hutchinson DW, Matejtschuk E 1985. The N-terminal sequence of albumin Redhill, a variant of human serum albumin. FEBS Lett 193:211-212.
    • (1985) FEBS Lett , vol.193 , pp. 211-212
    • Hutchinson, D.W.1    Matejtschuk, E.2
  • 47
    • 0021926611 scopus 로고
    • Localization of the amino acid substitution site in a fast migrating variant of human serum albumin
    • Iadarola P, Minchiotti L, Galliano M. 1985. Localization of the amino acid substitution site in a fast migrating variant of human serum albumin. FEBS Lett 180:85-88.
    • (1985) FEBS Lett , vol.180 , pp. 85-88
    • Iadarola, P.1    Minchiotti, L.2    Galliano, M.3
  • 49
    • 33847165024 scopus 로고    scopus 로고
    • S-Nitrosylation of human variant albumin Liprizzi (R410C) confers potent antibacterial and cytoprotective properties
    • Ishima Y, Sawa T, Kragh-Hansen U, Miyamoto Y, Matsushita S, Akaike T, Otagiri M. 2007. S-Nitrosylation of human variant albumin Liprizzi (R410C) confers potent antibacterial and cytoprotective properties. J Pharmacol Exp Ther 320:969-977.
    • (2007) J Pharmacol Exp Ther , vol.320 , pp. 969-977
    • Ishima, Y.1    Sawa, T.2    Kragh-Hansen, U.3    Miyamoto, Y.4    Matsushita, S.5    Akaike, T.6    Otagiri, M.7
  • 50
    • 0011780172 scopus 로고
    • Die Doppel-albuminaemie, eine neue erbliche Proteinanomalie.
    • Knedel M. 1957. Die Doppel-albuminaemie, eine neue erbliche Proteinanomalie. Blut 3:129-131.
    • (1957) Blut , vol.3 , pp. 129-131
    • Knedel, M.1
  • 51
    • 0025157284 scopus 로고
    • Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations
    • Kragh-Hansen U, Brennan SO, Galliano M, Sugita O. 1990a. Binding of warfarin, salicylate, and diazepam to genetic variants of human serum albumin with known mutations. Mol Pharmacol 37:238-242.
    • (1990) Mol Pharmacol , vol.37 , pp. 238-242
    • Kragh-Hansen, U.1    Brennan, S.O.2    Galliano, M.3    Sugita, O.4
  • 55
    • 0035956278 scopus 로고    scopus 로고
    • The glycan structure of albumin Redhill, a glycosylated variant of human serum albumin
    • Kragh-Hansen U, Donaldson D, Jensen PH. 2001. The glycan structure of albumin Redhill, a glycosylated variant of human serum albumin. Biochim Biophys Acta 1550:20-26.
    • (2001) Biochim Biophys Acta , vol.1550 , pp. 20-26
    • Kragh-Hansen, U.1    Donaldson, D.2    Jensen, P.H.3
  • 58
    • 33749254842 scopus 로고    scopus 로고
    • Chain length-dependent binding of fatty acid anions to human serum albumin studied by site-directed mutagenesis
    • Kragh-Hansen U, Watanabe H, Nakajou K, Iwao Y, Otagiri M. 2006. Chain length-dependent binding of fatty acid anions to human serum albumin studied by site-directed mutagenesis. J Mol Biol 363:702-712.
    • (2006) J Mol Biol , vol.363 , pp. 702-712
    • Kragh-Hansen, U.1    Watanabe, H.2    Nakajou, K.3    Iwao, Y.4    Otagiri, M.5
  • 59
    • 0021748272 scopus 로고
    • Bilirubin binding by variant albumins in Yanomama Indians
    • Lorey FW, Ahlfors CE, Smith DG, Neel JV. 1984. Bilirubin binding by variant albumins in Yanomama Indians. Am J Hum Genet 36:1112-1120.
    • (1984) Am J Hum Genet , vol.36 , pp. 1112-1120
    • Lorey, F.W.1    Ahlfors, C.E.2    Smith, D.G.3    Neel, J.V.4
  • 62
    • 0022762133 scopus 로고
    • Structure and properties of albumin Tokushima and its proteolytic processing by cathepsin B in vitro
    • Matsuda Y, Ogushi F, Ogawa K, Katunuma N. 1986. Structure and properties of albumin Tokushima and its proteolytic processing by cathepsin B in vitro. J Biochem 100:375-379.
    • (1986) J Biochem , vol.100 , pp. 375-379
    • Matsuda, Y.1    Ogushi, F.2    Ogawa, K.3    Katunuma, N.4
  • 66
    • 0026506728 scopus 로고
    • Two alloalbumins with identical electrophoretic mobility are produced by differently charged amino acid substitutions
    • Minchiotti L, Galliano M, Stoppini M, Ferri G, Crespeau H, Rochu D, Porta F. 1992. Two alloalbumins with identical electrophoretic mobility are produced by differently charged amino acid substitutions. Biochim Biophys Acta 1119:232-238.
    • (1992) Biochim Biophys Acta , vol.1119 , pp. 232-238
    • Minchiotti, L.1    Galliano, M.2    Stoppini, M.3    Ferri, G.4    Crespeau, H.5    Rochu, D.6    Porta, F.7
  • 67
    • 0027210458 scopus 로고
    • The structural characterization and bilirubin-binding properties of albumin Herborn, a (Lys240 → Glu) albumin mutant
    • Minchiotti L, Galliano M, Zapponi MC, Tenni R. 1993. The structural characterization and bilirubin-binding properties of albumin Herborn, a (Lys240 → Glu) albumin mutant. Eur J Biochem 214: 437-444.
    • (1993) Eur J Biochem , vol.214 , pp. 437-444
    • Minchiotti, L.1    Galliano, M.2    Zapponi, M.C.3    Tenni, R.4
  • 68
    • 0028897148 scopus 로고
    • A genetic variant of albumin (albumin Asola; TyrHO → Cys) with no free -SH group but with an additional disulfide bridge
    • Minchiotti L, Galliano M, Kragh-Hansen U, Watkins S, Madison J, Putnam FW 1995. A genetic variant of albumin (albumin Asola; TyrHO → Cys) with no free -SH group but with an additional disulfide bridge. Eur J Biochem 228:155-159.
    • (1995) Eur J Biochem , vol.228 , pp. 155-159
    • Minchiotti, L.1    Galliano, M.2    Kragh-Hansen, U.3    Watkins, S.4    Madison, J.5    Putnam, F.W.6
  • 70
    • 0032961853 scopus 로고    scopus 로고
    • Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin
    • Minchiotti L, Kragh-Hansen U, Nielsen H, Hardy E, Mercier AY, Galliano M. 1999. Structural characterization, stability and fatty acid-binding properties of two French genetic variants of human serum albumin. Biochim Biophys Acta 1431:223-231.
    • (1999) Biochim Biophys Acta , vol.1431 , pp. 223-231
    • Minchiotti, L.1    Kragh-Hansen, U.2    Nielsen, H.3    Hardy, E.4    Mercier, A.Y.5    Galliano, M.6
  • 74
    • 34250929445 scopus 로고
    • Uber das erbliche Augtreten einer Albuminspaltung im Elektrophoresediagramm.
    • Nennstiel HJ, Becht T. 1957. Uber das erbliche Augtreten einer Albuminspaltung im Elektrophoresediagramm. Klin Wochenschr 35:689.
    • (1957) Klin Wochenschr , vol.35 , pp. 689
    • Nennstiel, H.J.1    Becht, T.2
  • 76
    • 8344260789 scopus 로고
    • Su di un caso di analbuminemia congenita (Ital.).
    • Papi N, Castiglioni A, Reale A. 1983. Su di un caso di analbuminemia congenita (Ital.). Riv Ital Pediatr 9:85-87.
    • (1983) Riv Ital Pediatr , vol.9 , pp. 85-87
    • Papi, N.1    Castiglioni, A.2    Reale, A.3
  • 77
    • 0025775608 scopus 로고
    • Structural characterization of a glycoprotein variant of human serum albumin: Albumin Casebrook (494 Asp → Asn)
    • Peach RJ, Brennan SO. 1991. Structural characterization of a glycoprotein variant of human serum albumin: albumin Casebrook (494 Asp → Asn). Biochim Biophys Acta 1097:49-54.
    • (1991) Biochim Biophys Acta , vol.1097 , pp. 49-54
    • Peach, R.J.1    Brennan, S.O.2
  • 78
    • 0026701954 scopus 로고
    • Albumin Rugby Park: A truncated albumin variant caused by a G → C splice-site mutation in intron 13
    • Peach RJ, Fellowes AP, Brennan SO, George PM. 1992. Albumin Rugby Park: a truncated albumin variant caused by a G → C splice-site mutation in intron 13. Biochim Biophys Acta 1180:107-110.
    • (1992) Biochim Biophys Acta , vol.1180 , pp. 107-110
    • Peach, R.J.1    Fellowes, A.P.2    Brennan, S.O.3    George, P.M.4
  • 80
    • 0028338869 scopus 로고
    • A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia
    • Petersen CE, Scottolini AG, Cody LR, Mandel M, Reimer N, Bhagavan NV. 1994. A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia. J Med Genet 31:355-359.
    • (1994) J Med Genet , vol.31 , pp. 355-359
    • Petersen, C.E.1    Scottolini, A.G.2    Cody, L.R.3    Mandel, M.4    Reimer, N.5    Bhagavan, N.V.6
  • 81
  • 82
    • 0033625049 scopus 로고    scopus 로고
    • Familial dysalbuminemic hyperthyroxinemia may result in altered warfarin pharmacokinetics
    • Petersen CE, Ha C-E, Harohalli K, Park DS, Bhagavan NV 2000. Familial dysalbuminemic hyperthyroxinemia may result in altered warfarin pharmacokinetics. Chem Biol Interact 124:161-172.
    • (2000) Chem Biol Interact , vol.124 , pp. 161-172
    • Petersen, C.E.1    Ha, C.-E.2    Harohalli, K.3    Park, D.S.4    Bhagavan, N.V.5
  • 83
    • 49149099839 scopus 로고
    • Le variazoni della sieroalbumina: Aspetti biologici e clinici.
    • Porta E 1983. Le variazoni della sieroalbumina: aspetti biologici e clinici. Federazione Medica 36:917-923.
    • (1983) Federazione Medica , vol.36 , pp. 917-923
    • Porta, E.1
  • 84
    • 49149108909 scopus 로고
    • Alloalbumine come marcatore genetico in Italia
    • Porta F, Galliano M, Rossi A. 1992. Alloalbumine come marcatore genetico in Italia. Boll Osp Varese 21:580-590.
    • (1992) Boll Osp Varese , vol.21 , pp. 580-590
    • Porta, F.1    Galliano, M.2    Rossi, A.3
  • 87
    • 0025363483 scopus 로고
    • Genetic characterization of an alloalbumin, albumin Kashmir, using gene amplification and allele-specific oligonucleotides
    • Savva D, Tárnoky AL, Vickers MF. 1990. Genetic characterization of an alloalbumin, albumin Kashmir, using gene amplification and allele-specific oligonucleotides. Biochem J 266:615-617.
    • (1990) Biochem J , vol.266 , pp. 615-617
    • Savva, D.1    Tárnoky, A.L.2    Vickers, M.F.3
  • 88
    • 0032559538 scopus 로고    scopus 로고
    • Genetic variation in human serum albumin: A 313 Lys → Asn mutation in Albumin Reading identified by PCR analysis
    • Savva D, Li B, Kragh-Hansen U, Galliano M, Minchiotti L, Tárnoky AL. 1998. Genetic variation in human serum albumin: a 313 Lys → Asn mutation in Albumin Reading identified by PCR analysis. Clin Chim Acta 270, 195-201.
    • (1998) Clin Chim Acta , vol.270 , pp. 195-201
    • Savva, D.1    Li, B.2    Kragh-Hansen, U.3    Galliano, M.4    Minchiotti, L.5    Tárnoky, A.L.6
  • 89
    • 0000421962 scopus 로고
    • Über Serumeiweissveranderungen beim Diabetes mellitus.
    • Scheurlen PG. 1955. Über Serumeiweissveranderungen beim Diabetes mellitus. Klin Wochenschr 33:198-205.
    • (1955) Klin Wochenschr , vol.33 , pp. 198-205
    • Scheurlen, P.G.1
  • 91
  • 92
    • 0028024140 scopus 로고
    • An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families
    • Sunthornthepvarakul T, Angkeow P, Weiss RE, Hayashi Y, Refetoff S. 1994. An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families. Biochem Biophys Res Commun 202:781-787.
    • (1994) Biochem Biophys Res Commun , vol.202 , pp. 781-787
    • Sunthornthepvarakul, T.1    Angkeow, P.2    Weiss, R.E.3    Hayashi, Y.4    Refetoff, S.5
  • 94
    • 0023220769 scopus 로고
    • Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning
    • Takahashi N, Takahashi Y, Blumberg BS, Putnam FW. 1987a. Amino acid substitutions in genetic variants of human serum albumin and in sequences inferred from molecular cloning. Proc Natl Acad Sci USA 84:4413-4417.
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 4413-4417
    • Takahashi, N.1    Takahashi, Y.2    Blumberg, B.S.3    Putnam, F.W.4
  • 96
    • 0023449817 scopus 로고
    • Structural changes and metal binding by prealbumins and other amino-terminal genetic variants of human serum albumin
    • Takahashi N, Takahashi Y, Putnam FW. 1987c. Structural changes and metal binding by prealbumins and other amino-terminal genetic variants of human serum albumin. Proc Natl Acad Sci USA 84:7403-7407.
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 7403-7407
    • Takahashi, N.1    Takahashi, Y.2    Putnam, F.W.3
  • 97
    • 0020620321 scopus 로고
    • Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes
    • Treisman R, Orkin SH, Maniatis T. 1983. Specific transcription and RNA splicing defects in five cloned beta-thalassaemia genes. Nature 302:591-596.
    • (1983) Nature , vol.302 , pp. 591-596
    • Treisman, R.1    Orkin, S.H.2    Maniatis, T.3
  • 98
    • 0026686834 scopus 로고
    • High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end
    • Vestberg K, Galliano M, Minchiotti L, Kragh-Hansen U. 1992. High-affinity binding of warfarin, salicylate and diazepam to natural mutants of human serum albumin modified in the C-terminal end. Biochem Pharmacol 44:1515-1521.
    • (1992) Biochem Pharmacol , vol.44 , pp. 1515-1521
    • Vestberg, K.1    Galliano, M.2    Minchiotti, L.3    Kragh-Hansen, U.4
  • 99
    • 0030920437 scopus 로고    scopus 로고
    • A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred
    • Wada N, Chiba H, Shimizu C, Kijima H, Kubo M, Koike T. 1997. A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred. J Clin Endocrinol Metab 82:3246-3250.
    • (1997) J Clin Endocrinol Metab , vol.82 , pp. 3246-3250
    • Wada, N.1    Chiba, H.2    Shimizu, C.3    Kijima, H.4    Kubo, M.5    Koike, T.6
  • 103
  • 104
    • 0015528056 scopus 로고
    • Amino acid substitution in two identical inherited human serum albumin variants: Albumin Oliphant and albumin Ann Arbor
    • Winter WP, Weitkamp LR, Rucknagel DL. 1972. Amino acid substitution in two identical inherited human serum albumin variants: albumin Oliphant and albumin Ann Arbor. Biochemistry 11:889-896.
    • (1972) Biochemistry , vol.11 , pp. 889-896
    • Winter, W.P.1    Weitkamp, L.R.2    Rucknagel, D.L.3
  • 105
    • 49149103759 scopus 로고
    • Albumindoppelzacken als vererbbere Bluteisweissanomalie
    • Wuhrmann F. 1959. Albumindoppelzacken als vererbbere Bluteisweissanomalie. Schweiz Med Wochenschr 89:150-152.
    • (1959) Schweiz Med Wochenschr , vol.89 , pp. 150-152
    • Wuhrmann, F.1
  • 106
    • 0027221812 scopus 로고
    • Protein and gene structure analysis of an albumin genetic variant: Proalbumin Wu Yang (-2 Arg → His)
    • Zan WC, Xu WF, Chi CW. 1993. Protein and gene structure analysis of an albumin genetic variant: Proalbumin Wu Yang (-2 Arg → His). Int J Pept Prot Res 41:441-446.
    • (1993) Int J Pept Prot Res , vol.41 , pp. 441-446
    • Zan, W.C.1    Xu, W.F.2    Chi, C.W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.