메뉴 건너뛰기




Volumn 20, Issue 2, 1999, Pages 153-158

Brain uptake of iodinated l-meta-tyrosine, a metabolically stable amino acid derivative

Author keywords

[No Author keywords available]

Indexed keywords

IODINE 123; IODINE 125; META TYROSINE;

EID: 0032922963     PISSN: 01433636     EISSN: 14735628     Source Type: Journal    
DOI: 10.1097/00006231-199902000-00007     Document Type: Article
Times cited : (7)

References (12)
  • 1
    • 0019512445 scopus 로고
    • Biopterin in human brain and urine from controls and parkinsonian patients: Application of a new radioimmunoassay
    • Nagatsu T, Yamaguchi T, Kato T et al. Biopterin in human brain and urine from controls and parkinsonian patients: Application of a new radioimmunoassay. Clin Chim Acta 1981; 109: 305-311.
    • (1981) Clin Chim Acta , vol.109 , pp. 305-311
    • Nagatsu, T.1    Yamaguchi, T.2    Kato, T.3
  • 2
    • 0023588252 scopus 로고
    • Decreased tyrosine transport in fibroblast from schizophrenic patients
    • Hagenfeldt L, Venizelos N, Bjerkenstedt L, Wiesel FA. Decreased tyrosine transport in fibroblast from schizophrenic patients. Life Sci 1987; 41: 2749-2757.
    • (1987) Life Sci , vol.41 , pp. 2749-2757
    • Hagenfeldt, L.1    Venizelos, N.2    Bjerkenstedt, L.3    Wiesel, F.A.4
  • 3
    • 0025829583 scopus 로고
    • A strategy for the study of cerebral amino acid transport using iodine-123-labeled amino acid radiopharmaceutical: 3-iodo-alpha-methyl-L-tyrosine
    • Kawai K, Fujibayashi Y, Saji H et al. A strategy for the study of cerebral amino acid transport using iodine-123-labeled amino acid radiopharmaceutical: 3-iodo-alpha-methyl-L-tyrosine. J Nucl Med 1991; 32: 819-824.
    • (1991) J Nucl Med , vol.32 , pp. 819-824
    • Kawai, K.1    Fujibayashi, Y.2    Saji, H.3
  • 4
    • 44949266593 scopus 로고
    • Monoiodo-D-Tyrosine, an artificial amino acid radiopharmaceutical for selective measurement of membrane amino acid transport in the pancreas
    • Kawai K, Fujibayashi Y, Saji H, Konishi J, Kubodera A, Yokoyama A. Monoiodo-D-Tyrosine, an artificial amino acid radiopharmaceutical for selective measurement of membrane amino acid transport in the pancreas. Nucl Med Biol 1990; 17: 369-376.
    • (1990) Nucl Med Biol , vol.17 , pp. 369-376
    • Kawai, K.1    Fujibayashi, Y.2    Saji, H.3    Konishi, J.4    Kubodera, A.5    Yokoyama, A.6
  • 5
    • 0026761454 scopus 로고
    • An artificial amino acid radiopharmaceutical for single photon emission computed tomographic study of pancreatic amino acid transports: 123I-3-iodo-alpha-methyl-L-tyrosine
    • Kawai K, Fujibayashi Y, Yonekura Y et al. An artificial amino acid radiopharmaceutical for single photon emission computed tomographic study of pancreatic amino acid transports: 123I-3-iodo-alpha-methyl-L-tyrosine. Ann Nucl Med 1992; 6: 169-175.
    • (1992) Ann Nucl Med , vol.6 , pp. 169-175
    • Kawai, K.1    Fujibayashi, Y.2    Yonekura, Y.3
  • 6
    • 0029888884 scopus 로고    scopus 로고
    • Synthesis and evaluation of radioiodinated 6-iodo-L-DOPA as a cerebral L-amino acid transport marker
    • Kawai K, Ohta H, Kubodera A, Channing A, Eckelman WC. Synthesis and evaluation of radioiodinated 6-iodo-L-DOPA as a cerebral L-amino acid transport marker. Nucl Med Biol 1996; 23: 251-255.
    • (1996) Nucl Med Biol , vol.23 , pp. 251-255
    • Kawai, K.1    Ohta, H.2    Kubodera, A.3    Channing, A.4    Eckelman, W.C.5
  • 7
    • 0001308227 scopus 로고
    • Substrate specificity of steady-state amino acid transport in mouse brain slices
    • Blasberg R, Lajtha A. Substrate specificity of steady-state amino acid transport in mouse brain slices. Arch Biochem Biophys 1965; 112: 361-377.
    • (1965) Arch Biochem Biophys , vol.112 , pp. 361-377
    • Blasberg, R.1    Lajtha, A.2
  • 8
    • 0025127396 scopus 로고
    • Synthesis of L-6-[1231]iodo-m-tyrosine, a potential SPECT brain imaging agent
    • Adams MJ, Ponce YZ, Berry JM. Synthesis of L-6-[1231]iodo-m-tyrosine, a potential SPECT brain imaging agent. J Labelled Compds Radiopharm 1989; 28: 1065-1072.
    • (1989) J Labelled Compds Radiopharm , vol.28 , pp. 1065-1072
    • Adams, M.J.1    Ponce, Y.Z.2    Berry, J.M.3
  • 9
    • 0015183409 scopus 로고
    • Studies on the metabolism of D-and L-isomers of 3, 4-dihydroxyphenylalanine (DOPA). I. Autoradiographic study on the distribution of 14C-labeled D-and l-DOPA and dopamine after intravenous administration in rats
    • Shindo H, Miyakoshi N, Takahashi I. Studies on the metabolism of D-and L-isomers of 3, 4-dihydroxyphenylalanine (DOPA). I. Autoradiographic study on the distribution of 14C-labeled D-and l-DOPA and dopamine after intravenous administration in rats. Chem Pharm Bull 1971; 19: 2490-2500.
    • (1971) Chem Pharm Bull , vol.19 , pp. 2490-2500
    • Shindo, H.1    Miyakoshi, N.2    Takahashi, I.3
  • 10
    • 0017410888 scopus 로고
    • Incorporation pattern of L-, D-, and DL-amino acids into the pancreas of mice
    • Goto R, Tezuka M, Tamemasa O. Incorporation pattern of L-, D-, and DL-amino acids into the pancreas of mice. Chem Pharm Bull 1977; 25: 1574-1581.
    • (1977) Chem Pharm Bull , vol.25 , pp. 1574-1581
    • Goto, R.1    Tezuka, M.2    Tamemasa, O.3
  • 11
    • 0013510464 scopus 로고
    • The metabolism of iodotyrosine. I. The fate of mono-and di-iodotyrosine in normal subjects and in patients with various diseases
    • Stanbury JB, Kassenaar A AH, Meijer JWA. The metabolism of iodotyrosine. I. The fate of mono-and di-iodotyrosine in normal subjects and in patients with various diseases. J Clin Endocrinol Metab 1956; 25: 1574-1581.
    • (1956) J Clin Endocrinol Metab , vol.25 , pp. 1574-1581
    • Stanbury, J.B.1    Kassenaar, A.2    Meijer, J.W.A.3
  • 12
    • 0020656758 scopus 로고
    • A new perfusion imaging agent: [I-123]HIPDM: N, JV, N’-trimethyl-N’-[2-hydroxy-3-methyl-5-iodobenzyl]-l,3-propanediamine
    • Kung HF, Tramposch KM, Blau M. A new perfusion imaging agent: [I-123]HIPDM: N, JV, N’-trimethyl-N’-[2-hydroxy-3-methyl-5-iodobenzyl]-l,3-propanediamine. J Nucl Med 1983; 24: 66-72.
    • (1983) J Nucl Med , vol.24 , pp. 66-72
    • Kung, H.F.1    Tramposch, K.M.2    Blau, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.