Zobrazeno 1 - 10 of 41 pro vyhledávání: '"Toshiyuki Yanase"'
1
A High Level of Colony-Stimulating Activity in a Lung Cancer Patient with Extensive Leucocytosis, and the Establishment of a CSA Producing Cell Line (KONT)
Autor: Toshiyuki Yanase, Yoshiyuki Niho, Nobuhiro Kimura
Publikováno v: Scandinavian Journal of Haematology. 28:417-424
Colony-stimulating activity (CSA) was demonstrated in materials taken from a patient suffering from lung cancer associated with excessive leucocytosis. CSA was detected not only in his urine, serum and pleural effusion but also in the supernatant of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::341c1a9d57b6630850b0ef6efb5d417b
https://doi.org/10.1111/j.1600-0609.1982.tb00547.x
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5
Structure of cloned δ-globin genes from a normal subject and a patient with δ-thabssemia; sequence polymorphisms found in the δ-globin gene region of Japanese individuals
Autor: Eiji Matsunaga, Yasuyuki Takagi, Yoshiro Ohta, Takanori Nakamura, Toshiyuki Yanase, Takashi Imamura, Toshikazu Matsuo, Toshinobu Fujiyoshi, Akinori Kimura
Publikováno v: Nucleic Acids Research. 10:5725-5732
The delta-globin genes of a normal Japanese and a Japanese patient with homozygous delta-thalassemia were cloned, and the nucleotide sequence of a region including the gene was determined. Comparison of the nucleotide sequences of these two individua
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f62e7eecc9a9cca005e137bbad21c1b
https://doi.org/10.1093/nar/10.19.5725
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6
A new electrophoretic variant of hemoglobin (Ogi) in which a leucine residue is replaced by an arginine residue at position 34 of the α-chain
Autor: Taiji Imoto, Jun Sugihara, Ikuo Sumida, Toshikazu Matsuo, Takashi Imamura, Toshiyuki Yanase, Hidenori Yamada
Publikováno v: Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 701:45-48
Hemoglobin Ogi, in which an arginine is substituted for a leucine residue at position 34 of the alpha-chain, was detected in a Japanese family. Although slightly increased oxygen affinity is associated with this amino acid substitution in the alpha 1
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64b46facae789d85a3627ebcc597d0d
https://doi.org/10.1016/0167-4838(82)90310-7
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7
Regulation of N-Acetylneuraminic Acid Synthesis Following Injury and Partial Hepatectomy
Autor: Hiromi Ishibashi, Hideo Okubo, Toshiyuki Yanase, Katsunori Shibata
Publikováno v: Experimental Biology and Medicine. 155:152-156
SummaryChanges in hepatic UDP-GlcNAc 2'-epimerase specific activity and concentration of CMP-NANA were measured as a function of time following injury and partial hepatectomy. Injured rats exhibited an increase in the enzyme specific activity at 24 h
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d4063406a65997ca3efb484bca89b3
https://doi.org/10.3181/00379727-155-39763
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8
Beta-thalassemia Intermedia From Two Japanese Families
Autor: Kiyohide Nunoi, Jun Sasaki, Katsunori Shibata, Kotaro Yamaoka, Takashi Imamura, Toshiyuki Yanase
Publikováno v: Japanese Journal of Medicine. 16:375-382
Two cases of heterozygous β-thalassemia with unusually severe anemia and hepatosplenomegaly are described. Their Hb A2 and Hb F levels were shown to be in the range of the typical β-thalassemia trait. Bone marrow examinations showed marked erythroi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::66eb261b5cabfc3aebe1082399959c47
https://doi.org/10.2169/internalmedicine1962.16.375
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9
Frequency and Distribution of Structural Variants of Hemoglobin and Thalassemic States in Western Japan
Autor: Toshikazu Matsuo, Jun Sugihara, I. Sunrida, Toshiyuki Yanase, Kotaro Yamaoka, Toru Maruyama, Yoshiro Ohta, Takashi Imamura
Publikováno v: Hemoglobin. 4:409-415
Hemolysates from 100,000 people who visited the Kyushu University Hospital and affiliated hospitals during the past 15 years were screened for hemoglobinopathies using electrophoresis on thin-layer starch gel; those exhibiting an abnormality were cha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c0387e47ff1985e6a85b0e82c503dfb
https://doi.org/10.3109/03630268008996221
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10
Hereditary spherocytosis associated with a variant of band 3 protein in the erythrocyte membrane
Autor: Toshikazu Matsuo, Toshiyuki Yanase, Shunjiro Kagiyama, Takashi Imamura
Publikováno v: Japanese Journal of Medicine. 23:216-219
A 17-year-old woman with hereditary spherocytosis was found to be heterozygous for an unusual variant of the band 3 protein in erythrocyte membranes. The variant had a molecular weight of 95, 000 daltons which was larger by about 3, 000 daltons than
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a67cb90959a3b68d2d086e2f250b511
https://doi.org/10.2169/internalmedicine1962.23.216
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