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Results: 1-24 |
Results: 24
HRG TOKUSHIMA - MOLECULAR AND CELLULAR CHARACTERIZATION OF HISTIDINE-RICH GLYCOPROTEIN (HRG) DEFICIENCY
Authors: SHIGEKIYO T YOSHIDA H MATSUMOTO K AZUMA H WAKABAYASHI S SAITO S FUJIKAWA K KOIDE T
Citation: T. Shigekiyo et al., HRG TOKUSHIMA - MOLECULAR AND CELLULAR CHARACTERIZATION OF HISTIDINE-RICH GLYCOPROTEIN (HRG) DEFICIENCY, Blood, 91(1), 1998, pp. 128-133
A CASE OF DERMATOMYOSITIS COMPLICATED BY THROMBOTIC THROMBOCYTOPENIC PURPURA
Authors: MIYAOKA Y URANO Y NAMEDA Y SHIGEKIYO T HORIE T SANO N ARASE S
Citation: Y. Miyaoka et al., A CASE OF DERMATOMYOSITIS COMPLICATED BY THROMBOTIC THROMBOCYTOPENIC PURPURA, Dermatology, 194(1), 1997, pp. 68-71
RADIOIMMUNOASSAY FOR THROMBIN RECEPTOR FRAGMENT (ARG27-ARG41)
Authors: MIYAMOTO K AZUMA H SHINTANI Y SHIGEKIYO T SAITO S
Citation: K. Miyamoto et al., RADIOIMMUNOASSAY FOR THROMBIN RECEPTOR FRAGMENT (ARG27-ARG41), Thrombosis and haemostasis, 1997, pp. 254-254
CONGENITAL HISTIDINE-RICH GLYCOPROTEIN (HRG) DEFICIENCY - A SINGLE MISSENSE MUTATION (G85E) IN EXON-3 OF THE HRG GENE
Authors: SHIGEKIYO T MATSUMOTO K AZUMA H WAKABAYASHI S SAITO S FUJIKAWA K KOIDE T
Citation: T. Shigekiyo et al., CONGENITAL HISTIDINE-RICH GLYCOPROTEIN (HRG) DEFICIENCY - A SINGLE MISSENSE MUTATION (G85E) IN EXON-3 OF THE HRG GENE, Thrombosis and haemostasis, 1997, pp. 602-602
AN IN-VITRO SYSTEM FOR IDENTIFYING AGENTS CAPABLE OF CHANGING SERUM-LIPOPROTEIN (A) CONCENTRATION BY REGULATING THE TRANSCRIPTIONAL ACTIVITY OF THE APOLIPOPROTEIN (A) GENE PROMOTER
Authors: WATANABE A AZUMA H YAMAGUCHI H MIYAMOTO K KANAGAWA Y SHIGEKIYO T SAITO S
Citation: A. Watanabe et al., AN IN-VITRO SYSTEM FOR IDENTIFYING AGENTS CAPABLE OF CHANGING SERUM-LIPOPROTEIN (A) CONCENTRATION BY REGULATING THE TRANSCRIPTIONAL ACTIVITY OF THE APOLIPOPROTEIN (A) GENE PROMOTER, Thrombosis and haemostasis, 1997, pp. 1334-1334
MOLECULAR PATHOGENESIS OF TYPE-I CONGENITAL PLASMINOGEN DEFICIENCY
Authors: AZUMA H YAMAGUCHI H KANAGAWA Y WATANABE A MIYAMOTO K SHIGEKIYO T SALTO S
Citation: H. Azuma et al., MOLECULAR PATHOGENESIS OF TYPE-I CONGENITAL PLASMINOGEN DEFICIENCY, Thrombosis and haemostasis, 1997, pp. 3050-3050
A NOVEL MISSENSE MUTATION IN THE ENDOGLIN GENE IN HEREDITARY HEMORRHAGIC TELANGIECTASIA
Authors: YAMAGUCHI H AZUMA H SHIGEKIYO T INOUE H SAITO S
Citation: H. Yamaguchi et al., A NOVEL MISSENSE MUTATION IN THE ENDOGLIN GENE IN HEREDITARY HEMORRHAGIC TELANGIECTASIA, Thrombosis and haemostasis, 77(2), 1997, pp. 243-247
MOLECULAR PATHOGENESIS OF TYPE-I CONGENITAL PLASMINOGEN DEFICIENCY - EXPRESSION OF RECOMBINANT HUMAN MUTANT PLASMINOGENS IN MAMMALIAN-CELLS
Authors: AZUMA H MIMA N SHIRAKAWA M MIYAMOTO K YAMAGUCHI H MITSUI T SHIGEKIYO T SAITO S
Citation: H. Azuma et al., MOLECULAR PATHOGENESIS OF TYPE-I CONGENITAL PLASMINOGEN DEFICIENCY - EXPRESSION OF RECOMBINANT HUMAN MUTANT PLASMINOGENS IN MAMMALIAN-CELLS, Blood, 89(1), 1997, pp. 183-190
INTERFERON ALPHA-2A THERAPY FOR DISSEMINATED INTRAVASCULAR COAGULATION IN A PATIENT WITH BLUE RUBBER BLEB NEVUS SYNDROME - A CASE-REPORT
Authors: KUNISHIGE M AZUMA H MASUDA K SHIGEKIYO T ARII Y KAWAI H SAITO S
Citation: M. Kunishige et al., INTERFERON ALPHA-2A THERAPY FOR DISSEMINATED INTRAVASCULAR COAGULATION IN A PATIENT WITH BLUE RUBBER BLEB NEVUS SYNDROME - A CASE-REPORT, Angiology, 48(3), 1997, pp. 273-277
EFFECT OF INDOMETHACIN FARNESIL, A PRODRUG OF INDOMETHACIN, ON PLATELET-AGGREGATION IN HUMANS
Authors: SHIGEKIYO T SHIRAKAWA M KANAZUKA M MIYAMOTO K MIMA N AZUMA H SAITO S
Citation: T. Shigekiyo et al., EFFECT OF INDOMETHACIN FARNESIL, A PRODRUG OF INDOMETHACIN, ON PLATELET-AGGREGATION IN HUMANS, Clinical drug investigation, 11(2), 1996, pp. 114-116
A NOVEL MISSENSE MUTATION IN 2 FAMILIES WITH CONGENITAL PLASMINOGEN DEFICIENCY - IDENTIFICATION OF AN ALA(675) TO THR(675) SUBSTITUTION
Authors: MIMA N AZUMA H SHIGEKIYO T SAITO S
Citation: N. Mima et al., A NOVEL MISSENSE MUTATION IN 2 FAMILIES WITH CONGENITAL PLASMINOGEN DEFICIENCY - IDENTIFICATION OF AN ALA(675) TO THR(675) SUBSTITUTION, Thrombosis and haemostasis, 75(1), 1996, pp. 96-100
INCREASE IN PLASMA THROMBOMODULIN LEVEL IN PATIENTS WITH VIBRATION SYNDROME
Authors: KANAZUKA M SHIGEKIYO T TOIBANA N SAITO S
Citation: M. Kanazuka et al., INCREASE IN PLASMA THROMBOMODULIN LEVEL IN PATIENTS WITH VIBRATION SYNDROME, Thrombosis research, 82(1), 1996, pp. 51-56
AN IN-VITRO SYSTEM FOR IDENTIFYING AGENTS CAPABLE OF CHANGING SERUM LIPOPROTEIN(A) CONCENTRATION BY REGULATING THE TRANSCRIPTIONAL ACTIVITYOF THE APOLIPOPROTEIN(A) GENE PROMOTER
Authors: AZUMA H YAMAGUCHI H MIMA N SHIRAKAWA M MIYAMOTO K KANAGAWA Y WATANABE A SHIGEKIYO T SAITO S
Citation: H. Azuma et al., AN IN-VITRO SYSTEM FOR IDENTIFYING AGENTS CAPABLE OF CHANGING SERUM LIPOPROTEIN(A) CONCENTRATION BY REGULATING THE TRANSCRIPTIONAL ACTIVITYOF THE APOLIPOPROTEIN(A) GENE PROMOTER, Biochemical and biophysical research communications, 227(2), 1996, pp. 570-575
TAKAYASUS-ARTERITIS ASSOCIATED WITH ANTIPHOSPHOLIPID ANTIBODIES - REPORT OF 2 CASES
Authors: YOKOI K HOSOI E AKAIKE M SHIGEKIYO T SAITO S
Citation: K. Yokoi et al., TAKAYASUS-ARTERITIS ASSOCIATED WITH ANTIPHOSPHOLIPID ANTIBODIES - REPORT OF 2 CASES, Angiology, 47(3), 1996, pp. 315-319
CONGENITAL DEFICIENCY OF HISTIDINE-RICH GLYCOPROTEIN - FAILURE TO IDENTIFY ABNORMALITIES IN ROUTINE LABORATORY ASSAYS OF HEMOSTATIC FUNCTION, IMMUNOLOGICAL FUNCTION AND TRACE-ELEMENTS
Authors: SHIGEKIYO T KANAZUKA M AZUMA H OSHIMA T KUSAKA K SAITO S
Citation: T. Shigekiyo et al., CONGENITAL DEFICIENCY OF HISTIDINE-RICH GLYCOPROTEIN - FAILURE TO IDENTIFY ABNORMALITIES IN ROUTINE LABORATORY ASSAYS OF HEMOSTATIC FUNCTION, IMMUNOLOGICAL FUNCTION AND TRACE-ELEMENTS, The Journal of laboratory and clinical medicine, 125(6), 1995, pp. 719-723
FAMILIAL OCCURRENCE OF 2 PATIENTS WITH MALIGNANT RHEUMATOID-ARTHRITIS
Authors: YOKOI K HOSOI E NAKANISHI M UMEMOTO K SHIGEKIYO T SAITO S
Citation: K. Yokoi et al., FAMILIAL OCCURRENCE OF 2 PATIENTS WITH MALIGNANT RHEUMATOID-ARTHRITIS, Journal of internal medicine, 236(4), 1994, pp. 469-472
PROTEIN-S TOKUSHIMA - ABNORMAL-MOLECULE WITH A SUBSTITUTION OF GLU FOR LYS-155 IN THE 2ND EPIDERMAL GROWTH FACTOR-LIKE DOMAIN OF PROTEIN-S
Authors: HAYASHI T NISHIOKA J SHIGEKIYO T SAITO S SUZUKI K
Citation: T. Hayashi et al., PROTEIN-S TOKUSHIMA - ABNORMAL-MOLECULE WITH A SUBSTITUTION OF GLU FOR LYS-155 IN THE 2ND EPIDERMAL GROWTH FACTOR-LIKE DOMAIN OF PROTEIN-S, Blood, 83(3), 1994, pp. 683-690
PROTEIN-S TOKUSHIMA - AN ABNORMAL PROTEIN-S FOUND IN A JAPANESE FAMILY WITH THROMBOSIS
Authors: SHIGEKIYO T UNO Y KAWAUCHI S SAITO S HONDO H NISHIOKA J HAYASHI T SUZUKI K
Citation: T. Shigekiyo et al., PROTEIN-S TOKUSHIMA - AN ABNORMAL PROTEIN-S FOUND IN A JAPANESE FAMILY WITH THROMBOSIS, Thrombosis and haemostasis, 70(2), 1993, pp. 244-246
CONGENITAL HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY
Authors: SHIGEKIYO T OHSHIMA T OKA H TOMONARI A AZUMA H SAITO S
Citation: T. Shigekiyo et al., CONGENITAL HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY, Thrombosis and haemostasis, 70(2), 1993, pp. 263-265
CONGENITAL PLASMINOGEN DEFICIENCY IN A FAMILY WITH THROMBOSIS CAUSED BY A SER-572 TO PRO MUTATION
Authors: AZUMA H MIMA N MIYAMOTO K KONDOH T TOYOTA K SHIGEKIYO T SAITO S
Citation: H. Azuma et al., CONGENITAL PLASMINOGEN DEFICIENCY IN A FAMILY WITH THROMBOSIS CAUSED BY A SER-572 TO PRO MUTATION, Thrombosis and haemostasis, 69(6), 1993, pp. 575-575
PROTEIN-S TOKUSHIMA - ABNORMAL-MOLECULE WITH A SUBSTITUTION OF GLU FOR LYS-155 IN THE 2ND EPIDERMAL GROWTH-FACTOR-LIKE DOMAIN OF PROTEIN-S
Authors: HAYASHI T NISHIOKA J SHIGEKIYO T SAITO S SUZUKI K
Citation: T. Hayashi et al., PROTEIN-S TOKUSHIMA - ABNORMAL-MOLECULE WITH A SUBSTITUTION OF GLU FOR LYS-155 IN THE 2ND EPIDERMAL GROWTH-FACTOR-LIKE DOMAIN OF PROTEIN-S, Thrombosis and haemostasis, 69(6), 1993, pp. 1251-1251
CONGENITAL HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY ASSOCIATED WITH THROMBOSIS
Authors: SHIGEKIYO T OHSHIMA T OKA H TOMONARI A AZUMA H SAITO S
Citation: T. Shigekiyo et al., CONGENITAL HISTIDINE-RICH GLYCOPROTEIN DEFICIENCY ASSOCIATED WITH THROMBOSIS, Thrombosis and haemostasis, 69(6), 1993, pp. 1256-1256
SPONTANEOUS VERSUS SECONDARY THROMBOSIS IN CONGENITAL HETEROZYGOUS PLASMINOGEN DEFICIENCY - REBUTTAL
Authors: SHIGEKIYO T
Citation: T. Shigekiyo, SPONTANEOUS VERSUS SECONDARY THROMBOSIS IN CONGENITAL HETEROZYGOUS PLASMINOGEN DEFICIENCY - REBUTTAL, Thrombosis and haemostasis, 69(5), 1993, pp. 531-531
CONGENITAL PLASMINOGEN DEFICIENCY CAUSED BY A SER(572) TO PRO MUTATION
Authors: AZUMA H UNO Y SHIGEKIYO T SAITO S
Citation: H. Azuma et al., CONGENITAL PLASMINOGEN DEFICIENCY CAUSED BY A SER(572) TO PRO MUTATION, Blood, 82(2), 1993, pp. 475-480
Risultati: 1-24 |