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Results: 1-8 |
Results: 8
HOMOZYGOUS MISSENSE MUTATION (BAND-3 FUKUOKA-G130R) - A MILD FORM OF HEREDITARY SPHEROCYTOSIS WITH NEAR-NORMAL BAND-3 CONTENT AND MINIMAL CHANGES OF MEMBRANE ULTRASTRUCTURE DESPITE MODERATE PROTEIN-4.2 DEFICIENCY
Authors: INOUE T KANZAKI A KAKU M YAWATA A TAKEZONO M OKAMOTO N WADA H SUGIHARA T YAMADA O KATAYAMA Y NAGATA N YAWATA Y
Citation: T. Inoue et al., HOMOZYGOUS MISSENSE MUTATION (BAND-3 FUKUOKA-G130R) - A MILD FORM OF HEREDITARY SPHEROCYTOSIS WITH NEAR-NORMAL BAND-3 CONTENT AND MINIMAL CHANGES OF MEMBRANE ULTRASTRUCTURE DESPITE MODERATE PROTEIN-4.2 DEFICIENCY, British Journal of Haematology, 102(4), 1998, pp. 932-939
PHENOTYPIC-EXPRESSION IN HEREDITARY SPHEROCYTOSIS AGGRAVATED BY COMBINED BAND-3 MUTATIONS (G714R, K56E AND P854L G130R)/
Authors: YAWATA Y YAWATA A KANZAKI A KAKU M TAKEZONO M INOUE T OKAMOTO N
Citation: Y. Yawata et al., PHENOTYPIC-EXPRESSION IN HEREDITARY SPHEROCYTOSIS AGGRAVATED BY COMBINED BAND-3 MUTATIONS (G714R, K56E AND P854L G130R)/, British Journal of Haematology, 102(1), 1998, pp. 303-303
MOLECULAR AND GENETIC-CHARACTERISTICS IN JAPANESE PATIENTS WITH HEREDITARY SPHEROCYTOSIS - FREQUENT BAND-3 MUTATIONS AND RARER ANKYRIN MUTATIONS
Authors: KANZAKI A TAKEZONO M KAKU M YAWATA A OZCAN R KUGLER W EBER SW YAWATA Y
Citation: A. Kanzaki et al., MOLECULAR AND GENETIC-CHARACTERISTICS IN JAPANESE PATIENTS WITH HEREDITARY SPHEROCYTOSIS - FREQUENT BAND-3 MUTATIONS AND RARER ANKYRIN MUTATIONS, Blood, 90(10), 1997, pp. 2709-2709
QUANTITATIVE ELECTRON-MICROSCOPY DEMONSTRATES AN EXCELLENT CORRELATION WITH THE EXTENT OF TRUNCATION OF C-TERMINAL REGION OF HUMAN ERYTHROID BETA-SPECTRINS BY EXON SKIPPING
Authors: YAWATA A KANZAKI A YAWATA Y KAKU M TAKEZONO M
Citation: A. Yawata et al., QUANTITATIVE ELECTRON-MICROSCOPY DEMONSTRATES AN EXCELLENT CORRELATION WITH THE EXTENT OF TRUNCATION OF C-TERMINAL REGION OF HUMAN ERYTHROID BETA-SPECTRINS BY EXON SKIPPING, Blood, 90(10), 1997, pp. 2718-2718
THE METHYLATION STATE OF THE GENOMIC DNA OF RED-CELL MEMBRANE-PROTEIN(PROTEIN-4.2, BAND-3 AND BETA-SPECTRIN) DURING ERYTHROID-DIFFERENTIATION
Authors: YAWATA Y ZESCHNIGK M REMUS R DOERFLER W WADA H TAKEZONO M KAKU M KANZAKI A YATA K SUGIHARA T YAMADA O YAWATA A
Citation: Y. Yawata et al., THE METHYLATION STATE OF THE GENOMIC DNA OF RED-CELL MEMBRANE-PROTEIN(PROTEIN-4.2, BAND-3 AND BETA-SPECTRIN) DURING ERYTHROID-DIFFERENTIATION, Blood, 90(10), 1997, pp. 2719-2719
HEREDITARY XEROCYTOSIS IS A PHENOTYPICALLY DIFFERENT ENTITY FROM HEREDITARY HIGH RED-CELL MEMBRANE PHOSPHATIDYLCHOLINE HEMOLYTIC-ANEMIA
Authors: YAWATA Y KANZAKI A YAWATA A KAKU M TAKEZONO M SUGIHARA T WADA H YATA K YAMADA O
Citation: Y. Yawata et al., HEREDITARY XEROCYTOSIS IS A PHENOTYPICALLY DIFFERENT ENTITY FROM HEREDITARY HIGH RED-CELL MEMBRANE PHOSPHATIDYLCHOLINE HEMOLYTIC-ANEMIA, Blood, 90(10), 1997, pp. 7-7
EVEN PARTIAL DEFICIENCY OF PROTEIN-4.2 IS CRITICAL FOR INTEGRITY OF SKELETAL NETWORK IN-SITU AND INTRAMEMBRANE PARTICLES IN A HOMOZYGOUS BAND-3 FUKUOKA (G130R) WITH ITS IMPAIRED BINDING TO PROTEIN-4.2
Authors: INOUE T KANZAKI A YAWATA A KAKU M TAKEZONO M WADA H SUGIHARA T YAMADA O KATAYAMA Y NAGATA N YAWATA Y
Citation: T. Inoue et al., EVEN PARTIAL DEFICIENCY OF PROTEIN-4.2 IS CRITICAL FOR INTEGRITY OF SKELETAL NETWORK IN-SITU AND INTRAMEMBRANE PARTICLES IN A HOMOZYGOUS BAND-3 FUKUOKA (G130R) WITH ITS IMPAIRED BINDING TO PROTEIN-4.2, Blood, 88(10), 1996, pp. 2748-2748
POSTTRANSLATIONAL MODIFICATION OF PROTEIN-4.2 - A PROTEIN-4.2 DOUBLETNAGANO WITH ITS 72 AND 74KDS
Authors: YAWATA Y KANZAKI A INOUE T KAKU M YAWATA A TAKEZONO M SHIMOHIRA Y ISHIDA F KOBAYASHI H
Citation: Y. Yawata et al., POSTTRANSLATIONAL MODIFICATION OF PROTEIN-4.2 - A PROTEIN-4.2 DOUBLETNAGANO WITH ITS 72 AND 74KDS, Blood, 88(10), 1996, pp. 2758-2758
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