HEREDITARY ELLIPTOCYTOSIS DUE TO BOTH QUALITATIVE AND QUANTITATIVE DEFECTS IN MEMBRANE SKELETAL PROTEIN 4.1

被引：37
作者：
CONBOY, JG [1 ]
SHITAMOTO, R [1 ]
PARRA, M [1 ]
WINARDI, R [1 ]
KABRA, A [1 ]
SMITH, J [1 ]
MOHANDAS, N [1 ]
机构：
[1] KANSAS STATE UNIV AGR & APPL SCI,DEPT PATHOL,MANHATTAN,KS 66506
来源：
BLOOD | 1991年 / 78卷 / 09期
关键词：
D O I：
10.1182/blood.V78.9.2438.bloodjournal7892438
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：2438 / 2443
页数：6
相关论文
共 50 条
  • [41] Deficiency of a membrane skeletal protein, 4.1G, results in myelin abnormalities in the peripheral nervous system
    Yurika Saitoh
    Nobuhiko Ohno
    Junji Yamauchi
    Takeharu Sakamoto
    Nobuo Terada
    Histochemistry and Cell Biology, 2017, 148 : 597 - 606
  • [42] Deficiency of a membrane skeletal protein, 4.1G, results in myelin abnormalities in the peripheral nervous system
    Saitoh, Yurika
    Ohno, Nobuhiko
    Yamauchi, Junji
    Sakamoto, Takeharu
    Terada, Nobuo
    HISTOCHEMISTRY AND CELL BIOLOGY, 2017, 148 (06) : 597 - 606
  • [43] Enhanced haemolysis with β-thalassaemia trait due to the unstable β chain variant, Hb Gunma, accompanied by hereditary elliptocytosis due to protein 4•1 deficiency in a Japanese family
    Maehara, T
    Tsukamoto, N
    Nojima, Y
    Karasawa, M
    Murakami, H
    Hattori, Y
    Ideguchi, H
    BRITISH JOURNAL OF HAEMATOLOGY, 2002, 117 (01) : 193 - 197
  • [44] Membrane cation and anion transport activities in erythrocytes of hereditary spherocytosis: Effects of different membrane protein defects
    DeFranceschi, L
    Olivieri, O
    delGiudice, EM
    Perrotta, S
    Sabato, V
    Corrocher, R
    Iolascon, A
    AMERICAN JOURNAL OF HEMATOLOGY, 1997, 55 (03) : 121 - 128
  • [45] Modulation of the postprandial utilization of dietary protein by both qualitative and quantitative factors of the protein intake in humans
    Juillet, B
    Fouillet, H
    Bos, C
    Gaudichon, C
    Tomé, D
    FASEB JOURNAL, 2006, 20 (04) : A9 - A9
  • [46] Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis
    Demiralp, Duygu Ozel
    Peker, Selen
    Turgut, Burhan
    Akar, Nejat
    PROTEOMICS CLINICAL APPLICATIONS, 2012, 6 (7-8) : 403 - 411
  • [47] Erythroid membrane protein defects in hereditary spherocytosis. A study of 62 Spanish cases
    Ricard, MP
    Gilsanz, F
    Millan, I
    HAEMATOLOGICA, 2000, 85 (09) : 994 - 995
  • [48] MOLECULAR-CLONING AND CHARACTERIZATION OF THE GENE CODING FOR RED-CELL MEMBRANE SKELETAL PROTEIN-4.1
    CONBOY, JG
    BIORHEOLOGY, 1986, 23 (03) : 218 - 218
  • [49] DISTANCE BETWEEN SKELETAL PROTEIN-4.1 AND THE ERYTHROCYTE-MEMBRANE BILAYER MEASURED BY RESONANCE ENERGY-TRANSFER
    SHAHROKH, Z
    VERKMAN, AS
    SHOHET, SB
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1991, 266 (18) : 12082 - 12089
  • [50] MEMBRANE SKELETAL PROTEIN-4.1 OF AVIAN ERYTHROCYTES IS COMPOSED OF MULTIPLE VARIANTS THAT EXHIBIT TISSUE-SPECIFIC EXPRESSION
    GRANGER, BL
    LAZARIDES, E
    CELL, 1984, 37 (02) : 595 - 607
12345