A novel ENU-induced mutation in Ankyrin I provides new insights into hereditary spherocytosis

被引：0
|
作者：
Anderson, N.
Hughes, M.
Milenkovic, Z.
Wong, J.
Wang, C.
McNagny, K.
Stanford, W.
机构：
[1] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[2] Univ British Columbia, Biomed Res Ctr, Vancouver, BC, Canada
[3] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON, Canada
[4] Univ Toronto, Inst Biomat & Biomed Engn, Toronto, ON, Canada
来源：
EXPERIMENTAL HEMATOLOGY | 2007年 / 35卷 / 09期
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：108 / 108
页数：1
相关论文
共 50 条
  • [31] Identification of a novel SPTB gene splicing mutation in hereditary spherocytosis: a case report and diagnostic insights
    Li, Xiaobing
    Zhang, Tingqiang
    Li, Xuemei
    Wang, Li
    Li, Qian
    Liu, Qianqian
    He, Chengyin
    Zhang, Li
    Liu, Yongsheng
    Tang, Junling
    FRONTIERS IN GENETICS, 2025, 15
  • [32] New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse
    Koichiro Abe
    Helmut Fuchs
    Thomas Lisse
    Wolfgang Hans
    Martin Hrabé de Angelis
    Mammalian Genome, 2006, 17 : 915 - 926
  • [33] Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report
    Jun-Fang Wang
    Li Ma
    Xiao-Hui Gong
    Cheng Cai
    Jing-Jing Sun
    World Journal of Clinical Cases, 2021, 9 (19) : 5245 - 5251
  • [34] An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice
    Morag A Lewis
    Elizabeth Quint
    Anne M Glazier
    Helmut Fuchs
    Martin Hrabé De Angelis
    Cordelia Langford
    Stijn van Dongen
    Cei Abreu-Goodger
    Matias Piipari
    Nick Redshaw
    Tamas Dalmay
    Miguel Angel Moreno-Pelayo
    Anton J Enright
    Karen P Steel
    Nature Genetics, 2009, 41 : 614 - 618
  • [35] Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report
    Wang, Jun-Fang
    Ma, Li
    Gong, Xiao-Hui
    Cai, Cheng
    Sun, Jing-Jing
    WORLD JOURNAL OF CLINICAL CASES, 2021, 9 (19) : 5245 - 5251
  • [36] hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse
    Tian, Meng
    Campagna, Dean R.
    Woodward, Lanette S.
    Justice, Monica J.
    Fleming, Mark D.
    BLOOD, 2008, 112 (10) : 4308 - 4313
  • [37] An ENU-induced mutation causing arrest of spermatocytes before first meiotic division.
    Sun, Fengyun
    Handel, Mary Ann
    BIOLOGY OF REPRODUCTION, 2006, : 83 - 84
  • [38] New ENU-induced semidominant mutation, Ali18, causes inflammatory arthritis, dermatitis, and osteoporosis in the mouse
    Abe, Koichiro
    Fuchs, Helmut
    Lisse, Thomas
    Hans, Wolfgang
    de Angelis, Martin Hrabe
    MAMMALIAN GENOME, 2006, 17 (09) : 915 - 926
  • [39] A study of ENU-induced mutagenesis in the mouse using the restriction site mutation (RSM) assay
    Jenkins, GJS
    Takahashi, N
    Parry, JM
    TERATOGENESIS CARCINOGENESIS AND MUTAGENESIS, 1999, 19 (04): : 281 - 292
  • [40] An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice
    Lewis, Morag A.
    Quint, Elizabeth
    Glazier, Anne M.
    Fuchs, Helmut
    De Angelis, Martin Hrabe
    Langford, Cordelia
    van Dongen, Stijn
    Abreu-Goodger, Cei
    Piipari, Matias
    Redshaw, Nick
    Dalmay, Tamas
    Angel Moreno-Pelayo, Miguel
    Enright, Anton J.
    Steel, Karen P.
    NATURE GENETICS, 2009, 41 (05) : 614 - 618
12345