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
  • [41] Novel 15 mutations of the ankyrin gene pathognomonic for hereditary spherocytosis in the Japanese population.
    Yawata, Y
    Nakanishi, H
    Kanzaki, A
    Yawata, A
    Yamada, O
    BLOOD, 2000, 96 (11) : 594A - +
  • [42] A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy
    Hines, Timothy J.
    Bailey, Janice
    Liu, Hedi
    Guntur, Anyonya R.
    Seburn, Kevin L.
    Pratt, Samia L.
    Funke, Jonathan R.
    Tarantino, Lisa M.
    Burgess, Robert W.
    BIOLOGY-BASEL, 2023, 12 (07):
  • [43] Novel ENU-induced eye mutations in the mouse: models for human eye disease
    Thaung, C
    West, K
    Clark, BJ
    McKie, L
    Morgan, JE
    Arnold, K
    Nolan, PM
    Peters, J
    Hunter, AJ
    Brown, SDM
    Jackson, IJ
    Cross, SH
    HUMAN MOLECULAR GENETICS, 2002, 11 (07) : 755 - 767
  • [44] Effect of nucleoticle excision repair on ENU-induced mutation in female germ cells of Drosophila melanogaster
    Alvarez, L
    Comendador, MA
    Sierra, LM
    ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2003, 41 (04) : 270 - 279
  • [45] Fast Homozygosity Mapping and Identification of a Zebrafish ENU-Induced Mutation by Whole-Genome Sequencing
    Voz, Marianne L.
    Coppieters, Wouter
    Manfroid, Isabelle
    Baudhuin, Ariane
    Von Berg, Virginie
    Charlier, Carole
    Meyer, Dirk
    Driever, Wolfgang
    Martial, Joseph A.
    Peers, Bernard
    PLOS ONE, 2012, 7 (04):
  • [46] An ENU-induced mutation in Rs1h causes disruption of retinal structure and function
    Jablonski, MM
    Dalke, C
    Wang, XF
    Lu, L
    Manly, KF
    Pretsch, W
    Favor, J
    Pardue, MT
    Rinchik, EM
    Williams, RW
    Goldowitz, D
    Graw, J
    MOLECULAR VISION, 2005, 11 (67): : 569 - 581
  • [47] A recurring frameshift mutation of the ankyrin-1 gene associated with severe hereditary spherocytosis in Brazil.
    Gallagher, PG
    Ferreira, JDS
    Saad, STO
    Kerbally, J
    Costa, FF
    Forget, B
    BLOOD, 1996, 88 (10) : 11 - 11
  • [48] A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination
    Noveroske, JK
    Hardy, R
    Dapper, JD
    Vogel, H
    Justice, MJ
    MAMMALIAN GENOME, 2005, 16 (09) : 672 - 682
  • [49] A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination
    Janice K. Noveroske
    Rebecca Hardy
    Jason D. Dapper
    Hannes Vogel
    Monica J. Justice
    Mammalian Genome, 2005, 16 : 672 - 682
  • [50] New mutation in the β-spectrin gene in hereditary spherocytosis: A case report
    Jin, Changyu
    Hu, Huijie
    Li, Qingqing
    Lai, Yanli
    Wang, Jiaping
    Mu, Qitian
    Ouyang, Guifang
    Sheng, Lixia
    GENE REPORTS, 2024, 37
12345