Beneficial Effects of Nucleoside Treatment in Zebrafish Models of Diamond Blackfan Anemia Deficient in Ribosomal Proteins L11 or S19

被引：0
|
作者：
Danilova, Nadia [1 ]
Sakamoto, Kathleen M. [2 ]
Lin, Shuo [1 ]
机构：
[1] Univ Calif Los Angeles, Dept Mol Cell & Dev Biol, Los Angeles, CA USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA
来源：
BLOOD | 2011年 / 118卷 / 21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：1470 / 1470
页数：1
相关论文
共 50 条
  • [31] Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia
    Hamaguchi, I
    Ooka, A
    Brun, A
    Richter, J
    Dahl, N
    Karlsson, S
    BLOOD, 2002, 100 (08) : 2724 - 2731
  • [32] Mutations in ribosomal protein S19 gene account for Diamond Blackfan anemia phenotype in 58 out of 216 affected families.
    Willig, TN
    Draptchinskaia, N
    Dianzani, I
    Ball, S
    Niemeyer, C
    Ramenghi, U
    Orfali, K
    Gustavsson, P
    Garelli, E
    Brusco, A
    Tiemann, C
    Dahl, N
    Mohandas, N
    Tchernia, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A498 - A498
  • [33] 5′UTR Variants of Ribosomal Protein S19 Transcript Determine Translational Efficiency: Implications for Diamond-Blackfan Anemia and Tissue Variability
    Badhai, Jitendra
    Schuster, Jens
    Gidlof, Olof
    Dahl, Niklas
    PLOS ONE, 2011, 6 (03):
  • [34] Variable expressivity and incomplete penetrance in a large family with non-classical Diamond-Blackfan anemia associated with ribosomal protein L11 splicing variant
    Carlston, Colleen M.
    Afify, Zeinab A.
    Palumbos, Janice C.
    Bagley, Heidi
    Barbagelata, Carlos
    Wooderchak-Donahue, Whitney L.
    Mao, Rong
    Carey, John C.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (10) : 2622 - 2627
  • [35] The Frequency and Characteristics of the Ribosomal Protein L5 (RPL5) and Ribosomal Protein L11 (RPL11) Gene Mutations in Patients with Diamond-Blackfan Anemia in the Czech National Registry
    Pospisilova, Dagmar
    Cmejla, Radek
    Cmejlova, Jana
    Handrkova, Helena
    Stary, Jan
    Cerna, Zdenka
    BLOOD, 2008, 112 (11) : 1064 - 1065
  • [36] Two distinct mechanisms are responsible for regulation of ribosomal protein S19 expression level in diamond-blackfan anemia by NF-κB pathway
    Hurtaud, Corinne
    Cretein, Aurore
    Clayette, Valerie
    Pisani, Didier
    Giraudier, Stephane
    Leblanc, Thierry
    Delaunay, Jean
    Tchernia, Gil
    Mohandas, Narla
    Da Costa, Lydie
    BLOOD, 2007, 110 (11) : 502A - 502A
  • [37] Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia
    Flygare, J
    Kiefer, T
    Miyake, K
    Utsugisawa, T
    Hamaguchi, I
    Da Costa, L
    Richter, J
    Davey, EJ
    Matsson, H
    Dahl, N
    Wiznerowicz, M
    Trono, D
    Karlsson, S
    BLOOD, 2005, 105 (12) : 4627 - 4634
  • [38] Overexpression of the ribosomal protein S19(RPS19) in CD34+cells leads to an increase in erythroid progenitors in Diamond-Blackfan anemia patients with mutated RPS19.
    Hamaguchi, I
    Ooka, A
    Richter, J
    Dahl, N
    Karlsson, S
    BLOOD, 2000, 96 (11) : 802A - 802A
  • [39] New insights in Diamond-Blackfan anemia (DBA):: Two mutations in the ribosomal protein S19 (RPS19) gene identified in DBA perturb the nucleolar localization of RPS19.
    Da Costa, LM
    Gascard, P
    Lo, A
    Meerpohl, J
    Niemeyer, CM
    Tchernia, GJ
    Chasis, JA
    Fixler, J
    Mohandas, N
    BLOOD, 2002, 100 (11) : 8A - 8A
  • [40] Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia
    Miyake, Koich
    Utsugisawa, Taiju
    Flygare, Johan
    Kiefer, Thomas
    Hamaguchi, Isao
    Richter, Johan
    Karlsson, Stefan
    STEM CELLS, 2008, 26 (02) : 323 - 329
12345