Translation initiation defect and gene profiles linked to depletion of Shwachman-Diamond syndrome gene product.

被引:0
|
作者
Liu, JM
Nihrane, A
Ellis, SR
机构
[1] Schneider Childrens Hosp, Dept Pediat, New Hyde Pk, NY USA
[2] Univ Louisville, Dept Biochem & Mol Biol, Louisville, KY 40292 USA
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
3072
引用
收藏
页码:859A / 860A
页数:2
相关论文
共 50 条
  • [21] Characterization of SD01, the budding yeast ortholog of the Shwachman-Diamond gene
    Garrido-Lecca, A
    Shimamura, A
    Huang, J
    MOLECULAR BIOLOGY OF THE CELL, 2004, 15 : 94A - 94A
  • [22] Knockdown of the Shwachman-Diamond syndrome gene, SBDS, induces galectin-1 expression and impairs cell growth
    Yamaguchi, Masafumi
    Sera, Yukihiro
    Toga-Yamaguchi, Hanae
    Kanegane, Hirokazu
    Iguchi, Yusuke
    Fujimura, Kingo
    INTERNATIONAL JOURNAL OF HEMATOLOGY, 2024, 119 (04) : 383 - 391
  • [23] Identification of a novel AluSx-mediated deletion of exon 3 in the SBDS gene in a patient with Shwachman-Diamond syndrome
    Costa, Elisio
    Duque, Frederico
    Oliveira, Jorge
    Garcia, Paula
    Goncalves, Isabel
    Diogo, Luisa
    Santos, Rosario
    BLOOD CELLS MOLECULES AND DISEASES, 2007, 39 (01) : 96 - 101
  • [24] Knockdown of the Shwachman-Diamond syndrome gene, SBDS, induces galectin-1 expression and impairs cell growth
    Masafumi Yamaguchi
    Yukihiro Sera
    Hanae Toga-Yamaguchi
    Hirokazu Kanegane
    Yusuke Iguchi
    Kingo Fujimura
    International Journal of Hematology, 2024, 119 : 383 - 391
  • [25] Gene Disruption of Zebrafish Sbds Phenocopies Human Shwachman-Diamond Syndrome but Suggests More Global and Lineage Defects
    Oyarbide, Usua
    Kell, Margaret J.
    Farinas, Javier
    Topczewski, Jacek
    Corey, Seth
    BLOOD, 2016, 128 (22)
  • [26] Compound heterozygous mutations of the SBDS gene in a patient with shwachman-diamond syndrome, type 1 diabetes mellitus and osteoporosis
    Rosendahl, Jonas
    Teich, Niels
    Moessner, Joachim
    Edelmann, Jeanett
    Koch, Christian A.
    PANCREATOLOGY, 2006, 6 (06) : 549 - 554
  • [27] Mitotic abnormalities and spindle assembly checkpoint inactivation in a cell model of Shwachman-Diamond syndrome with mutations in the Shwachman-Bodian-Diamond syndrome gene, 258+2T > C
    Sera, Yukihiro
    Imanaka, Tsuneo
    Iguchi, Yusuke
    Yamaguchi, Masafumi
    DRUG DISCOVERIES AND THERAPEUTICS, 2024,
  • [28] Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients
    Minelli, Antonella
    Nacci, Lucia
    Valli, Roberto
    Pietrocola, Giampiero
    Ramenghi, Ugo
    Locatelli, Franco
    Brescia, Letizia
    Nicolis, Elena
    Cipolli, Marco
    Danesino, Cesare
    BLOOD CELLS MOLECULES AND DISEASES, 2016, 60 : 33 - 35
  • [29] Knockdown of Shwachman-Diamond Syndrome Gene, SBDS, Induces Increased Expression of Galectin-1 and Impaired Cell Growth
    Yamaguchi, Masafumi
    Fujimura, Kingo
    Kanegane, Hirokazu
    Toga-Yamaguchi, Hanae
    Okamura, Naoki
    BLOOD, 2012, 120 (21)
  • [30] Prenatal Diagnosis of Shwachman-Diamond Syndrome: Fetal Compound Heterozygous Variants in the SBDS Gene Associated With Mildly Straight Ribs
    Zhu, Linyan
    Wang, Xuhong
    Shi, Yubo
    Huang, Xiaxi
    Ding, Huiqing
    PRENATAL DIAGNOSIS, 2025,