GENE EXPRESSION PROFILE IN THE BRAIN OF A MOUSE MODEL FOR CACH/VWM DISEASE DUE TO A POINT MUTATION IN EIF2B5

被引：0
|
作者：
Marom, L. [1 ]
Geva, M. [1 ]
Elroy-Stein, O. [1 ]
机构：
[1] Tel Aviv Univ, IL-69978 Tel Aviv, Israel
来源：
GLIA | 2009年 / 57卷 / 13期
关键词：
D O I：
暂无
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
引用
收藏
页码：S48 / S49
页数：2
相关论文
共 50 条
  • [31] Mutation Analysis and Expression of the Mottled Gene in the Macular Mouse Model of Menkes Disease
    Yoshiko Murata
    Hiroko Kodama
    Toshiaki Abe
    Norio Ishida
    Masahiko Nishimura
    Barbara Levinson
    Jane Gitschier
    Seymour Packman
    Pediatric Research, 1997, 42 : 436 - 442
  • [32] Mutation analysis and expression of the mottled gene in the macular mouse model of Menkes disease
    Murata, Y
    Kodama, H
    Abe, T
    Ishida, N
    Nishimura, M
    Levinson, B
    Gitschier, J
    Packman, S
    PEDIATRIC RESEARCH, 1997, 42 (04) : 436 - 442
  • [33] A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature
    Parisa Nourmohammadi
    Mostafa Asadollahi
    Arezou Karamzade
    Yeganeh Eshaghkhani
    Meisam Babaei
    Zahra Golchehre
    Seyedeh Roksana Taheri
    Sepideh Hasani
    Mahdieh Taghizadeh
    Mohammad Keramatipour
    Journal of Genetics, 102
  • [34] Distinct spatial profile of inflammatory gene expression in the brain of a mouse model of neuropsychiatric lupus
    Aw, Ernest
    Zhang, Yingying
    Carroll, Michael
    JOURNAL OF IMMUNOLOGY, 2021, 206
  • [35] Pulmonary Veno-Occlusive Disease Due to Biallelic EIF2AK4 Gene Mutation
    Cullivan, S.
    Alameeri, A.
    McCullagh, B.
    Gaine, S. P.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2021, 203 (09)
  • [36] A novel missense variant in EIF2B5 identified in a consanguineous Iranian family with vanishing white matter disease and a brief review of the literature
    Nourmohammadi, Parisa
    Asadollahi, Mostafa
    Karamzade, Arezou
    Eshaghkhani, Yeganeh
    Babaei, Meisam
    Golchehre, Zahra
    Taheri, Seyedeh Roksana
    Hasani, Sepideh
    Taghizadeh, Mahdieh
    Keramatipour, Mohammad
    JOURNAL OF GENETICS, 2023, 102 (02)
  • [37] Altered bone microarchitecture and gene expression profile due to calcium deficiency in a mouse model of myeloma
    Libouban, Helene
    Chappard, Daniel
    MICRON, 2017, 96 : 77 - 85
  • [38] CircAHNAK upregulates EIF2B5 expression to inhibit the progression of ovarian cancer by modulating the JAK2/STAT3 signaling pathway
    He, Si-Li
    Zhao, Xingping
    Yi, Shui-Jing
    CARCINOGENESIS, 2022, 43 (10) : 941 - 955
  • [39] VANISHING WHITE MATTER DISEASE DUE TO VARIANT MUTATIONS IN THE EIF2B-1 GENE
    Priya, Bangalore
    Ian, Berry R.
    John, Livingston
    Dan, Warren
    David, Nicholl J.
    Mary, O'Driscoll
    Tom, Hayton
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2018, 89 (10):
  • [40] The Arg113His mutation of the translation initiation factor (eIF2B5) associated with the adult onset of vanishing white matter is not present in multiple sclerosis
    Lucas, M
    Suárez, R
    Marcos, A
    García-Sánchez, MI
    Solano, F
    Venegas, A
    Izquierdo, G
    MULTIPLE SCLEROSIS, 2005, 11 : S116 - S116
12345