EFTUD2, The Gene Responsible For Mandibulofacial Dysostosis With Microcephaly (MFDM), Is Required For Implantation And Craniofacial Development In Mouse

被引：0
|
作者：
Beauchamp, Marie-Claude
Djedid, Anissa
Daupin, Kevin
Clokie, Kayla
Majewski, Jacek
Majewska, Loydie Jerome
机构：
来源：
FASEB JOURNAL | 2019年 / 33卷
基金：
加拿大健康研究院;
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
774.20
引用
收藏
页数：2
相关论文
共 37 条
  • [21] Phenotype analysis of Polish patients with mandibulofacial dysostosis type Guion-Almeida associated with esophageal atresia and choanal atresia caused by EFTUD2 gene mutations
    Smigiel, Robert
    Bezniakow, Natalia
    Jakubiak, Aleksandra
    Bloch, Michal
    Patkowski, Dariusz
    Obersztyn, Ewa
    Sasiadek, Maria M.
    JOURNAL OF APPLIED GENETICS, 2015, 56 (02) : 199 - 204
  • [22] Array-CGH is an effective first-tier diagnostic test for EFTUD2-associated congenital mandibulofacial dysostosis with microcephaly
    Gandomi, S. K.
    Parra, M.
    Reeves, D.
    Yap, V.
    Gau, C. -L.
    CLINICAL GENETICS, 2015, 87 (01) : 80 - 84
  • [23] A rare genetic syndrome with a new splice mutation detected in the EFTUD2 gene; mandibulofacial disostosis, guion-almeida type
    Gerik-Celebi, B.
    Ceylaner, S.
    Cam, S.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 957 - 957
  • [24] The Core Splicing Factors EFTUD2, SNRPB and TXNL4A Are Essential for Neural Crest and Craniofacial Development
    Park, Byung-Yong
    Tachi-Duprat, Melanie
    Ihewulezi, Chibuike
    Devotta, Arun
    Saint-Jeannet, Jean-Pierre
    JOURNAL OF DEVELOPMENTAL BIOLOGY, 2022, 10 (03)
  • [25] The mouse Jagged2 gene is required for craniofacial, limb and thymic development
    Lan, Y
    Jiang, RL
    Chapman, H
    Norton, C
    Serreze, D
    Gridley, T
    DEVELOPMENTAL BIOLOGY, 1998, 198 (01) : 207 - 207
  • [26] Expression Analyses of Cep152, a Responsible Gene Product for Autosomal Recessive Primary Microcephaly, during Mouse Brain Development
    Hamada, Nanako
    Noda, Mariko
    Ito, Hidenori
    Iwamoto, Ikuko
    Nagata, Koh-ichi
    DEVELOPMENTAL NEUROSCIENCE, 2022, 44 (03) : 162 - 170
  • [27] The mouse Ovol2 gene is required for cranial neural tube development
    Mackay, DR
    Hu, M
    Li, BA
    Rhéaume, C
    Dai, X
    DEVELOPMENTAL BIOLOGY, 2006, 291 (01) : 38 - 52
  • [28] GENOMIC IMPRINTING OF MASH2, A MOUSE GENE REQUIRED FOR TROPHOBLAST DEVELOPMENT
    GUILLEMOT, F
    CASPARY, T
    TILGHMAN, SM
    COPELAND, NG
    GILBERT, DJ
    JENKINS, NA
    ANDERSON, DJ
    JOYNER, AL
    ROSSANT, J
    NAGY, A
    NATURE GENETICS, 1995, 9 (03) : 235 - 242
  • [29] Expression Analyses of Polo-Like Kinase 4, a Gene Product Responsible for Autosomal Recessive Microcephaly and Seckel Syndrome, during Mouse Brain Development
    Hamada, Nanako
    Iwamoto, Ikuko
    Noda, Mariko
    Nishikawa, Masashi
    Nagata, Koh-ichi
    DEVELOPMENTAL NEUROSCIENCE, 2022, 44 (06) : 643 - 650
  • [30] The Mouse Homeobox Gene Gbx2 Is Required for the Development of Cholinergic Interneurons in the Striatum
    Chen, Li
    Chatterjee, Mallika
    Li, James Y. H.
    JOURNAL OF NEUROSCIENCE, 2010, 30 (44): : 14824 - 14834
1234