DEVELOPMENT The many faces of NKX2-1

被引：0
|
作者：
Whalley, Katherine
机构：
来源：
NATURE REVIEWS NEUROSCIENCE | 2008年 / 9卷 / 11期
关键词：
D O I：
10.1038/nrn2519
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
[No abstract available]
引用
收藏
页码：802+803 / 803
页数：1
相关论文
共 50 条
  • [31] NKX2-1 New Mutation Associated With Myoclonus, Dystonia, and Pituitary Involvement
    Balicza, Peter
    Grosz, Zoltan
    Molnar, Viktor
    Illes, Anett
    Csaban, Dora
    Gezsi, Andras
    Dezsi, Livia
    Zadori, Denes
    Vecsei, Laszlo
    Molnar, Maria Judit
    FRONTIERS IN GENETICS, 2018, 9
  • [32] NKX2-1 mutation in a family diagnosed with ataxic dyskinetic cerebral palsy
    McMichael, Gai
    Haan, Eric
    Gardner, Alison
    Yap, Tzu Ying
    Thompson, Suzanna
    Ouvrier, Robert
    Dale, Russell C.
    Gecz, Jozef
    MacLennan, Alastair H.
    EUROPEAN JOURNAL OF MEDICAL GENETICS, 2013, 56 (09) : 506 - 509
  • [33] In vivo role of different domains and of phosphorylation in the transcription factor Nkx2-1
    Silberschmidt, Daniel
    Rodriguez-Mallon, Alina
    Mithboakar, Prathiba
    Cali, Gaetano
    Amendola, Elena
    Sanges, Remo
    Zannini, Mariastella
    Scarfo, Marzia
    De Luca, Pasquale
    Nitsch, Lucio
    Di Lauro, Roberto
    De Felice, Mario
    BMC DEVELOPMENTAL BIOLOGY, 2011, 11
  • [34] Nkx2-1 Represses a Latent Gastric Differentiation Program in Lung Adenocarcinoma
    Snyder, Eric L.
    Watanabe, Hideo
    Magendantz, Margaret
    Hoersch, Sebastian
    Chen, Tiffany A.
    Wang, Diana G.
    Crowley, Denise
    Whittaker, Charles A.
    Meyerson, Matthew
    Kimura, Shioko
    Jacks, Tyler
    MOLECULAR CELL, 2013, 50 (02) : 185 - 199
  • [35] Predicting the pathogenicity of NKX2-1 and IGSF1 variants with in silico bioinformatic tools
    Narumi, Satoshi
    CLINICAL PEDIATRIC ENDOCRINOLOGY, 2020, 29 (03) : 123 - 126
  • [36] The Prognostic Value of TTF-1/NKX2-1 in Lung Squamous Cell Carcinoma
    Liao, Yida
    Yang, Fan
    Li, Xiao
    Chen, Kezhong
    Wang, Jun
    APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY, 2023, 31 (06) : 414 - 420
  • [37] Neurologic and systemic variability in benign hereditary chorea due to NKX2-1 mutations
    Coon, E. A.
    Milone, M.
    Niu, Z.
    Patterson, M. C.
    Ahlskog, J. E.
    MOVEMENT DISORDERS, 2015, 30 : S139 - S139
  • [38] NKX2-1 expression defines Wnt dependency patterns in human lung adenocarcinoma
    Hamamoto, Junko
    Emoto, Katsura
    Terai, Hideki
    Kawada, Ichiro
    Soejima, Kenzo
    Yasuda, Hiroyuki
    Sato, Toshiro
    CANCER SCIENCE, 2024, 115 : 1867 - 1867
  • [39] A case of permanent congenital hypothyroidism with NKX2-1 mutation and optic nerve thickness
    Yang, Jaejin
    Chung, Woo Yeong
    Oh, Seung Hwan
    Seo, Go Hun
    Kim, Jeong Rye
    Yu, Jeesuk
    HORMONE RESEARCH IN PAEDIATRICS, 2022, 95 (SUPPL 2): : 587 - 587
  • [40] MicroRNA-365 regulates NKX2-1, a key mediator of lung cancer
    Kang, Sung-Min
    Lee, Heon-Jin
    Cho, Je-Yoel
    CANCER LETTERS, 2013, 335 (02) : 487 - 494
12345