Understanding the roles and the regulation of the Mowat-Wilson Syndrome transcription factor ZEB2 during development and disease

被引:0
|
作者
Birkhoff, J. [1 ]
Korporaal, A.
Caraffi, S. G. [2 ]
Ivanovski, I. [2 ]
Garcia-Minaur, S. [3 ]
Kolovos, P. [4 ]
Brouwer, R. [1 ]
van Ijcken, W. [1 ]
Garavelli, L. [2 ]
Huylebroeck, D. [1 ]
Conidi, A. [1 ]
机构
[1] Erasmus MC, Rotterdam, Netherlands
[2] IRCSS Reggio Emilia, Reggio Emilia, Italy
[3] La Paz Hosp, Madrid, Spain
[4] BRIC Inst, Copenhagen, Denmark
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
C02.6
引用
收藏
页码:1083 / 1083
页数:1
相关论文
共 50 条
  • [1] Understanding the roles and the regulation of the Mowat-Wilson Syndrome transcription factor ZEB2 during development and disease
    Birkhoff, J.
    Korporaal, A.
    Caraffi, S. G.
    Ivanovski, I.
    Garcia-Minaur, S.
    Kolovos, P.
    Brouwer, R.
    van Ijcken, W.
    Garavelli, L.
    Huylebroeck, D.
    Conidi, A.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1082 - 1083
  • [2] ZEB2, the Mowat-Wilson Syndrome Transcription Factor: Confirmations, Novel Functions, and Continuing Surprises
    Birkhoff, Judith C.
    Huylebroeck, Danny
    Conidi, Andrea
    GENES, 2021, 12 (07)
  • [3] Ophthalmologic Abnormalities in Mowat-Wilson Syndrome and a Mutation in ZEB2
    Ariss, Michelle
    Natan, Kristina
    Friedman, Neil
    Traboulsi, Elias I.
    OPHTHALMIC GENETICS, 2012, 33 (03) : 159 - 160
  • [4] A Novel Partial Duplication of ZEB2 and Review of ZEB2 Involvement in Mowat-Wilson Syndrome
    Baxter, Adrianne L.
    Vivian, Jay L.
    Hagelstrom, R. Tanner
    Hossain, Waheeda
    Golden, Wendy L.
    Wassman, E. Robert
    Vanzo, Rena J.
    Butler, Merlin G.
    MOLECULAR SYNDROMOLOGY, 2017, 8 (04) : 211 - 218
  • [5] The Spectrum of ZEB2 Mutations Causing the Mowat-Wilson Syndrome in Japanese Populations
    Yamada, Yasukazu
    Nomura, Noriko
    Yamada, Kenichiro
    Matsuo, Mari
    Suzuki, Yuka
    Sameshima, Kiyoko
    Kimura, Reiko
    Yamamoto, Yuto
    Fukushi, Daisuke
    Fukuhara, Yayoi
    Ishihara, Naoko
    Nishi, Eriko
    Imataka, George
    Suzumura, Hiroshi
    Hamano, Shin-Ichiro
    Shimizu, Kenji
    Iwakoshi, Mie
    Ohama, Kazunori
    Ohta, Akira
    Wakamoto, Hiroyuki
    Kajita, Mitsuharu
    Miura, Kiyokuni
    Yokochi, Kenji
    Kosaki, Kenjiro
    Kuroda, Tatsuo
    Kosaki, Rika
    Hiraki, Yoko
    Saito, Kayoko
    Mizuno, Seiji
    Kurosawa, Kenji
    Okamoto, Nobuhiko
    Wakamatsu, Nobuaki
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2014, 164 (08) : 1899 - 1908
  • [6] Recurrence of Mowat-Wilson Syndrome in Siblings With a Novel Mutation in the ZEB2 Gene
    Cecconi, Massimiliano
    Forzano, Francesca
    Garavelli, Livia
    Pantaleoni, Chiara
    Grasso, Marina
    Bricarelli, Franca Dagna
    Perroni, Lucia
    Di Maria, Emilio
    Faravelli, Francesca
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2008, 146A (23) : 3095 - 3099
  • [7] Novel Alu insertion in the ZEB2 gene causing Mowat-Wilson syndrome
    Barington, Maria
    Bak, Mads
    Kjartansdottir, Kristin Ros
    Hansen, Thomas van Overeem
    Birkedal, Ulf
    Ostergaard, Elsebet
    Hove, Hanne Buciek
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2024, 194 (08)
  • [8] Congenital tracheal stenosis in Mowat-Wilson syndrome with nonsense mutation of ZEB2 gene
    Lin, Lun-Chin
    Wen, Wan-Hsin
    Chen, Peir-Taur
    PEDIATRICS AND NEONATOLOGY, 2024, 65 (02): : 202 - 203
  • [9] A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome
    Hu, Yuan
    Peng, Qi
    Ma, Keze
    Li, Siping
    Rao, Chunbao
    Zhong, Baimao
    Lu, Xiaomei
    JOURNAL OF CLINICAL LABORATORY ANALYSIS, 2020, 34 (09)
  • [10] A Chinese Boy with Mowat-Wilson Syndrome Caused by a 10 bp Deletion in the ZEB2 Gene
    Wei, Lin
    Han, Xiao
    Li, Xue
    Han, Bingjuan
    Nie, Wenying
    PHARMACOGENOMICS & PERSONALIZED MEDICINE, 2021, 14 : 1041 - 1045