An in vivo gain-of-function screening identified the Williams-Beuren syndrome gene GTF2IRD1 as a mammary tumor promoter

被引：0

作者：

Huo, Yongliang ^{[1
]}

Su, Yinghao ^{[1
]}

Cai, Qiuyin ^{[1
]}

Macara, Ian ^{[1
]}

机构：

[1] Vanderbilt Univ, 221 Kirkland Hall, Nashville, TN 37235 USA

来源：

CANCER RESEARCH | 2016年 / 76卷

关键词：

D O I：

10.1158/1538-7445.FBCR15-A27

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

A27

引用

页数：2

共 32 条

[21] Gtf2i and Gtf2ird1 mutation do not account for the full phenotypic effect of the Williams syndrome critical region in mouse models
Kopp, Nathan
McCullough, Katherine
Maloney, Susan E.
Dougherty, Joseph D.
HUMAN MOLECULAR GENETICS, 2019, 28 (20) : 3443 - 3465
[22] Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome
Schneider, Tomasz
Skitt, Zara
Liu, Yiwen
Deacon, Robert M. J.
Flint, Jonathan
Karmiloff-Smith, Annette
Rawlins, J. Nick P.
Tassabehji, May
BEHAVIOURAL BRAIN RESEARCH, 2012, 233 (02) : 458 - 473
[23] A mouse single-copy gene, Gtf2i, the homolog of human GTF2I, that is duplicated in the Williams-Beuren syndrome deletion region
Wang, YK
Pérez-Jurado, LA
Francke, U
GENOMICS, 1998, 48 (02) : 163 - 170
[24] Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome
Borralleras, Cristina
Sahun, Ignasi
Perez-Jurado, Luis A.
Campuzano, Victoria
MOLECULAR THERAPY, 2015, 23 (11) : 1691 - 1699
[25] The Transcription Factor GTF2IRD1 Regulates the Topology and Function of Photoreceptors by Modulating Photoreceptor Gene Expression across the Retina
Masuda, Tomohiro
Zhang, Xiaodong
Berlinicke, Cindy
Wan, Jun
Yerrabelli, Anitha
Conner, Elizabeth A.
Kjellstrom, Sten
Bush, Ronald
Thorgeirsson, Snorri S.
Swaroop, Anand
Chen, Shiming
Zack, Donald J.
JOURNAL OF NEUROSCIENCE, 2014, 34 (46): : 15356 - 15368
[26] Williams Syndrome: evidence from atypical deletions links GTF21 and GTF2IRD1, but not FZD9, with posterior cortical structure and neural functions
Simon, AF
Yao, GM
Chen, XN
Mills, D
Rose, FE
Salandanan, LS
Reiss, A
Bellugi, U
Korenberg, JR
AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (05) : 514 - 514
[27] Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams–Beuren syndrome
Hannah J Tipney
Timothy A Hinsley
Andrew Brass
Kay Metcalfe
Dian Donnai
May Tassabehji
European Journal of Human Genetics, 2004, 12 : 551 - 560
[28] Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes
Fan, Chun Chieh
Schork, Andrew J.
Brown, Timothy T.
Spencer, Barbara E.
Akshoomoff, Natacha
Chen, Chi-Hua
Kuperman, Joshua M.
Hagler, Donald J., Jr.
Steen, Vidar M.
Le Hellard, Stephanie
Haberg, Asta Kristine
Espeseth, Thomas
Andreassen, Ole A.
Dale, Anders M.
Jernigan, Terry L.
Halgren, Eric
TRANSLATIONAL PSYCHIATRY, 2018, 8
[29] GTF2IRD1 on chromosome 7 is a novel oncogene regulating the tumor-suppressor gene TGFβR2 in colorectal cancer
Nambara, Sho
Masuda, Takaaki
Kobayashi, Yuta
Sato, Kuniaki
Tobo, Taro
Koike, Kensuke
Noda, Miwa
Ogawa, Yushi
Kuroda, Yousuke
Ito, Shuhei
Eguchi, Hidetoshi
Sugimachi, Keishi
Mimori, Koshi
CANCER SCIENCE, 2020, 111 (02) : 343 - 355
[30] Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes
Chun Chieh Fan
Andrew J. Schork
Timothy T. Brown
Barbara E. Spencer
Natacha Akshoomoff
Chi-Hua Chen
Joshua M. Kuperman
Donald J. Hagler
Vidar M. Steen
Stephanie Le Hellard
Asta Kristine Håberg
Thomas Espeseth
Ole A. Andreassen
Anders M. Dale
Terry L. Jernigan
Eric Halgren
Translational Psychiatry, 8

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