PMC Links for Gene (Select 6899) - PMC

Links from Gene

Items: 1 to 20 of 36

<< First< Prev

Page of 2

Next >Last >>

Select item 107786791.

Establishment of the Myeloid TBX-Code Reveals Aberrant Expression of T-Box Gene TBX1 in Chronic Myeloid Leukemia

Stefan Nagel, Josephine Haake, Claudia Pommerenke, Corinna Meyer, Roderick A. F. MacLeod

Int J Mol Sci. 2024 Jan; 25(1): 32. Published online 2023 Dec 19. doi: 10.3390/ijms25010032

PMCID:: PMC10778679

Article PDF–3.6M

Select item 88324092.

TBX1 functions as a putative oncogene of breast cancer through promoting cell cycle progression

Shuya Huang, Xiang Shu, Jie Ping, Jie Wu, Jifeng Wang, Chris Shidal, Xingyi Guo, Joshua A Bauer, Jirong Long, Xiao-Ou Shu, Wei Zheng, Qiuyin Cai

Carcinogenesis. 2022 Jan; 43(1): 12–20. Published online 2021 Dec 17. doi: 10.1093/carcin/bgab111

PMCID:: PMC8832409

Article PDF–54M

Select item 87947933.

Case Report: Unmanipulated Matched Sibling Donor Hematopoietic Cell Transplantation In TBX1 Congenital Athymia: A Lifesaving Therapeutic Approach When Facing a Systemic Viral Infection

Maria Chitty-Lopez, Carla Duff, Gretchen Vaughn, Jessica Trotter, Hector Monforte, David Lindsay, Elie Haddad, Michael D. Keller, Benjamin R. Oshrine, Jennifer W. Leiding

Front Immunol. 2021; 12: 721917. Published online 2022 Jan 14. doi: 10.3389/fimmu.2021.721917

PMCID:: PMC8794793

Article PDF–894K

Select item 61948094.

Heterozygous Mutations in TBX1 as a Cause of Isolated Hypoparathyroidism

Dong Li, Christopher T Gordon, Myriam Oufadem, Jeanne Amiel, Harsh S Kanwar, Marina Bakay, Tiancheng Wang, Hakon Hakonarson, Michael A Levine

J Clin Endocrinol Metab. 2018 Nov; 103(11): 4023–4032. Published online 2018 Aug 20. doi: 10.1210/jc.2018-01260

PMCID:: PMC6194809

Article

Select item 53411605.

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

Yuejuan Xu, Shaohai Fang, Erge Zhang, Tian Pu, Ruixue Cao, Qihua Fu, Fen Li, Sun Chen, Kun Sun, Rang Xu

Sci Rep. 2017; 7: 44165. Published online 2017 Mar 8. doi: 10.1038/srep44165

PMCID:: PMC5341160

Article PDF–1.1M

Select item 45354336.

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome

Carrie L. Heike, Jacqueline R. Starr, Mark J. Rieder, Michael L. Cunningham, Karen L. Edwards, Ian Stanaway, Dana C. Crawford

Birth Defects Res A Clin Mol Teratol. Author manuscript; available in PMC 2015 Aug 13.

Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2010 Jan; 88(1): 54–63. doi: 10.1002/bdra.20604

PMCID:: PMC4535433

Article PDF–662K

Select item 40992057.

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion

Yue-Juan Xu, Sun Chen, Jian Zhang, Shao-Hai Fang, Qian-Qian Guo, Jian Wang, Qi-Hua Fu, Fen Li, Rang Xu, Kun Sun

BMC Med Genet. 2014; 15: 78. Published online 2014 Jul 6. doi: 10.1186/1471-2350-15-78

PMCID:: PMC4099205

Article PDF–2.9M

Select item 39567588.

TBX1 Mutation Identified by Exome Sequencing in a Japanese Family with 22q11.2 Deletion Syndrome-Like Craniofacial Features and Hypocalcemia

Tsutomu Ogata, Tetsuya Niihori, Noriko Tanaka, Masahiko Kawai, Takeshi Nagashima, Ryo Funayama, Keiko Nakayama, Shinichi Nakashima, Fumiko Kato, Maki Fukami, Yoko Aoki, Yoichi Matsubara

PLoS One. 2014; 9(3): e91598. Published online 2014 Mar 17. doi: 10.1371/journal.pone.0091598

PMCID:: PMC3956758

Article PDF–893K

Select item 34921499.

The T-box transcription factor Brachyury regulates epithelial–mesenchymal transition in association with cancer stem-like cells in adenoid cystic carcinoma cells

Miyuki Shimoda, Tsuyoshi Sugiura, Ikumi Imajyo, Kotaro Ishii, Satomi Chigita, Katsuhiro Seki, Yousuke Kobayashi, Kanemitsu Shirasuna

BMC Cancer. 2012; 12: 377. Published online 2012 Aug 29. doi: 10.1186/1471-2407-12-377

PMCID:: PMC3492149

Article PDF–2.0M

Select item 347728110.

Overt Cleft Palate Phenotype and TBX1 Genotype Correlations in Velo-cardio-facial/DiGeorge/22q11.2 Deletion Syndrome Patients

Sean B. Herman, Tingwei Guo, Donna M. McDonald McGinn, Anna Blonska, Alan L. Shanske, Anne S. Bassett, Eva WC Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, M. Cristina Digilio, Bruno Marino, Bruno Dallapiccola, Courtney Carpenter, Xin Zheng, Jacob Johnson, Jonathan Chung, Anne Marie Higgins, Nicole Philip, Tony Simon, Karlene Coleman, Damian Heine-Suner, Jordi Rosell, Wendy Kates, Marcella Devoto, Elaine Zackai, Tao Wang, Robert Shprintzen, Beverly S. Emanuel, Bernice E. Morrow, International Chromosome 22q11.2 Consortium

Am J Med Genet A. Author manuscript; available in PMC 2013 Nov 1.

Published in final edited form as: Am J Med Genet A. 2012 Nov; 158A(11): 2781–2787. Published online 2012 Oct 3. doi: 10.1002/ajmg.a.35512

PMCID:: PMC3477281

Article PDF–1003K

Select item 319682411.

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio- facial/DiGeorge/22q11.2 deletion syndrome patients

Tingwei Guo, Donna McDonald McGinn, Anna Blonska, Alan Shanske, Anne Bassett, Eva Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, M. Cristina Digilio, Bruno Marino, Bruno Dallapiccola, Courtney Carpenter, Xin Zheng, Jacob Johnson, Jonathan Chung, Anne Marie Higgins, Nicole Philip, Tony J. Simon, Karlene Coleman, Damian Heine-Suner, Jordi Rosell, Wendy Kates, Marcella Devoto, Elizabeth Goldmuntz, Elaine Zackai, Tao Wang, Robert Shprintzen, Beverly Emanuel, Bernice Morrow, the International Chromosome 22q11.2 Consortium

Hum Mutat. Author manuscript; available in PMC 2012 Nov 1.

Published in final edited form as: Hum Mutat. 2011 Nov; 32(11): 1278–1289. Published online 2011 Sep 16. doi: 10.1002/humu.21568

PMCID:: PMC3196824

Article PDF–2.2M

Select item 297607612.

Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants

Helen R Griffin, Ana Töpf, Elise Glen, Christiane Zweier, A Graham Stuart, Jonathan Parsons, Ian Peart, John Deanfield, John O'Sullivan, Anita Rauch, Peter Scambler, John Burn, Heather J Cordell, Bernard Keavney, Judith A Goodship

Heart. 2010 Oct 15; 96(20): 1651–1655. Published online 2010 Oct 11. doi: 10.1136/hrt.2010.200121

PMCID:: PMC2976076

Article PDF–379K

Select item 281007213.

The T-box transcription factor Brachyury promotes epithelial-mesenchymal transition in human tumor cells

Romaine I. Fernando, Mary Litzinger, Paola Trono, Duane H. Hamilton, Jeffrey Schlom, Claudia Palena

J Clin Invest. 2010 Feb 1; 120(2): 533–544. Published online 2010 Jan 11. doi: 10.1172/JCI38379

PMCID:: PMC2810072

Article PDF–3.0M

Select item 195267414.

Analysis of TBX1 Variation in Patients with Psychotic and Affective Disorders

Birgit H Funke, Todd Lencz, Christine T Finn, Pamela DeRosse, G David Poznik, Alex M Plocik, John Kane, John Rogus, Anil K Malhotra, Raju Kucherlapati

Mol Med. 2007 Jul-Aug; 13(7-8): 407–414. doi: 10.2119/2006-00119.Funke

PMCID:: PMC1952674

Article PDF–1.6M

Select item 173478315.

Mutation analysis of TBX1 in non-deleted patients with features of DGS/VCFS or isolated cardiovascular defects

W. Gong, S. Gottlieb, J. Collins, A. Blescia, H. Dietz, E. Goldmuntz, D. McDonald-McGinn, E. Zackai, B. Emanuel, D. Driscoll, M. Budarf

J Med Genet. 2001 Dec; 38(12): e45. doi: 10.1136/jmg.38.12.e45

PMCID:: PMC1734783

Summary PDF–175K

Select item 880634116.

T-box transcription factor TBX1, targeted by microRNA-6727-5p, inhibits cell growth and enhances cisplatin chemosensitivity of cervical cancer cells through AKT and MAPK pathways

Haixia Liu, Mei Song, Xiaoyan Sun, Xin Zhang, Huayan Miao, Yankui Wang

Bioengineered. 2021; 12(1): 565–577. Published online 2021 Feb 8. doi: 10.1080/21655979.2021.1880732

PMCID:: PMC8806341

Article PDF–3.4M

Select item 735055717.

Transactivation of SOX5 by Brachyury promotes breast cancer bone metastasis

Ming Chen, Shitao Zou, Chao He, Jundong Zhou, Suoyuan Li, Minghong Shen, Rulei Cheng, Donglai Wang, Tianming Zou, Xueqi Yan, Ying Huang, Jun Shen

Carcinogenesis. 2020 Jul; 41(5): 551–560. Published online 2019 Nov 12. doi: 10.1093/carcin/bgz142

PMCID:: PMC7350557

Article PDF–91M

Select item 615106418.

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

Nanchao Hong, Erge Zhang, Qingjie Wang, Xiaoqing Zhang, Fen Li, Qihua Fu, Rang Xu, Yu Yu, Sun Chen, Yuejuan Xu, Kun Sun

J Transl Med. 2018; 16: 260. Published online 2018 Sep 21. doi: 10.1186/s12967-018-1633-1

PMCID:: PMC6151064

Article PDF–1.5M

Select item 537842019.

A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury

Bixiao Zhao, Qiongshi Lu, Yuwei Cheng, Justin M. Belcher, Edward D. Siew, David E. Leaf, Simon C. Body, Amanda A. Fox, Sushrut S. Waikar, Charles D. Collard, Heather Thiessen-Philbrook, T. Alp Ikizler, Lorraine B. Ware, Charles L. Edelstein, Amit X. Garg, Murim Choi, Jennifer A. Schaub, Hongyu Zhao, Richard P. Lifton, Chirag R. Parikh

Am J Respir Crit Care Med. 2017 Feb 15; 195(4): 482–490. Published online 2017 Feb 15. doi: 10.1164/rccm.201603-0518OC

PMCID:: PMC5378420

Article PDF–966K

Select item 325906420.

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

Yue-Juan Xu, Jian Wang, Rang Xu, Peng-Jun Zhao, Xi-Ke Wang, Heng-Juan Sun, Li-Ming Bao, Jie Shen, Qi-Hua Fu, Fen Li, Kun Sun

BMC Med Genet. 2011; 12: 169. Published online 2011 Dec 21. doi: 10.1186/1471-2350-12-169

PMCID:: PMC3259064

Article PDF–609K

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 36

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity