PubMed for id: 6899

Year	Number of Results
1992	1
1993	1
1997	1
1999	1
2000	1
2001	2
2002	1
2003	2
2004	1
2005	1
2006	3
2007	6
2008	1
2009	5
2010	8
2011	6
2012	7
2013	4
2014	8
2015	2
2017	5
2018	5
2019	2
2020	6
2021	7
2022	2
2023	3
2024	0

1

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

Nagel S, Haake J, Pommerenke C, Meyer C, MacLeod RAF. Nagel S, et al. Int J Mol Sci. 2023 Dec 19;25(1):32. doi: 10.3390/ijms25010032. Int J Mol Sci. 2023. PMID: 38203204 Free PMC article.

2

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

Chitty-Lopez M, Duff C, Vaughn G, Trotter J, Monforte H, Lindsay D, Haddad E, Keller MD, Oshrine BR, Leiding JW. Chitty-Lopez M, et al. Front Immunol. 2022 Jan 14;12:721917. doi: 10.3389/fimmu.2021.721917. eCollection 2021. Front Immunol. 2022. PMID: 35095830 Free PMC article.

3

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

Huang S, Shu X, Ping J, Wu J, Wang J, Shidal C, Guo X, Bauer JA, Long J, Shu XO, Zheng W, Cai Q. Huang S, et al. Carcinogenesis. 2022 Feb 11;43(1):12-20. doi: 10.1093/carcin/bgab111. Carcinogenesis. 2022. PMID: 34919666 Free PMC article.

4

SNP-mediated binding of TBX1 to the enhancer element of IL-10 reduces the risk of Behçet's disease.

Tan H, Su G, Tan X, Qin Y, Chen L, Yuan G, Kijlstra A, Yang P. Tan H, et al. Epigenomics. 2021 Oct;13(19):1523-1537. doi: 10.2217/epi-2021-0215. Epub 2021 Oct 6. Epigenomics. 2021. PMID: 34612069

5

Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study.

Deshpande DR, Demirdag YY, Marsh RA, Sullivan KE, Orange JS; USIDNET Consortium. Deshpande DR, et al. J Clin Immunol. 2021 Jan;41(1):29-37. doi: 10.1007/s10875-020-00854-y. Epub 2020 Sep 19. J Clin Immunol. 2021. PMID: 32949294

6

Genetic Variant of TBX1 Gene Is Functionally Associated With Adolescent Idiopathic Scoliosis in the Chinese Population.

Li Y, Wu Z, Xu L, Feng Z, Wang Y, Dai Z, Liu Z, Sun X, Qiu Y, Zhu Z. Li Y, et al. Spine (Phila Pa 1976). 2021 Jan 1;46(1):17-21. doi: 10.1097/BRS.0000000000003700. Spine (Phila Pa 1976). 2021. PMID: 32947497

7

Generation of human iPSC line from a patient with Tetralogy of Fallot, YAHKMUi001-A, carrying a mutation in TBX1 gene.

Han S, Zhang YY, Meng MY, Hou ZL, Meng P, Zhao YY, Gao H, Tang J, Liu Z, Yang LL, Jiang LH, Li YX. Han S, et al. Stem Cell Res. 2020 Jan;42:101687. doi: 10.1016/j.scr.2019.101687. Epub 2019 Dec 12. Stem Cell Res. 2020. PMID: 31869684 Free article.

8

Heterozygous Mutations in TBX1 as a Cause of Isolated Hypoparathyroidism.

Li D, Gordon CT, Oufadem M, Amiel J, Kanwar HS, Bakay M, Wang T, Hakonarson H, Levine MA. Li D, et al. J Clin Endocrinol Metab. 2018 Nov 1;103(11):4023-4032. doi: 10.1210/jc.2018-01260. J Clin Endocrinol Metab. 2018. PMID: 30137364 Free PMC article.

9

Expression, function, and regulation of the embryonic transcription factor TBX1 in parathyroid tumors.

Verdelli C, Avagliano L, Guarnieri V, Cetani F, Ferrero S, Vicentini L, Beretta E, Scillitani A, Creo P, Bulfamante GP, Vaira V, Corbetta S. Verdelli C, et al. Lab Invest. 2017 Dec;97(12):1488-1499. doi: 10.1038/labinvest.2017.88. Epub 2017 Sep 18. Lab Invest. 2017. PMID: 28920943 Free article.

10

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

Xu Y, Fang S, Zhang E, Pu T, Cao R, Fu Q, Li F, Chen S, Sun K, Xu R. Xu Y, et al. Sci Rep. 2017 Mar 8;7:44165. doi: 10.1038/srep44165. Sci Rep. 2017. PMID: 28272434 Free PMC article. Clinical Trial.

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