Suppr超能文献

相似文献

1
DiGeorge syndrome, Tbx1, and retinoic acid signaling come full circle.
Circ Res. 2010 Mar 5;106(4):630-2. doi: 10.1161/CIRCRESAHA.109.215319.
4
22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.
Pediatr Cardiol. 2010 Apr;31(3):378-90. doi: 10.1007/s00246-009-9613-0.
7
DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1.
Nat Genet. 2001 Mar;27(3):286-91. doi: 10.1038/85845.
8
Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency.
PLoS One. 2018 Nov 8;13(11):e0207251. doi: 10.1371/journal.pone.0207251. eCollection 2018.
9
The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
Wiley Interdiscip Rev Dev Biol. 2013 May-Jun;2(3):393-403. doi: 10.1002/wdev.75. Epub 2012 Jun 19.
10
MOZ regulates the Tbx1 locus, and Moz mutation partially phenocopies DiGeorge syndrome.
Dev Cell. 2012 Sep 11;23(3):652-63. doi: 10.1016/j.devcel.2012.07.010. Epub 2012 Aug 23.

引用本文的文献

1
A retinoic acid:YAP1 signaling axis controls atrial lineage commitment.
Cell Rep. 2025 May 27;44(5):115687. doi: 10.1016/j.celrep.2025.115687. Epub 2025 May 8.
3
A Retinoic Acid:YAP1 signaling axis controls atrial lineage commitment.
bioRxiv. 2024 Jul 12:2024.07.11.602981. doi: 10.1101/2024.07.11.602981.
4
Single-cell analysis reveals transcriptional dynamics in healthy primary parathyroid tissue.
Genome Res. 2024 Jul 23;34(6):837-850. doi: 10.1101/gr.278215.123.
5
Primary and secondary defects of the thymus.
Immunol Rev. 2024 Mar;322(1):178-211. doi: 10.1111/imr.13306. Epub 2024 Jan 16.
6
The Tbx20-TLE interaction is essential for the maintenance of the second heart field.
Development. 2023 Nov 1;150(21). doi: 10.1242/dev.201677. Epub 2023 Oct 30.
9
Current and Future Therapeutic Approaches for Thymic Stromal Cell Defects.
Front Immunol. 2021 Mar 18;12:655354. doi: 10.3389/fimmu.2021.655354. eCollection 2021.

本文引用的文献

2
Retinoic acid in development: towards an integrated view.
Nat Rev Genet. 2008 Jul;9(7):541-53. doi: 10.1038/nrg2340. Epub 2008 Jun 10.
5
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes.
Dev Cell. 2006 Jan;10(1):71-80. doi: 10.1016/j.devcel.2005.12.003.
6
Dissecting contiguous gene defects: TBX1.
Curr Opin Genet Dev. 2005 Jun;15(3):279-84. doi: 10.1016/j.gde.2005.03.001.
7
Retinoic acid down-regulates Tbx1 expression in vivo and in vitro.
Dev Dyn. 2005 Apr;232(4):928-38. doi: 10.1002/dvdy.20268.
9
Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice.
Proc Natl Acad Sci U S A. 2003 Feb 18;100(4):1763-8. doi: 10.1073/pnas.0437920100. Epub 2003 Jan 31.
10
A genetic link between Tbx1 and fibroblast growth factor signaling.
Development. 2002 Oct;129(19):4605-11. doi: 10.1242/dev.129.19.4605.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验