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Related Articles by Review for PMID: 16402211
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A SALL4 zinc finger missense mutation predicted to result in increased DNA binding affinity is associated with cranial midline defects and mild features of Okihiro syndrome.
Hum Genet. 2006 Mar;119(1-2):154-61. doi: 10.1007/s00439-005-0124-7. Epub 2006 Jan 3.
Hum Genet. 2006.
PMID: 16402211
[Progress of study on the transcription factor SALL4].
Lin J, Ji RB, Qian J.
Lin J, et al.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011 Jun;19(3):820-3.
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2011.
PMID: 21729579
Review.
Chinese.
Item in Clipboard
Two-timing zinc finger transcription factors liaising with RNA.
Burdach J, O'Connell MR, Mackay JP, Crossley M.
Burdach J, et al.
Trends Biochem Sci. 2012 May;37(5):199-205. doi: 10.1016/j.tibs.2012.02.001. Epub 2012 Mar 7.
Trends Biochem Sci. 2012.
PMID: 22405571
Review.
Item in Clipboard
HOXA1 mutations are not a common cause of Duane anomaly.
Tischfield MA, Chan WM, Grunert JF, Andrews C, Engle EC.
Tischfield MA, et al.
Am J Med Genet A. 2006 Apr 15;140(8):900-2. doi: 10.1002/ajmg.a.31167.
Am J Med Genet A. 2006.
PMID: 16528738
Free PMC article.
Review.
No abstract available.
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SALL4: engine of cell stemness.
Xiong J.
Xiong J.
Curr Gene Ther. 2014;14(5):400-11. doi: 10.2174/1566523214666140825125138.
Curr Gene Ther. 2014.
PMID: 25174577
Review.
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Integrative Role of the SALL4 Gene: From Thalidomide Embryopathy to Genetic Defects of the Upper Limb, Internal Organs, Cerebral Midline, and Pituitary.
Kodytková A, Dušátková P, Amaratunga SA, Plachý L, Průhová Š, Lebl J.
Kodytková A, et al.
Horm Res Paediatr. 2024;97(2):106-112. doi: 10.1159/000531452. Epub 2023 Jun 7.
Horm Res Paediatr. 2024.
PMID: 37285827
Free PMC article.
Review.
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SALL Proteins; Common and Antagonistic Roles in Cancer.
Álvarez C, Quiroz A, Benítez-Riquelme D, Riffo E, Castro AF, Pincheira R.
Álvarez C, et al.
Cancers (Basel). 2021 Dec 15;13(24):6292. doi: 10.3390/cancers13246292.
Cancers (Basel). 2021.
PMID: 34944911
Free PMC article.
Review.
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