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Items: 1 to 20 of 62

1.

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects.

Kamar A, Fahed AC, Shibbani K, El-Hachem N, Bou-Slaiman S, Arabi M, Kurban M, Seidman JG, Seidman CE, Haidar R, Baydoun E, Nemer G, Bitar F.

Front Genet. 2017 Dec 18;8:217. doi: 10.3389/fgene.2017.00217. eCollection 2017.

2.

SALL4 as a transcriptional and epigenetic regulator in normal and leukemic hematopoiesis.

Yang J.

Biomark Res. 2018 Jan 3;6:1. doi: 10.1186/s40364-017-0115-6. eCollection 2018. Review.

3.

Duane retraction syndrome: causes, effects and management strategies.

Kekunnaya R, Negalur M.

Clin Ophthalmol. 2017 Oct 30;11:1917-1930. doi: 10.2147/OPTH.S127481. eCollection 2017. Review.

4.

A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases.

Khalil A, Tanos R, El-Hachem N, Kurban M, Bouvagnet P, Bitar F, Nemer G.

Sci Rep. 2017 May 3;7(1):1416. doi: 10.1038/s41598-017-01641-3.

5.

The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.

Tao H, Kawakami Y, Hui CC, Hopyan S.

Wiley Interdiscip Rev Dev Biol. 2017 Jul;6(4). doi: 10.1002/wdev.270. Epub 2017 Mar 20. Review.

PMID:
28319333
6.

Sall4 controls differentiation of pluripotent cells independently of the Nucleosome Remodelling and Deacetylation (NuRD) complex.

Miller A, Ralser M, Kloet SL, Loos R, Nishinakamura R, Bertone P, Vermeulen M, Hendrich B.

Development. 2016 Sep 1;143(17):3074-84. doi: 10.1242/dev.139113. Epub 2016 Jul 28.

7.

Leukemic survival factor SALL4 contributes to defective DNA damage repair.

Wang F, Gao C, Lu J, Tatetsu H, Williams DA, Müller LU, Cui W, Chai L.

Oncogene. 2016 Nov 24;35(47):6087-6095. doi: 10.1038/onc.2016.146. Epub 2016 May 2.

8.

Role of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.

Elmakky A, Stanghellini I, Landi A, Percesepe A.

Curr Genomics. 2015 Aug;16(4):264-78. doi: 10.2174/1389202916666150528000412.

9.

SALL4, the missing link between stem cells, development and cancer.

Tatetsu H, Kong NR, Chong G, Amabile G, Tenen DG, Chai L.

Gene. 2016 Jun 15;584(2):111-9. doi: 10.1016/j.gene.2016.02.019. Epub 2016 Feb 16. Review.

10.

Sall1 in renal stromal progenitors non-cell autonomously restricts the excessive expansion of nephron progenitors.

Ohmori T, Tanigawa S, Kaku Y, Fujimura S, Nishinakamura R.

Sci Rep. 2015 Oct 29;5:15676. doi: 10.1038/srep15676.

11.

SALL4 Expression in Hepatocellular Carcinomas Is Associated with EpCAM-Positivity and a Poor Prognosis.

Park H, Lee H, Seo AN, Cho JY, Choi YR, Yoon YS, Han HS, Park YN, Kim H.

J Pathol Transl Med. 2015 Sep;49(5):373-81. doi: 10.4132/jptm.2015.07.09. Epub 2015 Aug 10.

12.

A cohesin-OCT4 complex mediates Sox enhancers to prime an early embryonic lineage.

Abboud N, Moore-Morris T, Hiriart E, Yang H, Bezerra H, Gualazzi MG, Stefanovic S, Guénantin AC, Evans SM, Pucéat M.

Nat Commun. 2015 Apr 8;6:6749. doi: 10.1038/ncomms7749.

13.

Genome-wide linkage analysis and association study identifies loci for polydactyly in chickens.

Sun Y, Liu R, Zhao G, Zheng M, Sun Y, Yu X, Li P, Wen J.

G3 (Bethesda). 2014 Apr 21;4(6):1167-72. doi: 10.1534/g3.114.011338.

14.

Sall1 maintains nephron progenitors and nascent nephrons by acting as both an activator and a repressor.

Kanda S, Tanigawa S, Ohmori T, Taguchi A, Kudo K, Suzuki Y, Sato Y, Hino S, Sander M, Perantoni AO, Sugano S, Nakao M, Nishinakamura R.

J Am Soc Nephrol. 2014 Nov;25(11):2584-95. doi: 10.1681/ASN.2013080896. Epub 2014 Apr 17.

15.

Spalt-like 4 promotes posterior neural fates via repression of pou5f3 family members in Xenopus.

Young JJ, Kjolby RA, Kong NR, Monica SD, Harland RM.

Development. 2014 Apr;141(8):1683-93. doi: 10.1242/dev.099374.

16.

Strabismus genetics across a spectrum of eye misalignment disorders.

Ye XC, Pegado V, Patel MS, Wasserman WW.

Clin Genet. 2014 Aug;86(2):103-11. doi: 10.1111/cge.12367. Epub 2014 Mar 26. Review.

17.

Aberrant expression of SALL4 in acute B cell lymphoblastic leukemia: mechanism, function, and implication for a potential novel therapeutic target.

Ueno S, Lu J, He J, Li A, Zhang X, Ritz J, Silberstein LE, Chai L.

Exp Hematol. 2014 Apr;42(4):307-316.e8. doi: 10.1016/j.exphem.2014.01.005. Epub 2014 Jan 23.

18.

Complex cytogenetic rearrangements at the DURS1 locus in syndromic Duane retraction syndrome.

Baris HN, Chan WM, Andrews C, Behar DM, Donovan DJ, Morton CC, Ranells J, Pal T, Ligon AH, Engle EC.

Clin Case Rep. 2013 Oct 1;1(1). doi: 10.1002/ccr3.11. No abstract available.

19.

Mutation of SALL2 causes recessive ocular coloboma in humans and mice.

Kelberman D, Islam L, Lakowski J, Bacchelli C, Chanudet E, Lescai F, Patel A, Stupka E, Buck A, Wolf S, Beales PL, Jacques TS, Bitner-Glindzicz M, Liasis A, Lehmann OJ, Kohlhase J, Nischal KK, Sowden JC.

Hum Mol Genet. 2014 May 15;23(10):2511-26. doi: 10.1093/hmg/ddt643. Epub 2014 Jan 9.

20.

Hox5 interacts with Plzf to restrict Shh expression in the developing forelimb.

Xu B, Hrycaj SM, McIntyre DC, Baker NC, Takeuchi JK, Jeannotte L, Gaber ZB, Novitch BG, Wellik DM.

Proc Natl Acad Sci U S A. 2013 Nov 26;110(48):19438-43. doi: 10.1073/pnas.1315075110. Epub 2013 Nov 11.

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