Similar articles for PMID: 18818376

Year	Number of Results
1980	1
1998	1
1999	3
2000	2
2001	2
2002	2
2003	4
2004	3
2005	5
2006	6
2007	6
2008	5
2009	5
2010	10
2011	6
2012	6
2013	3
2014	2
2015	2
2016	4
2017	6
2018	8
2019	3
2020	2
2021	5
2022	5
2023	2
2024	0

1

Sall1, sall2, and sall4 are required for neural tube closure in mice.

Böhm J, Buck A, Borozdin W, Mannan AU, Matysiak-Scholze U, Adham I, Schulz-Schaeffer W, Floss T, Wurst W, Kohlhase J, Barrionuevo F. Böhm J, et al. Am J Pathol. 2008 Nov;173(5):1455-63. doi: 10.2353/ajpath.2008.071039. Epub 2008 Sep 25. Am J Pathol. 2008. PMID: 18818376 Free PMC article.

2

Zinc finger protein sall2 is not essential for embryonic and kidney development.

Sato A, Matsumoto Y, Koide U, Kataoka Y, Yoshida N, Yokota T, Asashima M, Nishinakamura R. Sato A, et al. Mol Cell Biol. 2003 Jan;23(1):62-9. doi: 10.1128/MCB.23.1.62-69.2003. Mol Cell Biol. 2003. PMID: 12482961 Free PMC article.

3

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development.

Sakaki-Yumoto M, Kobayashi C, Sato A, Fujimura S, Matsumoto Y, Takasato M, Kodama T, Aburatani H, Asashima M, Yoshida N, Nishinakamura R. Sakaki-Yumoto M, et al. Development. 2006 Aug;133(15):3005-13. doi: 10.1242/dev.02457. Epub 2006 Jun 21. Development. 2006. PMID: 16790473

4

sall1 and sall4 repress pou5f3 family expression to allow neural patterning, differentiation, and morphogenesis in Xenopus laevis.

Exner CRT, Kim AY, Mardjuki SM, Harland RM. Exner CRT, et al. Dev Biol. 2017 May 1;425(1):33-43. doi: 10.1016/j.ydbio.2017.03.015. Epub 2017 Mar 18. Dev Biol. 2017. PMID: 28322736 Free article.

5

Genomic cloning, chromosomal mapping, and expression analysis of msal-2.

Kohlhase J, Altmann M, Archangelo L, Dixkens C, Engel W. Kohlhase J, et al. Mamm Genome. 2000 Jan;11(1):64-8. doi: 10.1007/s003350010012. Mamm Genome. 2000. PMID: 10602995

6

Genetic backgrounds and modifier genes of NTD mouse models: An opportunity for greater understanding of the multifactorial etiology of neural tube defects.

Leduc RY, Singh P, McDermid HE. Leduc RY, et al. Birth Defects Res. 2017 Jan 30;109(2):140-152. doi: 10.1002/bdra.23554. Birth Defects Res. 2017. PMID: 27768235 Review.

7

Expression of a truncated Sall1 transcriptional repressor is responsible for Townes-Brocks syndrome birth defects.

Kiefer SM, Ohlemiller KK, Yang J, McDill BW, Kohlhase J, Rauchman M. Kiefer SM, et al. Hum Mol Genet. 2003 Sep 1;12(17):2221-7. doi: 10.1093/hmg/ddg233. Epub 2003 Jul 15. Hum Mol Genet. 2003. PMID: 12915476

8

Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues.

De Castro SCP, Hirst CS, Savery D, Rolo A, Lickert H, Andersen B, Copp AJ, Greene NDE. De Castro SCP, et al. Dev Biol. 2018 Mar 15;435(2):130-137. doi: 10.1016/j.ydbio.2018.01.016. Epub 2018 Feb 2. Dev Biol. 2018. PMID: 29397878 Free PMC article.

9

Molecular cloning of a SALL1-related pseudogene and mapping to chromosome Xp11.2.

Kohlhase J, Köhler A, Jäckle H, Engel W, Stick R. Kohlhase J, et al. Cytogenet Cell Genet. 1999;84(1-2):31-4. doi: 10.1159/000015206. Cytogenet Cell Genet. 1999. PMID: 10343095

10

Regional neural tube closure defined by the Grainy head-like transcription factors.

Rifat Y, Parekh V, Wilanowski T, Hislop NR, Auden A, Ting SB, Cunningham JM, Jane SM. Rifat Y, et al. Dev Biol. 2010 Sep 15;345(2):237-45. doi: 10.1016/j.ydbio.2010.07.017. Epub 2010 Jul 21. Dev Biol. 2010. PMID: 20654612 Free article.

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