PubMed for id: 3211

Year	Number of Results
1975	1
1989	2
1990	1
1992	1
1994	1
1996	3
1998	3
1999	3
2000	2
2001	3
2002	4
2003	1
2007	3
2008	1
2009	2
2010	3
2011	3
2012	1
2015	2
2016	2
2017	2
2018	1
2019	1
2020	2
2021	2
2024	0

1

Analysis of HOXB1 gene in a cohort of patients with sporadic ventricular septal defect.

Pinard A, Eudes N, Mitchell J, Bajolle F, Grelet M, Okoronkwo J, Bonnet D, Collod-Béroud G, Zaffran S. Pinard A, et al. Mol Biol Rep. 2018 Oct;45(5):1507-1513. doi: 10.1007/s11033-018-4212-x. Epub 2018 Jun 19. Mol Biol Rep. 2018. PMID: 29923154

2

A novel homozygous HOXB1 mutation in a Turkish family with hereditary congenital facial paresis.

Sahin Y, Güngör O, Ayaz A, Güngör G, Sahin B, Yaykasli K, Ceylaner S. Sahin Y, et al. Brain Dev. 2017 Feb;39(2):166-170. doi: 10.1016/j.braindev.2016.09.002. Epub 2016 Sep 15. Brain Dev. 2017. PMID: 27640920

3

Homozygous HOXB1 loss-of-function mutation in a large family with hereditary congenital facial paresis.

Vogel M, Velleuer E, Schmidt-Jiménez LF, Mayatepek E, Borkhardt A, Alawi M, Kutsche K, Kortüm F. Vogel M, et al. Am J Med Genet A. 2016 Jul;170(7):1813-9. doi: 10.1002/ajmg.a.37682. Epub 2016 May 4. Am J Med Genet A. 2016. PMID: 27144914

4

HOXB1 founder mutation in humans recapitulates the phenotype of Hoxb1-/- mice.

Webb BD, Shaaban S, Gaspar H, Cunha LF, Schubert CR, Hao K, Robson CD, Chan WM, Andrews C, MacKinnon S, Oystreck DT, Hunter DG, Iacovelli AJ, Ye X, Camminady A, Engle EC, Jabs EW. Webb BD, et al. Am J Hum Genet. 2012 Jul 13;91(1):171-9. doi: 10.1016/j.ajhg.2012.05.018. Epub 2012 Jul 5. Am J Hum Genet. 2012. PMID: 22770981 Free PMC article.

5

Anterior Hox genes interact with components of the neural crest specification network to induce neural crest fates.

Gouti M, Briscoe J, Gavalas A. Gouti M, et al. Stem Cells. 2011 May;29(5):858-70. doi: 10.1002/stem.630. Stem Cells. 2011. PMID: 21433221 Free PMC article.

6

A genetic polymorphism in the human HOXB1 homeobox gene implying a 9bp tandem repeat in the amino-terminal coding region. Mutations in brief no. 200. Online.

Faiella A, Zortea M, Barbaria E, Albani F, Capra V, Cama A, Boncinelli E. Faiella A, et al. Hum Mutat. 1998;12(5):363. Hum Mutat. 1998. PMID: 10671062

7

Specification of distinct motor neuron identities by the singular activities of individual Hox genes.

Jungbluth S, Bell E, Lumsden A. Jungbluth S, et al. Development. 1999 Jun;126(12):2751-8. doi: 10.1242/dev.126.12.2751. Development. 1999. PMID: 10331985

8

MicroRNA-301b-3p facilitates cell proliferation and migration in colorectal cancer by targeting HOXB1.

Xiong J, Zhang L, Tang R, Zhu Z. Xiong J, et al. Bioengineered. 2021 Dec;12(1):5839-5849. doi: 10.1080/21655979.2021.1962483. Bioengineered. 2021. PMID: 34488545 Free PMC article.

9

The MicroRNA hsa-let-7g Promotes Proliferation and Inhibits Apoptosis in Lung Cancer by Targeting HOXB1.

Cui F, Zhou Q, Xiao K, Ma S. Cui F, et al. Yonsei Med J. 2020 Mar;61(3):210-217. doi: 10.3349/ymj.2020.61.3.210. Yonsei Med J. 2020. PMID: 32102121 Free PMC article.

10

HOXB1 Is a Tumor Suppressor Gene Regulated by miR-3175 in Glioma.

Han L, Liu D, Li Z, Tian N, Han Z, Wang G, Fu Y, Guo Z, Zhu Z, Du C, Tian Y. Han L, et al. PLoS One. 2015 Nov 13;10(11):e0142387. doi: 10.1371/journal.pone.0142387. eCollection 2015. PLoS One. 2015. PMID: 26565624 Free PMC article.

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