PubMed (GeneRIF) for id: 10483

Year	Number of Results
2002	1
2009	3
2010	4
2011	3
2012	1
2013	3
2014	3
2015	3
2016	1
2017	5
2018	4
2020	2
2021	4
2022	2
2023	2
2024	0

1

New Cases and Mutations in SEC23B Gene Causing Congenital Dyserythropoietic Anemia Type II.

Musri MM, Venturi V, Ferrer-Cortès X, Romero-Cortadellas L, Hernández G, Leoz P, Ricard Andrés MP, Morado M, Fernández Valle MDC, Beneitez Pastor D, Ortuño Cabrero A, Moreno Gamiz M, Senent Peris L, Perez-Valencia AI, Pérez-Montero S, Tornador C, Sánchez M. Musri MM, et al. Int J Mol Sci. 2023 Jun 9;24(12):9935. doi: 10.3390/ijms24129935. Int J Mol Sci. 2023. PMID: 37373084 Free PMC article.

2

Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.

Saptarshi AN, More TA, Dongerdiye R, Kedar P. Saptarshi AN, et al. Indian J Pediatr. 2023 Aug;90(8):840. doi: 10.1007/s12098-023-04662-1. Epub 2023 May 19. Indian J Pediatr. 2023. PMID: 37204595 No abstract available.

3

SEC23B Loss-of-Function Suppresses Hepcidin Expression by Impairing Glycosylation Pathway in Human Hepatic Cells.

Rosato BE, Marra R, D'Onofrio V, Del Giudice F, Della Monica S, Iolascon A, Andolfo I, Russo R. Rosato BE, et al. Int J Mol Sci. 2022 Jan 24;23(3):1304. doi: 10.3390/ijms23031304. Int J Mol Sci. 2022. PMID: 35163229 Free PMC article.

4

A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice.

Wei W, Liu Z, Zhang C, Khoriaty R, Zhu M, Zhang B. Wei W, et al. J Biol Chem. 2022 Jan;298(1):101536. doi: 10.1016/j.jbc.2021.101536. Epub 2021 Dec 24. J Biol Chem. 2022. PMID: 34954140 Free PMC article.

5

[Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia].

Feng Y, Shi P, Liu N, Kong X. Feng Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Aug 10;38(8):727-730. doi: 10.3760/cma.j.cn511374-20200327-00211. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 34365611 Chinese.

6

Compound heterozygosity for two novel mutations of the SEC23B gene in congenital dyserythropoietic anemia type II.

Chen S, Guo Z, Ye Y, Yang S, Huang G. Chen S, et al. Int J Hematol. 2021 Sep;114(3):390-394. doi: 10.1007/s12185-021-03155-1. Epub 2021 Apr 29. Int J Hematol. 2021. PMID: 33914262

7

Non-canonical role of wild-type SEC23B in the cellular stress response pathway.

Yehia L, Liu D, Fu S, Iyer P, Eng C. Yehia L, et al. Cell Death Dis. 2021 Mar 22;12(4):304. doi: 10.1038/s41419-021-03589-9. Cell Death Dis. 2021. PMID: 33753724 Free PMC article.

8

RAP-011 Rescues the Disease Phenotype in a Cellular Model of Congenital Dyserythropoietic Anemia Type II by Inhibiting the SMAD2-3 Pathway.

De Rosa G, Andolfo I, Marra R, Manna F, Rosato BE, Iolascon A, Russo R. De Rosa G, et al. Int J Mol Sci. 2020 Aug 4;21(15):5577. doi: 10.3390/ijms21155577. Int J Mol Sci. 2020. PMID: 32759740 Free PMC article.

9

Mutations in the coat complex II component SEC23B promote colorectal cancer metastasis.

Yang C, Chen N, Li X, Lu D, Hou Z, Li Y, Jin Y, Gu J, Yin Y. Yang C, et al. Cell Death Dis. 2020 Mar 2;11(3):157. doi: 10.1038/s41419-020-2358-7. Cell Death Dis. 2020. PMID: 32123160 Free PMC article.

10

The ULK1-FBXW5-SEC23B nexus controls autophagy.

Jeong YT, Simoneschi D, Keegan S, Melville D, Adler NS, Saraf A, Florens L, Washburn MP, Cavasotto CN, Fenyö D, Cuervo AM, Rossi M, Pagano M. Jeong YT, et al. Elife. 2018 Dec 31;7:e42253. doi: 10.7554/eLife.42253. Elife. 2018. PMID: 30596474 Free PMC article.

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