Bijun Zhang - Search Results

Year	Number of Results
2012	1
2013	2
2014	4
2015	5
2016	4
2017	6
2018	1
2019	2
2020	7
2021	7
2022	5
2023	1
2024	1

1

A sodium alginate-based sustained-release IPN hydrogel and its applications.

Zou Z, Zhang B, Nie X, Cheng Y, Hu Z, Liao M, Li S. Zou Z, et al. Among authors: zhang b. RSC Adv. 2020 Oct 30;10(65):39722-39730. doi: 10.1039/d0ra04316h. eCollection 2020 Oct 27. RSC Adv. 2020. PMID: 35515393 Free PMC article. Review.

2

20-HETE downregulates Na/K-ATPase α1 expression via the ubiquitination pathway.

Zhang B, Xu R, Fang G, Zhao Y. Zhang B, et al. Prostaglandins Other Lipid Mediat. 2021 Feb;152:106503. doi: 10.1016/j.prostaglandins.2020.106503. Epub 2020 Oct 24. Prostaglandins Other Lipid Mediat. 2021. PMID: 33199266

3

miR-137 downregulates c-kit expression in acute myeloid leukemia.

Hu Y, Dong X, Chu G, Lai G, Zhang B, Wang L, Zhao Y. Hu Y, et al. Among authors: zhang b. Leuk Res. 2017 Jun;57:72-77. doi: 10.1016/j.leukres.2017.01.028. Epub 2017 Feb 16. Leuk Res. 2017. PMID: 28314168

4

20-HETE regulated PSMB5 expression via TGF-β/Smad signaling pathway.

Lai G, Sun R, Wu J, Zhang B, Zhao Y. Lai G, et al. Among authors: zhang b. Prostaglandins Other Lipid Mediat. 2018 Jan;134:123-130. doi: 10.1016/j.prostaglandins.2017.08.005. Epub 2017 Aug 12. Prostaglandins Other Lipid Mediat. 2018. PMID: 28807746

5

Neddylation-mediated Nedd4-2 activation regulates ubiquitination modification of renal NBCe1.

Tu J, Zhang B, Fang G, Chang W, Zhao Y. Tu J, et al. Among authors: zhang b. Exp Cell Res. 2020 May 15;390(2):111958. doi: 10.1016/j.yexcr.2020.111958. Epub 2020 Mar 12. Exp Cell Res. 2020. PMID: 32173470 Free article.

6

Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome.

Zhang L, Liu X, Zhao Y, Wang Q, Zhang Y, Gao H, Zhang B, Cui W, Zhao Y. Zhang L, et al. Among authors: zhang b. Ital J Pediatr. 2022 Jul 23;48(1):121. doi: 10.1186/s13052-022-01319-1. Ital J Pediatr. 2022. PMID: 35870983 Free PMC article.

7

Nedd4-2 haploinsufficiency in mice causes increased seizure susceptibility and impaired Kir4.1 ubiquitination.

Liu X, Zhang H, Zhang B, Tu J, Li X, Zhao Y. Liu X, et al. Among authors: zhang b. Biochim Biophys Acta Mol Basis Dis. 2021 Jun 1;1867(6):166128. doi: 10.1016/j.bbadis.2021.166128. Epub 2021 Mar 13. Biochim Biophys Acta Mol Basis Dis. 2021. PMID: 33722745 Free article.

8

Decreased Amino Acid Concentrations are Involved in Congenital Heart Disease.

Lai G, Li X, Zhang B, Wang L, He R, Zhao Y. Lai G, et al. Among authors: zhang b. Ann Nutr Metab. 2019;74(3):257-263. doi: 10.1159/000499405. Epub 2019 Mar 27. Ann Nutr Metab. 2019. PMID: 30917366

9

Autosomal dominant hereditary spastic paraplegia caused by mutation of UBAP1.

Wang J, Hou Y, Qi L, Zhai S, Zheng L, Han L, Guo Y, Zhang B, Miao P, Lou Y, Xu X, Wang Y, Ren Y, Cao Z, Feng J. Wang J, et al. Among authors: zhang b. Neurogenetics. 2020 Jul;21(3):169-177. doi: 10.1007/s10048-020-00608-3. Epub 2020 Mar 28. Neurogenetics. 2020. PMID: 32222895

10

Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders.

Zhang Y, Liu X, Gao H, Cui W, Zhang B, Zhao Y. Zhang Y, et al. Among authors: zhang b. Mol Cytogenet. 2021 Dec 18;14(1):57. doi: 10.1186/s13039-021-00574-x. Mol Cytogenet. 2021. PMID: 34922566 Free PMC article.

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