Huizhi Zhao
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Explore the profile of Huizhi Zhao including associated specialties, affiliations and a list of published articles.
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33
Citations
507
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Recent Articles
11.
Li H, Wang X, Zhao H, Wang F, Bao Y, Guo J, et al.
Epigenomics
. 2019 Nov;
12(1):5-18.
PMID: 31769301
To know the cause of sequence variants in neural tube defect (NTD). We sequenced genes implicated in neural tube closure (NTC) in a Chinese cohort and elucidated the molecular mechanism-driving...
12.
Zhang J, Zhao H, Wu K, Peng Y, Han X, Zhang H, et al.
J Cell Mol Med
. 2019 May;
23(8):5076-5086.
PMID: 31144421
U2AF1 (U2AF35) is the small subunit of the U2 auxiliary factor (U2AF) that constitutes the U2 snRNP (small nuclear ribonucleoproteins) of the spliceosome. Here, we examined the function of U2AF1...
13.
Li W, Wang Y, Zhao H, Zhang H, Xu Y, Wang S, et al.
Blood
. 2019 May;
134(5):480-491.
PMID: 31101625
The erythroblastic island (EBI), composed of a central macrophage and surrounding erythroid cells, was the first hematopoietic niche discovered. The identity of EBI macrophages has thus far remained elusive. Given...
14.
Wang T, Zhang Y, Ping F, Zhao H, Yan L, Lin Q, et al.
Nephrology (Carlton)
. 2018 Dec;
24(10):1009-1016.
PMID: 30499223
Aim: Pulmonary infection (PI) is the leading cause of death in patients with primary membranous nephropathy on immunosuppressive therapy. A rating score was thus developed to foresee the risk of...
15.
Qu X, Zhang S, Wang S, Wang Y, Li W, Huang Y, et al.
Blood
. 2018 Sep;
132(22):2406-2417.
PMID: 30254129
Myelodysplastic syndromes (MDSs) are clonal hematopoietic stem cell disorders characterized by ineffective hematopoiesis. Anemia is the defining cytopenia of MDS patients, yet the molecular mechanisms for dyserythropoiesis in MDSs remain...
16.
Zhao H, Wu S
Photochem Photobiol
. 2018 Aug;
95(1):338-344.
PMID: 30160308
Nitric oxide ( ) plays an important role in the regulation of redox balance in keratinocytes post-UVB exposure. Since endothelial cells releases for a prolonged time post-UVB, we determined whether...
17.
Huang Y, Hale J, Wang Y, Li W, Zhang S, Zhang J, et al.
J Hematol Oncol
. 2018 Feb;
11(1):19.
PMID: 29433555
Background: SF3B1 is a core component of splicing machinery. Mutations in SF3B1 are frequently found in myelodysplastic syndromes (MDS), particularly in patients with refractory anemia with ringed sideroblasts (RARS), characterized...
18.
Shangguan S, Wang L, Chang S, Lu X, Wang Z, Wu L, et al.
Birth Defects Res A Clin Mol Teratol
. 2014 Aug;
103(1):37-44.
PMID: 25131656
Background: Animal models of neural tube defects (NTDs) have indicated roles for the Fzd3 gene and the planar cell polarity signaling pathway in convergent extension. We investigated the involvement of...
19.
Wang F, Wang J, Guo J, Chen X, Guan Z, Zhao H, et al.
Genes Nutr
. 2013 Aug;
8(6):581-7.
PMID: 23918616
The PCMT1 gene encodes the protein repair enzyme protein-L-isoaspartate (D-aspartate) O-methyltransferase, which is known to protect certain neural cells against Bax-induced apoptosis. Previous studies have produced inconsistent results regarding the...
20.
Wu L, Wang L, Shangguan S, Chang S, Wang Z, Lu X, et al.
Mol Cell Biochem
. 2013 May;
380(1-2):33-42.
PMID: 23690138
Neural tube defects (NTDs) are serious congenital malformation of fusion failure of the neural tube during early embryogenesis. DNA methylation disorders have been found in NTD-affected fetuses, and are correlated...