Xiang-Min Xu
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Explore the profile of Xiang-Min Xu including associated specialties, affiliations and a list of published articles.
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50
Citations
294
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Recent Articles
1.
Tan X, Liu Y, Shang X, Ye Y, Xu X
Hemoglobin
. 2022 Mar;
45(5):341-344.
PMID: 35322741
We here describe a novel hemoglobin (Hb) variant, Hb Liaobu [α107(G14)Val→Leu, : c.322G>C], in a Chinese family. The structurally abnormal α chain variant could not be detected using capillary electrophoresis...
2.
Dong X, Zhou J, Qin H, Xin B, Huang Z, Li Y, et al.
J Virol
. 2020 Jan;
94(8).
PMID: 31969440
The features of herpes simplex virus 1 (HSV-1) strain 129 (H129), including natural neurotropism and anterograde transneuronal trafficking, make it a potential tool for anterograde neural circuitry tracing. Recently anterograde...
3.
Sun S, Ma D, Li M, Zhang R, Huang C, Huang H, et al.
Brain
. 2019 Jun;
142(8):2215-2229.
PMID: 31199454
Charcot-Marie-Tooth disease is a hereditary motor and sensory neuropathy exhibiting great clinical and genetic heterogeneity. Here, the identification of two heterozygous missense mutations in the C1orf194 gene at 1p21.2-p13.2 with...
4.
Ye Y, Zhang Q, Zhong J, Li Y, Zhang L, Yu Q, et al.
Yi Chuan
. 2017 Apr;
39(3):232-240.
PMID: 28420619
β-thalassemia is an autosomal recessive monogenic disease that is caused by defects in the production of β-like globin chains. Activation of γ-globin gene and the increase in fetal hemoglobin expression...
5.
Yang Q, Chen W, Li Y, Chen C, Xu X, Zhang J
IEEE Trans Cybern
. 2017 Jan;
47(3):636-650.
PMID: 28113686
Taking the advantage of estimation of distribution algorithms (EDAs) in preserving high diversity, this paper proposes a multimodal EDA. Integrated with clustering strategies for crowding and speciation, two versions of...
6.
Li L, Zhou W, Fang P, Zhong Z, Xie J, Yan T, et al.
Clin Chem Lab Med
. 2016 Oct;
55(3):358-367.
PMID: 27754957
Background: Spinal muscular atrophy (SMA) is mainly caused by deletions in SMA-related genes. The objective of this study was to develop gene-dosage assays for diagnosing SMA. Methods: A multiplex, quantitative...
7.
Lin L, Chen D, Guo J, Zhou W, Xu X
Blood Cells Mol Dis
. 2015 May;
55(1):62-7.
PMID: 25976469
Thalassemia is an inherited autosomal recessive blood disorder characterized by the underproduction of globin chains as a consequence of globin gene defects, resulting in malfunctioning red blood cells and oxygen...
8.
Fang P, Li L, Zeng J, Zhou W, Wu W, Zhong Z, et al.
BMC Musculoskelet Disord
. 2015 Apr;
16:11.
PMID: 25888055
Background: Spinal muscular atrophy (SMA) is caused by SMN1 dysfunction, and the copy number of SMN2 and NAIP can modify the phenotype of SMA. The aim of this study was...
9.
Wang J, Xiao Q, Chen Y, Yi S, Liu D, Liu Y, et al.
Blood Cells Mol Dis
. 2014 Jun;
53(4):241-5.
PMID: 24958328
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked incompletely dominant enzyme deficiency that results from G6PD gene mutations. Women heterozygous for G6PD mutations exhibit variation in the loss of enzyme activity...
10.
Liu Y, Shang X, Li Z, Wu Y, Li L, Xu X
Gene
. 2013 Apr;
524(2):377-80.
PMID: 23624125
Pretibial epidermolysis bullosa (PEB) is an extremely rare subtype of dominant dystrophic epidermolysis bullosa (DDEB) caused by mutation of the COL7A1 gene. More than 730 mutations have been identified in...