Xiao-feng Wei

发表

Mutation in SSUH2 Causes Autosomal‐Dominant Dentin Dysplasia Type I

Qiuxia Yu, Lingling Hu, Xiangmin Xu, 2017, Human mutation.

KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia.

Tizhen Yan, Li Lin, N. Mohandas, 2014, Blood.

Identification of the Linkage of a 1.357 KB β-Globin Gene Deletion and A γ-Globin Gene Triplication in a Chinese Family

Xiang-min Xu, Ji-wei Huang, Qian Li, 2010, Hemoglobin.

Molecular characterization of a novel 27.6-kb deletion causing α+ thalassemia in a Chinese family

Xiang-min Xu, X. Shang, Xin-hua Zhang, 2010, Annals of Hematology.

Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin

Lihua Yu, Xiangmin Xu, X. Shang, 2015, European Journal of Human Genetics.

DNA hypermethylation and X chromosome inactivation are major determinants of phenotypic variation in women heterozygous for G6PD mutations.

Xiang-min Xu, F. Xiong, Xiang-cai Wei, 2014, Blood cells, molecules & diseases.

Investigation of the mechanism of copy number variations involving the α-globin gene cluster on chromosome 16: two case reports and literature review

X. Shang, Linlin Xu, Xiao-feng Wei, 2022, Molecular Genetics and Genomics.

Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with Hemoglobinopathies

Asan, Huanming Yang, Jian Wang, 2017, EBioMedicine.

Erythroid Krüppel-like factor mutations are relatively more common in a thalassemia endemic region and ameliorate the clinical and hematological severity of β-thalassemia

Tizhen Yan, Li Lin, N. Mohandas, 2014 .

RED CELLS , IRON , AND ERYTHROPOIESIS KLF 1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of b-thalassemia

Tizhen Yan, Li Lin, N. Mohandas, 2014 .

Identification of haemolytic anaemia caused by glucose phosphate isomerase deficiency in a thalassaemia‐endemic region: Correction of misdiagnosis and consideration of the cause of misdiagnosis

X. Shang, Xue-dong Wu, D. Zhu, 2022, British journal of haematology.

Unusual survival of a twin with homozygous α0-thalassemia due to chimerism

Decheng Cai, Xiangmin Xu, Fang Yang, 2020, Haematologica.

Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review

Dina Zhu, X. Shang, Min Liang, 2021, Frontiers in Genetics.

A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis.

Decheng Cai, X. Shang, Min Liang, 2020, Gene.

A compound heterozygous mutation of the alkaline phosphatase ALPL gene causes hypophosphatasia in a Han Chinese family

Xiangmin Xu, Hengbiao Sun, Jian Wang, 2020, Experimental and therapeutic medicine.

A combination of the (αα)GZ and ‐‐SEA deletions causing a severe form of hemoglobin H disease

Decheng Cai, Xiangmin Xu, X. Shang, 2019, International journal of laboratory hematology.

A melting curve analysis--based PCR assay for one-step genotyping of β-thalassemia mutations a multicenter validation.

Qingge Li, Xiaoyun Chen, Xiangmin Xu, 2011, The Journal of molecular diagnostics : JMD.

TEA domain transcription factor 4 modulates repression of fetal haemoglobin by direct binding to the γ‐globin gene promoters

Yuhua Ye, Xiangmin Xu, X. Shang, 2021, British journal of haematology.

GATA zinc finger domain‐containing protein 2A (GATAD2A) deficiency reactivates fetal haemoglobin in patients with β‐thalassaemia through impaired formation of methyl‐binding domain protein 2 (MBD2)‐containing nucleosome remodelling and deacetylation (NuRD) complex

Dali Li, Yukio Nakamura, R. Kurita, 2021, British journal of haematology.

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing

Wanjun Zhou, Tizhen Yan, Yuhua Ye, 2020, Molecular Genetics and Genomics.

A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family.

Xiang-min Xu, X. Shang, R. Cai, 2013, Blood cells, molecules & diseases.

Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual

Xiangmin Xu, Li Zhang, Xiao-feng Wei, 2018, Hemoglobin.

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.

Liang Li, Wanjun Zhou, Xiangmin Xu, 2013, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

J. Li, B. Tang, Wanjun Zhou, 2019, Brain : a journal of neurology.

A novel splicing mutation of ANK1 is associated with phenotypic heterogeneity of hereditary spherocytosis in a Chinese family.

Yang Zhang, X. Shang, Linlin Xu, 2022, Biochimica et biophysica acta. Molecular basis of disease.