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Journal of Clinical Laboratory Analysis|August 2, 2017
The prevalence and molecular characterization of (δβ)<sup>0</sup> -thalassemia and hereditary persistence of fetal hemoglobin in the Chinese Zhuang populationSheng He, Yuan Wei, Li Lin, et al.Molecular Genetics & Genomic Medicine|June 18, 2023
Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing-site variant and a missense variant in the ROBO3 geneSheng Yi, Zailong Qin, Xunzhao Zhou, et al.Hemoglobin|March 2, 2018
Characterization of Hb Bart's Hydrops Fetalis Caused by - -<sup>SEA</sup> and a Large Novel α<sup>0</sup>-Thalassemia DeletionSheng He, Jihui Li, Peng Huang, et al.Nanotechnology|December 2, 2016
Plasmonic nano-protrusions: hierarchical nanostructures for single-molecule Raman spectroscopySagnik Basuray, Avinash Pathak, Sangho Bok, et al.European Journal of Pharmacology|July 17, 2025
Koumine alters immune barrier function by targeting TGFβ-mediated collagen deposition in gastric cancerHailing Lin, Jingping Liu, Yuli Tang, et al.Journal of Clinical Pathology|September 14, 2022
Molecular characterisation of Hb Akron [β52 (D3) Asp→Val] combined with thalassaemia in a Chinese familySheng He, Bolian Wang, Shang Yi, et al.Hemoglobin|May 6, 2017
Complex Interaction of Hb Q-Thailand with α<sup>0</sup>- and β<sup>0</sup>-Thalassemia in a Chinese FamilySheng He, Qian Qin, Li Lin, et al.Gene|February 16, 2016
Prevalence and genetic analysis of α- and β-thalassemia in Baise region, a multi-ethnic region in southern ChinaSheng He, Qian Qin, Shang Yi, et al.Hemoglobin|August 6, 2016
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese FamilySheng He, Li Lin, Yuan Wei, et al.Hemoglobin|November 23, 2017
Characterization of a Large Novel α-Globin Gene Cluster Deletion Causing α<sup>0</sup>-Thalassemia in a Chinese FamilySheng He, Qian Qin, Peng Huang, et al.Pageof 5