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Frontiers in Oncology
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October 10, 2022
LncRNA MALAT1 regulates METTL3-mediated PD-L1 expression and immune infiltrates in pancreatic cancer
Zhengwei Song, Xiaoguang Wang, Fei Chen, et al.
Heliyon
|
March 25, 2024
Clinical and genetic analysis of trichohepatoneurodevelopmental syndrome caused by a <i>CCDC47</i> variant
Qi Yang, Xunzhao Zhou, Yeying Ling, et al.
Frontiers in Genetics
|
November 3, 2025
A novel dinucleotide variant at 5' splice sites in the <i>F8</i> gene causes exon 19 skipping in a Chinese family with hemophilia A
Xunzhao Zhou, Qi Yang, Qiuli Chen, et al.
Hemoglobin
|
April 4, 2017
A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T]
Li Lin, Biyan Chen, Shang Yi, et al.
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 population
Sheng 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 gene
Sheng Yi, Zailong Qin, Xunzhao Zhou, et al.
Scientific Reports
|
August 19, 2025
Machine learning based screening of biomarkers associated with cell death and immunosuppression of multiple life stages sepsis populations
Jie Yang, Fanyan Ou, Binbin Li, et al.
FEBS Open Bio
|
December 10, 2021
Optimised expression and purification of RBP4 and preparation of anti-RBP4 monoclonal antibody
Hui Li, Xiao He, Sha Wen, 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 Family
Sheng He, Qian Qin, Li Lin, et al.
Hemoglobin
|
August 6, 2016
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family
Sheng He, Li Lin, Yuan Wei, et al.
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of 9
Search research articles
Search
Showing results (41-50 of 88) with videos related to
Sort By:
Page
of 9
Frontiers in Oncology
|
October 10, 2022
LncRNA MALAT1 regulates METTL3-mediated PD-L1 expression and immune infiltrates in pancreatic cancer
Zhengwei Song, Xiaoguang Wang, Fei Chen, et al.
Heliyon
|
March 25, 2024
Clinical and genetic analysis of trichohepatoneurodevelopmental syndrome caused by a <i>CCDC47</i> variant
Qi Yang, Xunzhao Zhou, Yeying Ling, et al.
Frontiers in Genetics
|
November 3, 2025
A novel dinucleotide variant at 5' splice sites in the <i>F8</i> gene causes exon 19 skipping in a Chinese family with hemophilia A
Xunzhao Zhou, Qi Yang, Qiuli Chen, et al.
Hemoglobin
|
April 4, 2017
A Novel α2-Globin Gene Mutation: Hb Debao [α31(B12)Arg→Trp; HBA2: c.94A>T]
Li Lin, Biyan Chen, Shang Yi, et al.
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 population
Sheng 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 gene
Sheng Yi, Zailong Qin, Xunzhao Zhou, et al.
Scientific Reports
|
August 19, 2025
Machine learning based screening of biomarkers associated with cell death and immunosuppression of multiple life stages sepsis populations
Jie Yang, Fanyan Ou, Binbin Li, et al.
FEBS Open Bio
|
December 10, 2021
Optimised expression and purification of RBP4 and preparation of anti-RBP4 monoclonal antibody
Hui Li, Xiao He, Sha Wen, 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 Family
Sheng He, Qian Qin, Li Lin, et al.
Hemoglobin
|
August 6, 2016
Identification of a Novel β-Globin Mutation (HBB: C.189_195delTCATGGC) in a Chinese Family
Sheng He, Li Lin, Yuan Wei, et al.
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of 9