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Molecular Genetics and Genomics : MGG
|
January 4, 2020
Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α<sup>0</sup>-thalassemia by targeted next-generation sequencing
Zhiming Li, Xuan Shang, Shiqiang Luo, et al.
Hereditas
|
January 19, 2022
Cell-free DNA from plasma as a promising alternative for detection of gene mutations in patients with Maffucci syndrome
Yi Sun, Xindong Fan, Yamin Rao, et al.
Molecular Medicine Reports
|
December 8, 2021
Analysis of a family with mitochondrial trifunctional protein deficiency caused by <i>HADHA</i> gene mutations
Jinling Yang, Dejian Yuan, Xiaohui Tan, et al.
Journal of Clinical Laboratory Analysis
|
November 17, 2011
Detection of α-globin gene deletions using denaturing high-performance liquid chromatography and multiplex ligation-dependent probe amplification
Meiting Cao, Zhaolan Liu, Xingyuan Jia, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
January 17, 2018
[Clinical and cytogenetic study in a child with de novo chromosome 9 abnormality]
Bi-Yu Lu, Jian-Qiang Tan, De-Jian Yuan, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
December 15, 2012
Controlled synthesis of double-wall a-FePO4 nanotubes and their LIB cathode properties
Ren Cai, Hai Liu, Wenyu Zhang, et al.
International Journal of Clinical and Experimental Pathology
|
February 9, 2026
Swimming exercise reversed the loss of grip strength, muscle cross-sectional area and trabecular bone volume among type 1 diabetic rats independent of insulin therapy
Xinlu Li, Yiqun Xiao, Yuming Zheng, et al.
Nano Letters
|
June 10, 2025
Fully Wearable Devices for Real-Time Health Monitoring and Multimodal Sensing in Nanomedicine Using Multiplexed Green Biofuels
Futing Wang, Changxiao Song, Yujin Li, et al.
Blood Cells, Molecules & Diseases
|
March 14, 2013
A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family
Ji-Wei Huang, Xuan Shang, Ying Zhao, et al.
Nano Letters
|
October 7, 2025
Multifunctional PTCA/GO for a Glucose-Driven Electrochemiluminescence Biosensor
Jingxian Li, Ran Zhang, Suping Deng, et al.
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of 19
Search research articles
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Showing results (101-110 of 188) with videos related to
Sort By:
Page
of 19
Molecular Genetics and Genomics : MGG
|
January 4, 2020
Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α<sup>0</sup>-thalassemia by targeted next-generation sequencing
Zhiming Li, Xuan Shang, Shiqiang Luo, et al.
Hereditas
|
January 19, 2022
Cell-free DNA from plasma as a promising alternative for detection of gene mutations in patients with Maffucci syndrome
Yi Sun, Xindong Fan, Yamin Rao, et al.
Molecular Medicine Reports
|
December 8, 2021
Analysis of a family with mitochondrial trifunctional protein deficiency caused by <i>HADHA</i> gene mutations
Jinling Yang, Dejian Yuan, Xiaohui Tan, et al.
Journal of Clinical Laboratory Analysis
|
November 17, 2011
Detection of α-globin gene deletions using denaturing high-performance liquid chromatography and multiplex ligation-dependent probe amplification
Meiting Cao, Zhaolan Liu, Xingyuan Jia, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
January 17, 2018
[Clinical and cytogenetic study in a child with de novo chromosome 9 abnormality]
Bi-Yu Lu, Jian-Qiang Tan, De-Jian Yuan, et al.
Small (Weinheim an Der Bergstrasse, Germany)
|
December 15, 2012
Controlled synthesis of double-wall a-FePO4 nanotubes and their LIB cathode properties
Ren Cai, Hai Liu, Wenyu Zhang, et al.
International Journal of Clinical and Experimental Pathology
|
February 9, 2026
Swimming exercise reversed the loss of grip strength, muscle cross-sectional area and trabecular bone volume among type 1 diabetic rats independent of insulin therapy
Xinlu Li, Yiqun Xiao, Yuming Zheng, et al.
Nano Letters
|
June 10, 2025
Fully Wearable Devices for Real-Time Health Monitoring and Multimodal Sensing in Nanomedicine Using Multiplexed Green Biofuels
Futing Wang, Changxiao Song, Yujin Li, et al.
Blood Cells, Molecules & Diseases
|
March 14, 2013
A novel fusion gene and a common α(0)-thalassemia deletion cause hemoglobin H disease in a Chinese family
Ji-Wei Huang, Xuan Shang, Ying Zhao, et al.
Nano Letters
|
October 7, 2025
Multifunctional PTCA/GO for a Glucose-Driven Electrochemiluminescence Biosensor
Jingxian Li, Ran Zhang, Suping Deng, et al.
Page
of 19