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Journal of Human Genetics
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June 26, 2023
Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia
Jingpeng Zhao, Zhiyong Ji, Guiquan Meng, et al.
Cell Death & Disease
|
December 8, 2025
Noncanonical role of astrocytic mitochondrial Cx43: suppressing IDH3α to sustain glycolytic homeostasis against depression
Junrui Ye, Hongyun Wang, Ye Peng, et al.
Human Genetics
|
February 19, 2025
Decade-long application of preimplantation genetic testing for DMD/BMD: analysis of five clinical strategies and embryo recombination patterns
Weili Wang, Jing Dai, Xiao Hu, et al.
Frontiers in Cell and Developmental Biology
|
June 16, 2023
Novel homozygous variants in <i>TTC12</i> cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella
Lanlan Meng, Qiang Liu, Chen Tan, et al.
Human Mutation
|
January 12, 2026
RNA-Seq of Cultured Peripheral Blood Lymphocytes Improves Identification of Cryptic Splicing Defects in Rare Disease Diagnostics
Jinlin Ren, Congling Dai, Fei Meng, et al.
Journal of Assisted Reproduction and Genetics
|
January 24, 2024
Extended application of PGT-M strategies for small pathogenic CNVs
Xiao Hu, Weili Wang, Keli Luo, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
December 18, 2020
Distinct expression trend of signature antigens of Staphylococcus aureus osteomyelitis correlated with clinical outcomes
Wei Fu, Wenbin He, Youliang Ren, et al.
American Journal of Human Genetics
|
December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Chen Tan, Lanlan Meng, Mingrong Lv, et al.
Journal of Assisted Reproduction and Genetics
|
February 18, 2026
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics
Chen Tan, Tiantian Wang, Chaofeng Tu, et al.
Cell Discovery
|
August 21, 2023
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression
Chaofeng Tu, Junfei Wen, Weili Wang, et al.
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of 14
Search research articles
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Showing results (121-130 of 133) with videos related to
Sort By:
Page
of 14
Journal of Human Genetics
|
June 26, 2023
Identification of a missense variant of MND1 in meiotic arrest and non-obstructive azoospermia
Jingpeng Zhao, Zhiyong Ji, Guiquan Meng, et al.
Cell Death & Disease
|
December 8, 2025
Noncanonical role of astrocytic mitochondrial Cx43: suppressing IDH3α to sustain glycolytic homeostasis against depression
Junrui Ye, Hongyun Wang, Ye Peng, et al.
Human Genetics
|
February 19, 2025
Decade-long application of preimplantation genetic testing for DMD/BMD: analysis of five clinical strategies and embryo recombination patterns
Weili Wang, Jing Dai, Xiao Hu, et al.
Frontiers in Cell and Developmental Biology
|
June 16, 2023
Novel homozygous variants in <i>TTC12</i> cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella
Lanlan Meng, Qiang Liu, Chen Tan, et al.
Human Mutation
|
January 12, 2026
RNA-Seq of Cultured Peripheral Blood Lymphocytes Improves Identification of Cryptic Splicing Defects in Rare Disease Diagnostics
Jinlin Ren, Congling Dai, Fei Meng, et al.
Journal of Assisted Reproduction and Genetics
|
January 24, 2024
Extended application of PGT-M strategies for small pathogenic CNVs
Xiao Hu, Weili Wang, Keli Luo, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
December 18, 2020
Distinct expression trend of signature antigens of Staphylococcus aureus osteomyelitis correlated with clinical outcomes
Wei Fu, Wenbin He, Youliang Ren, et al.
American Journal of Human Genetics
|
December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice
Chen Tan, Lanlan Meng, Mingrong Lv, et al.
Journal of Assisted Reproduction and Genetics
|
February 18, 2026
A common cause of non-obstructive azoospermia: biallelic MEI1 variants and implications for infertility diagnostics
Chen Tan, Tiantian Wang, Chaofeng Tu, et al.
Cell Discovery
|
August 21, 2023
Loss-of-function variants in human C12orf40 cause male infertility by blocking meiotic progression
Chaofeng Tu, Junfei Wen, Weili Wang, et al.
Page
of 14