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Ge Lin

Showing results (641-650 of 711) with videos related to

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Diabetologia|May 20, 2018
Folate treatment of pregnant rat dams abolishes metabolic effects in female offspring induced by a paternal pre-conception unhealthy dietJian Li, Yong-Ping Lu, Oleg Tsuprykov, et al.
Molecular Genetics & Genomic Medicine|May 4, 2021
Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicismXiao Hu, Wen-Bin He, Shuo-Ping Zhang, et al.
Journal of Assisted Reproduction and Genetics|January 24, 2024
Extended application of PGT-M strategies for small pathogenic CNVsXiao Hu, Weili Wang, Keli Luo, et al.
Planta Medica|October 29, 2021
Novel Insights into Pyrrolizidine Alkaloid Toxicity and Implications for Risk Assessment: Occurrence, Genotoxicity, Toxicokinetics, Risk Assessment-A Workshop ReportDieter Schrenk, Jörg Fahrer, Ashley Allemang, et al.
Genes, Chromosomes & Cancer|May 13, 2008
Tumor progression of culture-adapted human embryonic stem cells during long-term cultureSheng Yang, Ge Lin, Yue-Qiu Tan, et al.
Human Vaccines & Immunotherapeutics|February 5, 2021
Safety and immunogenicity of a novel oral hexavalent rotavirus vaccine：a phase I clinical trialZhi-Wei Wu, Qing-Liang Li, Hai-Song Zhou, et al.
Science China. Life Sciences|June 2, 2025
GMNN mutations cause female infertility characterized by preimplantation embryo arrest through regulating DNA re-replicationHonghui Zhang, Wei Su, Xiaohong Jiang, et al.
Journal of Medical Genetics|February 5, 2022
RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disordersWen-Bin He, Wen-Juan Xiao, Cong-Ling Dai, et al.
Patterns (New York, N.Y.)|July 31, 2024
A generalized AI system for human embryo selection covering the entire IVF cycle via multi-modal contrastive learningGuangyu Wang, Kai Wang, Yuanxu Gao, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Pageof 72

Showing results (641-650 of 711) with videos related to

Sort By:
Pageof 72
Diabetologia|May 20, 2018
Folate treatment of pregnant rat dams abolishes metabolic effects in female offspring induced by a paternal pre-conception unhealthy dietJian Li, Yong-Ping Lu, Oleg Tsuprykov, et al.
Molecular Genetics & Genomic Medicine|May 4, 2021
Next-generation sequence-based preimplantation genetic testing for monogenic disease resulting from maternal mosaicismXiao Hu, Wen-Bin He, Shuo-Ping Zhang, et al.
Journal of Assisted Reproduction and Genetics|January 24, 2024
Extended application of PGT-M strategies for small pathogenic CNVsXiao Hu, Weili Wang, Keli Luo, et al.
Planta Medica|October 29, 2021
Novel Insights into Pyrrolizidine Alkaloid Toxicity and Implications for Risk Assessment: Occurrence, Genotoxicity, Toxicokinetics, Risk Assessment-A Workshop ReportDieter Schrenk, Jörg Fahrer, Ashley Allemang, et al.
Genes, Chromosomes & Cancer|May 13, 2008
Tumor progression of culture-adapted human embryonic stem cells during long-term cultureSheng Yang, Ge Lin, Yue-Qiu Tan, et al.
Human Vaccines & Immunotherapeutics|February 5, 2021
Safety and immunogenicity of a novel oral hexavalent rotavirus vaccine：a phase I clinical trialZhi-Wei Wu, Qing-Liang Li, Hai-Song Zhou, et al.
Science China. Life Sciences|June 2, 2025
GMNN mutations cause female infertility characterized by preimplantation embryo arrest through regulating DNA re-replicationHonghui Zhang, Wei Su, Xiaohong Jiang, et al.
Journal of Medical Genetics|February 5, 2022
RNA splicing analysis contributes to reclassifying variants of uncertain significance and improves the diagnosis of monogenic disordersWen-Bin He, Wen-Juan Xiao, Cong-Ling Dai, et al.
Patterns (New York, N.Y.)|July 31, 2024
A generalized AI system for human embryo selection covering the entire IVF cycle via multi-modal contrastive learningGuangyu Wang, Kai Wang, Yuanxu Gao, et al.
American Journal of Human Genetics|December 21, 2021
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and miceChen Tan, Lanlan Meng, Mingrong Lv, et al.
Pageof 72