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Ge Lin

Showing results (591-600 of 711) with videos related to

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Analytica Chimica Acta|November 2, 2010
A new approach for simultaneous screening and quantification of toxic pyrrolizidine alkaloids in some potential pyrrolizidine alkaloid-containing plants by using ultra performance liquid chromatography-tandem quadrupole mass spectrometryYan Zhou, Na Li, Franky Fung-Kei Choi, et al.
Human Reproduction (Oxford, England)|November 18, 2019
ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case reportCan Dai, Yongzhe Chen, Liang Hu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 22, 2025
Correcting a patient-specific Rhodopsin mutation with adenine base editor in a mouse modelXiaoxue He, Tong Yan, Zongming Song, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|February 5, 2021
A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertilityWen-Bin He, Ya-Xin Zhang, Chen Tan, et al.
The Journal of Biological Chemistry|February 15, 2023
Histone acetyltransferase KAT2A modulates neural stem cell differentiation and proliferation by inducing degradation of the transcription factor PAX6Zhangji Dong, Wei He, Ge Lin, et al.
Journal of Medical Genetics|August 16, 2019
Biallelic mutations in <i>CFAP65</i> lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformationsWeili Wang, Chaofeng Tu, Hongchuan Nie, et al.
BMC Surgery|April 2, 2025
No differences in IVF pregnancy outcomes following hysteroscopic polypectomy using a manual hysteroscopic tissue removal device versus conventional resectionChen Wang, Yangqin Peng, Qinmei Wang, et al.
American Journal of Human Genetics|February 24, 2021
Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and miceJing Dai, Tianlei Zhang, Jing Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
The Journal of Biological Chemistry|November 10, 2023
Adenine base editor-mediated splicing remodeling activates noncanonical splice sitesYuanyuan Liu, Qing Li, Tong Yan, et al.
Pageof 72

Showing results (591-600 of 711) with videos related to

Sort By:
Pageof 72
Analytica Chimica Acta|November 2, 2010
A new approach for simultaneous screening and quantification of toxic pyrrolizidine alkaloids in some potential pyrrolizidine alkaloid-containing plants by using ultra performance liquid chromatography-tandem quadrupole mass spectrometryYan Zhou, Na Li, Franky Fung-Kei Choi, et al.
Human Reproduction (Oxford, England)|November 18, 2019
ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case reportCan Dai, Yongzhe Chen, Liang Hu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|March 22, 2025
Correcting a patient-specific Rhodopsin mutation with adenine base editor in a mouse modelXiaoxue He, Tong Yan, Zongming Song, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|February 5, 2021
A recurrent mutation in TBPL2 causes diminished ovarian reserve and female infertilityWen-Bin He, Ya-Xin Zhang, Chen Tan, et al.
The Journal of Biological Chemistry|February 15, 2023
Histone acetyltransferase KAT2A modulates neural stem cell differentiation and proliferation by inducing degradation of the transcription factor PAX6Zhangji Dong, Wei He, Ge Lin, et al.
Journal of Medical Genetics|August 16, 2019
Biallelic mutations in <i>CFAP65</i> lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformationsWeili Wang, Chaofeng Tu, Hongchuan Nie, et al.
BMC Surgery|April 2, 2025
No differences in IVF pregnancy outcomes following hysteroscopic polypectomy using a manual hysteroscopic tissue removal device versus conventional resectionChen Wang, Yangqin Peng, Qinmei Wang, et al.
American Journal of Human Genetics|February 24, 2021
Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and miceJing Dai, Tianlei Zhang, Jing Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 4, 2019
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humansYue-Qiu Tan, Chaofeng Tu, Lanlan Meng, et al.
The Journal of Biological Chemistry|November 10, 2023
Adenine base editor-mediated splicing remodeling activates noncanonical splice sitesYuanyuan Liu, Qing Li, Tong Yan, et al.
Pageof 72