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Chaofeng Tu

Showing results (41-50 of 64) with videos related to

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Human Reproduction (Oxford, England)|May 16, 2023
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermiaWeili Wang, Lilan Su, Lanlan Meng, 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.
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.
Molecular Human Reproduction|April 29, 2022
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and miceWeili Wang, Lanlan Meng, Jiaxin He, et al.
Human Genetics|January 17, 2020
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCDChaofeng Tu, Hongchuan Nie, Lanlan Meng, et al.
Molecular Human Reproduction|January 23, 2024
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermiaSibing Yi, Weili Wang, Lilan Su, 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 flagellaLanlan Meng, Qiang Liu, Chen Tan, et al.
Frontiers of Medicine|June 14, 2023
Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and miceRongchun Wang, Danhui Yang, Chaofeng Tu, et al.
Human Molecular Genetics|July 7, 2021
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesisWeili Wang, Shixong Tian, Hongchuan Nie, et al.
Journal of Medical Genetics|January 2, 2023
Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOAShixiong Tian, Chaofeng Tu, Xiaojin He, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Human Reproduction (Oxford, England)|May 16, 2023
Biallelic variants in KCTD19 associated with male factor infertility and oligoasthenoteratozoospermiaWeili Wang, Lilan Su, Lanlan Meng, 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.
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.
Molecular Human Reproduction|April 29, 2022
Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and miceWeili Wang, Lanlan Meng, Jiaxin He, et al.
Human Genetics|January 17, 2020
Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCDChaofeng Tu, Hongchuan Nie, Lanlan Meng, et al.
Molecular Human Reproduction|January 23, 2024
Deleterious variants in X-linked RHOXF1 cause male infertility with oligo- and azoospermiaSibing Yi, Weili Wang, Lilan Su, 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 flagellaLanlan Meng, Qiang Liu, Chen Tan, et al.
Frontiers of Medicine|June 14, 2023
Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and miceRongchun Wang, Danhui Yang, Chaofeng Tu, et al.
Human Molecular Genetics|July 7, 2021
CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesisWeili Wang, Shixong Tian, Hongchuan Nie, et al.
Journal of Medical Genetics|January 2, 2023
Biallelic mutations in <i>CFAP54</i> cause male infertility with severe MMAF and NOAShixiong Tian, Chaofeng Tu, Xiaojin He, et al.
Pageof 7