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Nature Communications
|
March 17, 2022
CEP128 is involved in spermatogenesis in humans and mice
Xueguang Zhang, Lingbo Wang, Yongyi Ma, et al.
Journal of Medical Genetics
|
August 5, 2021
Homozygous mutations in <i>CCDC34</i> cause male infertility with oligoasthenoteratozoospermia in humans and mice
Jiangshan Cong, Xiong Wang, Amir Amiri-Yekta, et al.
The Journal of Clinical Investigation
|
November 15, 2024
MGA loss-of-function variants cause premature ovarian insufficiency
Shuyan Tang, Ting Guo, Chengcheng Song, et al.
Cell
|
December 14, 2019
A Translation-Activating Function of MIWI/piRNA during Mouse Spermiogenesis
Peng Dai, Xin Wang, Lan-Tao Gou, et al.
American Journal of Human Genetics
|
November 19, 2019
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice
Chunyu Liu, Xiaojin He, Wangjie Liu, et al.
Cell Research
|
April 22, 2017
CRISPR-Cas9-mediated genome editing in one blastomere of two-cell embryos reveals a novel Tet3 function in regulating neocortical development
Lingbo Wang, Min-Yin Li, Chao Qu, et al.
Human Reproduction Open
|
February 5, 2024
Bi-allelic variants in <i>DNAH3</i> cause male infertility with asthenoteratozoospermia in humans and mice
Gui-Quan Meng, Yaling Wang, Chen Luo, et al.
Science China. Life Sciences
|
December 20, 2024
Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice
Yiling Zhou, Chaofeng Tu, Charles Coutton, et al.
American Journal of Human Genetics
|
January 20, 2021
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility
Chunyu Liu, Chaofeng Tu, Lingbo Wang, et al.
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of 8
Search research articles
Search
Showing results (71-80 of 79) with videos related to
Sort By:
Page
of 8
You have reached the last page of results.
This site can display upto 79 results.
Nature Communications
|
March 17, 2022
CEP128 is involved in spermatogenesis in humans and mice
Xueguang Zhang, Lingbo Wang, Yongyi Ma, et al.
Journal of Medical Genetics
|
August 5, 2021
Homozygous mutations in <i>CCDC34</i> cause male infertility with oligoasthenoteratozoospermia in humans and mice
Jiangshan Cong, Xiong Wang, Amir Amiri-Yekta, et al.
The Journal of Clinical Investigation
|
November 15, 2024
MGA loss-of-function variants cause premature ovarian insufficiency
Shuyan Tang, Ting Guo, Chengcheng Song, et al.
Cell
|
December 14, 2019
A Translation-Activating Function of MIWI/piRNA during Mouse Spermiogenesis
Peng Dai, Xin Wang, Lan-Tao Gou, et al.
American Journal of Human Genetics
|
November 19, 2019
Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice
Chunyu Liu, Xiaojin He, Wangjie Liu, et al.
Cell Research
|
April 22, 2017
CRISPR-Cas9-mediated genome editing in one blastomere of two-cell embryos reveals a novel Tet3 function in regulating neocortical development
Lingbo Wang, Min-Yin Li, Chao Qu, et al.
Human Reproduction Open
|
February 5, 2024
Bi-allelic variants in <i>DNAH3</i> cause male infertility with asthenoteratozoospermia in humans and mice
Gui-Quan Meng, Yaling Wang, Chen Luo, et al.
Science China. Life Sciences
|
December 20, 2024
Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice
Yiling Zhou, Chaofeng Tu, Charles Coutton, et al.
American Journal of Human Genetics
|
January 20, 2021
Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility
Chunyu Liu, Chaofeng Tu, Lingbo Wang, et al.
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of 8