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Human Reproduction (Oxford, England)
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June 26, 2021
Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex
Pingping Chen, Hexige Saiyin, Ruona Shi, et al.
Oncotarget
|
September 2, 2016
Rottlerin exerts its anti-tumor activity through inhibition of Skp2 in breast cancer cells
Xuyuan Yin, Yu Zhang, Jingna Su, et al.
Human Molecular Genetics
|
February 27, 2026
Correlations between phenotype and gene region-specific episignatures in Rubinstein-Taybi syndrome and Menke-Hennekam syndrome
Yanan Tang, Xiantao Ye, Yongkun Zhan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 12, 2019
A Novel Nonsense Mutation of <i>PHF6</i> in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome
Xia Zhang, Yanjie Fan, Xiaomin Liu, et al.
Nature Communications
|
December 16, 2015
SCF(β-TRCP) promotes cell growth by targeting PR-Set7/Set8 for degradation
Zhiwei Wang, Xiangpeng Dai, Jiateng Zhong, et al.
Pediatric Research
|
October 2, 2025
Identification of novel NDUFA3 variants in a patient with mitochondrial disorders
Yu Sun, Xiujuan Wei, Bing Xiao, et al.
The New Phytologist
|
February 16, 2026
StHAB1-mediated ABA signaling potentiates the sensitivity to long-distance signal StSP6A to promote tuberization in potato
Enshuang Wang, Shenglin Jing, Liepeng Dong, et al.
The Plant Cell
|
July 15, 2026
Bifurcation of StCRY1-StHY5 axis orchestrates blue light-enhanced glycoalkaloid and chlorophyll accumulation in potato tubers
Jun Qin, Shenglin Jing, Shengxuan Liu, et al.
Clinical Chemistry
|
February 8, 2020
High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study
Yu Sun, Xiantao Ye, Yanjie Fan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
August 2, 2021
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration
Yu Sun, Xiujuan Wei, Fang Fang, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Human Reproduction (Oxford, England)
|
June 26, 2021
Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex
Pingping Chen, Hexige Saiyin, Ruona Shi, et al.
Oncotarget
|
September 2, 2016
Rottlerin exerts its anti-tumor activity through inhibition of Skp2 in breast cancer cells
Xuyuan Yin, Yu Zhang, Jingna Su, et al.
Human Molecular Genetics
|
February 27, 2026
Correlations between phenotype and gene region-specific episignatures in Rubinstein-Taybi syndrome and Menke-Hennekam syndrome
Yanan Tang, Xiantao Ye, Yongkun Zhan, et al.
Journal of Clinical Research in Pediatric Endocrinology
|
January 12, 2019
A Novel Nonsense Mutation of <i>PHF6</i> in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome
Xia Zhang, Yanjie Fan, Xiaomin Liu, et al.
Nature Communications
|
December 16, 2015
SCF(β-TRCP) promotes cell growth by targeting PR-Set7/Set8 for degradation
Zhiwei Wang, Xiangpeng Dai, Jiateng Zhong, et al.
Pediatric Research
|
October 2, 2025
Identification of novel NDUFA3 variants in a patient with mitochondrial disorders
Yu Sun, Xiujuan Wei, Bing Xiao, et al.
The New Phytologist
|
February 16, 2026
StHAB1-mediated ABA signaling potentiates the sensitivity to long-distance signal StSP6A to promote tuberization in potato
Enshuang Wang, Shenglin Jing, Liepeng Dong, et al.
The Plant Cell
|
July 15, 2026
Bifurcation of StCRY1-StHY5 axis orchestrates blue light-enhanced glycoalkaloid and chlorophyll accumulation in potato tubers
Jun Qin, Shenglin Jing, Shengxuan Liu, et al.
Clinical Chemistry
|
February 8, 2020
High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study
Yu Sun, Xiantao Ye, Yanjie Fan, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
August 2, 2021
HPDL deficiency causes a neuromuscular disease by impairing the mitochondrial respiration
Yu Sun, Xiujuan Wei, Fang Fang, et al.
Page
of 3