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Journal of Cellular Physiology
|
January 17, 2018
Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase
Jichun Yang, Jing Ma, Yu Xiong, et al.
International Journal of Pediatric Otorhinolaryngology
|
February 7, 2013
Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct
Gendong Yao, Shouxia Li, Dingli Chen, et al.
Acta Oto-Laryngologica
|
May 4, 2013
Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss
Gendong Yao, Dingli Chen, Huijun Wang, et al.
The International Journal of Biochemistry & Cell Biology
|
December 25, 2012
The alteration of protein profile induced by cigarette smoking via oxidative stress in mice epididymis
Zijue Zhu, Wangjie Xu, Jingbo Dai, et al.
Biochimica Et Biophysica Acta
|
December 11, 2012
Ubiquitin C-terminal Hydrolase 37, a novel predictor for hepatocellular carcinoma recurrence, promotes cell migration and invasion via interacting and deubiquitinating PRP19
Ying Fang, Da Fu, Wenqing Tang, et al.
Prenatal Diagnosis
|
March 21, 2012
Identification of novel candidate maternal serum protein markers for Down syndrome by integrated proteomic and bioinformatic analysis
Yuan Kang, Xinran Dong, Qiongjie Zhou, et al.
Fa Yi Xue Za Zhi
|
March 24, 2011
[Estimation of postmortem interval using microRNA and 18S rRNA degradation in rat cardiac muscle]
Wen-can Li, Kai-jun Ma, Ping Zhang, et al.
Pediatric Nephrology (Berlin, Germany)
|
May 25, 2021
Diagnostic and clinical utility of genetic testing in children with kidney failure
Jing Chen, Fang Lin, Yihui Zhai, et al.
Frontiers in Cell and Developmental Biology
|
July 16, 2021
SP1-Mediated Upregulation of Long Noncoding RNA ZFAS1 Involved in Non-syndromic Cleft Lip and Palate <i>via</i> Inactivating WNT/β-Catenin Signaling Pathway
Shiyu Chen, Zhonglin Jia, Ming Cai, et al.
Bone & Joint Research
|
September 21, 2019
Functional analysis of a <i>de novo</i> mutation c.1692 del A of the <i>PHEX</i> gene in a Chinese family with X-linked hypophosphataemic rickets
Jianbo Huang, Xiaogang Bao, Wenjun Xia, et al.
Page
of 23
Search research articles
Search
Showing results (171-180 of 230) with videos related to
Sort By:
Page
of 23
Journal of Cellular Physiology
|
January 17, 2018
Epigenetic regulation of megakaryocytic and erythroid differentiation by PHF2 histone demethylase
Jichun Yang, Jing Ma, Yu Xiong, et al.
International Journal of Pediatric Otorhinolaryngology
|
February 7, 2013
Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct
Gendong Yao, Shouxia Li, Dingli Chen, et al.
Acta Oto-Laryngologica
|
May 4, 2013
Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss
Gendong Yao, Dingli Chen, Huijun Wang, et al.
The International Journal of Biochemistry & Cell Biology
|
December 25, 2012
The alteration of protein profile induced by cigarette smoking via oxidative stress in mice epididymis
Zijue Zhu, Wangjie Xu, Jingbo Dai, et al.
Biochimica Et Biophysica Acta
|
December 11, 2012
Ubiquitin C-terminal Hydrolase 37, a novel predictor for hepatocellular carcinoma recurrence, promotes cell migration and invasion via interacting and deubiquitinating PRP19
Ying Fang, Da Fu, Wenqing Tang, et al.
Prenatal Diagnosis
|
March 21, 2012
Identification of novel candidate maternal serum protein markers for Down syndrome by integrated proteomic and bioinformatic analysis
Yuan Kang, Xinran Dong, Qiongjie Zhou, et al.
Fa Yi Xue Za Zhi
|
March 24, 2011
[Estimation of postmortem interval using microRNA and 18S rRNA degradation in rat cardiac muscle]
Wen-can Li, Kai-jun Ma, Ping Zhang, et al.
Pediatric Nephrology (Berlin, Germany)
|
May 25, 2021
Diagnostic and clinical utility of genetic testing in children with kidney failure
Jing Chen, Fang Lin, Yihui Zhai, et al.
Frontiers in Cell and Developmental Biology
|
July 16, 2021
SP1-Mediated Upregulation of Long Noncoding RNA ZFAS1 Involved in Non-syndromic Cleft Lip and Palate <i>via</i> Inactivating WNT/β-Catenin Signaling Pathway
Shiyu Chen, Zhonglin Jia, Ming Cai, et al.
Bone & Joint Research
|
September 21, 2019
Functional analysis of a <i>de novo</i> mutation c.1692 del A of the <i>PHEX</i> gene in a Chinese family with X-linked hypophosphataemic rickets
Jianbo Huang, Xiaogang Bao, Wenjun Xia, et al.
Page
of 23