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Acta Tropica
|
August 1, 2025
Mitochondrial genome characterization and phylogenetic position of a putative taeniid tapeworm (Taenia sp. QH-2023) isolated from Pseudois nayaur
Guodong Dai, Yan Su, Li Li, et al.
Nature Communications
|
October 12, 2021
Three chromosome-level duck genome assemblies provide insights into genomic variation during domestication
Feng Zhu, Zhong-Tao Yin, Zheng Wang, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Frontiers in Endocrinology
|
September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Chenxi Yu, Bobo Xie, Zhengye Zhao, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis
Xiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.
Kidney International
|
May 26, 2020
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome
Nan Yang, Nan Wu, Shuangshuang Dong, et al.
Journal of Medical Genetics
|
August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)
Kun Wang, Sen Zhao, Bowen Liu, et al.
Page
of 35
Search research articles
Search
Showing results (321-330 of 346) with videos related to
Sort By:
Page
of 35
Acta Tropica
|
August 1, 2025
Mitochondrial genome characterization and phylogenetic position of a putative taeniid tapeworm (Taenia sp. QH-2023) isolated from Pseudois nayaur
Guodong Dai, Yan Su, Li Li, et al.
Nature Communications
|
October 12, 2021
Three chromosome-level duck genome assemblies provide insights into genomic variation during domestication
Feng Zhu, Zhong-Tao Yin, Zheng Wang, et al.
Journal of Human Genetics
|
August 18, 2018
Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral-basilar artery dissection (IVAD)
Kun Wang, Sen Zhao, Qianqian Zhang, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
Xin Fan, Sen Zhao, Chenxi Yu, et al.
Journal of Human Genetics
|
December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosis
Mao Lin, Sen Zhao, Gang Liu, et al.
Human Genetics
|
July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease
Jiaqi Liu, Yangzhong Zhou, Sen Liu, et al.
Frontiers in Endocrinology
|
September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
Chenxi Yu, Bobo Xie, Zhengye Zhao, et al.
The Journal of Clinical Investigation
|
November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosis
Xiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.
Kidney International
|
May 26, 2020
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome
Nan Yang, Nan Wu, Shuangshuang Dong, et al.
Journal of Medical Genetics
|
August 19, 2018
Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)
Kun Wang, Sen Zhao, Bowen Liu, et al.
Page
of 35