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Human Genetics
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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.
Infectious Diseases and Therapy
|
July 11, 2023
Patient Biochemistry and Treatment Need in Chronic Hepatitis B Virus Infection Across Three Continents: Retrospective Cross-Sectional Cohort Studies
Iain A Gillespie, Eleanor Barnes, Ian C K Wong, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 31, 2025
Plasma p-tau217 and p-tau217/Aβ1-42 are effective biomarkers for identifying CSF- and PET imaging-diagnosed Alzheimer's disease: Insights for research and clinical practice
Xiaomei Zhong, Qiang Wang, Mingfeng Yang, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
October 27, 2015
Association between ADAMTS-4 gene polymorphism and lumbar disc degeneration in Chinese Han population
Sen Liu, Nan Wu, Jiaqi Liu, et al.
International Journal of Antimicrobial Agents
|
April 23, 2022
Genetic relatedness among azole-resistant Candida tropicalis clinical strains in Taiwan from 2014 to 2018
Zi-Li Zhou, Kuo-Yun Tseng, Yin-Zhi Chen, et al.
Journal of Cellular and Molecular Medicine
|
April 12, 2020
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia
Nan Wu, Zhen Zhang, Xi Zhou, et al.
NPJ Genomic Medicine
|
February 16, 2022
Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders
Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, et al.
Journal of Synchrotron Radiation
|
April 1, 2025
High-resolution in situ characterization of laser powder bed fusion via transmission X-ray microscopy at X-ray free-electron lasers
Zane Taylor, Tharun Reddy, Lichao Fang, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2019
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1
Mao Lin, Zhenlei Liu, Gang Liu, et al.
Elife
|
July 15, 2025
EPHA4 signaling dysregulation links abnormal locomotion and the development of idiopathic scoliosis
Lianlei Wang, Xinyu Yang, Sen Zhao, et al.
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of 82
Search research articles
Search
Showing results (801-810 of 817) with videos related to
Sort By:
Page
of 82
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.
Infectious Diseases and Therapy
|
July 11, 2023
Patient Biochemistry and Treatment Need in Chronic Hepatitis B Virus Infection Across Three Continents: Retrospective Cross-Sectional Cohort Studies
Iain A Gillespie, Eleanor Barnes, Ian C K Wong, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
January 31, 2025
Plasma p-tau217 and p-tau217/Aβ1-42 are effective biomarkers for identifying CSF- and PET imaging-diagnosed Alzheimer's disease: Insights for research and clinical practice
Xiaomei Zhong, Qiang Wang, Mingfeng Yang, et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society
|
October 27, 2015
Association between ADAMTS-4 gene polymorphism and lumbar disc degeneration in Chinese Han population
Sen Liu, Nan Wu, Jiaqi Liu, et al.
International Journal of Antimicrobial Agents
|
April 23, 2022
Genetic relatedness among azole-resistant Candida tropicalis clinical strains in Taiwan from 2014 to 2018
Zi-Li Zhou, Kuo-Yun Tseng, Yin-Zhi Chen, et al.
Journal of Cellular and Molecular Medicine
|
April 12, 2020
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia
Nan Wu, Zhen Zhang, Xi Zhou, et al.
NPJ Genomic Medicine
|
February 16, 2022
Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders
Sen Zhao, Yuanqiang Zhang, Sigrun Hallgrimsdottir, et al.
Journal of Synchrotron Radiation
|
April 1, 2025
High-resolution in situ characterization of laser powder bed fusion via transmission X-ray microscopy at X-ray free-electron lasers
Zane Taylor, Tharun Reddy, Lichao Fang, et al.
Molecular Genetics & Genomic Medicine
|
November 28, 2019
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1
Mao Lin, Zhenlei Liu, Gang Liu, et al.
Elife
|
July 15, 2025
EPHA4 signaling dysregulation links abnormal locomotion and the development of idiopathic scoliosis
Lianlei Wang, Xinyu Yang, Sen Zhao, et al.
Page
of 82