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Human genomics

Showing results (611-620 of 1,110) with videos related to

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Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Human Genomics|April 7, 2018
Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeatsN Nazaripanah, F Adelirad, A Delbari, et al.
Human Genomics|December 30, 2009
Cholinesterase inhibitors in Alzheimer's disease and Lewy body spectrum disorders: the emerging pharmacogenetic storyBenjamin Lam, Elizabeth Hollingdrake, James L Kennedy, et al.
Human Genomics|September 25, 2016
Major influence of repetitive elements on disease-associated copy number variants (CNVs)Ana R Cardoso, Manuela Oliveira, Antonio Amorim, et al.
Human Genomics|May 6, 2017
In silico prioritization and further functional characterization of SPINK1 intronic variantsWen-Bin Zou, Hao Wu, Arnaud Boulling, et al.
Human Genomics|September 10, 2016
MicroRNAs in acute kidney injuryPei-Chun Fan, Chia-Chun Chen, Yung-Chang Chen, et al.
Human Genomics|June 23, 2018
Computational analysis of mRNA expression profiling in the inner ear reveals candidate transcription factors associated with proliferation, differentiation, and deafnessKobi Perl, Ron Shamir, Karen B Avraham
Human Genomics|June 28, 2018
Caution needs to be taken when assigning transcription start sites to ends of protein-coding genes: a rebuttalNiv Sabath, Anna Vilborg, Joan A Steitz, et al.
Human Genomics|April 25, 2023
Identification of four novel large deletions and complex variants in the α-globin locus in Chinese populationXiuqin Bao, Jicheng Wang, Danqing Qin, et al.
Human Genomics|April 25, 2023
The spectrum of phenylalanine hydroxylase variants and genotype-phenotype correlation in phenylketonuria patients in Gansu, ChinaChuan Zhang, Pei Zhang, Yousheng Yan, et al.
Pageof 111

Showing results (611-620 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|September 28, 2016
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathiesDorota Monies, Hindi N Alhindi, Mohamed A Almuhaizea, et al.
Human Genomics|April 7, 2018
Genome-scale portrait and evolutionary significance of human-specific core promoter tri- and tetranucleotide short tandem repeatsN Nazaripanah, F Adelirad, A Delbari, et al.
Human Genomics|December 30, 2009
Cholinesterase inhibitors in Alzheimer's disease and Lewy body spectrum disorders: the emerging pharmacogenetic storyBenjamin Lam, Elizabeth Hollingdrake, James L Kennedy, et al.
Human Genomics|September 25, 2016
Major influence of repetitive elements on disease-associated copy number variants (CNVs)Ana R Cardoso, Manuela Oliveira, Antonio Amorim, et al.
Human Genomics|May 6, 2017
In silico prioritization and further functional characterization of SPINK1 intronic variantsWen-Bin Zou, Hao Wu, Arnaud Boulling, et al.
Human Genomics|September 10, 2016
MicroRNAs in acute kidney injuryPei-Chun Fan, Chia-Chun Chen, Yung-Chang Chen, et al.
Human Genomics|June 23, 2018
Computational analysis of mRNA expression profiling in the inner ear reveals candidate transcription factors associated with proliferation, differentiation, and deafnessKobi Perl, Ron Shamir, Karen B Avraham
Human Genomics|June 28, 2018
Caution needs to be taken when assigning transcription start sites to ends of protein-coding genes: a rebuttalNiv Sabath, Anna Vilborg, Joan A Steitz, et al.
Human Genomics|April 25, 2023
Identification of four novel large deletions and complex variants in the α-globin locus in Chinese populationXiuqin Bao, Jicheng Wang, Danqing Qin, et al.
Human Genomics|April 25, 2023
The spectrum of phenylalanine hydroxylase variants and genotype-phenotype correlation in phenylketonuria patients in Gansu, ChinaChuan Zhang, Pei Zhang, Yousheng Yan, et al.
Pageof 111