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Genes

Showing results (1481-1490 of 14,498) with videos related to

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Genes|September 23, 2022
Multinomial Convolutions for Joint Modeling of Regulatory Motifs and Sequence Activity ReadoutsMinjun Park, Salvi Singh, Samin Rahman Khan, et al.
Genes|September 23, 2022
The Benefits of Family Screening in Rare Diseases: Genetic Testing Reveals 165 New Cases of Fabry Disease among At-Risk Family Members of 83 Index PatientsSergey Moiseev, Ekaterina Tao, Alexey Moiseev, et al.
Genes|September 23, 2022
Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population ScreeningJörg Schmidtke
Genes|September 23, 2022
Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani FamiliesRaeesa Tehreem, Iris Chen, Mudassar Raza Shah, et al.
Genes|September 23, 2022
Salt and Metal Tolerance Involves Formation of Guttation Droplets in Species of the <i>Aspergillus versicolor</i> ComplexMarie Harpke, Sebastian Pietschmann, Nico Ueberschaar, et al.
Genes|September 23, 2022
Biallelic Loss of Function Mutation in Sodium Channel Gene <i>SCN10A</i> in an Autism Spectrum Disorder Trio from PakistanAnsa Rabia, Ricardo Harripaul, Anna Mikhailov, et al.
Genes|September 23, 2022
C-to-U RNA Editing: A Site Directed RNA Editing Tool for Restoration of Genetic CodeSonali Bhakta, Toshifumi Tsukahara
Genes|September 23, 2022
Interleukin-17 Family Cytokines in Metabolic Disorders and CancerEileen Victoria Meehan, Kepeng Wang
Genes|September 23, 2022
Recent Developments in Autism Genetic Research: A Scientometric Review from 2018 to 2022Mengyu Lim, Alessandro Carollo, Dagmara Dimitriou, et al.
Genes|September 23, 2022
Simultaneous SARS-CoV-2 Genome Sequencing of 384 Samples on an Illumina MiSeq Instrument through Protocol OptimizationNasserdine Papa Mze, Mamadou Beye, Idir Kacel, et al.
Pageof 1,450

Showing results (1481-1490 of 14,498) with videos related to

Sort By:
Pageof 1,450
Genes|September 23, 2022
Multinomial Convolutions for Joint Modeling of Regulatory Motifs and Sequence Activity ReadoutsMinjun Park, Salvi Singh, Samin Rahman Khan, et al.
Genes|September 23, 2022
The Benefits of Family Screening in Rare Diseases: Genetic Testing Reveals 165 New Cases of Fabry Disease among At-Risk Family Members of 83 Index PatientsSergey Moiseev, Ekaterina Tao, Alexey Moiseev, et al.
Genes|September 23, 2022
Twenty-Five Years of Contemplating Genotype-Based Hereditary Hemochromatosis Population ScreeningJörg Schmidtke
Genes|September 23, 2022
Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani FamiliesRaeesa Tehreem, Iris Chen, Mudassar Raza Shah, et al.
Genes|September 23, 2022
Salt and Metal Tolerance Involves Formation of Guttation Droplets in Species of the <i>Aspergillus versicolor</i> ComplexMarie Harpke, Sebastian Pietschmann, Nico Ueberschaar, et al.
Genes|September 23, 2022
Biallelic Loss of Function Mutation in Sodium Channel Gene <i>SCN10A</i> in an Autism Spectrum Disorder Trio from PakistanAnsa Rabia, Ricardo Harripaul, Anna Mikhailov, et al.
Genes|September 23, 2022
C-to-U RNA Editing: A Site Directed RNA Editing Tool for Restoration of Genetic CodeSonali Bhakta, Toshifumi Tsukahara
Genes|September 23, 2022
Interleukin-17 Family Cytokines in Metabolic Disorders and CancerEileen Victoria Meehan, Kepeng Wang
Genes|September 23, 2022
Recent Developments in Autism Genetic Research: A Scientometric Review from 2018 to 2022Mengyu Lim, Alessandro Carollo, Dagmara Dimitriou, et al.
Genes|September 23, 2022
Simultaneous SARS-CoV-2 Genome Sequencing of 384 Samples on an Illumina MiSeq Instrument through Protocol OptimizationNasserdine Papa Mze, Mamadou Beye, Idir Kacel, et al.
Pageof 1,450