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Human genomics

Showing results (61-70 of 1,248) with videos related to

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Human Genomics|September 7, 2022
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencingShasha Chen, Qinchun Jin, Shiqiang Hou, et al.
Human Genomics|August 26, 2022
On the relationship between tripartite motif-containing 22 single-nucleotide polymorphisms and COVID-19 infection severityNidhal Raheem Juhi Al-Kaabi, Sepideh Chodari Khameneh, Mohadeseh Montazeri, et al.
Human Genomics|August 29, 2025
Integrative single-cell and bulk transcriptomic analysis reveals the landscape of T cell mitotic catastrophe associated genes in esophageal squamous cell carcinomaShuang Li, Zheng Tao, Nan Wang, et al.
Human Genomics|June 6, 2020
COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic miceCathleen Lutz, Leigh Maher, Charles Lee, et al.
Human Genomics|August 7, 2021
LncRNA-TUG1 promotes the progression of infantile hemangioma by regulating miR-137/IGFBP5 axisLili Zhou, Xiao Jia, Xiangzheng Yang
Human Genomics|May 26, 2020
Gene X environment: the cellular environment governs the transcriptional response to environmental chemicalsAndreanna Burman, Rolando Garcia-Milian, Shannon Whirledge
Human Genomics|August 5, 2022
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variantsAnjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, et al.
Human Genomics|August 22, 2022
SCP2 variant is associated with alterations in lipid metabolism, brainstem neurodegeneration, and testicular defectsMelanie Galano, Shereen Ezzat, Vassilios Papadopoulos
Human Genomics|May 8, 2021
An application of slow feature analysis to the genetic sequences of coronaviruses and influenza virusesAnastasios A Tsonis, Geli Wang, Lvyi Zhang, et al.
Human Genomics|June 10, 2015
Complement regulator CD46: genetic variants and disease associationsM Kathryn Liszewski, John P Atkinson
Pageof 125

Showing results (61-70 of 1,248) with videos related to

Sort By:
Pageof 125
Human Genomics|September 7, 2022
Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencingShasha Chen, Qinchun Jin, Shiqiang Hou, et al.
Human Genomics|August 26, 2022
On the relationship between tripartite motif-containing 22 single-nucleotide polymorphisms and COVID-19 infection severityNidhal Raheem Juhi Al-Kaabi, Sepideh Chodari Khameneh, Mohadeseh Montazeri, et al.
Human Genomics|August 29, 2025
Integrative single-cell and bulk transcriptomic analysis reveals the landscape of T cell mitotic catastrophe associated genes in esophageal squamous cell carcinomaShuang Li, Zheng Tao, Nan Wang, et al.
Human Genomics|June 6, 2020
COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic miceCathleen Lutz, Leigh Maher, Charles Lee, et al.
Human Genomics|August 7, 2021
LncRNA-TUG1 promotes the progression of infantile hemangioma by regulating miR-137/IGFBP5 axisLili Zhou, Xiao Jia, Xiangzheng Yang
Human Genomics|May 26, 2020
Gene X environment: the cellular environment governs the transcriptional response to environmental chemicalsAndreanna Burman, Rolando Garcia-Milian, Shannon Whirledge
Human Genomics|August 5, 2022
1029 genomes of self-declared healthy individuals from India reveal prevalent and clinically relevant cardiac ion channelopathy variantsAnjali Bajaj, Vigneshwar Senthivel, Rahul Bhoyar, et al.
Human Genomics|August 22, 2022
SCP2 variant is associated with alterations in lipid metabolism, brainstem neurodegeneration, and testicular defectsMelanie Galano, Shereen Ezzat, Vassilios Papadopoulos
Human Genomics|May 8, 2021
An application of slow feature analysis to the genetic sequences of coronaviruses and influenza virusesAnastasios A Tsonis, Geli Wang, Lvyi Zhang, et al.
Human Genomics|June 10, 2015
Complement regulator CD46: genetic variants and disease associationsM Kathryn Liszewski, John P Atkinson
Pageof 125