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Michael E Zwick

Showing results (51-60 of 75) with videos related to

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Journal of Pediatric Gastroenterology and Nutrition|May 6, 2014
Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel diseaseDavid T Okou, Kajari Mondal, William A Faubion, et al.
Plos One|August 8, 2024
Correction: Signatures of somatic mutations and gene expression from p16INK4A positive head and neck squamous cell carcinomas (HNSCC)Nabil F Saba, Ashok R Dinasarapu, Kelly R Magliocca, et al.
Translational Psychiatry|February 18, 2022
Metabolic effects of the schizophrenia-associated 3q29 deletionRebecca M Pollak, Ryan H Purcell, Timothy P Rutkowski, et al.
G3 (Bethesda, Md.)|July 22, 2015
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal DefectsDhanya Ramachandran, Zhen Zeng, Adam E Locke, et al.
Plos One|September 3, 2010
Rapid identification of genetic modifications in Bacillus anthracis using whole genome draft sequences generated by 454 pyrosequencingPeter E Chen, Kristin M Willner, Amy Butani, et al.
American Journal of Human Genetics|August 5, 2022
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neuronsAlena Kozlova, Siwei Zhang, Alex V Kotlar, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Journal of Medical Genetics|May 15, 2012
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderJirair Krikor Bedoyan, Valerie M Schaibley, Weiping Peng, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 15, 2020
Metabolic Pathway Analysis and Effectiveness of Tamoxifen in Danish Breast Cancer PatientsThomas P Ahern, Lindsay J Collin, James W Baurley, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Pageof 8

Showing results (51-60 of 75) with videos related to

Sort By:
Pageof 8
Journal of Pediatric Gastroenterology and Nutrition|May 6, 2014
Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel diseaseDavid T Okou, Kajari Mondal, William A Faubion, et al.
Plos One|August 8, 2024
Correction: Signatures of somatic mutations and gene expression from p16INK4A positive head and neck squamous cell carcinomas (HNSCC)Nabil F Saba, Ashok R Dinasarapu, Kelly R Magliocca, et al.
Translational Psychiatry|February 18, 2022
Metabolic effects of the schizophrenia-associated 3q29 deletionRebecca M Pollak, Ryan H Purcell, Timothy P Rutkowski, et al.
G3 (Bethesda, Md.)|July 22, 2015
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal DefectsDhanya Ramachandran, Zhen Zeng, Adam E Locke, et al.
Plos One|September 3, 2010
Rapid identification of genetic modifications in Bacillus anthracis using whole genome draft sequences generated by 454 pyrosequencingPeter E Chen, Kristin M Willner, Amy Butani, et al.
American Journal of Human Genetics|August 5, 2022
Loss of function of OTUD7A in the schizophrenia- associated 15q13.3 deletion impairs synapse development and function in human neuronsAlena Kozlova, Siwei Zhang, Alex V Kotlar, et al.
Human Mutation|October 17, 2013
Variant ATRX syndrome with dysfunction of ATRX and MAGT1 genesYing Qiao, Kajari Mondal, Valentina Trapani, et al.
Journal of Medical Genetics|May 15, 2012
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorderJirair Krikor Bedoyan, Valerie M Schaibley, Weiping Peng, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|January 15, 2020
Metabolic Pathway Analysis and Effectiveness of Tamoxifen in Danish Breast Cancer PatientsThomas P Ahern, Lindsay J Collin, James W Baurley, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 26, 2022
Identification of <i>PSMB5</i> as a genetic modifier of fragile X-associated tremor/ataxia syndromeHa Eun Kong, Junghwa Lim, Alexander Linsalata, et al.
Pageof 8