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Showing results (921-930 of 967) with videos related to

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Frontiers in Neurology|March 21, 2019
Incidence, Recurrence, and Risk Factors for Peri-ictal Central Apnea and Sudden Unexpected Death in EpilepsyLaura Vilella, Nuria Lacuey, Johnson P Hampson, et al.
Frontiers in Oncology|October 22, 2024
Harnessing the power of AI in precision medicine: NGS-based therapeutic insights for colorectal cancer cohortVictor Murcia Pienkowski, Piotr Skoczylas, Agata Zaremba, et al.
Nucleic Acids Research|November 15, 2007
Enteropathogen Resource Integration Center (ERIC): bioinformatics support for research on biodefense-relevant enterobacteriaJeremy D Glasner, Guy Plunkett, Bradley D Anderson, et al.
Human Genetics|July 19, 2006
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's diseaseSilke Metzger, Peter Bauer, Jürgen Tomiuk, et al.
Nature Communications|November 15, 2017
NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autismShichun Tu, Mohd Waseem Akhtar, Rosa Maria Escorihuela, et al.
Parkinsonism & Related Disorders|July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.
Frontiers in Neurology|June 14, 2019
Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain StructureJanik Goltermann, Ronny Redlich, Katharina Dohm, et al.
Mbio|April 11, 2024
Outpatient treatment with concomitant vaccine-boosted convalescent plasma for patients with immunosuppression and COVID-19Juan G Ripoll, Sidna M Tulledge-Scheitel, Anthony A Stephenson, et al.
Neurogenetics|December 22, 2005
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's diseaseSilke Metzger, Peter Bauer, Juergen Tomiuk, et al.
Molecular Psychiatry|September 7, 2018
Cortical surface area alterations shaped by genetic load for neuroticismNils Opel, Azmeraw T Amare, Ronny Redlich, et al.
Pageof 97

Showing results (921-930 of 967) with videos related to

Sort By:
Pageof 97
Frontiers in Neurology|March 21, 2019
Incidence, Recurrence, and Risk Factors for Peri-ictal Central Apnea and Sudden Unexpected Death in EpilepsyLaura Vilella, Nuria Lacuey, Johnson P Hampson, et al.
Frontiers in Oncology|October 22, 2024
Harnessing the power of AI in precision medicine: NGS-based therapeutic insights for colorectal cancer cohortVictor Murcia Pienkowski, Piotr Skoczylas, Agata Zaremba, et al.
Nucleic Acids Research|November 15, 2007
Enteropathogen Resource Integration Center (ERIC): bioinformatics support for research on biodefense-relevant enterobacteriaJeremy D Glasner, Guy Plunkett, Bradley D Anderson, et al.
Human Genetics|July 19, 2006
Genetic analysis of candidate genes modifying the age-at-onset in Huntington's diseaseSilke Metzger, Peter Bauer, Jürgen Tomiuk, et al.
Nature Communications|November 15, 2017
NitroSynapsin therapy for a mouse MEF2C haploinsufficiency model of human autismShichun Tu, Mohd Waseem Akhtar, Rosa Maria Escorihuela, et al.
Parkinsonism & Related Disorders|July 24, 2021
Urine levels of the polyglutamine ataxin-3 protein are elevated in patients with spinocerebellar ataxia type 3Yuka Koike, Karen R Jansen-West, Rana Hanna Al-Shaikh, et al.
Frontiers in Neurology|June 14, 2019
Apolipoprotein E Homozygous ε4 Allele Status: A Deteriorating Effect on Visuospatial Working Memory and Global Brain StructureJanik Goltermann, Ronny Redlich, Katharina Dohm, et al.
Mbio|April 11, 2024
Outpatient treatment with concomitant vaccine-boosted convalescent plasma for patients with immunosuppression and COVID-19Juan G Ripoll, Sidna M Tulledge-Scheitel, Anthony A Stephenson, et al.
Neurogenetics|December 22, 2005
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's diseaseSilke Metzger, Peter Bauer, Juergen Tomiuk, et al.
Molecular Psychiatry|September 7, 2018
Cortical surface area alterations shaped by genetic load for neuroticismNils Opel, Azmeraw T Amare, Ronny Redlich, et al.
Pageof 97