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Velimir Gayevskiy

Showing results (11-20 of 47) with videos related to

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Neurogenetics|September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencingKishore R Kumar, G M Wali, Mahesh Kamate, et al.
Molecular & Cellular Proteomics : MCP|June 10, 2015
Global Phosphoproteomic Mapping of Early Mitotic Exit in Human Cells Identifies Novel Substrate Dephosphorylation MotifsRachael A McCloy, Benjamin L Parker, Samuel Rogers, et al.
Molecular Genetics and Metabolism Reports|August 11, 2018
Expanding the spectrum of <i>PEX16</i> mutations and novel insights into disease mechanismsKishore R Kumar, Gautam Wali, Ryan L Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Beyond the panel: preconception screening in consanguineous couples using the TruSight One "clinical exome"Edwin P Kirk, Kristine Barlow-Stewart, Arthavan Selvanathan, et al.
Lung Cancer (Amsterdam, Netherlands)|May 8, 2026
MORPHEUS-Lung: biomarkers and clinical response to atezolizumab + bevacizumab + stereotactic body radiotherapy in patients with metastatic non-small cell lung cancerByoung Chul Cho, Sun Min Lim, Sang Hoon Lee, et al.
Molecular Genetics and Metabolism|December 19, 2018
Cryptic intronic NBAS variant reveals the genetic basis of recurrent liver failure in a childRocio Rius, Lisa G Riley, Yiran Guo, et al.
Cerebellum (London, England)|May 20, 2019
Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome SequencingAryun Kim, Kishore R Kumar, Ryan L Davis, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Journal for Immunotherapy of Cancer|June 23, 2026
VEGF-A blockade overcomes liver metastases resistance to chemoimmunotherapy in patients with advanced non-squamous NSCLCMatthieu Roulleaux-Dugage, Andrey Yurchenko, Sergey Nikolaev, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Neurogenetics|September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencingKishore R Kumar, G M Wali, Mahesh Kamate, et al.
Molecular & Cellular Proteomics : MCP|June 10, 2015
Global Phosphoproteomic Mapping of Early Mitotic Exit in Human Cells Identifies Novel Substrate Dephosphorylation MotifsRachael A McCloy, Benjamin L Parker, Samuel Rogers, et al.
Molecular Genetics and Metabolism Reports|August 11, 2018
Expanding the spectrum of <i>PEX16</i> mutations and novel insights into disease mechanismsKishore R Kumar, Gautam Wali, Ryan L Davis, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Beyond the panel: preconception screening in consanguineous couples using the TruSight One "clinical exome"Edwin P Kirk, Kristine Barlow-Stewart, Arthavan Selvanathan, et al.
Lung Cancer (Amsterdam, Netherlands)|May 8, 2026
MORPHEUS-Lung: biomarkers and clinical response to atezolizumab + bevacizumab + stereotactic body radiotherapy in patients with metastatic non-small cell lung cancerByoung Chul Cho, Sun Min Lim, Sang Hoon Lee, et al.
Molecular Genetics and Metabolism|December 19, 2018
Cryptic intronic NBAS variant reveals the genetic basis of recurrent liver failure in a childRocio Rius, Lisa G Riley, Yiran Guo, et al.
Cerebellum (London, England)|May 20, 2019
Increased Diagnostic Yield of Spastic Paraplegia with or Without Cerebellar Ataxia Through Whole-Genome SequencingAryun Kim, Kishore R Kumar, Ryan L Davis, et al.
European Journal of Endocrinology|February 22, 2017
Germline variants in familial pituitary tumour syndrome genes are common in young patients and families with additional endocrine tumoursSunita M C De Sousa, Mark J McCabe, Kathy Wu, et al.
Human Mutation|December 18, 2018
Reanalysis and optimisation of bioinformatic pipelines is critical for mutation detectionMark J Cowley, Yu-Chi Liu, Karen L Oliver, et al.
Journal for Immunotherapy of Cancer|June 23, 2026
VEGF-A blockade overcomes liver metastases resistance to chemoimmunotherapy in patients with advanced non-squamous NSCLCMatthieu Roulleaux-Dugage, Andrey Yurchenko, Sergey Nikolaev, et al.
Pageof 5