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Tim Jeske

Showing results (1-10 of 11) with videos related to

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Plos Computational Biology|February 8, 2020
SmartPhase: Accurate and fast phasing of heterozygous variant pairs for genetic diagnosis of rare diseasesPaul Hager, Hans-Werner Mewes, Meino Rohlfs, et al.
Bioinformatics (Oxford, England)|June 23, 2019
DEUS: an R package for accurate small RNA profiling based on differential expression of unique sequencesTim Jeske, Peter Huypens, Laura Stirm, et al.
Bioinformatics (Oxford, England)|January 11, 2017
KNIME4NGS: a comprehensive toolbox for next generation sequencing analysisMaximilian Hastreiter, Tim Jeske, Jonathan Hoser, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 8, 2021
New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and DuodenumDemet Teker Duztas, Lina Al-Shadfan, Hakan Ozturk, et al.
Cells|December 24, 2021
TGF-β Induction of miR-143/145 Is Associated to Exercise Response by Influencing Differentiation and Insulin Signaling Molecules in Human Skeletal MuscleSimon I Dreher, Selina Höckele, Peter Huypens, et al.
Journal of Clinical Immunology|July 26, 2020
An RTEL1 Mutation Links to Infantile-Onset Ulcerative Colitis and Severe ImmunodeficiencyAlma Ziv, Lael Werner, Liza Konnikova, et al.
Immunological Investigations|July 8, 2020
Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR)Farzaneh Rahmani, Elham Rayzan, Mohammad Reza Rahmani, et al.
Clinical Genetics|February 18, 2021
FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs!Luise A Schuch, Maria Forstner, Christina K Rapp, et al.
Inflammatory Bowel Diseases|May 23, 2019
CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel DiseaseThomas Magg, Anna Shcherbina, Duran Arslan, et al.
Blood|October 12, 2022
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changesMonika I Linder, Yoko Mizoguchi, Sebastian Hesse, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Plos Computational Biology|February 8, 2020
SmartPhase: Accurate and fast phasing of heterozygous variant pairs for genetic diagnosis of rare diseasesPaul Hager, Hans-Werner Mewes, Meino Rohlfs, et al.
Bioinformatics (Oxford, England)|June 23, 2019
DEUS: an R package for accurate small RNA profiling based on differential expression of unique sequencesTim Jeske, Peter Huypens, Laura Stirm, et al.
Bioinformatics (Oxford, England)|January 11, 2017
KNIME4NGS: a comprehensive toolbox for next generation sequencing analysisMaximilian Hastreiter, Tim Jeske, Jonathan Hoser, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 8, 2021
New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and DuodenumDemet Teker Duztas, Lina Al-Shadfan, Hakan Ozturk, et al.
Cells|December 24, 2021
TGF-β Induction of miR-143/145 Is Associated to Exercise Response by Influencing Differentiation and Insulin Signaling Molecules in Human Skeletal MuscleSimon I Dreher, Selina Höckele, Peter Huypens, et al.
Journal of Clinical Immunology|July 26, 2020
An RTEL1 Mutation Links to Infantile-Onset Ulcerative Colitis and Severe ImmunodeficiencyAlma Ziv, Lael Werner, Liza Konnikova, et al.
Immunological Investigations|July 8, 2020
Clinical and Mutation Description of the First Iranian Cohort of Infantile Inflammatory Bowel Disease: The Iranian Primary Immunodeficiency Registry (IPIDR)Farzaneh Rahmani, Elham Rayzan, Mohammad Reza Rahmani, et al.
Clinical Genetics|February 18, 2021
FARS1-related disorders caused by bi-allelic mutations in cytosolic phenylalanyl-tRNA synthetase genes: Look beyond the lungs!Luise A Schuch, Maria Forstner, Christina K Rapp, et al.
Inflammatory Bowel Diseases|May 23, 2019
CARMIL2 Deficiency Presenting as Very Early Onset Inflammatory Bowel DiseaseThomas Magg, Anna Shcherbina, Duran Arslan, et al.
Blood|October 12, 2022
Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changesMonika I Linder, Yoko Mizoguchi, Sebastian Hesse, et al.
Pageof 2