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Janine Altmüller

Showing results (31-40 of 326) with videos related to

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Immunogenetics|April 8, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencingJanine Altmüller, Britta Haenisch, Amit Kawalia, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Genomic basis of syndromic short stature in an Algerian patient cohortShahida Moosa, Farida Chentli, Janine Altmüller, et al.
The EMBO Journal|April 22, 2022
Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decayDamaris Wallmeroth, Jan-Wilm Lackmann, Sabrina Kueckelmann, et al.
Plos Pathogens|June 23, 2016
The WOPR Protein Ros1 Is a Master Regulator of Sporogenesis and Late Effector Gene Expression in the Maize Pathogen Ustilago maydisMarie Tollot, Daniela Assmann, Christian Becker, et al.
Elife|May 31, 2016
Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunitJulia Hatzold, Filippo Beleggia, Hannah Herzig, et al.
American Journal of Human Genetics|February 22, 2023
Epigenetic regulation of plastin 3 expression by the macrosatellite DXZ4 and the transcriptional regulator CHD4Eike A Strathmann, Irmgard Hölker, Nikolai Tschernoster, et al.
Cytokine|May 22, 2010
Genetic determinants of circulating levels of tumor necrosis factor receptor II and their association with TNF-RII gene polymorphismsYulia Vistoropsky, Sergey Ermakov, Mohammad Reza Toliat, et al.
Plos Computational Biology|October 8, 2013
Sensitive detection of viral transcripts in human tumor transcriptomesSven-Eric Schelhorn, Matthias Fischer, Laura Tolosi, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicismShahida Moosa, Helena Böhrer-Rabel, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathySusann Weissbach, Marie-Christine Reinert, Janine Altmüller, et al.
Pageof 33

Showing results (31-40 of 326) with videos related to

Sort By:
Pageof 33
Immunogenetics|April 8, 2017
Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencingJanine Altmüller, Britta Haenisch, Amit Kawalia, et al.
American Journal of Medical Genetics. Part A|October 13, 2021
Genomic basis of syndromic short stature in an Algerian patient cohortShahida Moosa, Farida Chentli, Janine Altmüller, et al.
The EMBO Journal|April 22, 2022
Human UPF3A and UPF3B enable fault-tolerant activation of nonsense-mediated mRNA decayDamaris Wallmeroth, Jan-Wilm Lackmann, Sabrina Kueckelmann, et al.
Plos Pathogens|June 23, 2016
The WOPR Protein Ros1 Is a Master Regulator of Sporogenesis and Late Effector Gene Expression in the Maize Pathogen Ustilago maydisMarie Tollot, Daniela Assmann, Christian Becker, et al.
Elife|May 31, 2016
Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunitJulia Hatzold, Filippo Beleggia, Hannah Herzig, et al.
American Journal of Human Genetics|February 22, 2023
Epigenetic regulation of plastin 3 expression by the macrosatellite DXZ4 and the transcriptional regulator CHD4Eike A Strathmann, Irmgard Hölker, Nikolai Tschernoster, et al.
Cytokine|May 22, 2010
Genetic determinants of circulating levels of tumor necrosis factor receptor II and their association with TNF-RII gene polymorphismsYulia Vistoropsky, Sergey Ermakov, Mohammad Reza Toliat, et al.
Plos Computational Biology|October 8, 2013
Sensitive detection of viral transcripts in human tumor transcriptomesSven-Eric Schelhorn, Matthias Fischer, Laura Tolosi, et al.
American Journal of Medical Genetics. Part A|October 19, 2016
Smith-Kingsmore syndrome: A third family with the MTOR mutation c.5395G>A p.(Glu1799Lys) and evidence for paternal gonadal mosaicismShahida Moosa, Helena Böhrer-Rabel, Janine Altmüller, et al.
American Journal of Medical Genetics. Part A|August 18, 2017
A new CUL4B variant associated with a mild phenotype and an exceptional pattern of leukoencephalopathySusann Weissbach, Marie-Christine Reinert, Janine Altmüller, et al.
Pageof 33