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Helge Raeder

Showing results (21-30 of 34) with videos related to

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Pediatric Diabetes|July 20, 2011
HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver diseaseE Nazli Gonc, Burcu Bulum Ozturk, Ingfrid S Haldorsen, et al.
Diabetes Care|June 12, 2008
Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutationsMette Vesterhus, Helge Raeder, Harald Aurlien, et al.
Physiological Reports|June 10, 2021
Induction of alveolar and bronchiolar phenotypes in human lung organoidsLaurence Hoareau, Agnete S T Engelsen, Marianne Aanerud, et al.
Human Genetics|September 18, 2009
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesJanniche Torsvik, Stefan Johansson, Anders Johansen, et al.
Scientific Reports|February 9, 2026
Human bone marrow derived mesenchymal stem cells do not promote oral cancer cell growth in vitro and metastasis in vivoDiana Siyam, Himalaya Parajuli, Imane El Herch, et al.
Diabetes|May 30, 2006
A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registryHelge Raeder, Lise Bjørkhaug, Stefan Johansson, et al.
Diabetes|October 2, 2009
Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetesHana Lango Allen, Stefan Johansson, Sian Ellard, et al.
Stem Cell Reports|October 30, 2020
Leptin Receptor Signaling Regulates Protein Synthesis Pathways and Neuronal Differentiation in Pluripotent Stem CellsManoj K Gupta, Heidrun Vethe, Samir Softic, et al.
Nature Metabolism|January 21, 2022
Abnormal exocrine-endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8Sevim Kahraman, Ercument Dirice, Giorgio Basile, et al.
Diabetes|September 28, 2004
Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapyJørn V Sagen, Helge Raeder, Eba Hathout, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Pediatric Diabetes|July 20, 2011
HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver diseaseE Nazli Gonc, Burcu Bulum Ozturk, Ingfrid S Haldorsen, et al.
Diabetes Care|June 12, 2008
Neurological features and enzyme therapy in patients with endocrine and exocrine pancreas dysfunction due to CEL mutationsMette Vesterhus, Helge Raeder, Harald Aurlien, et al.
Physiological Reports|June 10, 2021
Induction of alveolar and bronchiolar phenotypes in human lung organoidsLaurence Hoareau, Agnete S T Engelsen, Marianne Aanerud, et al.
Human Genetics|September 18, 2009
Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetesJanniche Torsvik, Stefan Johansson, Anders Johansen, et al.
Scientific Reports|February 9, 2026
Human bone marrow derived mesenchymal stem cells do not promote oral cancer cell growth in vitro and metastasis in vivoDiana Siyam, Himalaya Parajuli, Imane El Herch, et al.
Diabetes|May 30, 2006
A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registryHelge Raeder, Lise Bjørkhaug, Stefan Johansson, et al.
Diabetes|October 2, 2009
Polygenic risk variants for type 2 diabetes susceptibility modify age at diagnosis in monogenic HNF1A diabetesHana Lango Allen, Stefan Johansson, Sian Ellard, et al.
Stem Cell Reports|October 30, 2020
Leptin Receptor Signaling Regulates Protein Synthesis Pathways and Neuronal Differentiation in Pluripotent Stem CellsManoj K Gupta, Heidrun Vethe, Samir Softic, et al.
Nature Metabolism|January 21, 2022
Abnormal exocrine-endocrine cell cross-talk promotes β-cell dysfunction and loss in MODY8Sevim Kahraman, Ercument Dirice, Giorgio Basile, et al.
Diabetes|September 28, 2004
Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapyJørn V Sagen, Helge Raeder, Eba Hathout, et al.
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