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Growth hormone receptor-deficient pigs resemble the pathophysiology of human Laron syndrome and reveal altered activation of signaling cascades in the liver
OBJECTIVE: Laron syndrome (LS) is a rare, autosomal recessive disorder in humans caused by loss-of-function mutations of the growth hormone receptor (GHR) gene. To establish a large animal model for LS, pigs with GHR knockout (KO) mutations were generated and characterized. METHODS: CRISPR/Cas9 tech...
Autores principales: | Hinrichs, Arne, Kessler, Barbara, Kurome, Mayuko, Blutke, Andreas, Kemter, Elisabeth, Bernau, Maren, Scholz, Armin M., Rathkolb, Birgit, Renner, Simone, Bultmann, Sebastian, Leonhardt, Heinrich, de Angelis, Martin Hrabĕ, Nagashima, Hiroshi, Hoeflich, Andreas, Blum, Werner F., Bidlingmaier, Martin, Wanke, Rüdiger, Dahlhoff, Maik, Wolf, Eckhard |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001387/ https://www.ncbi.nlm.nih.gov/pubmed/29678421 http://dx.doi.org/10.1016/j.molmet.2018.03.006 |
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