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Mice with gene alterations in the GH and IGF family.
Qian, Yanrong; Berryman, Darlene E; Basu, Reetobrata; List, Edward O; Okada, Shigeru; Young, Jonathan A; Jensen, Elizabeth A; Bell, Stephen R C; Kulkarni, Prateek; Duran-Ortiz, Silvana; Mora-Criollo, Patricia; Mathes, Samuel C; Brittain, Alison L; Buchman, Mat; Davis, Emily; Funk, Kevin R; Bogart, Jolie; Ibarra, Diego; Mendez-Gibson, Isaac; Slyby, Julie; Terry, Joseph; Kopchick, John J.
Afiliación
  • Qian Y; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Berryman DE; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Basu R; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • List EO; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Okada S; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Young JA; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Jensen EA; Department of Pediatrics, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • Bell SRC; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Kulkarni P; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • Duran-Ortiz S; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Mora-Criollo P; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • Mathes SC; Translational Biomedical Sciences Doctoral Program, Ohio University, Athens, OH, USA.
  • Brittain AL; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Buchman M; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • Davis E; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Funk KR; Department of Biological Sciences, College of Arts and Sciences, Ohio University, Athens, OH, USA.
  • Bogart J; Molecular and Cellular Biology Program, Ohio University, Athens, OH, USA.
  • Ibarra D; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Mendez-Gibson I; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Slyby J; Translational Biomedical Sciences Doctoral Program, Ohio University, Athens, OH, USA.
  • Terry J; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
  • Kopchick JJ; Edison Biotechnology Institute, Ohio University, Athens, OH, USA.
Pituitary ; 25(1): 1-51, 2022 Feb.
Article en En | MEDLINE | ID: mdl-34797529
ABSTRACT
Much of our understanding of GH's action stems from animal models and the generation and characterization of genetically altered or modified mice. Manipulation of genes in the GH/IGF1 family in animals started in 1982 when the first GH transgenic mice were produced. Since then, multiple laboratories have altered mouse DNA to globally disrupt Gh, Ghr, and other genes upstream or downstream of GH or its receptor. The ability to stay current with the various genetically manipulated mouse lines within the realm of GH/IGF1 research has been daunting. As such, this review attempts to consolidate and summarize the literature related to the initial characterization of many of the known gene-manipulated mice relating to the actions of GH, PRL and IGF1. We have organized the mouse lines by modifications made to constituents of the GH/IGF1 family either upstream or downstream of GHR or to the GHR itself. Available data on the effect of altered gene expression on growth, GH/IGF1 levels, body composition, reproduction, diabetes, metabolism, cancer, and aging are summarized. For the ease of finding this information, key words are highlighted in bold throughout the main text for each mouse line and this information is summarized in Tables 1, 2, 3 and 4. Most importantly, the collective data derived from and reported for these mice have enhanced our understanding of GH action.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Somatotropina / Hormona del Crecimiento Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Pituitary Asunto de la revista: ENDOCRINOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Somatotropina / Hormona del Crecimiento Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Pituitary Asunto de la revista: ENDOCRINOLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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