Journal: The FASEB Journal
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FASEB
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Publications1 - 10 of 55
- Quantitative proteomics and systems biologyItem type: Other Conference Item
The FASEB JournalAebersold, Ruedi (2007) - Internalization via Antennapedia protein transduction domain of an scFv antibody toward c-Myc proteinItem type: Journal Article
The FASEB JournalAvignolo, C.; Bagnasco, L.; Biasotti, B.; et al. (2008) - Vitamin A and iodine supplementation in African children with concurrent vitamin A and iodine deficiencyItem type: Other Conference Item
The FASEB JournalZimmermann, Michael; Jooste, Pieter; Mabapa, Ngoako; et al. (2007) - Creatine kinasesItem type: Other Journal Item
The FASEB Journal ~ FASEB JOURNALWallimann, Theo; Schlattner, Uwe (2010) - Structure of an anti-idiotypic Fab against feline peritonitis virus-neutralizing antibody and a comparison with the complexed FabItem type: Journal Article
The FASEB JournalBan, Nenad; Escobar, Carlos; Hasel, Karl W.; et al. (1995) - Thyroid hormone down regulates structural M band proteins in rat heartItem type: Other Conference Item
The FASEB JournalKato, P.N.; Garcia, A.S.; Perriard, J.C.; et al. (2005) - Control of pelage hair follicle development and cycling by complex interactions between follistatin and activinItem type: Journal Article
The FASEB JournalNakamura, Motonobu; Matzuk, Martin M.; Gerstmayer, Bernhard; et al. (2003)Members of the transforming growth factor β/bone morphogenetic protein (TGF‐β/BMP) family are involved in the control of hair follicle (HF) morphogenesis and cycling. The activities of several members of this family (activins and BMP‐2, ‐4, ‐7, and ‐11) are controlled by antagonists such as follistatin. Because follistatin‐deficient mice show abnormalities in vibrissae development, we explored the role of follistatin and activin in pelage HF development and cycling. We show here that during HF development follistatin mRNA was prominently expressed by hair matrix and outer root sheath keratinocytes as well as by interfollicular epidermal cells, whereas activin βA mRNA was mainly expressed in dermal papilla cells. Compared with age‐matched wild‐type controls, both follistatin knockout mice and activin βA transgenic mice showed a significant retardation of HF morphogenesis. Treatment of wild‐type embryonic skin explants with follistatin protein stimulated HF development. This effect was inhibited by addition of recombinant activin A protein. Activin βA transgenic mice demonstrated retardation of catagen entry, down‐regulation of BMP‐2, and up‐regulation of expression of its antagonist matrix GLA protein. These observations suggest that follistatin and activin interaction plays an important role in both HF development and cycling, possibly in part by regulating expression of BMP‐2 and its antagonist. - Increasing mitochondrial muscle fatty acid oxidation induces skeletal muscle remodeling toward an oxidative phenotypeItem type: Journal Article
The FASEB JournalHénique, Carole; Mansouri, Abdelhak; Vavrova, Eliska; et al. (2015) - Nitric oxide mediates lymphatic vessel activation via soluble guanylate cyclase α1β1-impact on inflammationItem type: Journal Article
The FASEB JournalKajiya, Kentaro; Huggenberger, Reto; Drinnenberg, Ines; et al. (2007) - Transient receptor potential vanilloid 2-mediated shear-stress responses in C2C12 myoblasts are regulated by serum and extracellular matrixItem type: Journal Article
The FASEB JournalKurth, Felix; Franco-Obregón, Alfredo; Casarosa, Marco; et al. (2015)
Publications1 - 10 of 55