Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Franziska, Peter"'
Publikováno v:
Global Ecology and Conservation, Vol 49, Iss , Pp e02782- (2024)
The increasing use of onshore wind energy is leading to an increased deployment of wind turbines in structurally rich habitats such as forests. Forest-affiliated bats, in turn, are at risk of colliding with the rotor blades. Due to the legal protecti
Externí odkaz:
https://doaj.org/article/effacbbc3bd74e5b80f53561ba58c2ea
Publikováno v:
Basic and Applied Ecology, Vol 59, Iss , Pp 44-58 (2022)
Wildflower areas are a popular agri-environment scheme to counteract agro-biodiversity loss. Yet, their benefits are controversially discussed. Since inconsistent benefits may be owed to landscape context and temporal dynamics, we applied a multi-yea
Externí odkaz:
https://doaj.org/article/3d1a88bf6e634c0fa4ee56e2f186d07b
Autor:
Christin Völkner, Franziska Peter, Maik Liedtke, Saskia Krohn, Iris Lindner, Hugo Murua Escobar, Chiara Cimmaruta, Jan Lukas, Andreas Hermann, Moritz J. Frech
Publikováno v:
Stem Cell Research, Vol 41, Iss , Pp - (2019)
Niemann-Pick disease Type C (NPC) is a rare progressive neurodegenerative disorder with an incidence of 1:120,000 caused by mutations in the NPC1 or NPC2 gene. Only 5% of NPC patients suffer from mutations of the NPC2 gene. Here we demonstrate the ge
Externí odkaz:
https://doaj.org/article/f019f925d49f4d1897c661f7dc354fb9
Publikováno v:
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Abstract Niemann-Pick disease Type C1 (NPC1) is a rare hereditary neurodegenerative disease. NPC1-patients suffer, amongst others, from ataxia, based on a loss of cerebellar Purkinje cells (PCs). Impaired expression/function of excitatory amino acid
Externí odkaz:
https://doaj.org/article/8a7a8cdad48c4320bb1096a908cfd2a0
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-14 (2017)
Abstract Background Niemann-Pick disease Type C1 (NPC1) is a rare progressive neurodegenerative disorder caused by mutations in the NPC1 gene. The pathological mechanisms, underlying NPC1 are not yet completely understood. Especially the contribution
Externí odkaz:
https://doaj.org/article/ec06a8851e404fcbadcc6c77f9f4492f
Publikováno v:
Data in Brief, Vol 12, Iss C, Pp 123-131 (2017)
Data presented in this article demonstrate the generation and characterization of two novel Niemann-Pick disease Type C1 (NPC1) patient-specific induced pluripotent stem cell (iPSC) lines, related to the research article Trilck et al. (Diversity of G
Externí odkaz:
https://doaj.org/article/159ce8fffd284fee8029a6c3a3e5cf44
Autor:
Maik Liedtke, Christin Völkner, Alexandra V. Jürs, Franziska Peter, Michael Rabenstein, Andreas Hermann, Moritz J. Frech
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 8, p 4009 (2021)
Niemann-Pick type C2 (NP-C2) disease is a rare hereditary disease caused by mutations in the NPC2 gene. NPC2 is a small, soluble protein consisting of 151 amino acids, primarily expressed in late endosomes and lysosomes (LE/LY). Together with NPC1, a
Externí odkaz:
https://doaj.org/article/de269c3b19fe4378a881f0a5ac0c3408
Autor:
Mariana Patino, Franziska Peter
Publikováno v:
SSRN Electronic Journal.
Autor:
Bonhoure, Isabelle, Perelló, Josep, Franziska, Peter, Arza, Valeria, Actis, Guillermina, Wintersteller, Teresa, Woehrer, Veronika, Mayer, Katja, Thomas, Stefan
Co-designing Citizen Social Science for Collective Action (CoAct) proposesa new understanding of Citizen Social Science (CSS) in topics relatedto Planetary Health: community mental health care, environmental justice,youth employment, and gender equal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56a316da13b7b68e501d3dcc86526b95
Worldwide, wind turbines are increasingly being built at forest sites to meet the goals of national climate strategies. Yet, the impact on biodiversity is barely understood. Bats may be heavily affected by wind turbines in forests, because many speci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175e920f3c2a77bb0949823db1683ab9
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