Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Madlen Merten"'
Autor:
Madlen Merten, Johannes F. W. Greiner, Tarek Niemann, Meike Grosse Venhaus, Daniel Kronenberg, Richard Stange, Dirk Wähnert, Christian Kaltschmidt, Thomas Vordemvenne, Barbara Kaltschmidt
Publikováno v:
Cells, Vol 11, Iss 5, p 823 (2022)
Female sex is increasingly associated with a loss of bone mass during aging and an increased risk of developing nonunion fractures. Hormonal factors and cell-intrinsic mechanisms are suggested to drive these sexual dimorphisms, although underlying mo
Externí odkaz:
https://doaj.org/article/8e869420784646b4a83e146e80d2aafd
Autor:
Anna L. Höving, Kazuko E. Schmidt, Madlen Merten, Jassin Hamidi, Ann-Katrin Rott, Isabel Faust, Johannes F. W. Greiner, Jan Gummert, Barbara Kaltschmidt, Christian Kaltschmidt, Cornelius Knabbe
Publikováno v:
Cells, Vol 9, Iss 6, p 1472 (2020)
During aging, senescent cells accumulate in various tissues accompanied by decreased regenerative capacities of quiescent stem cells, resulting in deteriorated organ function and overall degeneration. In this regard, the adult human heart with a gene
Externí odkaz:
https://doaj.org/article/245b264f33af44c19efd1b718d68202f
Autor:
Thomas Vordemvenne, Dirk Wähnert, Julian Koettnitz, Madlen Merten, Nadine Fokin, Andreas Becker, Björn Büker, Asaria Vogel, Daniel Kronenberg, Richard Stange, Günther Wittenberg, Johannes FW Greiner, Andreas Hütten, Christian Kaltschmidt, Barbara Kaltschmidt
Publikováno v:
Cells, Vol 9, Iss 3, p 654 (2020)
Scaffold materials for bone regeneration are crucial for supporting endogenous healing after accidents, infections, or tumor resection. Although beneficial impacts of microtopological or nanotopological cues in scaffold topography are commonly acknow
Externí odkaz:
https://doaj.org/article/9a09c97dfee643d3b0748c0d3d18d013
Publikováno v:
BIOspektrum. 26:50-53
Neurodegenerative diseases like Parkinson’s disease differ between the sexes in severity and occurrence. Next to hormons, increasing evidence suggests stem cell-intrinsic mechanisms to account for pathologic sex-specific differences. Here, we discu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43f9b1c26d364650eea98d79c72f448f
https://doi.org/10.1007/s12268-020-1333-2
https://doi.org/10.1007/s12268-020-1333-2
Human Sex Matters: Y-linked lysine demethylase 5D drives accelerated male osteogenic differentiation
Autor:
Madlen Merten, Johannes F. W. Greiner, Barbara Kaltschmidt, Dirk Wähnert, Meike Grosse Venhaus, Tarek Niemann, Christian Kaltschmidt, Thomas Vordemvenne, Daniel Kronenberg, Richard Stange
Female sex is increasingly associated to a loss of bone mass during aging and an increased risk for fractures developing nonunion. Hormonal factors and cell-intrinsic mechanisms are suggested to drive these sexual dimorphisms, although underlying mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ed60ecc1aada754ec2380465dfeb8d4a
https://doi.org/10.1101/2021.11.10.468047
https://doi.org/10.1101/2021.11.10.468047
Sexual dimorphisms contribute, at least in part, to the severity and occurrence of a broad range of neurodegenerative, cardiovascular, and bone disorders. In addition to hormonal factors, increasing evidence suggests that stem cell-intrinsic mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41abe5a42b6a49e928bcce9401d4d1a4
https://pub.uni-bielefeld.de/record/2937576
https://pub.uni-bielefeld.de/record/2937576
Autor:
Karina Brinkrolf, Yvonne Kutter, Andreas Tauch, Christian Rückert, Madlen Merten, Andreas Albersmeier
Publikováno v:
Genome Announcements
Corynebacterium singulare DSM 44357 is a urease-positive microorganism isolated from human semen. The complete genome sequence of C. singulare DSM 44357 comprises 2,830,519 bp with a mean G+C content of 60.12% and 2,581 protein-coding genes. The dedu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ceb7372f5c8a4f62ceb3df8fcf2bea2e
https://doi.org/10.1128/genomea.00183-15
https://doi.org/10.1128/genomea.00183-15