Zobrazeno 1 - 10
of 66
pro vyhledávání: '"Josephine T. Tauer"'
Development of a facile method to compute collagen network pathological anisotropy using AFM imaging
Autor:
Emilie Khattignavong, Mehrnoosh Neshatian, Mina Vaez, Amaury Guillermin, Josephine T. Tauer, Marianne Odlyha, Nimish Mittal, Svetlana V. Komarova, Hassan Zahouani, Laurent Bozec
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Type I collagen, a fundamental extracellular matrix (ECM) component, is pivotal in maintaining tissue integrity and strength. It is also the most prevalent fibrous biopolymer within the ECM, ubiquitous in mammalian organisms. This structural
Externí odkaz:
https://doaj.org/article/9afa8d0790d9407fbf35a5460f0e12b5
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Osteogenesis imperfecta (OI) is a rare bone disease that is associated with fractures and low bone mass. Sclerostin inhibition is being evaluated as a potential approach to increase bone mass in OI. We had previously found that in Col1a1 Jrt
Externí odkaz:
https://doaj.org/article/159067d733a54de487fe954a2d222d85
Autor:
Josephine T. Tauer, Hadil Al-Jallad, Mayumi Umebayashi, Dena Bakhsh, Damian Rauch, Simon D. Tran, Frank Rauch, Reggie Hamdy
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Pediatric patients with Osteogenesis Imperfecta (OI), a heritable connective tissue disorder, frequently suffer from long bone deformations. Surgical correction often results in bone non-unions, necessitating revision surgery with autogenous
Externí odkaz:
https://doaj.org/article/7e7d0b830fd74be392b333996d84d02c
Publikováno v:
Data in Brief, Vol 41, Iss , Pp 107961- (2022)
Male and female mice with a dominant severe bone fragility disorder, osteogenesis imperfecta, and their wild-type littermates (FVB background) were challenged with a long-term (26 weeks) high-fat diet to evaluate the development of obesity and glucos
Externí odkaz:
https://doaj.org/article/055443d8bf3046b3818fd8ba397ec3fb
Autor:
Rick Proschmann, Christoph Baldow, Tino Rothe, Meinolf Suttorp, Christian Thiede, Josephine T. Tauer, Martin C. Müller, Andreas Hochhaus, Ingo Roeder, Ingmar Glauche
Publikováno v:
Haematologica, Vol 102, Iss 2 (2017)
Externí odkaz:
https://doaj.org/article/2237626172cd400ebc0992aac09a5954
Autor:
Meinolf Suttorp, Christian Thiede, Josephine T. Tauer, Ursula Range, Brigitte Schlegelberger, Nils von Neuhoff
Publikováno v:
Haematologica, Vol 95, Iss 5 (2010)
Externí odkaz:
https://doaj.org/article/97ad41bc786343fdafd37559f11a94f7
Publikováno v:
Hämostaseologie.
The tyrosine kinase inhibitors (TKIs) imatinib, dasatinib, bosutinib, and nilotinib are established for first-line treatment of chronic myeloid leukemia (CML) but may cause side effects such as bleeding and thrombotic complications. We investigated t
Autor:
Josephine T. Tauer, Hadil Al-Jallad, Mayumi Umebayashi, Dena Bakhsh, Damian Rauch, Simon D. Tran, Frank Rauch, Reggie Hamdy
Publikováno v:
Scientific reports. 12(1)
Pediatric patients with Osteogenesis Imperfecta (OI), a heritable connective tissue disorder, frequently suffer from long bone deformations. Surgical correction often results in bone non-unions, necessitating revision surgery with autogenous bone gra
Publikováno v:
Data in brief. 41
Male and female mice with a dominant severe bone fragility disorder, osteogenesis imperfecta, and their wild-type littermates (FVB background) were challenged with a long-term (26 weeks) high-fat diet to evaluate the development of obesity and glucos
Publikováno v:
Journal of Bone and Mineral Research. 34:207-214
Osteogenesis imperfecta (OI) is a heritable bone fragility disorder that is usually caused by mutations affecting collagen type I encoding genes. Recent studies in mouse models of recessive OI, Crtap-/- mice, and dominant OI, +/G610C mice, found that