Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aya Kawanami"'
Autor:
Hideki Mochizuki, Jiro Takano, Makoto Saegusa, Yasuto Nakata, Masahiko Takada, Yoshikuni Mizuno, Takaomi C. Saido, Tetsuo Mikami, Tomoko Nihira, Aya Kawanami, Makiko Nagai, Hideki Hayakawa, Mieko Ogino, Junichi Hamada, Kazutoshi Nishiyama
Publikováno v:
Journal of Neural Transmission
We evaluated the immunohistochemical intensities of α-synuclein, phosphorylated α-synuclein (p-syn), dopamine- and cAMP-regulated phosphoprotein of 32 kDa (DARPP-32), calbindin-D 28k, calpain-cleaved carboxy-terminal 150-kDa spectrin fragment, and
Autor:
Shunichi Murakami, Arjun S. Sebastian, Aya Kawanami, Takehiko Matsushita, Gary E. Landreth, Susan Mackem
Publikováno v:
Journal of Orthopaedic Research. 29:375-379
Activating mutations in FGFR3 cause the most common forms of human dwarfism: achondroplasia and thanatophoric dysplasia. In mouse models of achondroplasia, recent studies have implicated the ERK MAPK pathway, a pathway activated by FGFR3, in creating
Autor:
Aya Kawanami, Gary E. Landreth, Gener Balmes, Yuk Yu Chan, Takehiko Matsushita, Shunichi Murakami
Publikováno v:
Molecular and Cellular Biology. 29:5843-5857
Osteoblasts and chondrocytes arise from common osteo-chondroprogenitor cells. We show here that inactivation of ERK1 and ERK2 in osteo-chondroprogenitor cells causes a block in osteoblast differentiation and leads to ectopic chondrogenic differentiat
Publikováno v:
Developmental Biology. 326:237-249
External guidance cues play a role in controlling neuronal cell turning in the developing brain, but little is known about whether intrinsic programs are also involved in controlling the turning. In this study, we examined whether granule cells under
Autor:
Hulya Bukulmez, David Givol, Pavel Krejci, William R. Wilcox, Takehiko Matsushita, Kazuyuki Otani, Shunichi Murakami, Isakichi Yamaura, Pertchoui B. Mekikian, Yuk Yu Chan, Aya Kawanami, Gener Balmes, Matthew L. Warman
Publikováno v:
Human Molecular Genetics. 18:227-240
Activating mutations in FGFR3 cause achondroplasia and thanatophoric dysplasia, the most common human skeletal dysplasias. In these disorders, spinal canal and foramen magnum stenosis can cause serious neurologic complications. Here, we provide evide
Autor:
Zhufeng Ouyang, Patrick Leahy, Aya Kawanami, Shunichi Murakami, Zhijun Chen, Masakazu Ishikawa, Xiuzhen Yue, Edward M. Greenfield
Publikováno v:
Bone. 58
Bones consist of a number of cell types including osteoblasts and their precursor cells at various stages of differentiation. To analyze cellular organization within the bone, we generated Col1a1CreER-DsRed transgenic mice that express, in osteoblast
We generated Prx1CreER-GFP transgenic mice that express tamoxifen-inducible Cre recombinase and GFP under the control of a 2.4 kb Prx1 promoter. The transgene is expressed in osteochondro progenitor cells in the developing limb buds and in a subpopul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8afb5b7aa67ee173c7898cc624b63e43
https://europepmc.org/articles/PMC2742350/
https://europepmc.org/articles/PMC2742350/