Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Noriko Funato"'
Autor:
Noriko Funato, Hiromi Yanagisawa
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract TBX1, which encodes a T-box transcription factor, is considered a candidate gene for DiGeorge syndrome, velocardiofacial syndrome, and conotruncal anomaly face syndrome. Transduction of TBX1 decreases cell proliferation in epithelial cancer
Externí odkaz:
https://doaj.org/article/12e2aa2f2b2d4d2b94069fecc739f2ac
Autor:
Yuki Taga, Yu Iwasaki, Chisa Tometsuka, Noriko Funato, Yasutaka Shigemura, Masashi Kusubata, Kazunori Mizuno
Publikováno v:
npj Science of Food, Vol 6, Iss 1, Pp 1-8 (2022)
Abstract There are increasing reports demonstrating high bioavailability of 4-hydroxyproline (4Hyp)-containing oligopeptides after oral ingestion of collagen hydrolysate and their bioactivity. In contrast, no study investigates the fate of another co
Externí odkaz:
https://doaj.org/article/77c7e3fbfea7434bb2228851544af551
Publikováno v:
Current Research in Food Science, Vol 4, Iss , Pp 175-181 (2021)
Collagen hydrolysate has various beneficial effects, such as bone strengthening, joint/skin protection and lipid metabolism regulation. In this study, the anti-obesity activity of ginger protease-degraded collagen hydrolysate (GDCH) was evaluated in
Externí odkaz:
https://doaj.org/article/133ffbf2a05c461bb2ce065bc2830ddf
Autor:
Noriko Funato
Publikováno v:
Journal of Developmental Biology, Vol 10, Iss 2, p 18 (2022)
The 22q11.2 deletion is one of the most common genetic microdeletions, affecting approximately 1 in 4000 live births in humans. A 1.5 to 2.5 Mb hemizygous deletion of chromosome 22q11.2 causes DiGeorge syndrome (DGS) and velocardiofacial syndrome (VC
Externí odkaz:
https://doaj.org/article/52c7c0df4eeb4a46b4190fb4ae712273
Autor:
Noriko Funato
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
The synchondroses formed via endochondral ossification in the cranial base are an important growth center for the neurocranium. Abnormalities in the synchondroses affect cranial base elongation and the development of adjacent regions, including the c
Externí odkaz:
https://doaj.org/article/9d631e177ee247ffa5c76f669d2b1d79
Publikováno v:
Journal of Functional Foods, Vol 46, Iss , Pp 456-462 (2018)
Oral ingestion of collagen hydrolysate leads to significantly high blood levels of various hydroxyproline (Hyp)-containing oligopeptides, such as Pro-Hyp that has been reported to promote osteoblast differentiation. Using ginger protease, we recently
Externí odkaz:
https://doaj.org/article/8e9832d7d3ac4cc0bc16af2ca9d096b5
Autor:
Noriko Funato, Yuki Taga, Lindsay E. Laurie, Chisa Tometsuka, Masashi Kusubata, Kiyoko Ogawa-Goto
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 22, p 8638 (2020)
Temporal and/or spatial alteration of collagen family gene expression results in bone defects. However, how collagen expression controls bone size remains largely unknown. The basic helix-loop-helix transcription factor HAND1 is expressed in developi
Externí odkaz:
https://doaj.org/article/7cf86ea21a8743babbbd9396a47a6349
Publikováno v:
Genomics Data, Vol 9, Iss C, Pp 60-62 (2016)
In this article, we further provide the data generated for the previously published research article “Specification of jaw identity by the Hand2 transcription factor.” To better understand the downstream genes of the basic helix-loop-helix transc
Externí odkaz:
https://doaj.org/article/ba64e29868a544089d809c5ff23467fc
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0150263 (2016)
The developing long bone is a model of endochondral ossification that displays the morphological layers of chondrocytes toward the ossification center of the diaphysis. Indian hedgehog (Ihh), a member of the hedgehog family of secreted molecules, reg
Externí odkaz:
https://doaj.org/article/cb0fe96fe515425ca6f444c8f58bbbf4
Autor:
Mariko Mizuguchi, Yuka Sasaki, Toshifumi Hara, Masaya Higuchi, Yuetsu Tanaka, Noriko Funato, Nobuyuki Tanaka, Masahiro Fujii, Masataka Nakamura
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0148217 (2016)
Tax1 encoded by the human T-cell leukemia virus type 1 (HTLV-1) has been believed to dysregulate the expression of cellular genes involved in cell survival and mortality, leading to the development of adult T-cell leukemia (ATL). The function of Tax1
Externí odkaz:
https://doaj.org/article/595f16f7f1ff40528fe896695cf058e7