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of 22
pro vyhledávání: '"Banyar Than Naing"'
Autor:
Akira Yoneda, Kazuya Okada, Hitoshi Okubo, Mitsutoshi Matsuo, Hiroki Kishikawa, Banyar Than Naing, Atsushi Watanabe, Takashi Shimada
Publikováno v:
Case Reports in Gastroenterology, Vol 8, Iss 2, Pp 175-181 (2014)
Ehlers-Danlos syndrome, vascular type (vEDS) (MIM #130050) is an autosomal dominant disorder caused by mutation in the type III collagen gene, COL3A1, leading to fragility of blood vessels, bowel and uterus that leads to spontaneous rupture. We repor
Externí odkaz:
https://doaj.org/article/262f4f2bfc4f4b909ec67f7d396ff09e
Autor:
Banyar Than, Naing, Takami, Takizawa, Takanobu, Sakurai, Chaw, Kyi-Tha-Thu, Toshihiro, Takizawa
Publikováno v:
Histochemistry and Cell Biology. 159:363-375
LncRNA H19 serves as a regulatory RNA in mouse placental development. However, there is little information available on the in situ expression of H19 in the late-gestation mouse placenta. In this study, we performed quantitative polymerase chain reac
Publikováno v:
Histochemistry and cell biology. 149(5)
Long non-coding RNAs (lncRNAs; > 200 nucleotides in length) have attracted attention as fine-tuners of gene expression. However, little is known about the cell- and stage-specific expression pattern and function of lncRNAs in spermatogenesis. The pur
Autor:
Banyar Than Naing, Takashi Shimada, Shinji Tanigaki, Masae Ono, Atsushi Watanabe, Mitsutoshi Iwashita
Publikováno v:
International Medical Case Reports Journal
The vascular type of Ehlers-Danlos syndrome (EDS), EDS type IV (Online Mendelian Inheritance in Man [MIM] #130050) is characterized by thin, translucent skin, easy bruising, and arterial, intestinal, and/or uterine fragility during pregnancy, which m
Autor:
Atsushi Watanabe, Banyar Than Naing, Takashi Shimada, Hideo Orimo, Shuhei Satoh, Atsushi Fujita
Publikováno v:
Bone. 60:93-97
Hypophosphatasia (HPP) is an inherited disorder characterized by defective bone mineralization caused by mutations in the alkaline phosphatase gene (ALPL). Clinically, the disease spans a great continuum of disease severity and six forms can be disti
Akademický článek
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Publikováno v:
Current Genetic Medicine Reports. 1:171-174
Pharmacogenomics (PGx) involves investigation into the genetic basis of interindividual differences in drug responses, such as efficacy, dose requirements, and adverse events. PGx can be used as a tool for personalizing health care on the basis of in
Autor:
Shinsuke Ninomiya, Banyar Than Naing, Yoshikazu Kuroki, Kazunobu Ouchi, Mitsuo Masuno, Yasunori Ueda, Eisei Kondo, Yasuko Yamanouchi, Wataru Fujimoto, Kazushige Kadota, Mika Inoue, Tatsuya Kotaka, Takashi Shimada, Atsushi Watanabe
Publikováno v:
Congenital Anomalies. 52:207-210
We report a 34-year-old Japanese female with the vascular type of Ehlers-Danlos syndrome. She had thin translucent skin, extensive bruising, toe joint hypermobility, left lower extremity varicose veins, and chronic wrist, knee and ankle joint pain. S
Autor:
Rei Ogawa, Satoshi Akaishi, Takashi Shimada, Banyar Than Naing, Hiko Hyakusoku, Atsushi Watanabe, Atsushi Fujita, Motoko Sasaki
Publikováno v:
Journal of Investigative Dermatology. 134(7):2041-2043
Correction to: Journal of Investigative Dermatology (2014) xxx, xxx–xxx; advance online publication 27 February 2014; doi: 10.1038/jid.2014.71
Publikováno v:
Placenta. 46:111-112