Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Ritsuko, Ozawa"'
Autor:
Nyambayar Dashtsoodol, Tomokuni Shigeura, Ritsuko Ozawa, Michishige Harada, Satoshi Kojo, Takashi Watanabe, Haruhiko Koseki, Manabu Nakayama, Osamu Ohara, Masaru Taniguchi
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0153347 (2016)
Invariant Vα14 natural killer T (NKT) cells, characterized by the expression of a single invariant T cell receptor (TCR) α chain encoded by rearranged Trav11 (Vα14)-Traj18 (Jα18) gene segments in mice, and TRAV10 (Vα24)-TRAJ18 (Jα18) in humans,
Externí odkaz:
https://doaj.org/article/24ca0c137363450ba05b3819008aee46
Autor:
Tulika Prakash, Vineet K Sharma, Naoki Adati, Ritsuko Ozawa, Naveen Kumar, Yuichiro Nishida, Takayoshi Fujikake, Tadayuki Takeda, Todd D Taylor
Publikováno v:
PLoS ONE, Vol 5, Iss 10, p e13284 (2010)
From the ENCODE project, it is realized that almost every base of the entire human genome is transcribed. One class of transcripts resulting from this arises from the conjoined gene, which is formed by combining the exons of two or more distinct (par
Externí odkaz:
https://doaj.org/article/c00a41db78e443b183a467cf488fce12
Autor:
Satoshi Kojo, Takashi Watanabe, Michishige Harada, Minako Aihara, Ritsuko Ozawa, Tomokuni Shigeura, Nyambayar Dashtsoodol, Masaru Taniguchi, Takaho A. Endo, Osamu Ohara
Publikováno v:
Nature Immunology. 18:274-282
Although invariant Vα14+ natural killer T cells (NKT cells) are thought to be generated from CD4+CD8+ double-positive (DP) thymocytes, the developmental origin of CD4-CD8- double-negative (DN) NKT cells still remains unresolved. Here we provide defi
Autor:
Nyambayar, Dashtsoodol, Tomokuni, Shigeura, Minako, Aihara, Ritsuko, Ozawa, Satoshi, Kojo, Michishige, Harada, Takaho A, Endo, Takashi, Watanabe, Osamu, Ohara, Masaru, Taniguchi
Publikováno v:
Nature immunology. 18(3)
Although invariant V
Autor:
Tomokuni Shigeura, Satoshi Kojo, Takashi Watanabe, Manabu Nakayama, Nyambayar Dashtsoodol, Ritsuko Ozawa, Osamu Ohara, Haruhiko Koseki, Michishige Harada, Masaru Taniguchi
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 4, p e0153347 (2016)
PLoS ONE, Vol 11, Iss 4, p e0153347 (2016)
Invariant Vα14 natural killer T (NKT) cells, characterized by the expression of a single invariant T cell receptor (TCR) α chain encoded by rearranged Trav11 (Vα14)-Traj18 (Jα18) gene segments in mice, and TRAV10 (Vα24)-TRAJ18 (Jα18) in humans,
Publikováno v:
Proceedings of the National Academy of Sciences. 98:4569-4574
Protein–protein interactions play crucial roles in the execution of various biological functions. Accordingly, their comprehensive description would contribute considerably to the functional interpretation of fully sequenced genomes, which are floo
Autor:
Satoru Kuhara, Ritsuko Ozawa, Kiyoshi Yamamoto, Tomoko Chiba, Takashi Ito, Yoshiyuki Sakaki, Shigeru Muta, Kosuke Tashiro, Mayumi Nishizawa
Publikováno v:
Proceedings of the National Academy of Sciences. 97:1143-1147
Protein–protein interactions play pivotal roles in various aspects of the structural and functional organization of the cell, and their complete description is indispensable to thorough understanding of the cell. As an approach toward this goal, he
Autor:
Naoki Adati, Tadayuki Takeda, Ritsuko Ozawa, Takayoshi Fujikake, Vineet K. Sharma, Tulika Prakash, Todd D. Taylor, Yuichiro Nishida, Naveen Kumar
Publikováno v:
PLoS ONE
PLoS ONE, Vol 5, Iss 10, p e13284 (2010)
PLoS ONE, Vol 5, Iss 10, p e13284 (2010)
From the ENCODE project, it is realized that almost every base of the entire human genome is transcribed. One class of transcripts resulting from this arises from the conjoined gene, which is formed by combining the exons of two or more distinct (par
Autor:
Tadayuki Takeda, Yuichiro Nishida, Yoshiyuki Sakaki, Ritsuko Ozawa, Aasami Maeda, Naoki Adati
Publikováno v:
BMC Research Notes
BMC Research Notes, Vol 1, Iss 1, p 95 (2008)
BMC Research Notes, Vol 1, Iss 1, p 95 (2008)
Background SH-SY5Y cells exhibit a neuronal phenotype when treated with all-trans retinoic acid (RA), but the molecular mechanism of activation in the signalling pathway mediated by phosphatidylinositol 3-kinase (PI3K) is unclear. To investigate this
Autor:
Satoru Noguchi, Rumi Kurokawa, Megumu Ogawa, Yukiko K. Hayashi, Ritsuko Ozawa, Hiroshi Matsumoto, Ikuya Nonaka, Ichizo Nishino
Publikováno v:
The American journal of pathology. 168(3)
Emery-Dreifuss muscular dystrophy is an inherited muscular disorder clinically characterized by slowly progressive weakness affecting humero-peroneal muscles, early joint contractures, and cardiomyopathy with conduction block. The X-linked recessive