Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Yuka Saito-Nanjo"'
Autor:
Masahiro Irie, Tetsuya Niihori, Tomohiro Nakano, Tasuku Suzuki, Saori Katayama, Kunihiko Moriya, Hidetaka Niizuma, Nobu Suzuki, Yuka Saito-Nanjo, Masaei Onuma, Takeshi Rikiishi, Atsushi Sato, Mayumi Hangai, Mitsuteru Hiwatari, Junji Ikeda, Reo Tanoshima, Norio Shiba, Yuki Yuza, Nobuyuki Yamamoto, Yoshiko Hashii, Motohiro Kato, Junko Takita, Miho Maeda, Yoko Aoki, Masue Imaizumi, Yoji Sasahara
Publikováno v:
International Journal of Hematology. 117:598-606
Mutations in the MECOM encoding EVI1 are observed in infants who have radioulnar synostosis with amegakaryocytic thrombocytopenia. MECOM-associated syndrome was proposed based on clinical heterogeneity. Allogeneic hematopoietic stem cell transplantat
Autor:
Hitoshi Terui, Setsuya Aiba, Akiko Hagiwara-Takita, Kenshi Yamasaki, Yuka Saito-Nanjo, Ryoko Shimada-Omori, Kenichiro Tsuchiyama, Takeshi Rikiishi, Yoji Sasahara
Publikováno v:
The Journal of dermatologyREFERENCES. 48(9)
Genome-wide association studies have identified more than 60 susceptibility loci for psoriasis, highlighting the role of genetics in psoriasis development. Although the HLA region is suggested as the most prominent susceptibility locus, the role of t
Autor:
Tetsuya Niihori, Reo Tanoshima, Yoji Sasahara, Atsushi Sato, Masahiro Irie, Yuka Saito-Nanjo, Ryo Funayama, Matsuyuki Shirota, Taiki Abe, Yuko Okuyama, Naoto Ishii, Keiko Nakayama, Shigeo Kure, Masue Imaizumi, Yoko Aoki
Publikováno v:
Blood advances. 6(18)
Autor:
Osamu Sakamoto, Kengo Kawano, Hiroshi Kitazawa, Hidetaka Niizuma, Shigeo Kure, Toru Uchiyama, Yoji Sasahara, Takeshi Rikiishi, Kunihiko Moriya, Yuka Saito-Nanjo, Yasuhiro Setoguchi
Publikováno v:
European Journal of Pediatrics. 172:953-957
Mutations in genes critical for surfactant metabolism, including surfactant protein C (SP-C) and ABCA3, are well-recognized causes of interstitial lung disease. Recessive mutations in ABCA3 were first attributed to fatal respiratory failure in full-t
Autor:
Masahiro Irie, Keiko Nakayama, Tetsuya Niihori, Takeshi Nagashima, Atsushi Sato, Takashi Kaneko, Yoko Aoki, Yoichi Matsubara, Shin Ichi Inoue, Yuka Saito-Nanjo, Meri Ouchi-Uchiyama, Yoji Sasahara, Ryo Funayama, Shigeo Kure, Keiichi Ozono, Masue Imaizumi, Yoshiko Hashii
Publikováno v:
American journal of human genetics. 97(6)
Radioulnar synostosis with amegakaryocytic thrombocytopenia (RUSAT) is an inherited bone marrow failure syndrome, characterized by thrombocytopenia and congenital fusion of the radius and ulna. A heterozygous HOXA11 mutation has been identified in tw
Autor:
Yuko Watanabe, Yu Katata, Mika Watanabe, Kosuke Shido, Shigeo Kure, Yoji Sasahara, Setsuya Aiba, Tetsuya Niihori, Hidetaka Niizuma, Daiju Oba, Yoko Aoki, Takeshi Rikiishi, Chie Iizuka, Ryuta Saito, Yukihiko Sonoda, Yuka Saito-Nanjo, Masaei Onuma, Teiji Tominaga, Kunihiko Moriya
Publikováno v:
American journal of medical genetics. Part A. (1)
Genetic mosaicism for somatic mutations of oncogenes is common in genodermatoses, which can be complicated with extra-cutaneous abnormalities. Here we describe an infant with a congenital anaplastic astrocytoma, a linear syringocystadenoma papillifer
Autor:
Keiichi Ozono, Yoji Sasahara, Takashi Kaneko, Meri Ouchi-Uchiyama, Ryo Funayama, Tetsuya Niihori, Shigeo Kure, Masahiro Irie, Atsushi Sato, Takeshi Nagashima, Yuka Saito-Nanjo, Yoshiko Hashii, Yoichi Matsubara, Keiko Nakayama, Yoko Aoki, Shin Ichi Inoue, Masue Imaizumi
Publikováno v:
Experimental Hematology. 44:S44-S45