Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Mitsunobu Shimadzu"'
Autor:
Hirotake Wakamatsu, Mitsunobu Shimadzu, Kosei Matsue, Yasuhito Suehara, Mamiko Sakata-Yanagimoto, Kota Fukumoto, Keiichiro Hattori, Daisuke Komori, Manabu Fujisawa, Sharna Tanzima Nuhat, Manabu Kusakabe, Shigeru Chiba
Publikováno v:
Cancer Science
Angioimmunoblastic T‐cell lymphoma (AITL) is a subtype of nodal peripheral T‐cell lymphoma (PTCL). Somatic RHOA mutations, most frequently found at the hotspot site c.50G > T, p.Gly17Val (G17V RHOA mutation) are a genetic hallmark of AITL. Detect
Publikováno v:
Bunseki kagaku. 66:445-451
Autor:
Eiju Negoro, Mitsunobu Shimadzu, Akira Yoshida, Shinji Kishi, Yoshimasa Urasaki, Katsunori Tai, Kazutaka Takagi, Satoshi Ikegaya, Takanori Ueda, Hiromichi Iwasaki, Takahiro Yamauchi
Publikováno v:
International Journal of Infectious Diseases. 17(4):e271-e276
Summary Objectives The rapid diagnosis of bacteremia is crucial for patient management including the choice of antimicrobial therapy, especially in cases of hematological disease, because neutropenia occurs frequently during antineoplastic chemothera
Autor:
Hiroshi Terasaki, Masayoshi Katano, Tomoaki Tamura, Satoshi Kawauchi, Junko Murase, Mitsunobu Shimadzu, Yoshiko Masuda
Publikováno v:
Genetic Testing and Molecular Biomarkers. 14:269-282
We developed a method of quality control and monitoring for the isolation of mesenchymal stem cells (MSCs) from bone marrow and their differentiation into osteoblasts. After dividing the cell culture process into five groups based on cell types such
Autor:
Hisatoshi Baba, Tsuyoshi Miyazaki, Norbert Orwotho, Yasuo Kokubo, Takafumi Yayama, Shigeru Kobayashi, Kenichi Takeno, Kenzo Uchida, Elisa S. Mwaka, Kohei Negoro, Hideaki Nakajima, Mitsunobu Shimadzu
Publikováno v:
Journal of Orthopaedic Science. 14:471-483
Molecular biological techniques such as the polymerase chain reaction (PCR) and DNA microarray are used for the detection/identification of microorganisms; however, few reports have discussed the clinical utility of microarray analysis for identifica
Autor:
Takashi Deguchi, Mitsunobu Shimadzu, Satomi Sekiguchi, Hiroaki Ishiko, Mitsuru Yasuda, Osamu Kozawa, Rie Matsushima-Nishiwaki, Akio Hayashi, Susumu Ochiai
Publikováno v:
Journal of Antimicrobial Chemotherapy. 60:54-60
Objectives In Neisseria gonorrhoeae, the mosaic structure of penicillin-binding protein 2 (PBP 2), composed of fragments of PBP 2 from Neisseria cinerea and Neisseria perflava, was significantly associated with decreased susceptibility to cephalospor
Autor:
Jun Inatomi, George Seki, Yoko Endo, Nobuo Moriyama, Mesiha Ekim, Takashi Igarashi, Hideomi Yamada, Lihadh Al-Gazali, Shoko Horita, Mitsunobu Shimadzu, Takashi Sekine, Majed Dasouki, Toshiro Fujita
Publikováno v:
Journal of the American Society of Nephrology. 16:2270-2278
Mutations in the Na+-HCO3- co-transporter (NBC1) cause permanent proximal renal tubular acidosis (pRTA) with ocular abnormalities. However, little has been known about the relationship between the degree of NBC1 inactivation and the severity of pRTA.
Autor:
Yasuhiro Takeshima, Toru Takumi, Takashi Igarashi, Fumiko Tozawa, Jun Inatomi, George Seki, Takashi Sekine, Hitoshi Endou, Norishige Yoshikawa, Hajime Nakamura, Toshikazu Takahashi, Mitsunobu Shimadzu
Publikováno v:
Journal of the American Society of Nephrology. 12:713-718
Permanent isolated proximal renal tubular acidosis (pRTA) with ocular abnormalities is a systemic disease involving short stature, isolated pRTA, mental retardation, and ocular abnormalities. Kidney Na + /HCO 3 - cotransporter (kNBC1) cDNA from perip
Autor:
Tadashi Hasegawa, Mitsunobu Shimadzu, Shunji Yamamori, Masafumi Kurosumi, Hitoshi Tsuda, Goi Sakamoto, B S Hiroshi Terasaki, Futoshi Akiyama
Publikováno v:
Cancer. 92:2965-2974
BACKGROUND Fluorescent in situ hybridization (FISH) has been shown to be one of the most reliable methods with which to estimate the status of the HER-2/neu (or c-erb B-2) oncogene at the DNA level. METHODS To study interobserver reproducibility and
Autor:
Jun Inatomi, Takashi Igarashi, Takashi Kuwahara, Mitsunobu Shimadzu, Rajesh V. Thakker, Toshio Ohara
Publikováno v:
Kidney International. 58:520-527
Clinical and genetic studies of CLCN5 mutations in Japanese families with Dent's disease. Background Dent's disease is an X-linked renal tubular disorder that is characterized by low molecular weight proteinuria, hypercalciuria, nephrolithiasis, and