Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Kazumi, Akimoto"'
Autor:
Haruka Kishi, Teruo Jojima, Takahiko Kogai, Toshie Iijima, Eriko Ohira, Dai Tanuma, Sachiyo Konno, Kanako Kato, Atsumi Kezuka, Kazumi Akimoto, Junko Sakumoto, Akira Hishinuma, Takuya Tomaru, Noriko Makita, Isao Usui, Yoshimasa Aso
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Abstract Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3,
Externí odkaz:
https://doaj.org/article/43c5c4f10fc74e1891a01b40795994bd
Autor:
Ken‐ichi Inoue, Satoko Kishimoto, Kazumi Akimoto, Masashi Sakuma, Shigeru Toyoda, Teruo Inoue, Ken‐ichiro Yoshida, Mitsugi Shimoda, Shuji Suzuki
Publikováno v:
Annals of Gastroenterological Surgery, Vol 3, Iss 4, Pp 416-425 (2019)
Abstract Aim Cancer‐associated fibroblasts (CAF) play a crucial role in angiogenesis in the complex tumor microenvironment. However, fibroblasts show extensive heterogeneity and their dynamic functions against stressors remain largely unknown. Meth
Externí odkaz:
https://doaj.org/article/04e9aa041d204f9786d0408fbb81f13b
Autor:
Sachiyo Konno, Dai Tanuma, Eriko Ohira, Takahiko Kogai, Takuya Tomaru, Isao Usui, Teruo Jojima, Akira Hishinuma, Junko Sakumoto, Haruka Kishi, Kazumi Akimoto, Yoshimasa Aso, Atsumi Kezuka, Toshie Iijima, Noriko Makita, Kanako Kato
Publikováno v:
Clinical Case Reports, Vol 8, Iss 12, Pp 2619-2624 (2020)
Clinical Case Reports
Clinical Case Reports
Autosomal dominant hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome are typically diagnosed by manifestations of the three features with a positive family history. Our case carried a de novo variant in causative gene, GATA3, but prese
Autor:
Toshie Iijima, Akira Hishinuma, Junko Sakumoto, Keisuke Ueki, Teruo Jojima, Shintaro Sakurai, Masaaki Sagara, Kazumi Akimoto, Yoshimasa Aso, Takahiko Kogai, Masato Kase, Atsumi Kezuka, Isao Usui, Takashi Namatame, Kanako Kato, Takao Kamai
Publikováno v:
European Journal of Endocrinology. 183:K7-K12
A monoallelic germline alteration of ARMC5 causes primary bilateral macronodular adrenal hyperplasia (PBMAH) with Cushing’s syndrome via its subsequent somatic alteration on the other allele as the second hit. PBMAH is sometimes complicated with me
Publikováno v:
Internal Medicine. 61:3309-3310
Autor:
Mitsugi Shimoda, Ken-ichi Inoue, Teruo Inoue, Satoko Kishimoto, Shigeru Toyoda, Kazumi Akimoto, Shuji Suzuki, Masashi Sakuma, Ken-Ichiro Yoshida
Publikováno v:
Annals of Gastroenterological Surgery, Vol 3, Iss 4, Pp 416-425 (2019)
Aim Cancer‐associated fibroblasts (CAF) play a crucial role in angiogenesis in the complex tumor microenvironment. However, fibroblasts show extensive heterogeneity and their dynamic functions against stressors remain largely unknown. Methods We co
Autor:
Kazumi Akimoto, Hiroki Matsuda
Publikováno v:
Journal of the Sedimentological Society of Japan. 77:121-126
Publikováno v:
Dokkyo Journal Of Medical Sciences. 45(2):43-51
RUNX1 and RUNX3 are master transcription factors in sensory neuron lineage specifications. Protein levels of such developmental regulators are tightly controlled during carcinogenesis, in order to block differentiation and drive proliferation. Here w
Autor:
Kohsuke Uchida, Kikuo Kasai, Toshie Iijima, Kazunori Yanagi, Takanori Tomotsune, Kunihiro Suzuki, Kazumi Akimoto, Yoshimasa Aso, Teruo Jojima
Publikováno v:
Atherosclerosis. 261:44-51
Background and aims Several studies have demonstrated that both native glucagon-like peptide-1 (GLP-1) and GLP-1 receptor agonists suppress the progression of atherosclerosis in animal models. Methods We investigated whether liraglutide, a GLP-1 anal
Publikováno v:
Cancer Medicine
NRF2 stabilizes redox potential through genes for glutathione and thioredoxin antioxidant systems. Whether blockade of glutathione and thioredoxin is useful in eliminating cancer stem cells remain unknown. We used xenografts derived from colorectal c