Pathophysiology of hypophosphatasia and the potential role of asfotase alfa

por Orimo, Hideo
Publicado 2016

Development of a novel chronic kidney disease mouse model to evaluate the progression of hyperphosphatemia and associated mineral bone disease

por Tani, Takashi, Orimo, Hideo, Shimizu, Akira, Tsuruoka, Shuichi
Publicado 2017

Frameshift Mutations and a Length Polymorphism in the hMSH3 Gene and the Spectrum of Microsatellite Instability in Sporadic Colon Cancer

por Orimo, Hideo, Nakajima, Eiitsu, Ikejima, Miyoko, Emi, Mitsuru, Shimada, Takashi
Publicado 1999

Immunoproteomic identification of anti-C9 autoimmune antibody in patients with seronegative obstetric antiphospholipid syndrome

por Kuwabara, Yoshimitsu, Katayama, Akira, Kurihara, Sachiko, Orimo, Hideo, Takeshita, Toshiyuki
Publicado 2018

Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity

por Hiraoka, Miki, Takahashi, Hiroshi, Orimo, Hideo, Hiraoka, Miina, Ogata, Tsutomu, Azuma, Noriyuki
Publicado 2010

Prolonged Survival and Phenotypic Correction of Akp2(−/−) Hypophosphatasia Mice by Lentiviral Gene Therapy

por Yamamoto, Seiko, Orimo, Hideo, Matsumoto, Tae, Iijima, Osamu, Narisawa, Sonoko, Maeda, Takahide, Millán, José Luis, Shimada, Takashi
Publicado 2011

Treatment with bone maturation and average lifespan of HPP model mice by AAV8-mediated neonatal gene therapy via single muscle injection

por Matsumoto, Tae, Miyake, Koichi, Miyake, Noriko, Iijima, Osamu, Adachi, Kumi, Narisawa, Sonoko, Millán, José Luis, Orimo, Hideo, Shimada, Takashi
Publicado 2021