Pharmacogenetics of asthma in children

Por Kondo, Naomi, Matsui, Eiko, Nishimura, Akane, Kaneko, Hideo
Publicado em 2010

The role of dendritic cells in the generation of CD4(+) CD25(HI) Foxp3(+) T cells induced by amino acid copolymers

Por Kawamoto, Norio, Ohnishi, Hidenori, Kondo, Naomi, Strominger, Jack L.
Publicado em 2013

Pediatric thioridazine poisoning as a result of a pharmacy compounding error

Por Kato, Zenichiro, Nakamura, Mitsuhiro, Yamagishi, Yuka, Teramoto, Takahide, Kondo, Naomi
Publicado em 2009

Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development

Por Orii, Kenji E., Lee, Youngsoo, Kondo, Naomi, McKinnon, Peter J.
Publicado em 2006

PEX3 Is the Causal Gene Responsible for Peroxisome Membrane Assembly–Defective Zellweger Syndrome of Complementation Group G

Por Ghaedi, Kamran, Honsho, Masanori, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicado em 2000

Relationship between the benefits of suplatast tosilate, a Th2 cytokine inhibitor, and gene polymorphisms in children with bronchial asthma

Por MATSUI, EIKO, SHINODA, SHINJI, FUKUTOMI, OSAMU, KANEKO, HIDEO, FUKAO, TOSHIYUKI, KONDO, NAOMI
Publicado em 2010

The clinical and genetic factors for predicting the response to inhaled corticosteroids

Por Nagase, Hiroyuki, Tsurikisawa, Naomi, Kamiyama, Asae, Matsui, Eiko, Kondo, Naomi, Akiyama, Kazuo, Ohta, Ken
Publicado em 2013

Positioning of autoimmune TCR-Ob.2F3 and TCR-Ob.3D1 on the MBP85–99/HLA-DR2 complex

Por Kato, Zenichiro, Stern, Joel N. H., Nakamura, Hironori K., Kuwata, Kazuo, Kondo, Naomi, Strominger, Jack L.
Publicado em 2008

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

Por Tamura, Shigehiko, Okumoto, Kanji, Toyama, Ryusuke, Shimozawa, Nobuyuki, Tsukamoto, Toshiro, Suzuki, Yasuyuki, Osumi, Takashi, Kondo, Naomi, Fujiki, Yukio
Publicado em 1998

Refractory Chronic Pleurisy Caused by Helicobacter equorum-Like Bacterium in a Patient with X-Linked Agammaglobulinemia

Por Funato, Michinori, Kaneko, Hideo, Ohkusu, Kiyofumi, Sasai, Hideo, Kubota, Kazuo, Ohnishi, Hidenori, Kato, Zenichiro, Fukao, Toshiyuki, Kondo, Naomi
Publicado em 2011

Purification, crystallization and preliminary X-ray crystallographic analysis of human IL-18 and its extracellular complexes

Por Kimura, Takeshi, Tsutsumi, Naotaka, Arita, Kyohei, Ariyoshi, Mariko, Ohnishi, Hidenori, Kondo, Naomi, Shirakawa, Masahiro, Kato, Zenichiro, Tochio, Hidehito
Publicado em 2014

Intermittent and episode-driven use of pranlukast to reduce the frequency of wheezing in atopic children: a randomized, double-blind, placebo-controlled trial

Por Ebisawa, Motohiro, Terada, Akihiko, Sato, Kazuki, Kurosaka, Fumitake, Kondo, Naomi, Sugizaki, Chizuko, Morikawa, Akihiro, Nishima, Sankei, Urashima, Mitsuyoshi
Publicado no World Allergy Organ J (2015)

Structural basis for the multiple interactions of the MyD88 TIR domain in TLR4 signaling

Por Ohnishi, Hidenori, Tochio, Hidehito, Kato, Zenichiro, Orii, Kenji E., Li, Ailian, Kimura, Takeshi, Hiroaki, Hidekazu, Kondo, Naomi, Shirakawa, Masahiro
Publicado em 2009

Lymphocyte Responses to Chymotrypsin- or Trypsin V-Digested β-Lactoglobulin in Patients with Cow's Milk Allergy

Por Kondo Masashi, Fukao Toshiyuki, Shinoda Shinji, Kawamoto Norio, Kaneko Hideo, Kato Zenichiro, Matsui Eiko, Teramoto Takahide, Nakano Taku, Kondo Naomi
Publicado em 2007-03-01

Lymphocyte Responses to Chymotrypsin- or Trypsin V-Digested β-Lactoglobulin in Patients with Cow's Milk Allergy

Por Kondo, Masashi, Fukao, Toshiyuki, Shinoda, Shinji, Kawamoto, Norio, Kaneko, Hideo, Kato, Zenichiro, Matsui, Eiko, Teramoto, Takahide, Nakano, Taku, Kondo, Naomi
Publicado em 2007

Mutations in Novel Peroxin Gene PEX26 That Cause Peroxisome-Biogenesis Disorders of Complementation Group 8 Provide a Genotype-Phenotype Correlation

Por Matsumoto, Naomi, Tamura, Shigehiko, Furuki, Satomi, Miyata, Non, Moser, Ann, Shimozawa, Nobuyuki, Moser, Hugo W., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicado em 2003

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

Por Matsuzono, Yuji, Kinoshita, Naohiko, Tamura, Shigehiko, Shimozawa, Nobuyuki, Hamasaki, Maho, Ghaedi, Kamran, Wanders, Ronald J. A., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicado em 1999

PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

Por Okumoto, Kanji, Shimozawa, Nobuyuki, Kawai, Atsusi, Tamura, Shigehiko, Tsukamoto, Toshiro, Osumi, Takashi, Moser, Hugo, Wanders, Ronald J. A., Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicado em 1998

Defining the Pathway for Tat-mediated Delivery of β-Glucuronidase in Cultured Cells and MPS VII Mice

Por Orii, Koji O., Grubb, Jeffrey H., Vogler, Carole, Levy, Beth, Tan, Yun, Markova, Kamelia, Davidson, Beverly L., Mao, Q., Orii, Tadao, Kondo, Naomi, Sly, William S.
Publicado em 2005

Deaths Associated with Pandemic (H1N1) 2009 among Children, Japan, 2009–2010

Por Okumura, Akihisa, Nakagawa, Satoshi, Kawashima, Hisashi, Muguruma, Takashi, Saito, Osamu, Fujimoto, Jun-ichi, Toida, Chiaki, Kuga, Shuji, Imamura, Toshihiro, Shimizu, Toshiaki, Kondo, Naomi, Morishima, Tsuneo
Publicado em 2011