Pharmacogenetics of asthma in children

per Kondo, Naomi, Matsui, Eiko, Nishimura, Akane, Kaneko, Hideo
Publicat 2010

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

per Kawamoto, Norio, Ohnishi, Hidenori, Kondo, Naomi, Strominger, Jack L.
Publicat 2013

Pediatric thioridazine poisoning as a result of a pharmacy compounding error

per Kato, Zenichiro, Nakamura, Mitsuhiro, Yamagishi, Yuka, Teramoto, Takahide, Kondo, Naomi
Publicat 2009

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

per Orii, Kenji E., Lee, Youngsoo, Kondo, Naomi, McKinnon, Peter J.
Publicat 2006

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

per Ghaedi, Kamran, Honsho, Masanori, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Kondo, Naomi, Fujiki, Yukio
Publicat 2000

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

per MATSUI, EIKO, SHINODA, SHINJI, FUKUTOMI, OSAMU, KANEKO, HIDEO, FUKAO, TOSHIYUKI, KONDO, NAOMI
Publicat 2010

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

per Nagase, Hiroyuki, Tsurikisawa, Naomi, Kamiyama, Asae, Matsui, Eiko, Kondo, Naomi, Akiyama, Kazuo, Ohta, Ken
Publicat 2013

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

per Kato, Zenichiro, Stern, Joel N. H., Nakamura, Hironori K., Kuwata, Kazuo, Kondo, Naomi, Strominger, Jack L.
Publicat 2008

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

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

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

per Funato, Michinori, Kaneko, Hideo, Ohkusu, Kiyofumi, Sasai, Hideo, Kubota, Kazuo, Ohnishi, Hidenori, Kato, Zenichiro, Fukao, Toshiyuki, Kondo, Naomi
Publicat 2011

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

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

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

per Ebisawa, Motohiro, Terada, Akihiko, Sato, Kazuki, Kurosaka, Fumitake, Kondo, Naomi, Sugizaki, Chizuko, Morikawa, Akihiro, Nishima, Sankei, Urashima, Mitsuyoshi
Publicat a World Allergy Organ J (2015)

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

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

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

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

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

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

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

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

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

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

TGF-β Concentration in Breast Milk is Associated With the Development of Eczema in Infants

per Morita, Yoshinori, Campos-Alberto, Eduardo, Yamaide, Fumiya, Nakano, Taiji, Ohnisi, Hidenori, Kawamoto, Minako, Kawamoto, Norio, Matsui, Eiko, Kondo, Naomi, Kohno, Yoichi, Shimojo, Naoki
Publicat a Front Pediatr (2018)

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

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

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

per 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.
Publicat 2005