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1
The effect of targeted rheumatoid arthritis therapies on anti‐citrullinated protein autoantibody levels and B cell responses
The effect of targeted rheumatoid arthritis therapies on anti‐citrullinated protein autoantibody levels and B cell responses
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The effect of targeted rheumatoid arthritis therapies on anti‐citrullinated protein autoantibody levels and B cell responses

Modi, S. ; Soejima, M. ; Levesque, M. C.

Clinical and experimental immunology, 2013-07, Vol.173 (1), p.8-17 [Periódico revisado por pares]

England: Oxford University Press

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2
Anti-enolase１antibodies from a patient with systemic lupus erythematosus accompanied by pulmonary arterial hypertension promote migration of pulmonary artery smooth muscle cells
Anti-enolase１antibodies from a patient with systemic lupus erythematosus accompanied by pulmonary arterial hypertension promote migration of pulmonary artery smooth muscle cells
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Anti-enolase１antibodies from a patient with systemic lupus erythematosus accompanied by pulmonary arterial hypertension promote migration of pulmonary artery smooth muscle cells

Kato, Y. ; Kasama, T. ; Soejima, M. ; Kubota, T.

Immunology letters, 2020-02, Vol.218, p.22-29 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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3
Association study of a polymorphism of the CTGF gene and susceptibility to systemic sclerosis in the Japanese population
Association study of a polymorphism of the CTGF gene and susceptibility to systemic sclerosis in the Japanese population
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Association study of a polymorphism of the CTGF gene and susceptibility to systemic sclerosis in the Japanese population

Kawaguchi, Y ; Ota, Y ; Kawamoto, M ; Ito, I ; Tsuchiya, N ; Sugiura, T ; Katsumata, Y ; Soejima, M ; Sato, S ; Hasegawa, M ; Fujimoto, M ; Takehara, K ; Kuwana, M ; Yamanaka, H ; Hara, M

Annals of the rheumatic diseases, 2009-12, Vol.68 (12), p.1921-1924 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd and European League Against Rheumatism

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4
Genetic polymorphisms in the surfactant proteins in systemic sclerosis in Japanese: T/T genotype at 1580 C/T (Thr131Ile) in the SP-B gene reduces the risk of interstitial lung disease
Genetic polymorphisms in the surfactant proteins in systemic sclerosis in Japanese: T/T genotype at 1580 C/T (Thr131Ile) in the SP-B gene reduces the risk of interstitial lung disease
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Genetic polymorphisms in the surfactant proteins in systemic sclerosis in Japanese: T/T genotype at 1580 C/T (Thr131Ile) in the SP-B gene reduces the risk of interstitial lung disease

Sumita, Y. ; Sugiura, T. ; Kawaguchi, Y. ; Baba, S. ; Soejima, M. ; Murakawa, Y. ; Hara, M. ; Kamatani, N.

Rheumatology (Oxford, England), 2008-03, Vol.47 (3), p.289-291 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Molecular basis for secretor type α(1,2)-fucosyltransferase gene deficiency in a Japanese Population : A fusion gene generated by unequal crossover responsible for the enzyme deficiency
Molecular basis for secretor type α(1,2)-fucosyltransferase gene deficiency in a Japanese Population : A fusion gene generated by unequal crossover responsible for the enzyme deficiency
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Molecular basis for secretor type α(1,2)-fucosyltransferase gene deficiency in a Japanese Population : A fusion gene generated by unequal crossover responsible for the enzyme deficiency

KODA, Y ; SOEJIMA, M ; LIU, Y ; KIMURA, H

American journal of human genetics, 1996-08, Vol.59 (2), p.343-350 [Periódico revisado por pares]

Chicago, IL: University of Chicago Press

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6
Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene
Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene
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Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene

Koda, Y. ; Tachida, H. ; Soejima, M. ; Takenaka, O. ; Kimura, H.

Annals of human genetics, 2004-03, Vol.68 (2), p.110-119 [Periódico revisado por pares]

9600 Garsington Road , Oxford OX4 2DQ , UK: Blackwell Science Ltd

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7
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathy
Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathy
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Selective expression of MHC class I in the affected muscle of a patient with idiopathic inflammatory myopathy

Gono, T ; Katsumata, Y ; Kawaguchi, Y ; Soejima, M ; Wakasugi, D ; Miyawaki, M ; Tsukahara, S ; Yamanaka, H ; Hara, M

Clinical rheumatology, 2009-07, Vol.28 (7), p.873-876 [Periódico revisado por pares]

London: London : Springer-Verlag

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8
Nucleotide Sequence Analyses of Human Complement 6 (C6) Gene Suggest Balancing Selection
Nucleotide Sequence Analyses of Human Complement 6 (C6) Gene Suggest Balancing Selection
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Nucleotide Sequence Analyses of Human Complement 6 (C6) Gene Suggest Balancing Selection

Soejima, M. ; Tachida, H. ; Tsuneoka, M. ; Takenaka, O. ; Kimura, H. ; Koda, Y.

Annals of human genetics, 2005-05, Vol.69 (3), p.239-252 [Periódico revisado por pares]

350 Main Street , Malden , MA 02148 , USA , and 9600 Garsington Road , Oxford OX4 2DQ , UK: Blackwell Science Ltd

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9
A−61C and C−101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana
A−61C and C−101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana
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A−61C and C−101G Hp gene promoter polymorphisms are, respectively, associated with ahaptoglobinaemia and hypohaptoglobinaemia in Ghana

Teye, K ; Quaye, IKE ; Koda, Y ; Soejima, M ; Tsuneoka, M ; Pang, H ; Ekem, I ; Amoah, AGB ; Adjei, A ; Kimura, H

Clinical genetics, 2003-11, Vol.64 (5), p.439-443 [Periódico revisado por pares]

Oxford, UK: Munksgaard International Publishers

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10
Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)
Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)
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Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1)

PANG, H. ; KODA, Y. ; SOEJIMA, M. ; KIMURA, H.

Annals of human genetics, 2002-03, Vol.66 (2), p.139-144 [Periódico revisado por pares]

Cambridge, UK: Cambridge University Press

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