Mutations in the TRKA /NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis
Indo, Yasuhiro, Tsuruta, Motoko, Hayashida, Yumi, Karim, Mohammad Azharul, Ohta, Kohji, Kawano, Tomoyasu, Mitsubuchi, Hiroshi, Tonoki, Hidefumi, Awaya, Yutaka, Matsuda, Ichiro
Published in Nature genetics (01.08.1996)
Published in Nature genetics (01.08.1996)
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Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families
MIURA, Y, MARDY, S, AWAYA, Y, NIHEI, K, ENDO, F, MATSUDA, I, INDO, Y
Published in Human genetics (01.01.2000)
Published in Human genetics (01.01.2000)
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No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V
Toscano, Ennio, Simonati, Alessandro, Indo, Yasuhiro, Andria, Generoso
Published in Annals of neurology (01.08.2002)
Published in Annals of neurology (01.08.2002)
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Multisystem involvement in congenital insensitivity to pain with anhidrosis (CIPA), a nerve growth factor receptor(Trk A)-related disorder
Toscano, E, della Casa, R, Mardy, S, Gaetaniello, L, Sadile, F, Indo, Y, Pignata, C, Andria, G
Published in Neuropediatrics (01.02.2000)
Published in Neuropediatrics (01.02.2000)
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Metabolic regulation of osteoclast differentiation and function
Indo, Yoriko, Takeshita, Sunao, Ishii, Kiyo‐Aki, Hoshii, Takayuki, Aburatani, Hiroyuki, Hirao, Atsushi, Ikeda, Kyoji
Published in Journal of bone and mineral research (01.11.2013)
Published in Journal of bone and mineral research (01.11.2013)
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Molecular cloning and nucleotide sequence of cDNAs encoding the precursors of rat long chain acyl-coenzyme A, short chain acyl-coenzyme A, and isovaleryl-coenzyme A dehydrogenases. Sequence homology of four enzymes of the acyl-CoA dehydrogenase family
MATSUBARA, Y, INDO, Y, NAITO, E, OZASA, H, GLASSBERG, R, VOCKLEY, J, IKEDA, Y, KRAUS, J, TANAKA, K
Published in The Journal of biological chemistry (25.09.1989)
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Published in The Journal of biological chemistry (25.09.1989)
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Primary structure and gene localization of human prolidase
Endo, F, Tanoue, A, Nakai, H, Hata, A, Indo, Y, Titani, K, Matsuda, I
Published in The Journal of biological chemistry (15.03.1989)
Published in The Journal of biological chemistry (15.03.1989)
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Journal Article
Mutation and polymorphism analysis of the TRKA (NTRK1) gene encoding a high-affinity receptor for nerve growth factor in congenital insensitivity to pain with anhidrosis (CIPA) families
Miura, Y., Mardy, S., Awaya, Y., Nihei, K., Endo, F., Matsuda, I., Indo, Y.
Published in Human genetics (01.01.2000)
Published in Human genetics (01.01.2000)
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Molecular basis of intermittent maple syrup urine disease: novel mutations in the E2 gene of the branched-chain alpha-keto acid dehydrogenase complex
Tsuruta, M, Mitsubuchi, H, Mardy, S, Miura, Y, Hayashida, Y, Kinugasa, A, Ishitsu, T, Matsuda, I, Indo, Y
Published in Journal of human genetics (01.01.1998)
Published in Journal of human genetics (01.01.1998)
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Altered kinetic properties of the branched-chain α-keto acid dehydrogenase complex due to mutation of the β-subunit of the branched-chain α-keto acid decarboxylase (E1) component in lymphoblastoid cells derived from patients with maple syrup urine disease
INDO, Y, KITANO, A, ENDO, F, AKABOSHI, I, MATSUDA, I
Published in The Journal of clinical investigation (01.07.1987)
Published in The Journal of clinical investigation (01.07.1987)
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Gene analysis of Mennonite maple syrup urine disease kindred using primer-specified restriction map modification
Mitsubuchi, H, Matsuda, I, Nobukuni, Y, Heidenreich, R, Indo, Y, Endo, F, Mallee, J, Segal, S
Published in Journal of inherited metabolic disease (01.03.1992)
Published in Journal of inherited metabolic disease (01.03.1992)
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Immunochemical analysis of prolidase deficiency and molecular cloning of cDNA for prolidase of human liver
Endo, F, Hata, A, Indo, Y, Motohara, K, Matsuda, I
Published in Journal of inherited metabolic disease (01.09.1987)
Published in Journal of inherited metabolic disease (01.09.1987)
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Journal Article
Maple syrup urine disease: clinical and biochemical significance of gene analysis
Nobukuni, Y, Mitsubuchi, H, Akaboshi, I, Indo, Y, Endo, F, Matsuda, I
Published in Journal of inherited metabolic disease (01.09.1991)
Published in Journal of inherited metabolic disease (01.09.1991)
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