Search Results - "Indo, Yasuhiro"
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Neurobiology of pain, interoception and emotional response: lessons from nerve growth factor-dependent neurons
Published in The European journal of neuroscience (01-02-2014)“…Although nerve growth factor (NGF) is a well‐known neurotrophic factor, it also acts as a mediator of pain, itch and inflammation. Congenital insensitivity to…”
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Nerve growth factor and the physiology of pain: the relationships among interoception, sympathetic neurons and the emotional response indicated by the molecular pathophysiology of congenital insensitivity to pain with anhidrosis
Published in No to hattatsu (01-05-2015)“…Nerve growth factor (NGF) is a neurotrophic factor essential for the survival and maintenance of neurons. Congenital insensitivity to pain with anhidrosis…”
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Chronic Thromboembolic Pulmonary Hypertension Complicated with Homocystinuria
Published in Internal Medicine (01-01-2014)“…A 17-year-old boy with homocystinuria was found to have a systolic murmur during a routine examination. Echocardiography demonstrated pulmonary hypertension…”
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NGF-dependent neurons and neurobiology of emotions and feelings: Lessons from congenital insensitivity to pain with anhidrosis
Published in Neuroscience and biobehavioral reviews (01-04-2018)“…•Congenital insensitivity to pain with anhidrosis (CIPA) is a rare genetic disorder.•People with CIPA lack NGF-dependent neurons in otherwise intact…”
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Nerve growth factor, interoception, and sympathetic neuron: Lesson from congenital insensitivity to pain with anhidrosis
Published in Autonomic neuroscience (11-05-2009)“…Abstract Nerve growth factor (NGF) is a well-known neurotrophic factor essential for the survival and maintenance of sensory and sympathetic neurons…”
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Genetics of congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV. Clinical, biological and molecular aspects of mutations in TRKA(NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor
Published in Clinical autonomic research (01-05-2002)“…Congenital insensitivity to pain with anhidrosis (CIPA) or hereditary sensory and autonomic neuropathy type IV (HSAN-IV) is an autosomal recessive disorder…”
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Maple syrup urine disease
Published in Nihon rinshō (01-04-2002)Get more information
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Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis
Published in Clinical genetics (01-10-2012)“…Congenital insensitivity to pain with anhidrosis (CIPA) is an autosomal recessive genetic disorder characterized by insensitivity to pain, anhidrosis (the…”
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Nerve growth factor, pain, itch and inflammation: lessons from congenital insensitivity to pain with anhidrosis
Published in Expert review of neurotherapeutics (01-11-2010)“…NGF is a well-known neurotrophic factor essential for the survival and maintenance of primary afferent neurons and sympathetic neurons. NGF is also an…”
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Molecular basis of congenital insensitivity to pain with anhidrosis (CIPA): Mutations and polymorphisms in TRKA (NTRK1) gene encoding the receptor tyrosine kinase for nerve growth factor
Published in Human mutation (01-12-2001)“…Congenital insensitivity to pain with anhidrosis (CIPA), also referred to as hereditary sensory and autonomic neuropathy type IV (HSAN‐IV), is an autosomal…”
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Human ESP1/CRP2, a Member of the LIM Domain Protein Family: Characterization of the cDNA and Assignment of the Gene Locus to Chromosome 14q32.3
Published in Genomics (San Diego, Calif.) (15-01-1996)“…The LIM domain is present in a wide variety of proteins with diverse functions and exhibits characteristic arrangements of Cys and His residues with a novel…”
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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
Published in Journal of human genetics (01-01-1998)“…The E2 gene of the branched-chain alpha-keto acid dehydrogenase (BCKDH) complex was studied at the molecular level in three patients with intermittent maple…”
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Molecular cloning and nucleotide sequence of cDNAs encoding human long-chain acyl-CoA dehydrogenase and assignment of the location of its gene (ACADL) to chromosome 2
Published in Genomics (San Diego, Calif.) (01-11-1991)“…Long-chain acyl-CoA dehydrogenase (LCAD) catalyzes the first reaction of the mitochondrial beta-oxidation of fatty acids. We isolated and sequenced three cDNA…”
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Mutations in the TRKA /NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis
Published in Nature genetics (01-08-1996)“…Congenital insensitivity to pain with anhidrosis (CIPA; MIM 256800) is an autosomal-recessive disorder characterized by recurrent episodes of unexplained…”
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Congenital insensitivity to pain with anhidrosis (CIPA) : effect of TRKA (NTRK1) missense mutations on autophosphorylation of the receptor tyrosine kinase for nerve growth factor
Published in Human molecular genetics (01-02-2001)“…Human TRKA (NTRK1) encodes the receptor tyrosine kinases (RTKs) for nerve growth factor (NGF) and is the gene responsible for congenital insensitivity to pain…”
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Congenital Insensitivity to Pain with Anhidrosis: Novel Mutations in the TRKA ( NTRK1) Gene Encoding A High-Affinity Receptor for Nerve Growth Factor
Published in American journal of human genetics (01-06-1999)“…Congenital insensitivity to pain with anhidrosis (CIPA) is characterized by recurrent episodes of unexplained fever, anhidrosis (inability to sweat), absence…”
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Structure and organization of the human TRKA gene encoding a high affinity receptor for nerve growth factor
Published in The Japanese journal of human genetics (01-06-1997)“…Nerve growth factor (NGF) induces neurite outgrowth and promotes survival of embryonic sensory and sympathetic neurons. TRKA, a receptor tyrosine kinase cloned…”
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