INT181495
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
TRPV3 immunoreactivity was detected most strongly in basal keratinocytes in normal skin, sometimes continuously along the length of the epidermis (Fig 8A) whilst diabetic skin showed weaker cells (Fig 8B). | |||||||||||||||
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In accord, there was strong TRPV3 immunoreactivity, mostly in large calibre fibres, in ventral (Fig 6D) but not dorsal spinal roots. | |||||||||||||||
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The weak TRPV3 immunoreactivity in dorsal roots is consistent with a preferential transport peripherally rather than centrally. | |||||||||||||||
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TRPV3 immunoreactivity was not detected in fibres in any sample. | |||||||||||||||
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The aim of the present study was to investigate the distribution of the vanilloid receptors TRPV1, TRPV3, TRPV4, and TRPM8 in normal and injured human peripheral nerves and spinal nerve roots and in normal and neuropathic (painful neuroma and diabetes) skin and spinal cord,
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TRPV3 immunoreactivity in the ventral roots was largely lost three to four weeks following injury. | |||||||||||||||
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TRPV3 immunoreactivity was detected in basal keratinocytes and occasional suprabasal cells throughout the epidermis. | |||||||||||||||
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The role of TRPV3 and TRPV4 changes in keratinocytes deserve further study.
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The aim of the present study was to investigate the distribution of the vanilloid receptors TRPV1, TRPV3, TRPV4, and TRPM8 in normal and injured human peripheral nerves and spinal nerve roots and in normal and neuropathic (painful neuroma and diabetes) skin and spinal cord,
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General Comments
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