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  • Electronic Resource  (2)
  • Brain recognition  (1)
  • Key words Deafness  (1)
  • 1
    ISSN: 1438-2199
    Keywords: Amino acids ; Brain recognition ; Functional MRI ; Lateral hypothalamic area ; l-Lysine deficiency ; Neural plasticity ; Preference and appetite control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Eachl-amino acid (AA) in plasma and brain remains unchanged all day long while normal diet is available. But once restriction ofl-lysine (Lys) was introduced, strong anorexia happened. When Lys deficient diet was offered to rats, their growth were decreased depending upon dietary Lys intake, and they ingested Lys solution in choice quantitatively and both appetite and growth normalized. The recognition site for the deficit in rat's brain was identified by brain oxygenation using a functional MRI that higher signals in the ventromedial hypothalamus and lateral hypothalamic area (LHA) appeared, at 30–50 minutes after Lys injection i.p. and then recovered. Degree of Lys hunger, assayed by bar-pressing (50mg pellet of normal diet/30 presses), was suppressed by Lys micro-injection into the LHA, similar to free Lys ingestion but any other AA never did, suggesting the LHA as recognition site for Lys deficit in rats with Lys deficiency due to AA homeostasis.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-232X
    Keywords: Key words Deafness ; Onychodystrophy ; Autosomal dominant inheritance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The disease "deafness and onychodystrophy" (DOD) is characterized by congenital hearing impairment and dystrophic or absent nails and teeth. The autosomal dominant form of the disorder has been previously reported only in one family. We describe here another family in which three members in three generations (a girl, her mother, and her maternal grandfather) were affected with DOD. Our finding is consistent with an autosomal dominant mode of inheritance and confirms autosomal dominant DOD (DDOD, MIM *124480) as a recognizable clinical entity.
    Type of Medium: Electronic Resource
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