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  • 1990-1994  (2)
  • Atrial natriuretic factor  (1)
  • Hypospadias  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 8 (1993), S. 496-499 
    ISSN: 1437-9813
    Keywords: Hypospadias ; Epipadias ; Urethral replacement ; Transplants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract We present two experimental models consisting of two groups of 16 dogs each in which we performed venous and arterial autotransplants in the urethra using the same surgical technique and the same sutures. As a substitute for the urethra, 4 to 5 cm of either superficial femoral artery or vein were used. Clinical, radiologic, and histologic evaluations were performed 15, 30, 90, and 180 days following the autotransplants. Total re-epithelialization of the venous graft, good micturitional flow, and suitable distension of the neourethra during micturition were observed. the arterial graft also underwent total re-epithelialization, but was very rigid, so that the caliber of the neourethra decreased over a period of several months, causing a number of complications after 6 months of follow-up. We compare this transplant technique with the generally used techniques for hypospadias repair such as the use of skin, bladder mucosa, tunica vaginalis, and ureter. The results were statistically analyzed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0878
    Keywords: Heart ; Atrial natriuretic factor ; Cardiomyopathic animals ; Golden hamster (Mesocricetus auratus)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The secretory pathways of atrial natriuretic factor have been investigated in atrial and ventricular cardiocytes of control and cardiomyopathic Syrian hamsters in severe congestive heart failure with four antibodies: a monoclonal antibody (2H2) against rat synthetic atrial natriuretic factor (101–126), which is directed against region 101–103 of rat atrial natriuretic factor (99–126), and polyclonal, affinity-purified antibodies produced in rabbits against synthetic C-terminal atrial natriuretic factor (101–126), synthetic N-terminal atrial natriuretic factor (11–37) or the putative cleavage site of atrial natriuretic factor (98–99): atrial natriuretic factor (94–103). Application of the immunogold technique on thin frozen sections (immunocryoultramicrotomy) revealed an identical picture with the four antibodies. In atria of both control and cardiomyopathic hamsters where atrial natriuretic factor secretion is regulated, the atrial natriuretic factor propeptide travels, uncleaved, from the Golgi complex to immature and mature secretory granules. In ventricles of control hamsters, where secretion is constitutive, the atrial natriuretic factor propeptide travels from the Golgi complex to secretory vesicles. In the ventricles of hamsters with severe congestive heart failure, the Golgi complex is larger, secretory vesicles more abundant and a few secretory granules are present in ∼20% of cardiocytes. Here again, the peptide travels uncleaved in all these pathways. These results reveal the pathways of secretion of atrial natriuretic factor in atrial and ventricular cardiocytes and indicate that the propeptide is not cleaved intracellularly.
    Type of Medium: Electronic Resource
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