Results 211 to 220 of about 2,398 (262)
Storage, ultrastructural targeting and function of toposomes and hyalin in sea urchin embryogenesis
Mechanisms of Development, 1991 This study compares by immunogold labeling the ultrastructural localization of a hexameric 22S glycoprotein, called toposome, with that of hyalin in unfertilized eggs and cells of hatched sea urchin blastulae. Nearly all hyalin is present in the electron
L Lorand, E Kellenberger
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Immunochemical studies on alcoholic hyalin
Gastroenterologia Japonica, 1979 Kazunori Matsumoto +2 more
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Juvenile non‐hyaline fibromatosis: juvenile hyaline fibromatosis without prominent hyaline changes
Journal of Cutaneous Pathology, 2005Abstract: Juvenile hyaline fibromatosis (JHF) is a rare autosomal recessive disease of the connective tissue. It is characterized by papulonodular skin lesions, soft tissue masses, gingival hypertrophy, osteolytic bone lesions and flexion contractures of the large joints.
Rana Yavuzer, Anadolu +3 more
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Der Hautarzt, 1997
Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller +3 more
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Juvenile hyaline fibromatosis is a rare autosomal recessive connective tissue disease first described in 1873 by Murray. Major diagnostic criteria are multiple cutaneous tumors and gingival hypertrophy; minor criteria include contractures, osteolytic lesions and a positive family history.
M, Schaller +3 more
openaire +2 more sources
The British Journal of Radiology, 1981
A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D A, Stringer, C M, Hall
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A case of juvenile hyaline fibromatosis in a ten-year-old Asian girl is presented. This autosomal recessively inherited condition has not previously been described in the radiological literature. This patient demonstrates well the characteristic radiological appearance.
D A, Stringer, C M, Hall
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Histochemistry of sarcoidotic-hyaline
Pneumonologie Pneumonology, 1976On account of its weaker reactions for tryptophan, tyrosine, proteolipids, and lipoproteins, sarcoidotic-hyaline (Sa. Hy.) is immediately distinguishable from caseosis. However, protein histochemistry fails to differentiate Sa. Hy. from normal (fixed and insoluble postfixed) and pericaseous collagen. Evidence of this is provided by the present study on
G, Barbolini, S, Battaglia
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Pediatrics, 1961
Pulmonary hyaline membranes were studied by observations on their dissolution in vitro by proteolytic enzymes, by streptokinase and by urea with and without added thioglycollic acid. Pepsin, trypsin and chymotrypsin dissolved the hyaline membranes both in sections of human lungs as well as in sections of mouse lung with the experimentally produced ...
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Pulmonary hyaline membranes were studied by observations on their dissolution in vitro by proteolytic enzymes, by streptokinase and by urea with and without added thioglycollic acid. Pepsin, trypsin and chymotrypsin dissolved the hyaline membranes both in sections of human lungs as well as in sections of mouse lung with the experimentally produced ...
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Hyaline matrix in hyalinizing trabecular tumor
Diagnostic Cytopathology, 2014Hyalinizing trabecular tumor (HTT) is a rare neoplasm which usually follows an indolent clinical course. The cytologic diagnosis of HTT can be challenging as these neoplasms share cytomorphological features with other thyroid neoplasms and paraganglioma.
Elwira, Bakuła-Zalewska +3 more
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Splenic arteriolar hyalin in children
Journal of Pathology, 1986 Roger P. Lindley
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