Zobrazeno 1 - 10 of 28 pro vyhledávání: '"G H, Sack"'
1
Hyperphosphatasia with massive osteoectasia: a 45-year follow-up
Autor: G. H. Sack, E. F. McCarthy
Publikováno v: Skeletal Radiology. 36:2-6
Hyperphosphatasia is a heterogeneous group of disorders characterized by a generalized skeletal disease and increased alkaline phosphatase. Increased bone remodeling secondary to increased osteoclastic activity appears to be the underlying feature of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efe105be7033c7aa3d83a4ad68bef7c3
https://doi.org/10.1007/s00256-006-0176-3
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3
A fusion protein between serum amyloid A and staphylococcal nuclease--synthesis, purification, and structural studies
Autor: A K, Meeker, G H, Sack
Publikováno v: Proteins. 30(4)
We developed a recombinant DNA system to overexpress a fusion protein between the small, minimally soluble acute phase serum protein, serum amyloid A (SAA), and the bacterial enzyme staphylococcal nuclease (SN). This fusion protein is very soluble an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b0b8227104cffff612d06b8430c2e782
https://pubmed.ncbi.nlm.nih.gov/9533622
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6
Visual pigment gene changes in adrenoleukodystrophy
Autor: G H, Sack, J C, Morrell
Publikováno v: Investigative ophthalmologyvisual science. 34(9)
The gene for X-linked adrenoleukodystrophy, a neurodegenerative disorder, is closely linked to the red/green color pigment genes on the distal X-chromosome Xq28 and one kindred is known to have a genetic change affecting both loci. The purpose of thi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ca71ecfb2ded02249a8d60c3fa6eb699
https://pubmed.ncbi.nlm.nih.gov/8344786
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7
Serum amyloid A gene transcription in synovial cells during retroviral arthritis
Autor: G H, Sack, M C, Zink
Publikováno v: The American journal of pathology. 141(3)
In situ hybridization was used to demonstrate serum amyloid A (SAA) gene expression in arthritic joint tissue from lentivirus-infected sheep and goats. SAA gene transcription occurs in isolated individual synovial cells and occasional giant cells but
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9997fb3b05c4eeb456cd7c47b7c7c75e
https://pubmed.ncbi.nlm.nih.gov/1519661
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8
Highly polymorphic domains of the human serum amyloid A (SAA) gene GSAA1
Autor: C. C. Talbot Jr., G. H. Sack Jr.
Publikováno v: Scandinavian journal of immunology. 33(4)
The DNA of the human serum amyloid A (SAA) gene GSAA1 contains several repetitive regions within its introns. We have studied length variations al one such region in the 2nd intron by selective amplification using the polymerase chain reaction (PCR)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89cf1399b52257e967415f7ce437d6d6
https://pubmed.ncbi.nlm.nih.gov/2017667
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10
Hereditary canine spinal muscular atrophy: canine motor neuron disease
Autor: L C, Cork, D L, Price, J W, Griffin, G H, Sack
Publikováno v: Canadian journal of veterinary research = Revue canadienne de recherche veterinaire. 54(1)
Motor neuron diseases, manifest as weakness and atrophy of skeletal muscles, occur in infancy, childhood, and adult life. Some forms of this disease are inherited. Motor neurons are selectively affected and exhibit cytoskeletal pathology, primarily e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1bd1098893106a6f13f41942f8cffe92
https://pubmed.ncbi.nlm.nih.gov/2306675
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