Výsledky vyhledávání - "Mordechai Prass"

Inhibition of cell adhesion to glycoproteins of the extracellular matrix by peptides corresponding to serum amyloid A. Toward understanding the physiological role of an enigmatic protein

Autor: Ofer Lider, David Levartowsky, Mati Fridkin, Mordechai Prass, Liana Preciado-Patt, Rami Hershkoviz

Publikováno v: European Journal of Biochemistry. 223:35-42

Synthetic peptides related to amino acid residues 29-42 of human serum amyloid A (SAA), Tyr-Ile-Gly-Ser-Asp-Lys-Tyr-Phe-His-Ala-Arg-Gly-Asn-Tyr, were found to inhibit the adhesion of human T-lymphocytes and of mouse M4 melanoma cells to surfaces coat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c018e88e5cfffb31a452c8ac3d60c69c
https://doi.org/10.1111/j.1432-1033.1994.tb18963.x

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Autor: Liana Preciado-Patt, Ofer Lider, Hershkoviz Rami, Mati Fridkin, David Levartowsky, Mordechai Prass

Publikováno v: Peptides 1992 ISBN: 9789401046466
Peptides 1992

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f51bb673649cfd50cd6d8f9d030ba60f
https://doi.org/10.1007/978-94-011-1470-7_43

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Genetics of Familial Mediterranean Fever (FMF)

Autor: Mordechai Prass, Joram Heller, Harry Heller, Ezra Sohar

Publikováno v: Archives of Internal Medicine. 107:529

Introduction It has been stated in former papers1,2that Familial Mediterranean Fever (FMF) is a genetic disorder practically restricted to people from the wider Mediterranean area. This being of basic importance in the understanding of the disease an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::eb41b356f2b8acf9680e8c80ac2afbb3
https://doi.org/10.1001/archinte.1961.03620040055006

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Low-Fat Diet in Familial Mediterranean Fever

Autor: Moshe Chaimow, Mordechai Prass, Joseph Gafni, Ezra Sohar, Harry Heller

Publikováno v: Archives of Internal Medicine. 110:150

Familial Mediterranean fever (FMF) is a genetic disorder with complete autosomal recessive inheritance. It is prevalent in peoples of Mediterranean stock, particularly Sephardi Jews and Armenians.1,2The disease is manifested by 2 independent phenotyp

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11102f1ecd4102028316ab868676f33b
https://doi.org/10.1001/archinte.1962.03620200010003

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