Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Constantina Repa"'
Autor:
Argiris Symeonidis, N. Zoumbos, N. Anagnostopoulos, Alexandra Kouraklis-Symeonidis, Theodoros Marinakis, V. Vlacha, Constantina Repa, Ilina Micheva
Publikováno v:
Blood Cells, Molecules, and Diseases. 36:298-307
Gaucher disease is a lysosomal storage disorder, in which undigested glucosylceramide is deposited in the cytoplasm of mature macrophages, which accumulate in the bone marrow and the reticuloendothelial system. Dendritic cells are bone marrow-derived
Autor:
Christos Sotiropoulos, Eugenia Verigou, G. L. Theodorou, Theodoros Marinakis, Argiris Symeonidis, Constantina Repa, Marina Karakantza, Elena E. Solomou
Publikováno v:
JIMD Reports ISBN: 9783662448625
We investigated peripheral blood T-lymphocyte subpopulations and intracellular expression of IFN-γ, IL-4, IL-10, and IL-13, by whole blood flow cytometry, in 22 type I Gaucher disease (GD) patients. Results were compared with those of 19 sex- and ag
Autor:
Alice Maniatis, Marina Stamatelou, Argyris Simeonidis, George V.Z. Dedoussis, Athanasia Mouzaki, Maria-Christina Kyrtsonis, Constantina Repa
Publikováno v:
Medical Oncology. 15:124-128
The expansion of myeloma cells is regulated by cytokines, among which IL-6 is a major growth factor. It has been recently suggested that serum transforming growth factor beta 1 (TGF beta 1), a cytokine found in large amounts in alpha-granules of plat
Autor:
Constantinos Papanastasiou, Christos Papaconstantinou, Stefanos I. Papadhimitriou, Constantinos Pangalos, Danae Abazis, Marina Stamatelou, Constantina Repa
Publikováno v:
Cancer Genetics and Cytogenetics. 85:75-77
We report a case of chronic myelomonocytic leukemia in which cytogenetic analysis revealed a 47,XY, +1, + der(7)del(7)(q32q36)ins(7;1)(q32;p36.3p22) chromosomal constitution. This abnormal karyotype, which as a whole is new to any myeloid malignancy,
Autor:
Alexandra Kouraklis, G. L. Theodorou, Theodore Marinakis, Panayiotis Tsaftaridis, Argiris Symeonidis, Nicholas C. Zoumbos, Marina Karakantza, Constantina Repa
Publikováno v:
Blood. 112:4915-4915
Patients with Gaucher disease exhibit substantial evidence of impairment of their immune system, namely, increased serum levels of proinflammatory cytokines and immunoglobulins, and increased incidence of B-cell malignancies, such as non-Hodgkin’s
Autor:
Constantina Repa, Nikolaos Anagnostopoulos, Nicholas C. Zoumbos, Alexandra Kouraklis, Ilina Mitseva, Argiris Symeonidis, Theodoros Marinakis
Publikováno v:
Publons
Introduction - Aims: Gaucher’s disease is a lysosomal storage disorder, in which undigested glucocerebroside is deposited in the cytoplasm of mature macrophages, which accumulate in the bone marrow and the reticuloendothelial system. Dendritic cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a081bf11c60bebbbd27a66e777c37b2f
https://publons.com/publon/21672854/
https://publons.com/publon/21672854/