نتایج جستجو برای: vi mps

تعداد نتایج: 47894  

Journal: :archives of medical laboratory sciences 0
mohamad ali esmaili zohreh sharifi fatemeh yari

background: activated platelets shed microparticles (mps) in vivo and certainly in vitro under storage. like platelets, platelet-derived mps contribute to hemostatic and inflammatory responses. we sought to determine the interactions between platelet mps and peripheral b lymphocytes in the healthy blood circulation to propose a possible role for platelet mps in the functioning of b cells.   mat...

Journal: :Environmental Science and Technology Letters 2022

The unexpectedly high affinity of microplastics (MPs) for heavy metals has attracted increasing attention in recent years. However, there is a scarcity information on the effects coexisting constituents plastic–metal interactions, especially terms metal speciation. This study aimed to explore role benzophenone-type UV filters sorption, oxidation state, and toxicity chromium (Cr) by pristine UV-...

2012
Cem Sayilgan Lale Yuceyar Sedat Akbas Hulya Erolcay

Mucopolysaccharidoses (MPSs) are a group of metabolic diseases transmitted in an autosomal recessive fashion. MPSs are due to deficiencies of the specific enzymes responsible for the catabolism of dermatan sulfate, heparin sulfate, and keratan sulfate, resulting in the accumulation of glycosaminoglycans (GAGs). MPSs have a chronic, progressive course with multisystemic involvement. The incidenc...

Journal: :Investigative ophthalmology & visual science 1989
G Constantopoulos J A Scott R M Shull

Corneal opacification associated with glycosaminoglycan (GAG) deposition occurs in canine mucopolysaccharidosis I (MPS I), a deficiency of the lysosomal enzyme alpha-L-iduronidase. In affected dogs corneal lesions appear similar to those in children with the same disease. Transplantation of bone marrow from unaffected littermates was performed in 5 MPS I affected dogs at 5 months of age. In thr...

Journal: :archives of medical laboratory sciences 0
mohammad ali esmaeili department of hematology, school of allied medical sciences, iran university of medical sciences, tehran, iran fatemeh yari blood transfusion research center, high institute for research and education in transfusion medicine, tehran, iran ali amini department of hematology, school of allied medical sciences, iran university of medical sciences, tehran, iran mohammad reza rezvani department of hematology, faculty of allied medicine, iran university of medical science, tehran, iran

this article reviews will focus on the concept and formation of micro particles (mps) in circulation and their role in transfusion medicine and immune system. mps are cell membrane derived vesicles which express markers of their parent cells and are found in circulation at low levels. exact functions of mps are unclear. in here, physiological almost all types of circulating mps including platel...

Fatemeh Yari, Saeideh Milani,

Background: Microparticles (MPs) are small vesicles released from the cell membrane. Accordingly, these contain active molecules to mediate biological processes, including cell proliferation and cell cycle progression. The fusion of myeloma cell lines with immunized B lymphocytes is a critical step of hybridoma technology. MPs modulate lymphoproliferation, thereby facilitating B cell expansion ...

Journal: :Frontiers in Genetics 2023

Mucopolysaccharidoses (MPSs) are inherited lysosomal storage disorders (LSDs). MPSs caused by excessive accumulation of mucopolysaccharides due to missing or deficiency enzymes required for the degradation specific macromolecules. MPS I-IV, VI, VII, and IX sub-types mucopolysaccharidoses. Among these, III (also known as Sanfilippo) IV (Morquio) syndromes lethal prevalent sub-types. This study a...

2018
Catalina Burbano Juan Villar-Vesga Janine Orejuela Carlos Muñoz Adriana Vanegas Gloria Vásquez Mauricio Rojas Diana Castaño

Microparticles (MPs) are vesicles derived from the plasma membrane of different cells, are considered a source of circulating autoantigens, and can form immune complexes (MPs-ICs). The number of MPs and MPs-ICs increases in patients with systemic lupus erythematosus (SLE). MPs activate myeloid cells by inducing IL-6 and TNF-α in both SLE and other diseases. Therefore, we propose that the recogn...

Journal: :Pediatrics 2005
Paul Harmatz David Ketteridge Roberto Giugliani Natalie Guffon Elisa Leão Teles M Clara Sá Miranda Zi-Fan Yu Stuart J Swiedler John J Hopwood

OBJECTIVE Mucopolysaccharidosis VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disease caused by a deficiency of the enzyme N-acetylgalactosamine 4-sulfatase (ASB). This enzyme deficiency leads to a progressive disorder with multiple tissue and organ involvement. The disease is rare and is heterogeneous in its clinical presentation and progression. A potential treatment for this di...

Journal: :BMJ 1992

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