Results 51 to 60 of about 75,555 (208)

FADS Gene Cluster Polymorphisms: Important Modulators of Fatty Acid Levels and Their Impact on Atopic Diseases [PDF]

open access: yes, 2009
Long-chain polyunsaturated fatty acids (LC-PUFAs) play an important role in several physiological processes and their concentration in phospholipids has been associated with several complex diseases, such as atopic disease.
Heinrich, Joachim   +3 more
core   +1 more source

Metabolic Abnormalities of Erythrocytes in Severe Iron Deficiency [PDF]

open access: yesBlood, 1971
Abstract Severe iron deficiency was induced in rabbits by repeated phlebotomy and maintenance on an iron-deficient diet. Erythrocytes from these animals were studied at periods of 2-10 wk following the cessation of bloodletting and were found to have a shortened survival in vivo by the 51Cr technique.
R T, Card, L R, Weintraub
openaire   +2 more sources

Sublytic Terminal Complement Components Induce Eryptosis in Autoimmune Haemolytic Anaemia Related to IgM Autoantibodies [PDF]

open access: yes, 2019
BACKGROUND/AIMS: Eryptosis, the suicidal death of red blood cells (RBCs), is characterized by phosphatidylserine (PS) exposure at the cell surface. It can be catalysed by a variety of abnormal conditions and diseases.
Balola, Abdelwahab Hassan Ahmed   +3 more
core   +1 more source

Study on impacts of direct supplementation of choline into semi-intensive fish culture system based on haematopoietic alterations

open access: yesEnvironmental and Sustainability Indicators, 2021
The present study investigated the impact of choline chloride at the dose of 350 ​g bigha−1 fortnightly for 90 days culture on Indian Major Carps (IMCs) (Labeo rohita, Catla catla) and Air-breathing fishes (Clarias batracus and Anabas testudineus) in ...
Subhas Das   +7 more
doaj   +1 more source

Orotic Aciduria [PDF]

open access: yes, 2018
Orotic acid is an intermediate found in the pathway for pyrimidine synthesis. The mitochondrial enzyme dihydroorotate dehydrogenase (DHODH) catalyzes the production of orotic acid by the conversion of the compound dihydroorotate to orotic acid.
Fonteh, Aliah L
core   +1 more source

Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span

open access: yes, 2014
Transmembrane lipid transporters are believed to establish and maintain phospholipid asymmetry in biological membranes; however, little is known about the in vivo function of the specific transporters involved.
Bröer, Stefan   +9 more
core   +1 more source

Abnormal Erythrocyte Anion Exchange in Alzheimer Disease

open access: yesArchives of Pathology & Laboratory Medicine, 2000
AbstractContext.—Several abnormalities have been described in red blood cells of patients with Alzheimer disease (AD), but to date none of these has been confirmed by a second, independent study. Erythrocyte anion exchange has been reported to be abnormal in AD; we have developed a new technique for measuring anion exchange.Objectives.—To confirm the ...
F A, Greco, A, Satlin, A K, Solomon
openaire   +2 more sources

Phosphorylation in erythrocyte membranes from abnormally shaped cells [PDF]

open access: yesBlood, 1976
Erythrocyte protein phosphorylation was examined in membrane preparations of 25 patients with hereditary spherocytosis (HS). Reduced phosphorylation in substrate polypeptides was observed in 22 HS erythrocyte membranes for both splenectomized and nonsplenectomized patients.
A C, Greenquist, S B, Shohet
openaire   +3 more sources

Subchronic Toxicity of Green Algae (Spyrogyra SP.) Ethanolic Extract on Hematologic Parameters [PDF]

open access: yes, 2016
Green Algae, an organism with active substance such as phytomelatonin, has potential to be developed as Indonesian traditional medicine. As the long term addition of Green Algae ethanol extract (Ekstrak etanol ganggang hijau, EEGH) influences the ...
Devi, A. (Anggita)   +5 more
core  

Drugs for preventing red blood cell dehydration in people with sickle cell disease. [PDF]

open access: yes, 2016
BACKGROUND: Sickle cell disease is an inherited disorder of hemoglobin, resulting in abnormal red blood cells. These are rigid and may block blood vessels leading to acute painful crises and other complications.
Ballas, Samir K., Nagalla, Srikanth
core   +2 more sources

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