Cargando…

Proteome of Stored RBC Membrane and Vesicles from Heterozygous Beta Thalassemia Donors

Genetic characteristics of blood donors may impact the storability of blood products. Despite higher basal stress, red blood cells (RBCs) from eligible donors that are heterozygous for beta-thalassemia traits (βThal(+)) possess a differential nitrogen-related metabolism, and cope better with storage...

Descripción completa

Detalles Bibliográficos
Autores principales:	Tzounakas, Vassilis L., Anastasiadi, Alkmini T., Dzieciatkowska, Monika, Karadimas, Dimitrios G., Stamoulis, Konstantinos, Papassideri, Issidora S., Hansen, Kirk C., D’Alessandro, Angelo, Kriebardis, Anastasios G., Antonelou, Marianna H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8037027/ https://www.ncbi.nlm.nih.gov/pubmed/33806028 http://dx.doi.org/10.3390/ijms22073369

Ejemplares similares

Innate Variability in Physiological and Omics Aspects of the Beta Thalassemia Trait-Specific Donor Variation Effects
por: Anastasiadi, Alkmini T., et al.
Publicado: (2022)

Red Blood Cell Proteasome in Beta-Thalassemia Trait: Topology of Activity and Networking in Blood Bank Conditions
por: Anastasiadi, Alkmini T., et al.
Publicado: (2021)

Deciphering the Relationship Between Free and Vesicular Hemoglobin in Stored Red Blood Cell Units
por: Tzounakas, Vassilis L., et al.
Publicado: (2022)

Early and Late-Phase 24 h Responses of Stored Red Blood Cells to Recipient-Mimicking Conditions
por: Tzounakas, Vassilis L., et al.
Publicado: (2022)

Corpuscular Fragility and Metabolic Aspects of Freshly Drawn Beta-Thalassemia Minor RBCs Impact Their Physiology and Performance Post Transfusion: A Triangular Correlation Analysis In Vitro and In Vivo
por: Anastasiadi, Alkmini T., et al.
Publicado: (2022)

The Post-Storage Performance of RBCs from Beta-Thalassemia Trait Donors Is Related to Their Storability Profile
por: Anastasiadi, Alkmini T., et al.
Publicado: (2021)

Beta thalassemia minor is a beneficial determinant of red blood cell storage lesion
por: Tzounakas, Vassilis L., et al.
Publicado: (2021)

The time-course linkage between hemolysis, redox, and metabolic parameters during red blood cell storage with or without uric acid and ascorbic acid supplementation
por: Anastasiadi, Alkmini T., et al.
Publicado: (2023)

Supplementation with uric and ascorbic acid protects stored red blood cells through enhancement of non-enzymatic antioxidant activity and metabolic rewiring
por: Tzounakas, Vassilis L., et al.
Publicado: (2022)

Data on how several physiological parameters of stored red blood cells are similar in glucose 6-phosphate dehydrogenase deficient and sufficient donors
por: Tzounakas, Vassilis L., et al.
Publicado: (2016)

Progressive oxidation of cytoskeletal proteins and accumulation of denatured hemoglobin in stored red cells
por: Kriebardis, Anastasios G, et al.
Publicado: (2007)

Metabolic Linkage and Correlations to Storage Capacity in Erythrocytes from Glucose 6-Phosphate Dehydrogenase-Deficient Donors
por: Reisz, Julie A., et al.
Publicado: (2018)

Redox Status, Procoagulant Activity, and Metabolome of Fresh Frozen Plasma in Glucose 6-Phosphate Dehydrogenase Deficiency
por: Tzounakas, Vassilis L., et al.
Publicado: (2018)

Apolipoprotein J/Clusterin Is a Novel Structural Component of Human Erythrocytes and a Biomarker of Cellular Stress and Senescence
por: Antonelou, Marianna H., et al.
Publicado: (2011)

Apolipoprotein J/Clusterin in Human Erythrocytes Is Involved in the Molecular Process of Defected Material Disposal during Vesiculation
por: Antonelou, Marianna H., et al.
Publicado: (2011)

The Multi-Faced Extracellular Vesicles in the Plasma of Chronic Kidney Disease Patients
por: Georgatzakou, Hara T., et al.
Publicado: (2020)

Red Blood Cell Metabolism In Vivo and In Vitro
por: D’Alessandro, Angelo, et al.
Publicado: (2023)

In Sickness and in Health: Erythrocyte Responses to Stress and Aging
por: Antonelou, Marianna H., et al.
Publicado: (2022)

The Arising Role of Extracellular Vesicles in Cholangiocarcinoma: A Rundown of the Current Knowledge Regarding Diagnostic and Therapeutic Approaches
por: Trifylli, Eleni-Myrto, et al.
Publicado: (2023)

Stratification of β(S)β(+) Compound Heterozygotes Based on L-Glutamine Administration and RDW: Focusing on Disease Severity
por: Giannaki, Aimilia, et al.
Publicado: (2023)

Hypoxia modulates the purine salvage pathway and decreases red blood cell and supernatant levels of hypoxanthine during refrigerated storage
por: Nemkov, Travis, et al.
Publicado: (2018)

Blood Cell-Derived Microvesicles in Hematological Diseases and beyond
por: Georgatzakou, Hara T., et al.
Publicado: (2022)

Is RBC discrimination index suitable for differentiating between α- and β- thalassemias?
por: Gorakshakar, Ajit C., et al.
Publicado: (2011)

Polycythemia Vera in a Patient With Heterozygous Beta-Thalassemia: Coincidence or Causal Relationship?
por: Kottas, Konstantinos, et al.
Publicado: (2020)

Sphingosine 1-phosphate has a negative effect on RBC storage quality
por: Hay, Ariel, et al.
Publicado: (2022)

5613475 ADVERSE REACTIONS TO RBC TRANSFUSION: A SINGLE THALASSEMIA AND SICKLE CELL DISEASE DEPARTMENT’S EXPERIENCE
por: Xydaki, A.X., et al.
Publicado: (2023)

β-Thalassemia Intermedia: Interaction of α-Globin Gene Triplication With β-thalassemia Heterozygous in Spain
por: Ropero, Paloma, et al.
Publicado: (2022)

Reliability of Different RBC Indices and Formulas in Discriminating between β-Thalassemia Minor and other Microcytic Hypochromic Cases
por: Bordbar, Elahe, et al.
Publicado: (2015)

Deuterated Linoleic Acid Attenuates the RBC Storage Lesion in a Mouse Model of Poor RBC Storage
por: Kim, Christopher Y., et al.
Publicado: (2022)

RBC-NOS-Dependent S-Nitrosylation of Cytoskeletal Proteins Improves RBC Deformability
por: Grau, Marijke, et al.
Publicado: (2013)

Anemia and RBC Transfusion
por: Marik, Paul Ellis
Publicado: (2009)

Hexapeptide-11 is a novel modulator of the proteostasis network in human diploid fibroblasts
por: Sklirou, Aimilia D., et al.
Publicado: (2015)

Could Heterozygous Beta Thalassemia Provide Protection Against Multiple Sclerosis?
por: Cikrikcioglu, Mehmet Ali, et al.
Publicado: (2016)

A new red cell index and portable RBC analyzer for screening of iron deficiency and Thalassemia minor in a Chinese population
por: Tong, Lieshu, et al.
Publicado: (2017)

PB2238: ΒETA-THALASSEMIA INTERMEDIA: INTERACTION OF ΑLPHA-GLOBIN GENE TRIPLICATION WITH ΒETA-THALASSEMIA HETEROZYGOUS IN SPAIN
por: Ropero, P., et al.
Publicado: (2022)

Coagulation Abnormalities in Renal Pathology of Chronic Kidney Disease: The Interplay between Blood Cells and Soluble Factors
por: Pavlou, Efthimia G., et al.
Publicado: (2021)

Proteasome dysfunction induces excessive proteome instability and loss of mitostasis that can be mitigated by enhancing mitochondrial fusion or autophagy
por: Tsakiri, Eleni N., et al.
Publicado: (2019)

Molecular responses to therapeutic proteasome inhibitors in multiple myeloma patients are donor-, cell type- and drug-dependent
por: Papanagnou, Eleni-Dimitra, et al.
Publicado: (2018)

Red algal Rubisco fails to accumulate in transplastomic tobacco expressing Griffithsia monilis RbcL and RbcS genes
por: Lin, Myat T., et al.
Publicado: (2018)

Identification of Rubisco rbcL and rbcS in Camellia oleifera and their potential as molecular markers for selection of high tea oil cultivars
por: Chen, Yongzhong, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_p1rjj0v3k7713sv2paedmhm8hj