Blood group A is a negative risk factor for peripheric blood stem cell mobilization in allogeneic donorsdoi:10.36472/MSD.V7I6.382Tue Nur YigenoluMehmet BakrtaSemih BacBahar Uncu UluDerya ahinAli KlnFatma Nurbüke arklaDicle skenderNurgül zcan...
What is a heme group? What does Rh negative mean? What blood types can donate blood to whom? What is the ABO blood classification based on? What is the most common blood type in the world? What is Rhesus sensitization? An individual who is blood type AB negative can receive blood from...
Background and ObjectivesPreviously, a weak phenotype A<sub>m</sub> or B<sub>m</sub> was assumed to be caused by a reduction of A or B gene expression in bone marrow cells, but not in mucus-secreting cells. However, ABO expression has not been examined in erythroid progenitor cells of...
Background Blood group O of ABO blood group system is considered as a risk factor for various bleeding events, but the relationship with endoscopic treatment-associated bleeding has yet to be investigated. This study aimed to evaluate whether blood group O is associated with delayed bleeding after...
We have identified a possible mutation which characterizes A2 alleles (a minor subtype of A) at the human histo-blood group ABO locus based on polymerase chain reaction (PCR) of genomic DNA, followed by nucleotide sequencing of the amplified fragments. The A2 subtype has a single base deletion...
The lack of a specific and sensitive positron emission tomography (PET) probe to detect inflammation is a critical challenge. To bridge this gap, we present CD45-PET imaging, which detects inflammation with exceptional sensitivity and clarity in several preclinical models. Notably, the intensity of...
The short answer: AB negative is the rarest of the eight main blood types. Less than 1 percent of American donors are AB negative, according to the American Red Cross. AB negative blood is a rare blood type across the world, though percentages can range from 0.06 percent to 3 percent of...
A case of isoimmunisation in pregnancy caused by antibodies to the Kpa red blood cell antigen is described. The preceding pregnancy had resulted in fetal hydrops for which no cause was found as the antibody screening cells used to investigate the fetal hydrops were Kpa negative. This case ...
Fabry disease is a rare inherited condition characterized by the toxic accumulation of a fatty substance called globotriaosylceramide (Gb3) in the body’s cells. This buildup impairs organ function, especially in the kidneys and heart. The disease is also known as Anderson-Fabry disease, after...
targeted approaches are constrained by the fact that they only sample a small number of human genome equivalents, possibly leading to an inflated false negative rate. In response, an alternative group of approaches centred around shallow WGS and compendiums of patient-specific somatic mutations to gu...