Results 11 to 20 of about 26,628,314 (173)

Characterization of blood group variants in an Omani population by comparison of whole genome sequencing and serology. [PDF]

open access: yesTransfusion
Abstract Background Although blood group variation was first described over a century ago, our understanding of the genetic variation affecting antigenic expression on the red blood cell surface in many populations is lacking. This deficit limits the ability to accurately type patients, especially as serological testing is not available for all ...
Haffener PE   +7 more
europepmc   +2 more sources

Urine Proteomic Profiling at Admission Reveals Complement Biomarkers Linked to Alcohol-Associated Liver Disease. [PDF]

open access: yesAlcohol Clin Exp Res (Hoboken)
Patients with alcohol‐associated hepatitis (AH) and alcohol‐cirrhosis (AC) show perturbations in complement. Complement activation pathways are perturbed in the urine of patients with AH and AC, and distinguish severe AH from AC. Complement perturbations can help physicians and researchers to understand the liver–kidney crosstalk in severe AH and AC ...
Prado L   +11 more
europepmc   +2 more sources

Analysis of red blood cell blood group gene polymorphism and applicability evaluation of PCR-TaqMan technology in the Hui ethnic blood donor population in Suzhou

open access: yesZhongguo shuxue zazhi
[Objective] To investigate the characteristics of allele frequencies for 9 red blood cell (RBC) blood group systems in the Hui ethnic voluntary blood donor population of Suzhou using real-time fluorescence PCR technology, so as to provide technical ...
JIANG Jia   +4 more
doaj   +1 more source

Distribution of clinically relevant erythrocyte antigens among blood donors of the Republic of Srpska [PDF]

open access: yesScripta Medica, 2015
Introduction: Identifying voluntary blood donors with rare phenotype characteristics is the basic precondition for creating a registry of blood donors with rare blood groups.
Guzijan Gordana   +5 more
doaj  

The anti-Mia antibody – Report of four cases in a tertiary care hospital with review of literature

open access: yesGlobal Journal of Transfusion Medicine, 2019
Anti – Mia antibody is antibody reacting with Mi III phenotype of the Miltenberger (Mi) subsystem. It is rarely reported in the West, however, it is common in Chinese and South East Asian populations. Very few cases have been reported in India.
Sangeeta Pahuja   +4 more
doaj   +1 more source

STRATEGY FOR OPEN HEART SURGERY IN A NON-CROSS MATCHABLE BLOOD SCENARIO

open access: yesPakistan Armed Forces Medical Journal, 2016
To date thirty-three different blood group systems (including the ABO and Rh systems) have so far been recognized by the International Society of Blood Transfusion (ISBT)1. The commonest is ABO followed by the Rhesus (D) system.
Syed Shahid Nafees Zaidi   +4 more
doaj   +2 more sources

Torture and scepticism in Papua New Guinea witch hunts Torture et scepticisme dans les chasses aux sorcières en Papouasie‐Nouvelle‐Guinée

open access: yesJournal of the Royal Anthropological Institute, EarlyView.
For over a century, anthropologists have documented the many institutions that exist to respond to witchcraft and the uncanny that it names: oracles that attempt to produce certainty by naming the witch; moots in which grievances are aired; trials in magistrates’ courts that attempt to satisfy the community while preserving the life of the accused ...
Chloe Nahum‐Claudel
wiley   +1 more source

Application of combined NGS and TGS technologies in red blood cell blood group bank construction: a preliminary study

open access: yesZhongguo shuxue zazhi
[Objective] This study employed next-generation sequencing (NGS) for large-scale genotyping of 42 blood group systems in blood donors to evaluate its applicability in multi-system blood group identification and rare blood type repository construction ...
DING Mengyuan   +5 more
doaj   +1 more source

A genetic and historical perspective on the origins of keratitis fugax hereditaria

open access: yesActa Ophthalmologica, EarlyView.
Abstract Purpose To investigate the genetic and genealogical background of keratitis fugax hereditaria (KFH), a periodic corneal disease caused by the heterozygous pathogenic variant c.61G>C in the NLRP3 gene. KFH is characterized by recurrent unilateral autoinflammatory attacks alternating between the eyes and permanent corneal opacities.
Annamari T. Immonen   +7 more
wiley   +1 more source

Rethinking Merit in Calvin's Doctrine of the Atonement: Beyond Possessive Individualism

open access: yesInternational Journal of Systematic Theology, EarlyView.
Abstract Joan Lockwood O'Donovan argues that the Reformation doctrine of grace entails a rejection of the proprietary anthropology of self‐owning individuals and its attendant notion of justice – what C. B. Macpherson termed the “theory of possessive individualism.” Although O'Donovan praises Calvin's anthropology and his account of law for its non ...
John Walker
wiley   +1 more source

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