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Immucor Inc rhce beadchip array
Rhce Beadchip Array, supplied by Immucor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
rhce beadchip array - by Bioz Stars, 2026-10
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Article Title: Recurrent pregnancy loss in a patient with anti-Rh17.
Article Snippet: Department of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan Red Cell Reference Laboratory, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia Research and Development, Clinical Services and Research, Australian Red Cross Lifeblood, Kelvin Grove, Queensland, Australia School of Biomedical Sciences, Faculty of Health, Queensland University of Technology, Brisbane, Queensland, Australia School of Health and Behavioural Sciences, University of the Sunshine Coast, Sippy Downs, Queensland, Australia

Article Title: The novel c.634+4A>G splicing variant in RHCE results in weak C and e antigen expression in a pregnant woman originated from Japan.
Article Snippet: Funding information This work was supported by the Association Gaétan Saleün, the Etablissement français du sang (EFS) – Bretagne, and the Institut National de la Santé et de la Recherche Médicale (Inserm).. Abstract Background: In the RH blood group genes, molecular variants that alter antigen expression with potential clinical relevance are frequently identified and reported in the literature.. Study Design and Methods: A pregnant woman in her first pregnancy, who originates from Japan, was typed by routine serological testing.

Polymerase Chain Reaction:

Article Title: Variant RHD alleles and Rh immunization in patients with sickle cell disease.
Article Snippet: Transfusion management for sickle cell disease (SCD) is often complicated by alloimmunization due to exposure to multiple donor units, differences in the red blood cell (RBC) antigens expressed between recipient (primarily African) and donor (primarily European) populations, and underlying inflammation that leads to immune dysregulation and antibody formation.. 5 Sensitization to Rh antigens (D, C/c, E/e) and K represent the majority of the RBC antibodies formed in individuals with SCD.. Although serologic Rh and Kmatched red cells are recommended, 9 Rh immunization remains problematic due to RH genetic diversity.

Article Title: 2024 Poster Information.
Article Snippet: Poster Presentations: Blood Center/Blood Hospital-Based Donor Center P-BC-1 | Blood Inflammatory Markers Depend on Blood Donors Stress Type Feelings F. Cognasse, M. Heestermans, J. Charioni, B. Danic, P. Tiberghien, C. Morand, E. Huis In'T Veld, B. Masser, A. Duchez, H. Hamzeh-Cognasse 1 French National Blood Establishment EFS/AuvergneRhone-Alpes Regional Branch & INSERM 1059 St Etienne University, Health Innovation Campus of Saint-Etienne, 2 French Blood Establishment & INSERM 1059— SAINBIOSE, 3 UMR7268, ADES, EFS, CNRS, Université d'Aix Marseille & Etablissement Français du Sang PACA Corse, 4 Etablissement Français du Sang Bretagne, 5 Etablissement Français du Sang, La Plaine St Denis, France; Unité Mixte de Recherche, INSERM, Université de Franche-Comté, Besançon, France, 6 Etablissement Français du Sang Auvergne Rhône Alpes, 7 Department of Cognitive Science and Artificial Intelligence, Tilburg University & Donor Medicine Research, Sanquin Research, Amsterdam, The Netherlands, 8 Clinical Services and Research, Australia Red Cross Lifeblood & School of Psychology, The University of Queensland, Brisbane & National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Cambridge, UK, 9 INSERM 1059—SAINBIOSE Background/Case Studies: Labile blood products can occasionally trigger inflammatory responses in recipients.. Psychosocial stressors, which are identified as a risk for mental health disorders, may also contribute to neuroinflammation.. Stressful life events have been associated with elevated levels of proinflammatory molecules.

Article Title: Plenary Oral Abstract Session
Article Snippet: Poster Presentations: Hematology and Coagulation P-HC-1 | Hemeand Iron-triggered Defective Macrophage Functionality Contributes to the Pathophysiology of Hemolytic Anemias Francesca Vinchi, Richa Sharma, Steven Zebulon Vance and Karina Yazdanbakhsh New York Blood Center, Iron Research Laboratory, Weill Cornell Medicine, New York Blood Center, Complement

Software:

Article Title: 2022 Plenary, Oral, and Poster Abstract Presentations
Article Snippet: Author Poster Presentations Abstract Poster Presentations: Blood Bank/Blood CenterPoster Presentations: Blood Bank/Blood Center P-BB-1 | Characterization of Residual Cell Populations in Leukoreduction System (LRS) Disposable Sets Following Apheresis Platelet Collections Kathleen Kelly, Sharon Sen, Brandon Brown, Larry J Dumont and Susanne Marschner Vitalant Research Institute, Pathology, University of

Multiplex Assay:

Article Title: 2024 Poster Information.
Article Snippet: Poster Presentations: Blood Center/Blood Hospital-Based Donor Center P-BC-1 | Blood Inflammatory Markers Depend on Blood Donors Stress Type Feelings F. Cognasse, M. Heestermans, J. Charioni, B. Danic, P. Tiberghien, C. Morand, E. Huis In'T Veld, B. Masser, A. Duchez, H. Hamzeh-Cognasse 1 French National Blood Establishment EFS/AuvergneRhone-Alpes Regional Branch & INSERM 1059 St Etienne University, Health Innovation Campus of Saint-Etienne, 2 French Blood Establishment & INSERM 1059— SAINBIOSE, 3 UMR7268, ADES, EFS, CNRS, Université d'Aix Marseille & Etablissement Français du Sang PACA Corse, 4 Etablissement Français du Sang Bretagne, 5 Etablissement Français du Sang, La Plaine St Denis, France; Unité Mixte de Recherche, INSERM, Université de Franche-Comté, Besançon, France, 6 Etablissement Français du Sang Auvergne Rhône Alpes, 7 Department of Cognitive Science and Artificial Intelligence, Tilburg University & Donor Medicine Research, Sanquin Research, Amsterdam, The Netherlands, 8 Clinical Services and Research, Australia Red Cross Lifeblood & School of Psychology, The University of Queensland, Brisbane & National Institute for Health and Care Research Blood and Transplant Research Unit in Donor Cambridge, UK, 9 INSERM 1059—SAINBIOSE Background/Case Studies: Labile blood products can occasionally trigger inflammatory responses in recipients.. Psychosocial stressors, which are identified as a risk for mental health disorders, may also contribute to neuroinflammation.. Stressful life events have been associated with elevated levels of proinflammatory molecules.

DNA Sequencing:

Article Title: Plenary Oral Abstract Session
Article Snippet: Poster Presentations: Hematology and Coagulation P-HC-1 | Hemeand Iron-triggered Defective Macrophage Functionality Contributes to the Pathophysiology of Hemolytic Anemias Francesca Vinchi, Richa Sharma, Steven Zebulon Vance and Karina Yazdanbakhsh New York Blood Center, Iron Research Laboratory, Weill Cornell Medicine, New York Blood Center, Complement

Sequencing:

Article Title: Plenary Oral Abstract Session
Article Snippet: Poster Presentations: Hematology and Coagulation P-HC-1 | Hemeand Iron-triggered Defective Macrophage Functionality Contributes to the Pathophysiology of Hemolytic Anemias Francesca Vinchi, Richa Sharma, Steven Zebulon Vance and Karina Yazdanbakhsh New York Blood Center, Iron Research Laboratory, Weill Cornell Medicine, New York Blood Center, Complement



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Alloimmunization and genotype-predicted Rh antigen expression among chronically transfused patients with thalassemia receiving prophylactic C, E, and K matched red cells. (A) Antibody specificities detected among 40 chronically transfused patients with thalassemia. Columns for each specificity indicate patients’ corresponding antigen status (positive or negative) as reported by standard serologic typing methods. <t>RHD</t> <t>and</t> <t>RHCE</t> genotype-predicted Rh antigen expression among 5 Black (B) and 35 non-Black (C) patients with thalassemia. Partial antigens predicted from genotypes associated with alleles that result in Rh epitope(s) missing and absence of conventional antigen. RHD*DAU0 or RHCE*ce48C has not been shown to encode Rh proteins lacking epitopes and is considered altered antigens.
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Alloimmunization and genotype-predicted Rh antigen expression among chronically transfused patients with thalassemia receiving prophylactic C, E, and K matched red cells. (A) Antibody specificities detected among 40 chronically transfused patients with thalassemia. Columns for each specificity indicate patients’ corresponding antigen status (positive or negative) as reported by standard serologic typing methods. RHD and RHCE genotype-predicted Rh antigen expression among 5 Black (B) and 35 non-Black (C) patients with thalassemia. Partial antigens predicted from genotypes associated with alleles that result in Rh epitope(s) missing and absence of conventional antigen. RHD*DAU0 or RHCE*ce48C has not been shown to encode Rh proteins lacking epitopes and is considered altered antigens.

Journal: Blood Advances

Article Title: Rh alloimmunization in chronically transfused patients with thalassemia receiving RhD, C, E, and K matched transfusions

doi: 10.1182/bloodadvances.2020003732

Figure Lengend Snippet: Alloimmunization and genotype-predicted Rh antigen expression among chronically transfused patients with thalassemia receiving prophylactic C, E, and K matched red cells. (A) Antibody specificities detected among 40 chronically transfused patients with thalassemia. Columns for each specificity indicate patients’ corresponding antigen status (positive or negative) as reported by standard serologic typing methods. RHD and RHCE genotype-predicted Rh antigen expression among 5 Black (B) and 35 non-Black (C) patients with thalassemia. Partial antigens predicted from genotypes associated with alleles that result in Rh epitope(s) missing and absence of conventional antigen. RHD*DAU0 or RHCE*ce48C has not been shown to encode Rh proteins lacking epitopes and is considered altered antigens.

Article Snippet: RH genotyping was performed with RHD and RHCE BeadChip arrays (Bioarray/Immucor), and polymerase chain reaction–based assays, as described previously.

Techniques: Expressing

Alloimmunization and genotype-predicted Rh antigen expression among chronically transfused patients with SCD receiving prophylactic C, E, and K matched red cells by simple transfusion. (A) Antibody specificities detected among 48 chronically transfused patients with SCD. Columns for each specificity indicate patients’ corresponding antigen status (positive or negative) as reported by standard serologic or genotyping methods. (B) RHD and RHCE genotype-predicted Rh antigen expression among patients with SCD. Partial antigens predicted from genotypes with variant alleles that result in Rh epitope(s) missing and absence of conventional antigen. RHD*DAU0 or RHCE*ce48C has not been shown to encode Rh proteins lacking epitopes and is considered altered antigens.

Journal: Blood Advances

Article Title: Rh alloimmunization in chronically transfused patients with thalassemia receiving RhD, C, E, and K matched transfusions

doi: 10.1182/bloodadvances.2020003732

Figure Lengend Snippet: Alloimmunization and genotype-predicted Rh antigen expression among chronically transfused patients with SCD receiving prophylactic C, E, and K matched red cells by simple transfusion. (A) Antibody specificities detected among 48 chronically transfused patients with SCD. Columns for each specificity indicate patients’ corresponding antigen status (positive or negative) as reported by standard serologic or genotyping methods. (B) RHD and RHCE genotype-predicted Rh antigen expression among patients with SCD. Partial antigens predicted from genotypes with variant alleles that result in Rh epitope(s) missing and absence of conventional antigen. RHD*DAU0 or RHCE*ce48C has not been shown to encode Rh proteins lacking epitopes and is considered altered antigens.

Article Snippet: RH genotyping was performed with RHD and RHCE BeadChip arrays (Bioarray/Immucor), and polymerase chain reaction–based assays, as described previously.

Techniques: Expressing, Variant Assay