UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Epithelial Expression of Human ABO Blood Group Genes Is Dependent upon a Downstream Regulatory Element Functioning through an Epithelial Cell-specific Transcription Factor, Elf5

The Journal of biological chemistry, 2016-10, Vol.291 (43), p.22594-22606

2016

Volltextzugriff (PDF)

Integrative genome analysis identified the KANNO blood group antigen as prion protein

Transfusion (Philadelphia, Pa.), 2019-07, Vol.59 (7), p.2429-2435

2019

Volltextzugriff (PDF)

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11pt2), p.2917-2927

2013

Volltextzugriff (PDF)

Application of immortalized human erythroid progenitor cell line in serologic tests to detect red blood cell alloantibodies

Transfusion (Philadelphia, Pa.), 2018-11, Vol.58 (11), p.2675-2682

2018

Volltextzugriff (PDF)

Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population

Transfusion (Philadelphia, Pa.), 2019-08, Vol.59 (8), p.2519-2522

2019

Volltextzugriff (PDF)

A practical and effective strategy in East Asia to prevent anti‐D alloimmunization in patients by C/c phenotyping of serologic RhD‐negative blood donors

EJHaem, 2021-11, Vol.2 (4), p.750-756

2021

Volltextzugriff (PDF)

Is Bm5.8 specific to the Japanese population?

Vox sanguinis, 2019-02, Vol.114 (2), p.185-185

2019

Volltextzugriff (PDF)

Is B m 5.8 specific to the Japanese population?

Vox sanguinis, 2019-02, Vol.114 (2), p.185-185

2019

Volltextzugriff (PDF)

Review of ABO Expression and Variations based on Transcriptional Regulation of the ABO Blood Group Gene

Transfusion medicine and hemotherapy, 2024-08, Vol.51 (4), p.210-224

2024

Volltextzugriff (PDF)

Human ABO gene transcriptional regulation

Transfusion (Philadelphia, Pa.), 2020-04, Vol.60 (4), p.860-869

2020

Volltextzugriff (PDF)

DSLK and Kg: Antithetical antigens in the RHAG blood group system, and characterization of anti‐DSLK antibody

Vox sanguinis, 2023-05, Vol.118 (5), p.392-397

2023

Volltextzugriff (PDF)

Two new JK silencing alleles identified by single molecule sequencing with 20‐Kb long‐reads

Transfusion (Philadelphia, Pa.), 2023-08, Vol.63 (8), p.1441-1446

2023

Volltextzugriff (PDF)

Is Bm 5.8 specific to the Japanese population?

Vox sanguinis, 2019-02, Vol.114 (2), p.185-185

2019

Volltextzugriff (PDF)

GP.MOT: A novel glycophorin variant identified in a Japanese blood donor

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.2825-2829

2021

Volltextzugriff (PDF)

GP . MOT : A novel glycophorin variant identified in a Japanese blood donor

Transfusion (Philadelphia, Pa.), 2021-10, Vol.61 (10), p.2825-2829

2021

Volltextzugriff (PDF)

Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes

Immunogenetics (New York), 2001-05, Vol.53 (3), p.190-199

2001

Volltextzugriff (PDF)

A new antigen SUMI carried on glycophorin A encoded by the GYPAM with c.91A>C (p.Thr31Pro) belongs to the MNS blood group system

Transfusion (Philadelphia, Pa.), 2020-06, Vol.60 (6), p.1287-1293

2020

Volltextzugriff (PDF)

RUNX1 mutation in a patient with myelodysplastic syndrome and decreased erythrocyte expression of blood group A antigen

Transfusion (Philadelphia, Pa.), 2020-01, Vol.60 (1), p.184-196

2020

Volltextzugriff (PDF)

Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype

Transfusion (Philadelphia, Pa.), 2017-04, Vol.57 (4), p.1072-1077

2017

Volltextzugriff (PDF)

Genetic background of anti‐Xg a producers in Japanese blood donors

Vox sanguinis, 2022-10, Vol.117 (10), p.1235-1239

2022

Volltextzugriff (PDF)

A new antigen SUMI carried on glycophorin A encoded by the GYPAM with c. 91A> C (p. Thr31Pro ) belongs to the MNS blood group system

Transfusion (Philadelphia, Pa.), 2020-06, Vol.60 (6), p.1287-1293

2020

Volltextzugriff (PDF)

Anemic Disease of the Newborn With Little Increase in Hemolysis and Erythropoiesis Due to Maternal Anti-Jr a : A Case Study and Review of the Literature

Transfusion medicine reviews, 2019-07, Vol.33 (3), p.183

2019

Volltextzugriff (PDF)

An unusual variant glycophorin expressing protease‐resistant M antigen encoded by the GYPB‐E(2‐4)‐B hybrid gene

Vox sanguinis, 2020-10, Vol.115 (7), p.579-585

2020

Volltextzugriff (PDF)

The Kg‐antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn

British journal of haematology, 2020-12, Vol.191 (5), p.920-926

2020

Volltextzugriff (PDF)

Extensive polymorphism of ABO blood group gene : three major lineages of the alleles for the common ABO phenotypes

Human genetics, 1996-06, Vol.97 (6), p.777-783

1996

Volltextzugriff (PDF)

1 – 25 von 323

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(237)
Mit Volltextzugriff
(255)

Publikationsform

Sprache

Englisch
(284)
Japanisch
(58)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(9)

Menü

Weitere Dienste

Einstellungen

Epithelial Expression of Human ABO Blood Group Genes Is Dependent upon a Downstream Regulatory Element Functioning through an Epithelial Cell-specific Transcription Factor, Elf5

Integrative genome analysis identified the KANNO blood group antigen as prion protein

Mutation of the GATA site in the erythroid cell-specific regulatory element of the ABO gene in a Bm subgroup individual

Application of immortalized human erythroid progenitor cell line in serologic tests to detect red blood cell alloantibodies

Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population

A practical and effective strategy in East Asia to prevent anti‐D alloimmunization in patients by C/c phenotyping of serologic RhD‐negative blood donors

Is Bm5.8 specific to the Japanese population?

Is B m 5.8 specific to the Japanese population?

Review of ABO Expression and Variations based on Transcriptional Regulation of the ABO Blood Group Gene

Human ABO gene transcriptional regulation

DSLK and Kg: Antithetical antigens in the RHAG blood group system, and characterization of anti‐DSLK antibody

Two new JK silencing alleles identified by single molecule sequencing with 20‐Kb long‐reads

Is Bm 5.8 specific to the Japanese population?

GP.MOT: A novel glycophorin variant identified in a Japanese blood donor

GP . MOT : A novel glycophorin variant identified in a Japanese blood donor

Recombination and gene conversion-like events may contribute to ABO gene diversity causing various phenotypes

A new antigen SUMI carried on glycophorin A encoded by the GYPAM with c.91A>C (p.Thr31Pro) belongs to the MNS blood group system

RUNX1 mutation in a patient with myelodysplastic syndrome and decreased erythrocyte expression of blood group A antigen

Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype

Genetic background of anti‐Xg a producers in Japanese blood donors

A new antigen SUMI carried on glycophorin A encoded by the GYPAM with c. 91A> C (p. Thr31Pro ) belongs to the MNS blood group system

Anemic Disease of the Newborn With Little Increase in Hemolysis and Erythropoiesis Due to Maternal Anti-Jr a : A Case Study and Review of the Literature

An unusual variant glycophorin expressing protease‐resistant M antigen encoded by the GYPB‐E(2‐4)‐B hybrid gene

The Kg‐antigen, RhAG with a Lys164Gln mutation, gives rise to haemolytic disease of the newborn

Extensive polymorphism of ABO blood group gene : three major lineages of the alleles for the common ABO phenotypes

Suchergebnisse filtern