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8 Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis

Data up to Jan 2025

Published1993
Citations47
References39

Total Citations Per Year

Abstract

References (39)

Swainsonine inhibits the biosynthesis of complex glycoproteins by inhibition of Golgi mannosidase II.

1982 • 463 citations

Blood group ABH and Ii antigens of human erythrocytes: chemistry, polymorphism, and their developmental change.

1981 • 344 citations

Changes in cell surface antigen expression during hemopoietic differentiation

1982 • 260 citations

The distribution of repeating [Gal beta 1,4GlcNAc beta 1,3] sequences in asparagine-linked oligosaccharides of the mouse lymphoma cell lines BW5147 and PHAR 2.1.

1984 • 246 citations

Developmental change and genetic defect in the carbohydrate structure of band 3 glycoprotein of human erythrocyte membrane.

1979 • 230 citations

Hereditary Erythroblastic Multinuclearity Associated with a Positive Acidified‐Serum Test: a Type of Congenital Dyserythropoietic Anaemia

1969 • 217 citations

Biliary proteins. Unique inhibitors of cholesterol crystal nucleation in human gallbladder bile.

1984 • 210 citations

Congenital dyserythropoietic anemia with karyorrhexis and multinuclearity of erythroblasts.

1968 • 192 citations

Isolation and characterization of polyfucosylated lactosaminoglycan from human granulocytes.

1984 • 188 citations

Structure of fetal lactosaminoglycan. The carbohydrate moiety of Band 3 isolated from human umbilical cord erythrocytes.

1984 • 165 citations

Biosynthesis of blood group i-active polylactosaminoglycans. Partial purification and properties of an UDP-GlcNAc:N-acetyllactosaminide beta 1—-3-N-acetylglucosaminyltransferase from Novikoff tumor cell ascites fluid.

1988 • 156 citations

Isolation, characterization, and expression of cDNAs encoding murine alpha-mannosidase II, a Golgi enzyme that controls conversion of high mannose to complex N-glycans.

1991 • 129 citations

Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II.

1987 • 105 citations

Immunochemistry of Ii-Active Glycosphingolipids of Erythrocytes

1979 • 102 citations

HEMPAS: Congenital Dyserythropoietic Anaemia (Type II)

1973 • 87 citations

Agglutinability of Red Cells by Anti-i in Patients with Thalassæmia Major and Other Hæmatological Disorders

1964 • 82 citations

Congenital Dyserythropoietic Anaemia, Types I and II: Aberrant Pattern of Erythrocyte Membrane Proteins in CDA II, as Revealed by Two‐dimensional Polyacrylamide Gel Electrophoresis

1977 • 79 citations

Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS)

1984 • 65 citations

Incomplete glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia Type II (CDA II)

1983 • 53 citations

Decreased glycosylation of band 3 and band 4‐5 glycoproteins of erythrocyte membrane in congenital dyserythropoietic anaemia type II

1982 • 51 citations

Isolation of a rat liver Golgi mannosidase II clone by mixed oligonucleotide-primed amplification of cDNA.

1989 • 51 citations

Red cell membrane protein anomalies in congenital dyserythropoietic anaemia, type II (HEMPAS)

1982 • 48 citations

Alterations of Globin Chain Synthesis and of Red Cell Membrane Proteins in Congenital Dyserythropoietic Anemia I and II

1982 • 48 citations

Incompletely processed N‐glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)

1992 • 45 citations

Severe Hemochromatosis: The Predominant Clinical Manifestation of Congenital Dyserythropoietic Anemia Type 2

1985 • 40 citations

Anomalous clustering of underglycosylated band 3 in erythrocytes and their precursor cells in congenital dyserythropoietic anemia type II

1986 • 36 citations

Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II)

1987 • 33 citations

Abnormal fatty acid composition of erythrocyte glycosphingolipids in congenital dyserythropoietic anemia type II.

1985 • 30 citations

Accumulation of glycolipids containing N-acetylglucosamine in erythrocyte stroma of patients with congenital dyserythropoietic anemia type II (HEMPAS)

1975 • 23 citations

Variants of congenital dyserythropoietic anaemia: an update.

1982 • 23 citations

Electron microscopy in the diagnosis of the bone marrow disorders of the erythroid series.

1981 • 22 citations

Erythrocyte membrane proteins in an unusual case of congenital dyserythropoietic anaemia type II (CDA II)

1982 • 21 citations

Congenital Dyserythropoietic Anaemia (CDA) with Severe Gout, Rare Kell Phenotype and Erythrocyte, Granulocyte and Platelet Membrane Reduplication: a New Variant of CDA Type II

1980 • 20 citations

Congenital dyserythropoietic anaemia type II (HEMPAS): characterization of aberrant intracellular organelles by immunogold electron microscopy

1987 • 19 citations

Isolation and characterization of poly-N-acetyllactosaminylceramides accumulated in the erythrocytes of congenital dyserythropoietic anemia type II patients

1986 • 18 citations

A variant of the congenital dyserythropoietic anaemia type II with structural abnormalities in the granulocytic series

1986 • 18 citations

Unclassified type of congenital dyserythropoietic anaemia (CDA) with prominent peripheral erythroblastosis

1985 • 13 citations

Normal Serum Ferritin Levels in a Patient with HEMPAS Syndrome and Iron Overload

1982 • 10 citations

Congenital dyserythropoietic anaemia type II (CDA‐II): chromosomal banding studies and adherent cell effects on erythroid colony (CFU‐E) and burst (BFU‐E) formation

1982 • 8 citations

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8 Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis (1993) – Baillière s Clinical Haematology | Metascience Observatory Explorer