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