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Anemia of inadequate production
Known as:
Dyserythropoietic anemia
, Anemia, dyshematopoietic
, dyshematopoietic anemia
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A kind of anemia characterized by inadequate production of erythrocytes. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
6 relations
Broader (1)
Anemia
Congenital dyserythropoietic anemia
Congenital dyserythropoietic anemia, type I
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, and Calvarial Hyperostosis
Hereditary Diseases
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene
P. Bianchi
,
E. Fermo
,
+6 authors
A. Zanella
Human Mutation
2009
Corpus ID: 11804195
Congenital dyserythropoietic anemia type II (CDAII) is an autosomal recessive disease characterized by ineffective erythropoiesis…
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Highly Cited
2005
Highly Cited
2005
Dyserythropoietic Anemia and Thrombocytopenia due to a Novel Mutation in GATA-1
G. D. Del Vecchio
,
L. Giordani
,
A. De Santis
,
D. De Mattia
Acta Haematologica
2005
Corpus ID: 41470002
Hematopoiesis is a complex process regulated by nuclear proteins that coordinate lineage-specific patterns of gene expression…
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Highly Cited
2003
Highly Cited
2003
Effects of the R216Q mutation of GATA-1 on erythropoiesis and megakaryocytopoiesis
C. Balduini
,
A. Pecci
,
+10 authors
A. Savoia
Thrombosis and Haemostasis
2003
Corpus ID: 33294453
Summary The transcription factor GATA-1, together with its cofactor FOG-1, regulates erythropoiesis and megakaryocytopoiesis…
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Highly Cited
2002
Highly Cited
2002
Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
O. Dgany
,
N. Avidan
,
+22 authors
H. Tamary
American Journal of Human Genetics
2002
Corpus ID: 23190559
Congenital dyserythropoietic anemias (CDAs) constitute a rare group of inherited red-blood-cell disorders associated with…
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Highly Cited
1997
Highly Cited
1997
Alpha-Mannosidase-II Deficiency Results in Dyserythropoiesis and Unveils an Alternate Pathway in Oligosaccharide Biosynthesis
D. Chui
,
M. Oh-eda
,
+7 authors
J. Marth
Cell
1997
Corpus ID: 6064567
Highly Cited
1997
Highly Cited
1997
Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search.
P. Gasparini
,
E. Giudice
,
+5 authors
A. Iolascon
American Journal of Human Genetics
1997
Corpus ID: 23541765
Congenital dyserythropoietic anemias (CDA) are genetic disorders characterized by anemia and ineffective erythropoiesis. Three…
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Highly Cited
1996
Highly Cited
1996
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulum.
N. Alloisio
,
P. Texier
,
+7 authors
J. Guichard
Blood
1996
Corpus ID: 13506367
We studied 20 individuals from 17 unrelated families with congenital dyserythropoietic anemia (type II; CDAII). The clinical…
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1991
1991
Dyserythropoiesis, polymyopathy, and cardiac disease in three related English springer spaniels.
C. T. Holland
,
P. Canfield
,
A. Watson
,
G. Allan
Journal of Veterinary Internal Medicine
1991
Corpus ID: 29248113
A polysystemic disorder was observed in three related English Springer Spaniel dogs that demonstrated regurgitation from an early…
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Highly Cited
1990
Highly Cited
1990
Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II.
Michiko N. Fukuda
,
K. Masri
,
Anne dell
,
Lucio Luzzatto
,
K. Moremen
Proceedings of the National Academy of Sciences…
1990
Corpus ID: 8059584
Congenital dyserythropoietic anemia type II, or hereditary erythroblastic multinuclearity with a positive acidified-serum-lysis…
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Highly Cited
1987
Highly Cited
1987
Primary defect of congenital dyserythropoietic anemia type II. Failure in glycosylation of erythrocyte lactosaminoglycan proteins caused by lowered N-acetylglucosaminyltransferase II.
M. Fukuda
,
A. Dell
,
P. Scartezzini
Journal of Biological Chemistry
1987
Corpus ID: 33447892
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