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Hemoglobin C
Known as:
Hemoglobin C [Chemical/Ingredient]
, c hemoglobin
, haemoglobin c
A commonly occurring abnormal hemoglobin in which lysine replaces a glutamic acid residue at the sixth position of the beta chains. It results in…
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National Institutes of Health
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Related topics
Related topics
12 relations
Broader (1)
Hemoglobin
Hemoglobin C-Harlem:PrThr:Pt:Bld:Ord
Process of secretion
agonists
analogs & derivatives
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Narrower (2)
hemoglobin C Ziguinchor
hemoglobin C-Harlem
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2009
2009
Altered Membrane Structure and Surface Potential in Homozygous Hemoglobin C Erythrocytes
F. Tokumasu
,
G. Nardone
,
+4 authors
J. Dvorak
PLoS ONE
2009
Corpus ID: 4499909
Background Hemoglobin C differs from normal hemoglobin A by a glutamate-to-lysine substitution at position 6 of beta globin and…
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1999
1999
Glycohemoglobin results in samples with hemoglobin C or S trait: a comparison of four test systems.
William L. Roberts
,
Janelle M. Chiasera
,
Kory M. Ward-Cook
Clinical Chemistry
1999
Corpus ID: 44998963
A wide variety of commercial methods are available to measure glycohemoglobin (gHb). These methods measure various species of gHb…
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1997
1997
A technique for eliminating allele specific amplification failure during DNA amplification of heterozygous cells for preimplantation diagnosis.
N. el-Hashemite
,
J. Delhanty
Molecular human reproduction
1997
Corpus ID: 2401197
Advances in techniques of molecular biology have made possible the amplification of specific genes from single cells. This has a…
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1994
1994
Association of malonyl-CoA decarboxylase deficiency and heterozygote state for haemoglobin C disease
M. Krawinkel
,
H. Oldigs
,
René Santer
,
Willy Lehnert
,
U. Wendel
,
J. Schaub
Journal of Inherited Metabolic Disease
1994
Corpus ID: 37389329
Malonyl-CoA decarboxylase (EC 4.1.1.9) deficiency (McKusick 248360) is a rare inborn error of metabolism. Three cases (Brown et…
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1990
1990
Nocturnal enuresis in sickle cell haemoglobinopathies.
D. Readett
,
J. Morris
,
G. Serjeant
Archives of Disease in Childhood
1990
Corpus ID: 28306069
The prevalence of nocturnal enuresis (wet at least two nights a week) was investigated in children, aged 8, who were being…
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Highly Cited
1979
Highly Cited
1979
Low proportions of glycosylated hemoglobin associated with hemoglobin S and hemoglobin C.
H. Aleyassine
Clinical Chemistry
1979
Corpus ID: 22787796
Using a cation-exchange chromatographic method, we found normal or subnormal values for glycosylated hemoglobin in a few diabetic…
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1961
1961
Two Families Showing Interaction of Haemoglobin C or Thalassaemia with High Foetal Haemoglobin in Adults*
A. Kraus
,
B. Koch
,
L. Burckett
British medical journal
1961
Corpus ID: 37409517
The difference between the haemoglobin composition in heterozygous sickle-cell trait and in homozygous sickle-cell anaemia is…
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1957
1957
The Pathology of Sickle Cell Haemoglobin C Disease and Sickle Cell Anaemia
G. Edington
Journal of Clinical Pathology
1957
Corpus ID: 5102963
The purpose of this communication is to describe the necropsy findings in three patients dying of sickle cell haemoglobin C…
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1954
1954
Studies on abnormal hemoglobins. X. A new syndrome: hemoglobin C-thalassemia disease.
Karl Singer
,
Alfred P. Kraus
,
L. Singer
,
Herbert M. Rubinstein
,
Seymour R. Goldberg
Blood
1954
Corpus ID: 7534215
1. A Negro family is described in which several individuals exhibit either the manifestations of thalassemia, or of the…
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Review
1954
Review
1954
A case of sickle cell; haemoglobin C disease and a survey of haemoglobin C incidence in West Africa.
G. Edington
,
H. Lehmann
Transactions of the Royal Society of Tropical…
1954
Corpus ID: 37533770
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