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Sickle Cell Trait
Known as:
sickle and cell trait
, drepanocytosis
, cell sickle trait
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An individual who is heterozygous for the mutation that causes sickle cell anemia.
National Institutes of Health
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Related topics
Related topics
14 relations
Anemia
Hematopoietic and Lymphoid Cell
Hematopoietic and Lymphoid Tissue
Hemoglobin SS
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Broader (1)
Anemia, Hemolytic, Congenital
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Knowledge and Health Beliefs of Sickle Cell Disease and Sickle Cell Trait: The Influence on Acceptance of Genetic Screening for Sickle Cell Trait
Shanna L. Gustafson
2006
Corpus ID: 70683212
Sickle cell trait carriers are healthy; however, they are at risk to have children with sickle cell disease (SCD), a serious…
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2001
2001
Estimation of genetic parameters in a recurrent selection program in Apple
N. Oraguzie
,
M. E. Hofstee
,
L. Brewer
,
C. Howard
Euphytica
2001
Corpus ID: 33536495
Combining ability was estimated for 8 tree and 11 agronomic traits in a multi-location apple genetics population to select…
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1987
1987
Pulmonary function in sickle cell trait.
Thomas A. Dillard
,
John A. Kark
,
K. Rajagopal
,
J. A. Key
,
J. Canik
,
C. Ruehle
Annals of Internal Medicine
1987
Corpus ID: 12989105
Pulmonary function abnormalities, which have been reported to occur in persons with sickle cell trait (hemoglobin AS), could…
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1984
1984
The sickle cell trait in relation to the training and assignment of duties in the armed forces: III. Hyposthenuria, hematuria, sudden death, rhabdomyolysis, and acute tubular necrosis.
Diggs Lw
1984
Corpus ID: 77023168
: Although the sickle cell trait (SCT) is usually a benign and innocuous carrier state or condition rather than a disease, those…
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1978
1978
Competition of normal β chains and sickle haemoglobin β chains for α chains as a post-translational control mechanism
J. Shaeffer
,
R. Kingston
,
Melisenda J. McDonald
,
H. Franklin Bunn
Nature
1978
Corpus ID: 4329999
ADULT human haemoglobin (HbA) is a tetrameric protein with two α and two β polypeptide chains. Theoretically, individuals…
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1973
1973
Anesthetic risks in sickle cell trait.
P. McGarry
,
C. Duncan
Pediatrics
1973
Corpus ID: 2683797
Five Negro children with sickle cell trait died during or shortly after general anesthesia. Their ages were 18 months to 13 years…
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1972
1972
Translation of -globin m-RNA in -thalassemia and the S and C hemoglobinopathies.
R. F. Rieder
Journal of Clinical Investigation
1972
Corpus ID: 24792396
Genetic and biochemical evidence indicates that in beta-thalassemia there is impaired synthesis of the beta-globin chains of…
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1963
1963
AUTHORITARIANISM AND "TOLERANCE OF TRAIT INCONSISTENCY".
I. Steiner
,
H. H. Johnson
Journal of Abnormal Psychology
1963
Corpus ID: 30909192
1952
1952
Roentgen studies of the maxillae and mandible in sickle-cell anemia.
I. Robinson
,
B. Sarnat
Radiology
1952
Corpus ID: 1382661
There are a number of excellent reports describing the roentgenographic changes in the skull and long bones in sickle-cell anemia…
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1949
1949
Roentgen findings in sickle-cell anemia.
D. Carroll
,
John W. Evans
Radiology
1949
Corpus ID: 41803061
Sickle-cell anemia, which is inherited as a dominant mendelian characteristic, is found almost exclusively in Negroes, and is the…
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