Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,551,814 papers from all fields of science
Search
Sign In
Create Free Account
Hemoglobin E
Known as:
Hemoglobin E [Chemical/Ingredient]
, e hemoglobin
, haemoglobin e
An abnormal hemoglobin that results from the substitution of lysine for glutamic acid at position 26 of the beta chain. It is most frequently…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
13 relations
HBE1 gene
HBE1 wt Allele
Hemoglobin E:PrThr:Pt:Bld:Ord:Electrophoresis
Process of secretion
Expand
Narrower (1)
hemoglobin E Saskatoon
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Adaptation to anemia in hemoglobin E-ß thalassemia.
Angela Allen
,
C. Fisher
,
+6 authors
D. Weatherall
Blood
2010
Corpus ID: 206892803
Hemoglobin E β thalassemia is the commonest form of severe thalassemia in many Asian countries. Its remarkably variable clinical…
Expand
2009
2009
Hemoglobin E disorders in Eastern Uttar Pradesh.
S. Patne
,
J. Shukla
Indian Journal of Pathology and Microbiology
2009
Corpus ID: 1067889
The distribution of hemoglobin E (alpha2beta2 26Glu (R)Lys ) is mostly restricted to Northeastern India. While evaluating the…
Expand
2009
2009
The range of hemoglobin A(2) in hemoglobin E heterozygotes as determined by capillary electrophoresis.
Daniel D. Mais
,
R. Gulbranson
,
D. Keren
American Journal of Clinical Pathology
2009
Corpus ID: 37378373
Capillary electrophoresis (CE) is capable of distinguishing hemoglobin E (HbE) from hemoglobin A(2) (HbA(2)), thus permitting…
Expand
Review
2007
Review
2007
Sickle cell–haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study
Huxley Knox-Macaulay
,
M. M. Ahmed
,
D. Gravell
,
S. Alkindi
,
Anuradha Ganesh
International Journal of Laboratory Hematology
2007
Corpus ID: 24765215
The paucity of clinical reports in the world literature suggests that, as a disease entity, haemoglobin SE compound…
Expand
Highly Cited
2001
Highly Cited
2001
Simultaneous PCR detection of β – thalassemia and α – thalassemia 1 (SEA type) in prenatal diagnosis of complex thalassemia syndrome
N. Siriratmanawong
,
G. Fucharoen
,
K. Sanchaisuriya
,
T. Ratanasiri
,
S. Fucharoen
2001
Corpus ID: 71765656
1992
1992
Haemoglobin-E in the presence of oxidative substances from fava bean may be protective against Plasmodium falciparum malaria.
D. Kitayaporn
,
K. E. Nelson
,
P. Charoenlarp
,
T. Pholpothi
Transactions of the Royal Society of Tropical…
1992
Corpus ID: 5685260
Review
1972
Review
1972
Haemoglobin E-hereditary elliptocytosis in Malayan aborigines.
Luan Eng Lie-Injo
,
A. Fix
,
J. M. Bolton
,
R. Gilman
Acta Haematologica
1972
Corpus ID: 46823240
A survey was made of 1,384 Malayan aborigines for frequencies of abnormal haemoglobin and hereditary elliptocytosis. The subjects…
Expand
Highly Cited
1969
Highly Cited
1969
The Pattern of Disordered Haemoglobin Synthesis in Homozygous and Heterozygous β‐Thalassaemia *
D. Weatherall
,
J. Clegg
,
S. Na-nakorn
,
P. Wasi
British Journal of Haematology
1969
Corpus ID: 29495132
The rate of globin chain production has been studied in patients with homozygous β‐thalassaemia, heterozygous β‐thalassaemia…
Expand
1966
1966
The influence of hemoglobinopathies on reproduction.
J.Paul de V. Hendrickse
,
E.John Watson-Williams
American Journal of Obstetrics and Gynecology
1966
Corpus ID: 21653461
1965
1965
Hereditary Ovalocytosis and Haemoglobin E-Ovalocytosis in Malayan Aborigines
L. I. Eng
Nature
1965
Corpus ID: 4211117
THE red blood cells of mammalian vertebrates, including man, are normally round, except those of the camel, which are…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE