Literature DB >> 14888690

Familial differences in the proportion of abnormal hemoglobin present in the sickle cell trait.

J V NEEL, I C WELLS, H A ITANO.   

Abstract

Keywords:  ANEMIA, SICKLE CELL/heredity; HEMOGLOBIN/abnormalities

Mesh：

Substances：

Year:  1951        PMID： 14888690      PMCID： PMC436354          DOI： 10.1172/JCI102532

Source DB:  PubMed          Journal:  J Clin Invest        ISSN： 0021-9738            Impact factor:   14.808


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  6 in total

1.  The Inheritance of Sickle Cell Anemia.

Authors:  J V Neel
Journal:  Science       Date:  1949-07-15       Impact factor: 47.728

2.  The inheritance of the sickling phenomenon, with particular reference to sickle cell disease.

Authors:  J V NEEL
Journal:  Blood       Date:  1951-05       Impact factor: 22.113

3.  Ratio of sickle-cell anemia hemoglobin to normal hemoglobin in sicklemics.

Authors:  I C WELLS; H A ITANO
Journal:  J Biol Chem       Date:  1951-01       Impact factor: 5.157

4.  A new inherited abnormality of human hemoglobin.

Authors:  H A ITANO; J V NEEL
Journal:  Proc Natl Acad Sci U S A       Date:  1950-11       Impact factor: 11.205

5.  The occurrence in a family of Sicilian ancestry of the traits for both sickling and thalassemia.

Authors:  W N POWELL; J G RODARTE; J V NEEL
Journal:  Blood       Date:  1950-10       Impact factor: 22.113

6.  Sickle cell anemia a molecular disease.

Authors:  L PAULING; H A ITANO
Journal:  Science       Date:  1949-11-25       Impact factor: 47.728
  6 in total
  10 in total

1.  Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.

Authors:  J R Shaeffer; J DeSimone; L J Kleve
Journal:  Biochem Genet       Date:  1975-12       Impact factor: 1.890

2.  MALARIA AND STRESS IN RELATION TO HAEMOGLOBINS S AND C.

Authors:  G R THOMPSON
Journal:  Br Med J       Date:  1963-10-19

3.  STUDIES OF IN VITRO SYNTHESIS OF HETEROGENIC HEMOGLOBINS.

Authors:  J D HEYWOOD; M KARON; S WEISSMAN
Journal:  J Clin Invest       Date:  1964-12       Impact factor: 14.808

4.  QUANTITATIVE STUDIES ON A2, SICKLE CELL, AND FETAL HEMOGLOBINS IN NEGROES WITH MONGOLISM, WITH OBSERVATIONS ON TRANSLOCATION MONGOLISM IN NEGROES.

Authors:  E D WEINSTEIN; D L RUCKNAGEL; M W SHAW
Journal:  Am J Hum Genet       Date:  1965-09       Impact factor: 11.025

5.  Hypocatalasemia: a new genetic carrier state.

Authors:  S TAKAHARA; H B HAMILTON; J V NEEL; T Y KOBARA; Y OGURA; E T NISHIMURA
Journal:  J Clin Invest       Date:  1960-04       Impact factor: 14.808

6.  Electrophoretic components of the hemoglobin of red cell membranes.

Authors:  F A KLIPSTEIN; H M RANNEY
Journal:  J Clin Invest       Date:  1960-12       Impact factor: 14.808

7.  Qualitative and quantitative control of adult hemoglobin synthesis; a multiple allele hypothesis.

Authors:  H A ITANO
Journal:  Am J Hum Genet       Date:  1953-03       Impact factor: 11.025

8.  Thirty-year risk of ischemic stroke in individuals with sickle cell trait and modification by chronic kidney disease: The atherosclerosis risk in communities (ARIC) study.

Authors:  Melissa C Caughey; Vimal K Derebail; Nigel S Key; Alexander P Reiner; Rebecca F Gottesman; Abhijit V Kshirsagar; Gerardo Heiss
Journal:  Am J Hematol       Date:  2019-09-10       Impact factor: 10.047

9.  Aorta-coronary bypass in a patient with sickle cell trait.

Authors:  M Heiner; S J Teasdale; T David; A A Scott; M F Glynn
Journal:  Can Anaesth Soc J       Date:  1979-09

10.  Age trends in the prevalence of the sickle cell trait.

Authors:  D T Janerich; J H Kelly; F D Ziegler; S Selvin; I H Porter; J B Robinson; R C Herdman
Journal:  Health Serv Rep       Date:  1973-11
  10 in total

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