Literature DB >> 1100141

F-cells in the adult: normal values and levels in individuals with hereditary and acquired elevations of Hb F.

W G Wood, G Stamatoyannopoulos, G Lim, P E Nute.   

Abstract

Specific antibodies to human fetal hemoglobin were prepared and, after conjugation with a fluorescent dye, were used to determine the distribution of Hb F-containing cells in blood smears from normal adults and individuals with hereditary and acquired conditions associated with abnormal levels of Hb F. The mean proportion of F-cells in normal persons was 2.7% +/- 1.4%, with a range of 0.5%-7.0%. Proportions of F-cells were increased in persons with several acquired and inherited disorders that are associated with an increased percentage of Hb F in hemolysates. A strong linear correlation between the amount of Hb F and proportion of F-cells was observed. This technique may prove useful in studies of a variety of disorders associated with Hb F elevations and also in investigations of the mechanisms controlling the transition from fetal to adult hemoglobin during the course of human development.

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Year:  1975        PMID: 1100141

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  40 in total

1.  Hemoglobin ontogeny during normal mouse fetal development.

Authors:  T W Brotherton; D H Chui; J Gauldie; M Patterson
Journal:  Proc Natl Acad Sci U S A       Date:  1979-06       Impact factor: 11.205

Review 2.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Hematol Oncol Clin North Am       Date:  2010-02       Impact factor: 3.722

3.  Stimulation of fetal hemoglobin synthesis in bone marrow cultures from adult individuals.

Authors:  T H Papayannopoulou; M Brice; G Stamatoyannopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1976-06       Impact factor: 11.205

Review 4.  Control of globin gene expression during development and erythroid differentiation.

Authors:  George Stamatoyannopoulos
Journal:  Exp Hematol       Date:  2005-03       Impact factor: 3.084

5.  Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers.

Authors:  S L Thein; M Sampietro; K Rohde; J Rochette; D J Weatherall; G M Lathrop; F Demenais
Journal:  Am J Hum Genet       Date:  1994-02       Impact factor: 11.025

6.  Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Authors:  S H Boyer; L Margolet; M L Boyer; T H Huisman; W A Schroeder; W G Wood; D J Weatherall; J B Clegg; R Cartner
Journal:  Am J Hum Genet       Date:  1977-05       Impact factor: 11.025

7.  Detection of non-deletional type of hereditary persistence of fetal hemoglobin (HPFH) condition associated with 619 bp β(°)-thalassemia deletion.

Authors:  S M Husain; M P Anandaraj
Journal:  Indian J Clin Biochem       Date:  1997-07

8.  Reactivation of developmentally silenced globin genes by forced chromatin looping.

Authors:  Wulan Deng; Jeremy W Rupon; Ivan Krivega; Laura Breda; Irene Motta; Kristen S Jahn; Andreas Reik; Philip D Gregory; Stefano Rivella; Ann Dean; Gerd A Blobel
Journal:  Cell       Date:  2014-08-14       Impact factor: 41.582

9.  Reticulocyte parameters and hemoglobin F production in sickle cell disease patients undergoing hydroxyurea therapy.

Authors:  R Borba; C S P Lima; H Z W Grotto
Journal:  J Clin Lab Anal       Date:  2003       Impact factor: 2.352

10.  The prevalence of maternal F cells in a pregnant population and potential overestimation of foeto-maternal haemorrhage as a consequence.

Authors:  Deirdre Corcoran; Deirdre Murphy; Jennifer C Donnelly; Fionnuala Ni Ainle
Journal:  Blood Transfus       Date:  2013-06-12       Impact factor: 3.443

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