Literature DB >> 5645100

Acid-agar gel electrophoresis of human hemoglobins.

F Vella.   

Abstract

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Year:  1968        PMID： 5645100     DOI： 10.1093/ajcp/49.3_ts.440

Source DB:  PubMed          Journal:  Am J Clin Pathol        ISSN： 0002-9173            Impact factor:   2.493


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  6 in total

1.  Inheritance of the Bantu/Benin haplotype causes less severe hemolytic and oxidative stress in sickle cell anemia patients treated with hydroxycarbamide.

Authors:  Jéssika V Okumura; Danilo G H Silva; Lidiane S Torres; Edis Belini-Junior; Willian M Barberino; Renan G Oliveira; Gisele C S Carrocini; Gabriela B Gelaleti; Clarisse L C Lobo; Claudia R Bonini-Domingos
Journal:  J Hum Genet       Date:  2016-03-10       Impact factor: 3.172

2.  Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis.

Authors:  Lidiane de Souza Torres; Jéssika Viviani Okumura; Danilo Grünig Humberto da Silva; Claudia Regina Bonini-Domingos
Journal:  Rev Bras Hematol Hemoter       Date:  2015-02-23

3.  Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein.

Authors:  Lidiane S Torres; Jéssika V Okumura; Danilo G H Silva; Kallyne K O Mimura; Édis Belini-Júnior; Renan G Oliveira; Clarisse L C Lobo; Sonia M Oliani; Claudia R Bonini-Domingos
Journal:  PLoS One       Date:  2016-11-01       Impact factor: 3.240

4.  A model of genetic guidance for hemoglobinopathy patients and laboratory diagnosis of family members as educational and preventive measures.

Authors:  Tatiana Dela-Sávia Ferreira; Adriana Sousa Freire; Elisângela de Paula Silveira-Lacerda; Marco Túlio Antônio García-Zapata
Journal:  Rev Bras Hematol Hemoter       Date:  2012

5.  The influence of hydroxyurea on oxidative stress in sickle cell anemia.

Authors:  Lidiane de Souza Torres; Danilo Grünig Humberto da Silva; Edis Belini Junior; Eduardo Alves de Almeida; Clarisse Lopes de Castro Lobo; Rodolfo Delfini Cançado; Milton Artur Ruiz; Claudia Regina Bonini-Domingos
Journal:  Rev Bras Hematol Hemoter       Date:  2012

6.  Prevalence of β(S)-globin gene haplotypes, α-thalassemia (3.7 kb deletion) and redox status in patients with sickle cell anemia in the state of Paraná, Brazil.

Authors:  Eliana LitsukoTomimatsu Shimauti; Danilo Grunig Humberto Silva; Eniuce Menezes de Souza; Eduardo Alves de Almeida; Francismar Prestes Leal; Claudia Regina Bonini-Domingos
Journal:  Genet Mol Biol       Date:  2015-08-21       Impact factor: 1.771
  6 in total

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