Atypical β-S haplotypes: classification and genetic modulation in patients with sickle cell anemia

[1]  Sunetra Gupta,et al.  Understanding the contrasting spatial haplotype patterns of malaria-protective β-globin polymorphisms , 2015, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[2]  Jéssika V Okumura,et al.  Severity of Brazilian sickle cell disease patients: severity scores and feasibility of the Bayesian network model use. , 2015, Blood cells, molecules & diseases.

[3]  C. Bonini-Domingos,et al.  Screening of Transcription Factors Involved in Fetal Hemoglobin Regulation Using Phylogenetic Footprinting , 2015, Evolutionary bioinformatics online.

[4]  David J. Arenillas,et al.  JASPAR 2014: an extensively expanded and updated open-access database of transcription factor binding profiles , 2013, Nucleic Acids Res..

[5]  Janet S. Lee,et al.  The relationship between the severity of hemolysis, clinical manifestations and risk of death in 415 patients with sickle cell anemia in the US and Europe , 2013, Haematologica.

[6]  R. P. Gonçalves,et al.  DNA damage in leukocytes of sickle cell anemia patients is associated with hydroxyurea therapy and with HBB*S haplotype. , 2012, Mutation research.

[7]  Daniel E Bauer,et al.  Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders. , 2012, Blood.

[8]  D. Tuan,et al.  NF-Y Recruits Both Transcription Activator and Repressor to Modulate Tissue- and Developmental Stage-Specific Expression of Human γ-Globin Gene , 2012, PloS one.

[9]  M. Gladwin,et al.  Sickle-cell disease , 2010, The Lancet.

[10]  T. Boehm,et al.  Essential role of c-myb in definitive hematopoiesis is evolutionarily conserved , 2010, Proceedings of the National Academy of Sciences.

[11]  S. Orkin,et al.  Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6. , 2010, Genes & development.

[12]  María M. Abad-Grau,et al.  A network model to predict the risk of death in sickle cell disease. , 2007, Blood.

[13]  D. Kwiatkowski,et al.  Classical sickle beta-globin haplotypes exhibit a high degree of long-range haplotype similarity in African and Afro-Caribbean populations , 2007, BMC Genetics.

[14]  Mark A. Hall,et al.  The Role of p22 NF-E4 in Human Globin Gene Switching* , 2004, Journal of Biological Chemistry.

[15]  D. Labie,et al.  A novel sickle cell mutation of yet another origin in Africa: the Cameroon type , 1992, Human Genetics.

[16]  Wyeth W. Wasserman,et al.  JASPAR: an open-access database for eukaryotic transcription factor binding profiles , 2004, Nucleic Acids Res..

[17]  A. Schechter,et al.  Levels of GATA-1/GATA-2 transcription factors modulate expression of embryonic and fetal hemoglobins. , 2000, Gene.

[18]  J. Krieger,et al.  Atypical βs haplotypes are generated by diverse genetic mechanisms , 2000 .

[19]  M. Hutz,et al.  Atypical beta(s) haplotypes are generated by diverse genetic mechanisms. , 2000, American journal of hematology.

[20]  M L Terrin,et al.  Fetal hemoglobin in sickle cell anemia: determinants of response to hydroxyurea. Multicenter Study of Hydroxyurea. , 1997, Blood.

[21]  Graham R Serjeant,et al.  Sickle-cell disease , 1984, The Lancet.

[22]  D. Powars,et al.  Sickle cell anemia. Beta s gene cluster haplotypes as genetic markers for severe disease expression. , 1993, American journal of diseases of children.

[23]  D. Labie,et al.  A novel sickle gene of yet another origin in Africa: The Cameroon type , 1992 .

[24]  D. Powars.  Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features. , 1991, Hematology/oncology clinics of North America.

[25]  W. Schroeder,et al.  Beta S-gene-cluster haplotypes in sickle cell anemia: clinical implications. , 1990, The American journal of pediatric hematology/oncology.

[26]  R. Nagel,et al.  Polymerase chain reaction amplification applied to the determination of β‐like globin gene cluster haplotypes , 1989, American journal of hematology.

[27]  D. Labie,et al.  Atypical haplotypes linked to the βs gene in Africa are likely to be the product of recombination , 1988 .

[28]  D. Labie,et al.  The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level. , 1987, Blood.

[29]  A. Kulozik,et al.  Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation. , 1986, American journal of human genetics.

[30]  W. G. Hill,et al.  Nonuniform recombination within the human beta-globin gene cluster. , 1986, American journal of human genetics.

[31]  K. Mullis,et al.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.

[32]  K. Buetow,et al.  Nonuniform recombination within the human beta-globin gene cluster. , 1984, American journal of human genetics.

[33]  D. Labie,et al.  Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[34]  D. Labie,et al.  Sickle gene. Its origin and diffusion from West Africa. , 1981, The Journal of clinical investigation.

[35]  Y. Kan,et al.  Polymorphism of DNA sequence adjacent to human beta-globin structural gene: relationship to sickle mutation. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[36]  V. Ingram,et al.  Gene Mutations in Human Hæmoglobin: the Chemical Difference Between Normal and Sickle Cell Hæmoglobin , 1957, Nature.