Literature DB >> 14717773

Genetic insights into the clinical diversity of beta thalassaemia.

Swee Lay Thein1.   

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Year:  2004        PMID： 14717773     DOI： 10.1046/j.1365-2141.2003.04769.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  23 in total

Review 1.  Hemoglobin research and the origins of molecular medicine.

Authors:  Alan N Schechter
Journal:  Blood       Date:  2008-11-15       Impact factor: 22.113

2.  Phenotypic effect of α-globin gene numbers on Indian sickle β-thalassemia patients.

Authors:  Sanjay Kumar Pandey; Sweta Pandey; Ravi Ranjan; Vineet Shah; Rahasya Mani Mishra; Monica Sharma; Renu Saxena
Journal:  J Clin Lab Anal       Date:  2014-01-06       Impact factor: 2.352

3.  Alterations in expression and chromatin configuration of the alpha hemoglobin-stabilizing protein gene in erythroid Kruppel-like factor-deficient mice.

Authors:  Andre M Pilon; Douglas G Nilson; Dewang Zhou; Jose Sangerman; Tim M Townes; David M Bodine; Patrick G Gallagher
Journal:  Mol Cell Biol       Date:  2006-06       Impact factor: 4.272

4.  Terephthalamide-containing ligands: fast removal of iron from transferrin.

Authors:  Rebecca J Abergel; Kenneth N Raymond
Journal:  J Biol Inorg Chem       Date:  2007-11-08       Impact factor: 3.358

5.  Molecular basis of transfusion dependent beta-thalassemia major patients in Sabah.

Authors:  Lai Kuan Teh; Elizabeth George; Mei I Lai; Jin Ai Mary Anne Tan; Lily Wong; Patimah Ismail
Journal:  J Hum Genet       Date:  2013-12-26       Impact factor: 3.172

6.  Hypercoagulability in splenectomized thalassemic patients detected by whole-blood thromboelastometry, but not by thrombin generation in platelet-poor plasma.

Authors:  Armando Tripodi; Maria Domenica Cappellini; Veena Chantarangkul; Lidia Padovan; Maria Rosaria Fasulo; Alessia Marcon; Pier Mannuccio Mannucci
Journal:  Haematologica       Date:  2009-07-31       Impact factor: 9.941

7.  Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome.

Authors:  Anna Marrone; Amanda Walne; Hannah Tamary; Yuka Masunari; Michael Kirwan; Richard Beswick; Tom Vulliamy; Inderjeet Dokal
Journal:  Blood       Date:  2007-09-04       Impact factor: 22.113

8.  Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.

Authors:  L Jouini; C A Sahli; N Laaouini; F Ouali; I Ben Youssef; B Dakhlaoui; R Othmeni; F Ouennich; S Hadj Fredj; H Siala; M Becher; N E Toumi; S Fattoum; R Hafsia; A Bibi; T Messaoud
Journal:  Mol Biol Rep       Date:  2013-09-25       Impact factor: 2.316

Review 9.  β-Thalassemia intermedia: a comprehensive overview and novel approaches.

Authors:  Chingiz Asadov; Zohra Alimirzoeva; Tahira Mammadova; Gunay Aliyeva; Shahla Gafarova; Jeyhun Mammadov
Journal:  Int J Hematol       Date:  2018-01-29       Impact factor: 2.490

10.  Relaxed functional constraints on triplicate α-globin gene in the bank vole suggest a different evolutionary history from other rodents.

Authors:  S Marková; J B Searle; P Kotlík
Journal:  Heredity (Edinb)       Date:  2014-03-05       Impact factor: 3.821
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