Publications by authors named "Gift Pule"

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Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening.
Maddalena Martella, Mimma Campeggio, Gift Pulè, Ambroise Wonkam, Federica Menzato

Front Pediatr· April 2022

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Genetic modifiers of long-term survival in sickle cell anemia.
Ambroise Wonkam, Emile R Chimusa, Khuthala Mnika, Gift Dineo Pule, Valentina Josiane Ngo Bitoungui

Clin Transl Med· August 2020

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Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa.
Khuthala Mnika, Gaston K Mazandu, Mario Jonas, Gift D Pule, Emile R Chimusa

Front Genet· May 2019

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Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon.
Amy Geard, Gift D Pule, Bernard Chetcha Chemegni, Valentina J Ngo Bitoungui, Andre P Kengne

Br J Haematol· August 2017

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SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon.
Gift Dineo Pule, Valentina Josiane Ngo Bitoungui, Bernard Chetcha Chemegni, Andre Pascal Kengne, Ambroise Wonkam

BMC Res Notes· May 2017

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Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon.
Gift D Pule, Valentina J Ngo Bitoungui, Bernard Chetcha Chemegni, Andre P Kengne, Ambroise Wonkam

Hemoglobin· November 2016

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An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.
Khuthala Mnika, Gift D Pule, Collet Dandara, Ambroise Wonkam

OMICS· October 2016

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Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa.
Amy Geard, Gift D Pule, David Chelo, Valentina Josiane Ngo Bitoungui, Ambroise Wonkam

OMICS· October 2016

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Proceedings of a Sickle Cell Disease Ontology workshop - Towards the first comprehensive ontology for Sickle Cell Disease.
Nicola Mulder, Victoria Nembaware, Adekunle Adekile, Kofi A Anie, Baba Inusa, Gift Pule

Appl Transl Genom· June 2016

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Hydroxyurea down-regulates BCL11A, KLF-1 and MYB through miRNA-mediated actions to induce γ-globin expression: implications for new therapeutic approaches of sickle cell disease.
Gift Dineo Pule, Shaheen Mowla, Nicolas Novitzky, Ambroise Wonkam

Clin Transl Med· March 2016

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A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease.
Gift D Pule, Shaheen Mowla, Nicolas Novitzky, Charles S Wiysonge, Ambroise Wonkam

Expert Rev Hematol· October 2015

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Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions.
Gift Dineo Pule, Valentina Josiane Ngo Bitoungui, Bernard Chetcha Chemegni, Andre Pascal Kengne, Stylianos Antonarakis

OMICS· October 2015

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Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation?
Gift Pule, Ambroise Wonkam

Pan Afr Med J· June 2015

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Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?
Valentina J Ngo Bitoungui, Gift D Pule, Neil Hanchard, Jeanne Ngogang, Ambroise Wonkam

OMICS· March 2015

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