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Gift Dineo Pule
Observed names:
G D Pule,
G. D. Pule,
Gift D Pule,
Gift D. Pule,
Gift Pule,
Gift Pulè,
Pule, Gift
show all 7
Institution:
University of Cape Town
Observed institutions:
National Health Laboratory Service,
University of Cape Town,
Institute of Infectious Disease and Molecular Medicine
OpenAlex ID:
A5050201122
A systematic review of known mechanisms of hydroxyurea-induced fetal hemoglobin for treatment of sickle cell disease
2015
·
Gift D Pule
, Shaheen Mowla
, et al.
·
Expert Review of Hematology
·
97
Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon
2017
·
Amy Geard
, Gift D. Pule
, et al.
·
British Journal of Haematology
·
73
PDF
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
2016
·
Gift Dineo Pule
, Shaheen Mowla
, et al.
·
Clinical and Translational Medicine
·
55
PDF
Beta-Globin Gene Haplotypes Among Cameroonians and Review of the Global Distribution: Is There a Case for a Single Sickle Mutation Origin in Africa?
2015
·
Valentina J. Ngo Bitoungui
, Gift D. Pule
, et al.
·
OMICS A Journal of Integrative Biology
·
53
Genetic modifiers of long‐term survival in sickle cell anemia
2020
·
Ambroise Wonkam
, Emile R. Chimusa
, et al.
·
Clinical and Translational Medicine
·
35
Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa
2019
·
Khuthala Mnika
, Gaston K. Mazandu
, et al.
·
Frontiers in Genetics
·
28
PDF
Association between Variants at BCL11A Erythroid-Specific Enhancer and Fetal Hemoglobin Levels among Sickle Cell Disease Patients in Cameroon: Implications for Future Therapeutic Interventions
2015
·
Gift Dineo Pule
, Valentina Josiane Ngo Bitoungui
, et al.
·
OMICS A Journal of Integrative Biology
·
23
Proceedings of a Sickle Cell Disease Ontology workshop — Towards the first comprehensive ontology for Sickle Cell Disease
2016
·
Nicola Mulder
, Victoria Nembaware
, et al.
·
Applied & Translational Genomics
·
19
An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine
2016
·
Khuthala Mnika
, Gift D. Pule
, et al.
·
OMICS A Journal of Integrative Biology
·
17
Beta-globin gene haplotypes and selected Malaria-associated variants among black Southern African populations
2017
·
G. D. Pule
, E. R. Chimusa
, et al.
·
Global Health
·
14
PDF
Treatment for sickle cell disease in Africa: should we invest in haematopoietic stem cell transplantation?
2014
·
Gift Pule
, Ambroise Wonkam
·
Pan African Medical Journal
·
10
Distribution of HbS Allele and Haplotypes in a Multi-Ethnic Population of Guinea Bissau, West Africa: Implications for Public Health Screening
2022
·
Maddalena Martella
, Mimma Campeggio
, et al.
·
Frontiers in Pediatrics
·
9
Genetics of Sickle Cell-Associated Cardiovascular Disease: An Expert Review with Lessons Learned in Africa
2016
·
Amy Geard
, Gift D. Pule
, et al.
·
OMICS A Journal of Integrative Biology
·
8
Burden, genotype and phenotype profiles of adult patients with sickle cell disease in Cape Town, South Africa
2017
·
G D Pule
, K Mnica
, et al.
·
South African Medical Journal
·
7
PDF
Studies of novel variants associated with Hb F in Sardinians and Tanzanians in sickle cell disease patients from Cameroon
2016
·
Gift D. Pule
, Valentina J. Ngo Bitoungui
, et al.
·
Hemoglobin
·
5
SAR1a promoter polymorphisms are not associated with fetal hemoglobin in patients with sickle cell disease from Cameroon
2017
·
Gift Dineo Pule
, Valentina Josiane Ngo Bitoungui
, et al.
·
BMC Research Notes
·
4
PDF
Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease
2016
·
Gift D. Pule
·
Open University of Cape Town (University of Cape Town)
PDF
MOESM5 of 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
2016
·
Pule, Gift
, Mowla, Shaheen
, et al.
·
Figshare
MOESM3 of 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
2016
·
Pule, Gift
, Mowla, Shaheen
, et al.
·
Figshare
MOESM2 of 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
2016
·
Pule, Gift
, Mowla, Shaheen
, et al.
·
Figshare
MOESM1 of 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
2016
·
Pule, Gift
, Mowla, Shaheen
, et al.
·
Figshare
MOESM4 of 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
2016
·
Pule, Gift
, Mowla, Shaheen
, et al.
·
Figshare
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Works count:
28
Citation count:
461
H-index:
10
I10-index:
11
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