Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and HBG2[original query] |
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| DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America 2008 Aug 105 (33): 11869-74. Lettre Guillaume, Sankaran Vijay G, Bezerra Marcos André C, Araújo Aderson S, Uda Manuela, Sanna Serena, Cao Antonio, Schlessinger David, Costa Fernando F, Hirschhorn Joel N, Orkin Stuart |
| The XmnI (G)gamma polymorphism influences hemoglobin F synthesis contrary to BCL11A and HBS1L-MYB SNPs in a cohort of 57 beta-thalassemia intermedia patients. Blood cells, molecules & diseases 2010 Aug 45 (2): 124-7. Nguyen Thi Khanh Tien, Joly Philippe, Bardel Claire, Moulsma Mustapha, Bonello-Palot Nathalie, Francina Ala |
| Molecular analysis of ß-thalassemia patients: first identification of mutations HBB:c.93-2A>G and HBB:c.114G>A in Brazil. Hemoglobin 2011 35 (4): 358-66. Fernandes Andrea Cristina, Shimmoto Marily Maria Azevedo, Furuzawa Gilberto Koiti, Vicari Perla, Figueiredo Maria Stel |
| Genetic modifiers of ß-thalassemia and clinical severity as assessed by age at first transfusion. Haematologica 2012 Jul 97 (7): 989-93. Danjou Fabrice, Anni Franco, Perseu Lucia, Satta Stefania, Dessì Carlo, Lai Maria Eliana, Fortina Paolo, Devoto Marcella, Galanello Ren |
| Genetic variants at HbF-modifier loci moderate anemia and leukocytosis in sickle cell disease in Tanzania. American journal of hematology 2015 Jan 90 (1): E1-4. Mtatiro Siana Nkya, Makani Julie, Mmbando Bruno, Thein Swee Lay, Menzel Stephan, Cox Sharon |
| Genetics of fetal hemoglobin in tribal Indian patients with sickle cell anemia. Translational research : the journal of laboratory and clinical medicine 2015 Jun 165 (6): 696-703. Bhanushali Aparna A, Patra Pradip K, Pradhan Smarnika, Khanka Suraj S, Singh Sujata, Das Bibhu |
| The Impact of XmnI-HBG2, BCL11A and HBS1L-MYB Single Nucleotide Polymorphisms on Hb F Variation of Hematologically Normal Iranian Individuals. Hemoglobin 2016 Jun 40 (3): 198-201. Keyhani Elaheh, Jafari Vesiehsari Mahjoobeh, Talebi Kakroodi Setareh, Darabi Elham, Zamani Fahimeh, Karimlou Masoud, Kamali Koorosh, Neishabury Mary |
| The role of BCL11A and HMIP-2 polymorphisms on endogenous and hydroxyurea induced levels of fetal hemoglobin in sickle cell anemia patients from southern Brazil. Blood cells, molecules & diseases 2016 Nov 62 32-37. Friedrisch João Ricardo, Sheehan Vivien, Flanagan Jonathan M, Baldan Alessandro, Summarell Carly C Ginter, Bittar Christina Matzembacher, Friedrisch Bruno Kras, Wilke Ianaê Indiara, Ribeiro Camila Blos, Daudt Liane Esteves, da Rocha Silla Lucia Maria |
| Existence of HbF Enhancer Haplotypes at HBS1L-MYB Intergenic Region in Transfusion-Dependent Saudi ß-Thalassemia Patients. BioMed research international 2017 2017 1972429. Cyrus Cyril, Vatte Chittibabu, Borgio J Francis, Al-Rubaish Abdullah, Chathoth Shahanas, Nasserullah Zaki A, Jarrash Sana Al, Sulaiman Ahmed, Qutub Hatem, Alsaleem Hassan, Alzahrani Alhusain J, Steinberg Martin H, Ali Amein K |
| The Sickle ?-Thalassemia Phenotype. Journal of pediatric hematology/oncology 2017 Jan . Adekile Adekunle D, Akbulut Nagihan, Azab Asmaa F, Al-Sharida Sundus, Thomas Dia |
| The association of HBG2, BCL11A, and HMIP polymorphisms with fetal hemoglobin and clinical phenotype in Iraqi Kurds with sickle cell disease. International journal of laboratory hematology 2018 Sep . Al-Allawi Nasir, Qadir Shatha M A, Puehringer Helene, Chui David H K, Farrell John J, Oberkanins Christi |
| A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia. PloS one 2018 6 13 (6): e0197927. Adeyemo Titilope A, Ojewunmi Oyesola O, Oyetunji Idat A, Rooks Helen, Rees David C, Akinsulie Adebola O, Akanmu Alani S, Thein Swee Lay, Menzel Steph |
| g(HbF): a genetic model of fetal hemoglobin in sickle cell disease. Blood advances 2018 2 2 (3): 235-239. Gardner Kate, Fulford Tony, Silver Nicholas, Rooks Helen, Angelis Nikolaos, Allman Marlene, Nkya Siana, Makani Julie, Howard Jo, Kesse-Adu Rachel, Rees David C, Stuart-Smith Sara, Yeghen Tullie, Awogbade Moji, Sangeda Raphael Z, Mgaya Josephine, Patel Hamel, Newhouse Stephen, Menzel Stephan, Thein Swee L |
| Genetic modulators of fetal hemoglobin expression and ischemic stroke occurrence in African descendant children with sickle cell anemia. Annals of hematology 2019 9 98 (12): 2673-2681. Nicolau Marta, Vargas Sofia, Silva Marisa, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Kjöllerström Paula, Maia Raquel, Silva Rita, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Faustino Pau |
| Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in Tanzania. BMC medical genetics 2020 Jun 21 (1): 125. Nkya Siana, Mwita Liberata, Mgaya Josephine, Kumburu Happiness, van Zwetselaar Marco, Menzel Stephan, Mazandu Gaston Kuzamunu, Sangeda Raphael, Chimusa Emile, Makani Jul |
| Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA in ?-thalassaemia carriers. Archives of medical science : AMS 2021 8 17 (4): 1064-1074. Cyrus Cyril, Vatte Chittibabu, Chathoth Shahanas, Sayed Abdul Azeez, Borgio J Francis, Alrubaish Mohammed Abdullah, Alfalah Rawan, Alsaikhan Jana, Al Ali Amein |
| Genotypic Diversity among Angolan Children with Sickle Cell Anemia. International journal of environmental research and public health 2021 6 18 (10): . Delgadinho Mariana, Ginete Catarina, Santos Brígida, Miranda Armandina, Brito Migu |
| Detection of Transversions and Transitions in HBG2 Cis-Elements Associated with Sickle Cell Allele in Ghanaians. Biochemical genetics 2023 7 . G K Ababio, I Ekem, J Acquaye, S Y Oppong, A G B Amoah, J Brandful, I K Qua |
| Genotyping the BCL11A Single Nucleotide Polymorphism and Associated Levels of Fetal Hemoglobin in Mauritanian Sickle Cell Patients. Frontiers in bioscience (Scholar edition) 2024 6 16 (2): 11. Aminetou Taleb Brahim, Mariem Taleb, Harouna Soumaré, Sidi Mohamed Ghaber, Aminetou Mohamed, Ali Ould Mohamed Salem Boukha |
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