HuGE Literature Finder
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| The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation. Journal of human genetics 2021 Oct . Luo Shiqiang, Chen Xingyuan, Zeng Dingyuan, Tang Ning, Yuan Dejian, Zhong Qingyan, Mao Aiping, Xu Ruofan, Yan Tizh |
| Modulatory effect of single nucleotide polymorphism in Xmn1, BCL11A and HBS1L-MYB loci on foetal haemoglobin levels in ß-thalassemia major and Intermedia patients. JPMA. The Journal of the Pakistan Medical Association 2021 May 71 (5): 1394-1398. Bashir Shabnam, Mahmood Saqib, Mohsin Shahida, Tabassum Iqra, Ghafoor Mahmood, Sajjad Oshe |
| Association Between Genetic Polymorphisms and Hb F Levels in Heterozygous ß-Thalassemia 3.5?kb Deletions. Hemoglobin 2020 Sep 1-6. Tepakhan Wanicha, Kanjanaopas Sataron, Srewaradachpisal Kornt |
| Multi-Locus Models to Address Hb F Variability in Portuguese ß-Thalassemia Carriers. Hemoglobin 2020 Apr 1-5. Manco Licínio, Bento Celeste, Relvas Luís, Cunha Elisabete, Pereira Janet, Moreira Valeria, Alvarez Manuela, Maia Tabita, Ribeiro M Letíc |
| The association of HBG2, BCL11A, and HBS1L-MYB polymorphisms to thalidomide response in Chinese ß-thalassemia patients. Blood cells, molecules & diseases 2020 Apr 84 102442. Yang Kun, Wu Yi, Ma Yanni, Xiao Jian, Zhou Yali, Yin Xiaol |
| Molecular Analysis of Non-Transfusion Dependent Thalassemia Associated with Hemoglobin E-ß-Thalassemia Disease without a-Thalassemia. Mediterranean journal of hematology and infectious diseases 2019 11 (1): e2019038. Phanrahan Paramee, Yamsri Supawadee, Teawtrakul Nattiya, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Fucharoen Sup |
| Xmn1-158 ?GVariant in B-Thalassemia Intermediate Patients in South-East of Iran. International journal of hematology-oncology and stem cell research 2017 Apr 11 (2): 165-171. Miri-Moghaddam Ebrahim, Bahrami Sara, Naderi Majid, Bazi Ali, Karimipoor Morte |
| The Sickle ß-Thalassemia Phenotype. Journal of pediatric hematology/oncology 2017 Jan . Adekile Adekunle D, Akbulut Nagihan, Azab Asmaa F, Al-Sharida Sundus, Thomas Dia |
| 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 association between four SNPs (rs7482144, rs4671393, rs28384513 and rs4895441) and fetal hemoglobin levels in Chinese Zhuang ß-thalassemia intermedia patients. Blood cells, molecules & diseases 2017 03 63 52-57. Lai Yunli, Zhou Lin, Yi Sheng, Chen Yun, Tang Yanqing, Yi Shang, Yang Ze, Wei Hongwei, Zheng Chenguang, He She |
| A Multi-locus Approach to Characterization of Major Quantitative Trait Loci Influencing Hb F Regulation in Chinese ß-thalassemia Carriers. Hemoglobin 2016 Oct 1-12. Chan Nelson C N, Lau Kin-Mang, Cheng Kelvin C K, Chan Natalie P H, Ng Margaret H |
| Electromobility Shift Assay Reveals Evidence in Favor of Allele-Specific Binding of RUNX1 to the 5' Hypersensitive Site 4-Locus Control Region. Hemoglobin 2016 Aug 40 (4): 236-9. Dehghani Hossein, Ghobakhloo Sepideh, Neishabury Mary |
| 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 |
| A genetic score for the prediction of beta-thalassemia severity. Haematologica 2015 Apr 100 (4): 452-7. Danjou Fabrice, Francavilla Marcella, Anni Franco, Satta Stefania, Demartis Franca-Rosa, Perseu Lucia, Manca Matteo, Sollaino Maria Carla, Manunza Laura, Mereu Elisabetta, Marceddu Giuseppe, Pissard Serge, Joly Philippe, Thuret Isabelle, Origa Raffaella, Borg Joseph, Forni Gian Luca, Piga Antonio, Lai Maria Eliana, Badens Catherine, Moi Paolo, Galanello Ren |
| Polymorphic variations influencing fetal hemoglobin levels: association study in beta-thalassemia carriers and in normal individuals of Portuguese origin. Blood cells, molecules & diseases 2015 Apr 54 (4): 315-20. Pereira Clara, Relvas Luís, Bento Celeste, Abade Augusto, Ribeiro M Letícia, Manco Licín |
| Genetic Modifiers in ß-Thalassemia Intermedia: A Study on 102 Iraqi Arab Patients. Genetic testing and molecular biomarkers 2015 Mar . Al-Allawi Nasir A S, Puehringer Helene, Raheem Ruzaiqah A, Oberkanins Christi |
| 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 |
| Influence of Xmn 1(G)? (HBG2 c.-211 C ? T) Globin Gene Polymorphism on Phenotype of Thalassemia Patients of North India. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2014 Dec 30 (4): 286-90. Kumar Ravindra, Kaur Anupriya, Agarwal Sari |
| The influence of the BCL11A polymorphism on the phenotype of patients with beta thalassemia could be affected by the beta globin locus control region and/or the Xmn1-HBG2 genotypic background. Blood cells, molecules & diseases 2013 Aug 51 (2): 80-4. Neishabury Maryam, Zamani Fahimeh, Keyhani Elahe, Azarkeivan Azita, Abedini Seyedeh Sedigheh, Eslami Masumeh Sadat, Kakroodi Setareh Talebi, Vesiehsari Mahjoobeh Jafari, Najmabadi Hosse |
| 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 |
| 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 |
| 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 |
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- Page last updated:Jan 20, 2022
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