Records 1 - 5
| Functional polymorphisms of BCL11A and HBS1L-MYB genes affect both fetal hemoglobin level and clinical outcomes in a cohort of children with sickle cell anemia.
Annals of hematology 2020 May .
Sales Rahyssa Rodrigues, Belisário André Rolim, Faria Gabriela, Mendes Fabiola, Luizon Marcelo Rizzatti, Viana Marcos Bora
| Role of metabolic syndrome and its components as mediators of the genetic effect on type 2 diabetes: A family-based study in China.
Journal of diabetes 2019 Jul 11 (7): 552-562.
Song Jing, Jiang Xia, Juan Juan, Cao Yaying, Chibnik Lori B, Hofman Albert, Wu Tao, Hu Yongh
| Nine known and five novel mutations in the erythroid transcription factor KLF1 gene and phenotypic expression of fetal hemoglobin in hemoglobin E disorder.
Blood cells, molecules & diseases 2016 Jul 59 85-91.
Tepakhan Wanicha, Yamsri Supawadee, Sanchaisuriya Kanokwan, Fucharoen Goonnapa, Xu Xiangmin, Fucharoen Sup
| The Association of Type 2 Diabetes Loci Identified in Genome-Wide Association Studies with Metabolic Syndrome and Its Components in a Chinese Population with Type 2 Diabetes.
PloS one 2015 10 (11): e0143607.
Kong Xiaomu, Zhang Xuelian, Xing Xiaoyan, Zhang Bo, Hong Jing, Yang Wenyi
| Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysis.
Blood cells, molecules & diseases 0 53 (1-2): 11-5.
Pakdee Naruwat, Yamsri Supawadee, Fucharoen Goonnapa, Sanchaisuriya Kanokwan, Pissard Serge, Fucharoen Sup