Conlin L, Landrum M, Freimuth R, Funke B
Clin Chem. 2025; 71(1):45-53.
PMID: 39749501
PMC: 11695870.
DOI: 10.1093/clinchem/hvae195.
Shao C, Liu Q, Xu J, Zhang J, Zhang C, Xin Y
Mol Ther Nucleic Acids. 2024; 35(4):102371.
PMID: 39640014
PMC: 11617223.
DOI: 10.1016/j.omtn.2024.102371.
Wongkhammul N, Khamphikham P, Tongjai S, Tantiworawit A, Fanhchaksai K, Wongpalee S
Int J Mol Sci. 2024; 25(20).
PMID: 39457028
PMC: 11508986.
DOI: 10.3390/ijms252011246.
Panyasai S, Satthakarn S, Phasit A
Heliyon. 2023; 9(8):e19116.
PMID: 37649848
PMC: 10462817.
DOI: 10.1016/j.heliyon.2023.e19116.
Ho A, Hurst L
Genome Biol Evol. 2022; 14(8).
PMID: 35867377
PMC: 9348620.
DOI: 10.1093/gbe/evac115.
Unusual mammalian usage of TGA stop codons reveals that sequence conservation need not imply purifying selection.
Ho A, Hurst L
PLoS Biol. 2022; 20(5):e3001588.
PMID: 35550630
PMC: 9129041.
DOI: 10.1371/journal.pbio.3001588.
Alpha thalassemia genotypes in Kuwait.
Adekile A, Sukumaran J, Thomas D, DSouza T, Haider M
BMC Med Genet. 2020; 21(1):170.
PMID: 32831051
PMC: 7444039.
DOI: 10.1186/s12881-020-01105-y.
Effective Population Size Predicts Local Rates but Not Local Mitigation of Read-through Errors.
Ho A, Hurst L
Mol Biol Evol. 2020; 38(1):244-262.
PMID: 32797190
PMC: 7783166.
DOI: 10.1093/molbev/msaa210.
Trans-Species Polymorphism in Mitochondrial Genome of Camarodont Sea Urchins.
Balakirev E
Genes (Basel). 2019; 10(8).
PMID: 31387337
PMC: 6723515.
DOI: 10.3390/genes10080592.
Identification of MYLK3 mutations in familial dilated cardiomyopathy.
Tobita T, Nomura S, Morita H, Ko T, Fujita T, Toko H
Sci Rep. 2017; 7(1):17495.
PMID: 29235529
PMC: 5727479.
DOI: 10.1038/s41598-017-17769-1.
Translation readthrough mitigation.
Arribere J, Cenik E, Jain N, Hess G, Lee C, Bassik M
Nature. 2016; 534(7609):719-23.
PMID: 27281202
PMC: 5054982.
DOI: 10.1038/nature18308.
DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia.
Tan J, Kho S, Ngim C, Chua K, Goh A, Yeoh S
Sci Rep. 2016; 6:26994.
PMID: 27271331
PMC: 4897612.
DOI: 10.1038/srep26994.
Hemoglobin Constant Spring among Southeast Asian Populations: Haplotypic Heterogeneities and Phylogenetic Analysis.
Jomoui W, Fucharoen G, Sanchaisuriya K, Nguyen V, Fucharoen S
PLoS One. 2015; 10(12):e0145230.
PMID: 26683994
PMC: 4686174.
DOI: 10.1371/journal.pone.0145230.
Alpha-thalassemia mutations in adana province, southern Turkey: genotype-phenotype correlation.
Bozdogan S, Yuregir O, Buyukkurt N, Aslan H, Ozdemir Z, Gambin T
Indian J Hematol Blood Transfus. 2015; 31(2):223-8.
PMID: 25825562
PMC: 4375160.
DOI: 10.1007/s12288-014-0406-0.
AUF-1 and YB-1 independently regulate β-globin mRNA in developing erythroid cells through interactions with poly(A)-binding protein.
van Zalen S, Lombardi A, Jeschke G, Hexner E, Russell J
Mech Dev. 2015; 136:40-52.
PMID: 25720531
PMC: 4390516.
DOI: 10.1016/j.mod.2015.02.003.
A journey in science: early lessons from the hemoglobin field.
Weatherall D
Mol Med. 2014; 20:478-85.
PMID: 25548947
PMC: 4277548.
DOI: 10.2119/molmed.2014.00093.
Hemoglobin variants: biochemical properties and clinical correlates.
Thom C, Dickson C, Gell D, Weiss M
Cold Spring Harb Perspect Med. 2013; 3(3):a011858.
PMID: 23388674
PMC: 3579210.
DOI: 10.1101/cshperspect.a011858.
Molecular characterisation of Haemoglobin Constant Spring and Haemoglobin Quong Sze with a Combine-Amplification Refractory Mutation System.
Wee Y, Tan K, Chua K, George E, Tan J
Malays J Med Sci. 2012; 16(3):21-8.
PMID: 22589661
PMC: 3329134.
Abnormal haemoglobins: detection & characterization.
Wajcman H, Moradkhani K
Indian J Med Res. 2011; 134:538-46.
PMID: 22089618
PMC: 3237254.
An RNA-protein complex links enhanced nuclear 3' processing with cytoplasmic mRNA stabilization.
Ji X, Kong J, Liebhaber S
EMBO J. 2011; 30(13):2622-33.
PMID: 21623344
PMC: 3155305.
DOI: 10.1038/emboj.2011.171.
