Associated Papers
The CRISPR-Cas9 induced CCR5 Δ32 mutation as a potent gene therapy methodology for resistance to HIV-1 variant: a review.
Saifullah M et al.
European Review for Medical and Pharmacological Sciences, 2024
Bi-allelic mutation in SEC16B alters collagen trafficking and increases ER stress.
El-Gazzar A et al.
Embo Molecular Medicine, 2023
36916446 (PubMed )
Supplement: EMMM-15-e16834-s012.xlsx › WES_SEC16B_mutant
Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium.
Milne RL et al.
Human Molecular Genetics, 2014
Large-scale polymorphism discovery in macaque G-protein coupled receptors.
Goswami DB et al.
Bmc Genomics, 2013
24119066 (PubMed )
Supplement: 1471-2164-14-703-S4.xlsx › Sheet1
Inherited variants in regulatory T cell genes and outcome of ovarian cancer.
Goode EL et al.
Plos One, 2013
23382860 (PubMed )
Supplement: pone.0053903.s002.xlsx › Supplemental_Table_2
Role of exonic variation in chemokine receptor genes on AIDS: CCRL2 F167Y association with pneumocystis pneumonia.
An P et al.
Plos Genetics, 2011
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