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1.
Myocardial infarction biomarker discovery with integrated gene expression, pathways and biological networks analysis.
Genomics
; 112(6): 5072-5085, 2020 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-32920122
2.
Molecular insights into the coding region mutations of low-density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia.
J Gene Med
; 22(6): e3176, 2020 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-32073192
3.
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.
Hum Mol Genet
; 26(16): 3031-3045, 2017 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28521042
4.
Protein phenotype diagnosis of autosomal dominant calmodulin mutations causing irregular heart rhythms.
J Cell Biochem
; 119(10): 8233-8248, 2018 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-29932249
5.
Computational Analysis of Breast Cancer GWAS Loci Identifies the Putative Deleterious Effect of STXBP4 and ZNF404 Gene Variants.
J Cell Biochem
; 118(12): 4296-4307, 2017 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-28422318
6.
Comprehensive Computational Analysis of GWAS Loci Identifies CCR2 as a Candidate Gene for Celiac Disease Pathogenesis.
J Cell Biochem
; 118(8): 2193-2207, 2017 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-28059456
7.
Distribution of CYP2C8 and CYP2C9 amino acid substitution alleles in South Indian diabetes patients: A genotypic and computational protein phenotype study.
Clin Exp Pharmacol Physiol
; 44(12): 1171-1179, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28686288
8.
Replication of GWAS loci revealed the moderate effect of TNRC6B locus on susceptibility of Saudi women to develop uterine leiomyomas.
J Obstet Gynaecol Res
; 43(2): 330-338, 2017 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-27987337
9.
A Computational Protein Phenotype Prediction Approach to Analyze the Deleterious Mutations of Human MED12 Gene.
J Cell Biochem
; 117(9): 2023-35, 2016 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-26813965
10.
Evidence for the presence of somatic mitochondrial DNA mutations in right atrial appendage tissues of coronary artery disease patients.
Mol Genet Genomics
; 289(4): 533-40, 2014 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-24604425
11.
Paget's disease: a review of the epidemiology, etiology, genetics, and treatment.
Front Genet
; 14: 1131182, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37180975
12.
Combining machine learning and structure-based approaches to develop oncogene PIM kinase inhibitors.
Front Chem
; 11: 1137444, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36970406
13.
Identification and functional characterization of two rare LDLR stop gain variants (p.C231* and p.R744*) in Saudi familial hypercholesterolemia patients.
Panminerva Med
; 65(4): 479-490, 2023 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35274909
14.
Protein structural insights into a rare PCSK9 gain-of-function variant (R496W) causing familial hypercholesterolemia in a Saudi family: whole exome sequencing and computational analysis.
Front Physiol
; 14: 1204018, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37469559
15.
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot.
Gene
; 851: 146909, 2023 Jan 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-36162527
16.
Potential Biomarkers for Parkinson Disease from Functional Enrichment and Bioinformatic Analysis of Global Gene Expression Patterns of Blood and Substantia Nigra Tissues.
Bioinform Biol Insights
; 17: 11779322231166214, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37153842
17.
Rare variant burden analysis from exomes of three consanguineous families reveals LILRB1 and PRSS3 as potential key proteins in inflammatory bowel disease pathogenesis.
Front Med (Lausanne)
; 10: 1164305, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37215724
18.
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease.
Front Pediatr
; 10: 837957, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35237542
19.
Identification of miRNA-mRNA-TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches.
PLoS One
; 17(10): e0271262, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36264868
20.
Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer.
PLoS One
; 17(10): e0274629, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36194576