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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.
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
6.
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
7.
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
8.
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
9.
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
10.
Paget's disease: a review of the epidemiology, etiology, genetics, and treatment.
Front Genet
; 14: 1131182, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37180975
11.
The use of therapeutic drug monitoring for early identification of vedolizumab response in Saudi Arabian patients with inflammatory bowel disease.
Sci Rep
; 13(1): 1771, 2023 01 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-36720977
12.
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
13.
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
14.
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
15.
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
16.
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
17.
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
18.
Bioinformatics insights into the genes and pathways on severe COVID-19 pathology in patients with comorbidities.
Front Physiol
; 13: 1045469, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36589459
19.
A comparative mRNA- and miRNA transcriptomics reveals novel molecular signatures associated with metastatic prostate cancers.
Front Genet
; 13: 1066118, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36468011
20.
Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients.
Front Pediatr
; 10: 895074, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35692981