Detalles de la búsqueda
1.
Exploring the predictive power of jejunal microbiome composition in clinical and subclinical necrotic enteritis caused by Clostridium perfringens: insights from a broiler chicken model.
J Transl Med
; 22(1): 80, 2024 Jan 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-38243294
2.
Molecular design, synthesis and biological characterization of novel Resveratrol derivative as potential anticancer agent targeting NF-κB.
J Appl Biomed
; 18(1): 8-17, 2020 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-34907703
3.
Assessment of insertion/deletion polymorphism of ACE gene as a genetic risk marker for preeclampsia in pregnant women.
J Pak Med Assoc
; 70(5): 791-795, 2020 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-32400729
4.
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
5.
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
6.
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
7.
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
8.
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
9.
Variations in the GST activity are associated with single and combinations of GST genotypes in both male and female diabetic patients.
Mol Biol Rep
; 41(2): 841-8, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24381101
10.
Functional genomics based prioritization of potential nsSNPs in EPHX1, GSTT1, GSTM1 and GSTP1 genes for breast cancer susceptibility studies.
Genomics
; 99(6): 330-9, 2012 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-22564471
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.
Anti-angiogenic effect of nano-formulated water soluble kaempferol and combretastatin in an in vivo chick chorioallantoic membrane model and HUVEC cells.
Biomed Pharmacother
; 163: 114820, 2023 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-37141736
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.
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
16.
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
17.
No evidence for the role of somatic mutations and promoter hypermethylation of FH gene in the tumorigenesis of nonsyndromic uterine leiomyomas.
Tumour Biol
; 33(5): 1411-8, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-22528940
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.
Granulomatous hepatitis in a Saudi child with IL2RA defect: a case report and literature review.
Ther Adv Chronic Dis
; 13: 20406223221116798, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35968218