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1.
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
2.
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
3.
Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease.
Front Pediatr
; 10: 895298, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35783297
4.
Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen.
Front Med (Lausanne)
; 8: 694668, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34249980
5.
Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients.
Saudi J Biol Sci
; 27(1): 271-278, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31889847
6.
Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease.
Saudi J Biol Sci
; 27(6): 1494-1502, 2020 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-32489286
7.
Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects.
Saudi J Biol Sci
; 27(1): 324-334, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31889854
8.
In Silico Approach to Investigate the Structural and Functional Attributes of Familial Hypercholesterolemia Variants Reported in the Saudi Population.
J Comput Biol
; 25(2): 170-181, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29172679
9.
Interpreting the Mechanism of APOE (p.Leu167del) Mutation in the Incidence of Familial Hypercholesterolemia; An In-silico Approach.
Open Cardiovasc Med J
; 11: 84-93, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-29204218
10.
The Spectrum of Familial Hypercholesterolemia (FH) in Saudi Arabia: Prime Time for Patient FH Registry.
Open Cardiovasc Med J
; 11: 66-75, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28868092
11.
Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients.
PLoS One
; 12(5): e0176664, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28505210
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