Detalhe da pesquisa
1.
Inborn Errors of RNA Lariat Metabolism in Humans with Brainstem Viral Infection.
Cell
; 172(5): 952-965.e18, 2018 02 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29474921
2.
Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease.
Proc Natl Acad Sci U S A
; 118(15)2021 04 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-33876776
3.
Fulminant Viral Hepatitis in Two Siblings with Inherited IL-10RB Deficiency.
J Clin Immunol
; 43(2): 406-420, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36308662
4.
JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.
N Engl J Med
; 382(3): 256-265, 2020 01 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-31940699
5.
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease.
Nat Immunol
; 12(3): 213-21, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21278736
6.
Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency.
J Immunol
; 207(1): 133-152, 2021 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34183371
7.
A disorder clinically resembling cystic fibrosis caused by biallelic variants in the AGR2 gene.
J Med Genet
; 59(10): 993-1001, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34952832
8.
Enhanced Infiltration of Central Memory T Cells to the Lung Tissue during Allergic Lung Inflammation.
Int Arch Allergy Immunol
; 183(2): 127-141, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34818243
9.
Clinical and Immunological Characterization of Combined Immunodeficiency Due to TFRC Mutation in Eight Patients.
J Clin Immunol
; 40(8): 1103-1110, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32851577
10.
Graft Versus Host Disease Following HLA-Matched Sibling Donor Compared with Matched Related Donor for Hematopoietic Stem Cell Transplantation for the Treatment of Severe Combined Immunodeficiency Disease.
J Clin Immunol
; 39(4): 414-420, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31041574
11.
Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis.
Immunity
; 33(3): 400-11, 2010 Sep 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-20832341
12.
Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency.
Proc Natl Acad Sci U S A
; 113(51): E8277-E8285, 2016 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27930337
13.
Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.
J Clin Immunol
; 38(3): 278-282, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29589181
14.
Association of IL-13 rs20541 and rs1295686 variants with symptomatic asthma in a Saudi Arabian population.
J Asthma
; 55(11): 1157-1165, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29211635
15.
Impaired intrinsic immunity to HSV-1 in human iPSC-derived TLR3-deficient CNS cells.
Nature
; 491(7426): 769-73, 2012 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-23103873
16.
Th-17 regulatory cytokines IL-21, IL-23, and IL-6 enhance neutrophil production of IL-17 cytokines during asthma.
J Asthma
; 54(9): 893-904, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28635548
17.
Risk factors hindering asthma symptom control in Saudi children and adolescents.
Pediatr Int
; 59(6): 661-668, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28218986
18.
Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
J Allergy Clin Immunol
; 137(6): 1780-1787, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26915675
19.
Prevalence of UDP-glucuronosyltransferase polymorphisms (UGT1A6∗2, 1A7∗12, 1A8∗3, 1A9∗3, 2B7∗2, and 2B15∗2) in a Saudi population.
Saudi Pharm J
; 25(2): 224-230, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28344472
20.
Th-17 regulatory cytokines inhibit corticosteroid induced airway structural cells apoptosis.
Respir Res
; 17: 6, 2016 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-26772733