Detalhe da pesquisa
1.
Macrophage-mediated extracellular matrix remodeling controls host Staphylococcus aureus susceptibility in the skin.
Immunity
; 56(7): 1561-1577.e9, 2023 07 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37402364
2.
Disruption of the endopeptidase ADAM10-Notch signaling axis leads to skin dysbiosis and innate lymphoid cell-mediated hair follicle destruction.
Immunity
; 54(10): 2321-2337.e10, 2021 10 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34582748
3.
TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies.
J Allergy Clin Immunol
; 152(3): 736-747, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37277074
4.
Germline IKAROS dimerization haploinsufficiency causes hematologic cytopenias and malignancies.
Blood
; 137(3): 349-363, 2021 01 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32845957
5.
CARD9 Expression Pattern, Gene Dosage, and Immunodeficiency Phenotype Revisited.
J Clin Immunol
; 42(2): 336-349, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34791587
6.
Expression of CD40 Ligand on T Cells and Soluble CD40 Ligand in Children With Kawasaki Disease: A Single-Center Preliminary Study From North India.
J Clin Rheumatol
; 27(5): 194-200, 2021 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31985724
7.
Correction to: A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
J Clin Immunol
; 40(8): 1102, 2020 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-32901356
8.
A Nonsense N -Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
J Clin Immunol
; 40(8): 1093-1101, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32813180
9.
An Indian Family with Autosomal Dominant Hyper-IgE Syndrome Due to IL6ST Defect.
J Clin Immunol
; 44(4): 90, 2024 Apr 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38578568
10.
Clinical and molecular features of X-linked hyper IgM syndrome - An experience from North India.
Clin Immunol
; 195: 59-66, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-30053428
11.
Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.
J Clin Immunol
; 39(6): 611-615, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31338742
12.
Hyper-IgE syndrome with a novel STAT3 mutation-a single center study from India.
Asian Pac J Allergy Immunol
; 32(4): 321-7, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25543043
13.
Expression of γH2AX may help in defining a genetically more stable subtype of infiltrating ductal carcinoma of breast.
Indian J Med Res
; 137(4): 759-66, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23703345
14.
Single-nucleotide polymorphism and haplotype analysis of macrophage migration inhibitory factor gene and its correlation with serum macrophage migration inhibitory factor levels in North Indian psoriatic patients with moderate disease severity: A cross-sectional study.
Indian J Dermatol Venereol Leprol
; 89(2): 247-253, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-34114423
15.
Distinct use of super-enhancer elements controls cell type-specific CD25 transcription and function.
Sci Immunol
; 8(89): eadi8217, 2023 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37922339
16.
Large BTK gene mutation in a child with X-linked agammaglobulinemia and polyarthritis.
Clin Immunol
; 183: 109-111, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28807838
17.
Severe Aspergillus Pneumonia and Pulmonary Artery Hypertension in a Child with Autosomal Recessive Chronic Granulomatous Disease and Selective IgA Deficiency.
J Clin Immunol
; 37(4): 333-335, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28342009
18.
Flow cytometry analysis of the subpopulations of mouse keratinocytes and skin immune cells.
STAR Protoc
; 3(1): 101052, 2022 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-34977690
19.
STAT3-Mediated Transcriptional Regulation of Osteopontin in STAT3 Loss-of-Function Related Hyper IgE Syndrome.
Front Immunol
; 9: 1080, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29868029
20.
TH17 Cells in STAT3 Related Hyper-IgE Syndrome.
Indian J Pediatr
; 83(10): 1104-8, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27226025