Found: 16
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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
- Published in:
- Indian Journal of Dermatology, Venereology & Leprology, 2023, v. 89, n. 2, p. 247, doi. 10.25259/IJDVL_988_19
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- Publication type:
- Article
Spontaneously Occurring micronuclei in infiltrating ductal carcinoma of breast: A potential biomarker for aggressive phenotype detection?
- Published in:
- Diagnostic Cytopathology, 2013, v. 41, n. 4, p. 296, doi. 10.1002/dc.21836
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- Publication type:
- Article
Ileosigmoid Knotting Causing Double-Lumen Acute Intestinal Obstruction and Gangrene- Review and a Case Report.
- Published in:
- Journal of Clinical & Diagnostic Research, 2020, v. 14, n. 10, p. 6, doi. 10.7860/JCDR/2020/45118.14130
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- Publication type:
- Article
STAT3-Mediated Transcriptional Regulation of Osteopontin in STAT3 Loss-of-Function Related Hyper IgE Syndrome.
- Published in:
- Frontiers in Immunology, 2018, p. 1, doi. 10.3389/fimmu.2018.01080
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- Article
Isolated Gastric Perforation following Blunt Trauma Abdomen not to be Missed: A Case Series.
- Published in:
- 2024
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- Publication type:
- Case Study
Distinct use of super-enhancer elements controls cell type–specific CD25 transcription and function.
- Published in:
- Science Immunology, 2023, v. 8, n. 89, p. 1, doi. 10.1126/sciimmunol.adi8217
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- Publication type:
- Article
An Indian Family with Autosomal Dominant Hyper-IgE Syndrome Due to IL6ST Defect.
- Published in:
- Journal of Clinical Immunology, 2024, v. 44, n. 4, p. 1, doi. 10.1007/s10875-024-01695-9
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- Publication type:
- Article
CARD9 Expression Pattern, Gene Dosage, and Immunodeficiency Phenotype Revisited.
- Published in:
- Journal of Clinical Immunology, 2022, v. 42, n. 2, p. 336, doi. 10.1007/s10875-021-01173-6
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- Publication type:
- Article
Correction to: A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
- Published in:
- 2020
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- Publication type:
- Correction Notice
A Nonsense N –Terminus NFKB2 Mutation Leading to Haploinsufficiency in a Patient with a Predominantly Antibody Deficiency.
- Published in:
- Journal of Clinical Immunology, 2020, v. 40, n. 8, p. 1093, doi. 10.1007/s10875-020-00842-2
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- Publication type:
- Article
Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.
- Published in:
- 2019
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- Publication type:
- Letter
Severe Aspergillus Pneumonia and Pulmonary Artery Hypertension in a Child with Autosomal Recessive Chronic Granulomatous Disease and Selective IgA Deficiency.
- Published in:
- 2017
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- Publication type:
- Letter
Hyper-IgE syndrome with a novel STAT3 mutation-a single center study from India.
- Published in:
- Asian Pacific Journal of Allergy & Immunology, 2014, v. 32, n. 4, p. 321, doi. 10.12932/ap0456.32.4.2014
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- Publication type:
- Article
Novel Mutation in SH2 Domain of STAT3 (p.M660T) in Hyper-IgE Syndrome with Sterno-Clavicular and Paravertebral Abscesses.
- Published in:
- 2017
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- Publication type:
- Case Study
TH17 Cells in STAT3 Related Hyper-IgE Syndrome.
- Published in:
- 2016
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- Publication type:
- journal article
Expression of γH2AX may help in defining a genetically more stable subtype of infiltrating ductal carcinoma of breast.
- Published in:
- Indian Journal of Medical Research, 2013, v. 137, n. 4, p. 759
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- Publication type:
- Article