Found: 24
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Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1.
- Published in:
- Human Genetics, 2005, v. 118, n. 3/4, p. 348, doi. 10.1007/s00439-005-0036-6
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- Article
The Cxcr2<sup>+</sup> subset of the S100a8<sup>+</sup> gastric granylocytic myeloid-derived suppressor cell population (G-MDSC) regulates gastric pathology.
- Published in:
- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1147695
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- Article
Dual NADPH oxidases DUOX1 and DUOX2 synthesize NAADP and are necessary for Ca<sup>2+</sup> signaling during T cell activation.
- Published in:
- Science Signaling, 2021, v. 14, n. 709, p. 1, doi. 10.1126/scisignal.abe3800
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- Article
Helicobacter pylori Antimicrobial Susceptibility Testing-Guided Salvage Therapy in the USA: A Real Life Experience.
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- 2018
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- Publication type:
- journal article
Dual Oxidase 2 Bidirectional Promoter Polymorphisms Confer Differential Immune Responses in Airway Epithelia.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2012, v. 47, n. 4, p. 484, doi. 10.1165/rcmb.2012-0037oc
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- Article
Congenital Neonatal Hyperthyroidism Caused by Germline Mutations in the TSH Receptor Gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2008, v. 21, n. 5, p. 479, doi. 10.1515/jpem.2008.21.5.479
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- Article
Mutations in the NKX2.5 gene and the PAX8 promoter in a girl with thyroid dysgenesis.
- Published in:
- 2011
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- Publication type:
- journal article
A single copy of the recently identified dual oxidase maturation factor (DUOXA) 1 gene produces only mild transient hypothyroidism in a patient with a novel biallelic DUOXA2 mutation and monoallelic DUOXA1 deletion.
- Published in:
- 2011
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- Publication type:
- journal article
Loss-of-function mutations in the thyrotropin receptor gene as a major determinant of hyperthyrotropinemia in a consanguineous community.
- Published in:
- 2009
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- Publication type:
- journal article
Biallelic inactivation of the dual oxidase maturation factor 2 (DUOXA2) gene as a novel cause of congenital hypothyroidism.
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- 2008
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- Publication type:
- journal article
A Familial Thyrotropin (TSH) Receptor Mutation Provides in Vivo Evidence that the Inositol Phosphates/Ca<sup>2+</sup> Cascade Mediates TSH Action on Thyroid Hormone Synthesis.
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- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2816, doi. 10.1210/jc.2007-0366
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- Publication type:
- Article
C-Terminal Amino Acid Alteration rather than Late Termination Causes Complete Deficiency of Thyroxine-Binding Globulin CD-NeuIsenburg.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 3215, doi. 10.1210/jc.2005-2261
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- Publication type:
- Article
A Novel Thyroid Hormone Receptor-β Mutation That Fails to Bind Nuclear Receptor Corepressor in a Patient as an Apparent Cause of Severe, Predominantly Pituitary Resistance to Thyroid Hormone.
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- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 5, p. 1887, doi. 10.1210/jc.2005-2428
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- Article
Autosomal Dominant Resistance to Thyrotropin as a Distinct Entity in Five Multigenerational Kindreds: Clinical Characterization and Exclusion of Candidate Loci.
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- Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 7, p. 4025, doi. 10.1210/jc.2005-0572
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- Publication type:
- Article
Identification of Thyroxine-Binding Globulin-San Diego in a Family from Houston and Its Characterization by in Vitro Expression Using Xenopus Oocytes.
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- Journal of Clinical Endocrinology & Metabolism, 2000, v. 85, n. 1, p. 368, doi. 10.1210/jcem.85.1.6317
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- Publication type:
- Article
Identification of a Functional TPH1 Polymorphism Associated With Irritable Bowel Syndrome Bowel Habit Subtypes.
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- American Journal of Gastroenterology (Springer Nature), 2013, v. 108, n. 11, p. 1766, doi. 10.1038/ajg.2013.304
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- Article
Aberrant Cerebellar Development in Mice Lacking Dual Oxidase Maturation Factors.
- Published in:
- Thyroid, 2016, v. 26, n. 5, p. 741, doi. 10.1089/thy.2015.0034
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- Article
Two Cases of Thyroid Dysgenesis Caused by Different Novel PAX8 Mutations in the DNA-Binding Region: In Vitro Studies Reveal Different Pathogenic Mechanisms.
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- Thyroid, 2013, v. 23, n. 7, p. 791, doi. 10.1089/thy.2012.0141
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- Publication type:
- Article
A Somatic Gain-of-Function Mutation in the Thyrotropin Receptor Gene Producing a Toxic Adenoma in an Infant.
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- Thyroid, 2009, v. 19, n. 2, p. 187, doi. 10.1089/thy.2008.0302
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- Article
Resistance to Thyroid Hormone in a Patient with Thyroid Dysgenesis.
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- Thyroid, 2005, v. 15, n. 7, p. 730
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- Publication type:
- Article
CD4<sup>+</sup> Tissue-resident Memory T Cells Expand and Are a Major Source of Mucosal Tumour Necrosis Factor α in Active Crohn's Disease.
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- Journal of Crohn's & Colitis, 2019, v. 13, n. 7, p. 905, doi. 10.1093/ecco-jcc/jjz010
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- Publication type:
- Article
Dendritic cell‐derived TGF‐β mediates the induction of mucosal regulatory T‐cell response to Helicobacter infection essential for maintenance of immune tolerance in mice.
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- Helicobacter, 2020, v. 25, n. 6, p. 1, doi. 10.1111/hel.12763
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- Publication type:
- Article
Cochlear Structure and Hearing in Murine Congenital Hypothyroidism Caused by Targeted Gene Mutations in the Mouse Dual Oxidase A1 and A2 Genes.
- Published in:
- Laryngoscope, 2011, v. 121, n. S5, p. S324, doi. 10.1002/lary.22280
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- Article
DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease risk.
- Published in:
- Journal of Clinical Investigation, 2021, v. 131, n. 9, p. 1, doi. 10.1172/jci141676
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- Publication type:
- Article