147 results on '"Brown, Milton R."'
Search Results
2. Children with Neutrophil-Predominant Severe Asthma Have Proinflammatory Neutrophils With Enhanced Survival and Impaired Clearance
3. Resistin is elevated in cystic fibrosis sputum and correlates negatively with lung function
4. Systemic Corticosteroid Responses in Children with Severe Asthma: Phenotypic and Endotypic Features
5. Neutrophil Dysfunction in the Airways of Children with Acute Respiratory Failure Due to Lower Respiratory Tract Viral and Bacterial Coinfections
6. Cysteine oxidation impairs systemic glucocorticoid responsiveness in children with difficult-to-treat asthma
7. The effects of hydroxyurea and bone marrow transplant on Anti-Müllerian hormone (AMH) levels in females with sickle cell anemia
8. Molecular Basis of Multiple Pituitary Hormone Deficiency
9. Neutrophil-derived extracellular vesicles promote feed-forward inflammasome signaling in cystic fibrosis airways
10. Pilot study of inflammatory biomarkers in matched induced sputum and bronchoalveolar lavage of 2‐year‐olds with cystic fibrosis.
11. Functional and Transcriptional Adaptations of Blood Monocytes Recruited to the Cystic Fibrosis Airway Microenvironment In Vitro
12. Association of Glutathione-S-Transferase-P1 (GST-P1) Polymorphisms with Bronchopulmonary Dysplasia
13. Faster pharmacokinetics and increased patient acceptance of intradermal insulin delivery using a single hollow microneedle in children and adolescents with type 1 diabetes
14. Susceptibility to Childhood-Onset Rheumatoid Arthritis: Investigation of a Weighted Genetic Risk Score That Integrates Cumulative Effects of Variants at Five Genetic Loci
15. Hierarchy of risk of childhood-onset rheumatoid arthritis conferred by HLA–DRB1 alleles encoding the shared epitope
16. Distinct compartmentalization of immune cells and mediators characterizes bullous pemphigoid disease
17. A Mutational Hot Spot in the Prop-1 Gene in Russian Children with Combined Pituitary Hormone Deficiency
18. Association of Glutathione-S-Transferase-P1 (GSTP1) Polymorphism 105 Ile>Val with Chronic Lung Disease in Preterm Infants
19. Novel Patterns of Gene Expression in Pituitary Adenomas Identified by Complementary Deoxyribonucleic Acid Microarrays and Quantitative Reverse Transcription-Polymerase Chain Reaction*
20. Heritable Disorders of Pituitary Development*
21. Clinical and Biochemical Phenotype of Familial Anterior Hypopituitarism from Mutation of the PROP1 Gene*
22. Elastase Exocytosis by Airway Neutrophils Is Associated with Early Lung Damage in Children with Cystic Fibrosis
23. Genetic Polymorphisms Associated with Idiopathic Short Stature and First-Year Response to Growth Hormone Treatment
24. Exogenous Nitric Oxide Enhances Neutrophil Cell Death and DNA Fragmentation
25. The spectrum of growth-hormone insensitivity
26. Frontline Science: Pathological conditioning of human neutrophils recruited to the airway milieu in cystic fibrosis
27. Case-control Association Study of Autoimmunity Associated Variants in PDCD1 and Juvenile Idiopathic Arthritis
28. Transcription factors regulating pituitary development
29. Response
30. Children with Neutrophil-Predominant Severe Asthma Have Proinflammatory Neutrophils With Enhanced Survival and Impaired Clearance
31. Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations
32. Mature Cystic Fibrosis Airway Neutrophils Suppress T Cell Function: Evidence for a Role of Arginase 1 but Not Programmed Death-Ligand 1
33. Anti-Mullerian hormone levels in American girls by age and race/ethnicity
34. Meta-analysis confirms association between TNFA- G238A variant and JIA, and between PTPN22-C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA
35. Brief Report: Susceptibility to Childhood-Onset Rheumatoid Arthritis: Investigation of a Weighted Genetic Risk Score That Integrates Cumulative Effects of Variants at Five Genetic Loci
36. Anti-Mullerian hormone levels in American girls by age and race/ethnicity.
37. Association of Glutathione-S-Transferase-P1 (GST-P1) Polymorphisms with Bronchopulmonary Dysplasia
38. The spectrum of hypopituitarism caused by PROP1 mutations
39. Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations
40. Effect of Helicobacter pylori infection on mucin gene regulation in vitro
41. Short stature in carriers of recessive mutation causing familial isolated growth hormone deficiency
42. Meta-analysis confirms association between TNFAG238A variant and JIA, and between PTPN22- C1858T variant and oligoarticular, RF-polyarticular and RF-positive polyarticular JIA.
43. Mutations in PROP1 cause familial combined pituitary hormone deficiency
44. Central Hypothyroidism Reveals Compound Heterozygous Mutations in the Pit-1 Gene
45. Pituitary Adenomas: Screening for Gαq Mutations
46. MULTIPLE MUTATIONS IN A GH-R ALLELE. ▴ 514
47. Abnormalities of the Pituitary-specific Transcription Factor-1 Gene and Protein
48. Human Splicing Variation of PIT-1 mRNA in A Family with GH, PRL and TSH Deficiency
49. Abnormalities of the Human Growth Hormone Gene
50. Genetics of Growth Hormone Gene Expression
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.