Pediatría
Departamento
University of California, San Francisco
San Francisco, Estados UnidosPublicaciones en colaboración con investigadoras/es de University of California, San Francisco (12)
2023
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Admixture mapping of severe asthma exacerbations in Hispanic/Latino children and youth
Thorax, Vol. 78, Núm. 3, pp. 233-241
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Human genetics influences microbiome composition involved in asthma exacerbations despite inhaled corticosteroid treatment
Journal of Allergy and Clinical Immunology, Vol. 152, Núm. 3, pp. 799-806.e6
2022
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Multi-ancestry genome-wide association study of asthma exacerbations
Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, Vol. 33, Núm. 6, pp. e13802
2021
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Genome-wide association study of asthma exacerbations despite inhaled corticosteroid use
European Respiratory Journal, Vol. 57, Núm. 5
2020
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Rare Germline DICER1 Variants in Pediatric Patients With Cushing's Disease: What Is Their Role?
Frontiers in Endocrinology, Vol. 11
2014
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Interleukin-1 antagonism in type 1 diabetes of recent onset: Two multicenter, randomized double-masked, placebo-controlled trials
Diabetes Technology and Therapeutics
2013
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A novel method that improves sensitivity of protein detection in PAGE and Western blot
Electrophoresis, Vol. 34, Núm. 8, pp. 1148-1150
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Deletion of integrin-linked kinase from neural crest cells in mice results in aortic aneurysms and embryonic lethality
DMM Disease Models and Mechanisms, Vol. 6, Núm. 5, pp. 1205-1212
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Interleukin-1 antagonism in type 1 diabetes of recent onset: Two multicentre, randomised, double-blind, placebo-controlled trials
The Lancet, Vol. 381, Núm. 9881, pp. 1905-1915
2009
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Focal adhesion kinase is required for neural crest cell morphogenesis during mouse cardiovascular development
Journal of Clinical Investigation, Vol. 119, Núm. 8, pp. 2218-2230
2007
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CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders
American Journal of Human Genetics, Vol. 81, Núm. 1, pp. 104-113
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Deletion of integrin-linked kinase from skeletal muscles of mice resembles muscular dystrophy due to α7β1-integrin deficiency
American Journal of Pathology, Vol. 171, Núm. 6, pp. 1966-1977