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BMC Medical Genetics|June 4, 2009
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and reviewLuis Fernández, Julián Nevado, Fernando Santos, et al.
Journal of Immunology (Baltimore, Md. : 1950)|June 17, 2022
Profibrotic Role of Inducible Heat Shock Protein 90α Isoform in Systemic SclerosisJorge RuizdelRio, Pedro Muñoz, Patricia Carreira, et al.
Marine Pollution Bulletin|September 10, 2025
Remote sensing and image analysis of macro-plastic litter: A reviewShin'ichiro Kako, Tomoya Kataoka, Daisuke Matsuoka, et al.
Journal of the American Society of Nephrology : JASN|April 6, 2023
Unbiased Human Kidney Tissue Proteomics Identifies Matrix Metalloproteinase 7 as a Kidney Disease BiomarkerDaigoro Hirohama, Amin Abedini, Salina Moon, et al.
Frontiers in Public Health|May 25, 2026
Place your bet on change: the Young Adult Action Collective leading community-academic partnership efforts to understand and address gambling harms in Springfield, MAGeraldine Puerto, Theresa Glenn, Linnea A Evans, et al.
Pediatric Dermatology|April 3, 2025
Multifocal PIK3CA Related Congenital HemangiomaPatricia Andres-Ibarrola, Irune Méndez Maestro, Aitor Fernádez de Larrinoa Santamaría, et al.
Critical Reviews in Toxicology|May 26, 2021
Methodological considerations for measuring biofluid-based microRNA biomarkersBrian N Chorley, Elnaz Atabakhsh, Graeme Doran, et al.
Pediatric Dermatology|August 20, 2024
Segmental congenital vascular anomaly with atrophy, ulceration, and scarring (SeCVAUS): Case series and review of literatureMarta Ivars, Ilona J Frieden, Lauren Provini, et al.
The Journal of Experimental Medicine|December 29, 2018
Somatic activating mutations in <i>PIK3CA</i> cause generalized lymphatic anomalyLara Rodriguez-Laguna, Noelia Agra, Kristina Ibañez, et al.
Clinical Genetics|July 9, 2021
A standard of care for individuals with PIK3CA-related disorders: An international expert consensus statementSofia Douzgou, Myfanwy Rawson, Eulalia Baselga, et al.
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