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Frontiers in Immunology|December 3, 2025
Case Report: Durable response to tumor-infiltrating lymphocyte therapy in a patient with metastatic melanoma and chronic lymphocytic leukemia/small lymphocytic lymphomaLilit Karapetyan, Joel Kuriakose, Matthew C Perez, et al.
Clinical Endocrinology|July 5, 2022
Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia RegistryNeil Lawrence, Irina Bacila, Jeremy Dawson, et al.
The New England Journal of Medicine|May 5, 2015
Long-term effect of gene therapy on Leber's congenital amaurosisJames W B Bainbridge, Manjit S Mehat, Venki Sundaram, et al.
MMWR. Morbidity and Mortality Weekly Report|June 15, 2023
Genomic Surveillance for SARS-CoV-2 Variants: Circulation of Omicron Lineages - United States, January 2022-May 2023Kevin C Ma, Philip Shirk, Anastasia S Lambrou, et al.
Nature|June 6, 2020
A calcineurin-Hoxb13 axis regulates growth mode of mammalian cardiomyocytesNgoc Uyen Nhi Nguyen, Diana C Canseco, Feng Xiao, et al.
Human Genome Variation|February 5, 2021
Prevalence of pharmacogenomic variants in 100 pharmacogenes among Southeast Asian populations under the collaboration of the Southeast Asian Pharmacogenomics Research Network (SEAPharm)Chakkaphan Runcharoen, Koya Fukunaga, Insee Sensorn, et al.
European Journal of Endocrinology|October 14, 2023
Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort studyMariska A M Schröder, Mihaela Neacşu, Bas P H Adriaansen, et al.
La Clinica Terapeutica|April 28, 2026
Time-Threshold Dose-Response Relationship Between Duration of Premature Rupture of Membranes and Maternal, Neonatal, and Laboratory Evidence of Infection: A Systematic Review and Meta-AnalysisIman Shawky Hassan, Aziza Hussein Nassef, Mariam Salah Mohamed Emam, et al.
Cancer Cell|May 8, 2026
Dendritic cell redundancy enables priming of anti-tumor CD4<sup>+</sup> T cells in pancreatic cancerCourtney T S Kureshi, Michael J Walsh, Rakeeb Kureshi, et al.
Human Genetics|March 3, 2017
Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic featuresJing Zhang, Tomasz Gambin, Bo Yuan, et al.
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