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Acta Dermato-Venereologica|June 30, 2026
Distinctive Reactivity to the C-terminal Epitope of BP180 Characterizes Immune Checkpoint Inhibitor-associated Bullous Pemphigoid, and an ELISA Based on the BP180 Ectodomain Enables Prompt Diagnosis in a Subset of PatientsAnna Pira, Martina Merli, Feliciana Mariotti, et al.Frontiers in Psychiatry|March 9, 2026
The role of gene-environment interactions in endocrine-sensitive life stages for shaping mental health: focus on the RE-MEND projectKhawla Abualia, Andrea Cediel-Ulloa, Philip Allsopp, et al.Science (New York, N.Y.)|February 17, 2022
From cohorts to molecules: Adverse impacts of endocrine disrupting mixturesNicolò Caporale, Michelle Leemans, Lina Birgersson, et al.Nature Communications|April 21, 2021
Epigenomic landscape of human colorectal cancer unveils an aberrant core of pan-cancer enhancers orchestrated by YAP/TAZGiulia Della Chiara, Federica Gervasoni, Michaela Fakiola, et al.Nature Communications|October 9, 2020
JMJD3 acts in tandem with KLF4 to facilitate reprogramming to pluripotencyYinghua Huang, Hui Zhang, Lulu Wang, et al.SSM. Qualitative Research in Health|September 12, 2022
Democratic research: Setting up a research commons for a qualitative, comparative, longitudinal interview study during the COVID-19 pandemicBettina M Zimmermann, Hendrik Wagenaar, Katharina Kieslich, et al.ALTEX|April 16, 2025
Developmental neurotoxicity (DNT): A call for implementation of new approach methodologies for regulatory purposes: Summary of the 5th International Conference on DNT TestingIvana Celardo, Michael Aschner, Randolph S Ashton, et al.Ophthalmology and Therapy|January 31, 2022
Development and Implementation of the AIDA International Registry for Patients with Non-Infectious UveitisFrancesca Della Casa, Antonio Vitale, Silvana Guerriero, et al.Nature|September 7, 2020
LifeTime and improving European healthcare through cell-based interceptive medicineNikolaus Rajewsky, Geneviève Almouzni, Stanislaw A Gorski, et al.American Journal of Human Genetics|June 3, 2017
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin DysfunctionMichele Gabriele, Anneke T Vulto-van Silfhout, Pierre-Luc Germain, et al.Pageof 14