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Scientific Reports|October 8, 2020
Haploinsufficiency due to a novel ACO2 deletion causes mitochondrial dysfunction in fibroblasts from a patient with dominant optic nerve atrophyMarie Anne-Catherine Neumann, Dajana Grossmann, Simone Schimpf-Linzenbold, et al.
Translational Psychiatry|January 19, 2019
Fetal glucocorticoid receptor (Nr3c1) deficiency alters the landscape of DNA methylation of murine placenta in a sex-dependent manner and is associated to anxiety-like behavior in adulthoodMichaela Schmidt, Elad Lax, Rudy Zhou, et al.
Cancers|March 10, 2022
Randomized Phase 2 Study Comparing Pathological Responses of Resected Colorectal Cancer Metastases after Bevacizumab with mFOLFOX6 or FOLFIRI (BEV-ONCO Trial)Pamela Baldin, Javier Carrasco, Gabriela Beniuga, et al.
Nucleic Acids Research|October 17, 2017
Epigenetic mechanisms underlie the crosstalk between growth factors and a steroid hormoneYehoshua Enuka, Morris E Feldman, Animesh Chowdhury, et al.
Diabetes|April 24, 2019
Modified UCN2 Peptide Acts as an Insulin Sensitizer in Skeletal Muscle of Obese MiceMelissa L Borg, Julie Massart, Milena Schönke, et al.
Antioxidants & Redox Signaling|July 16, 2019
Mutations in RHOT1 Disrupt Endoplasmic Reticulum-Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's DiseaseDajana Grossmann, Clara Berenguer-Escuder, Marie Estelle Bellet, et al.
Clinical Kidney Journal|January 22, 2025
Current practices in prevention, screening, and treatment of diabetes in kidney transplant recipients: European survey highlights from the ERA DESCARTES Working GroupYassine Laghrib, Luuk Hilbrands, Gabriel C Oniscu, et al.
Journal of Chromatography. A|September 25, 2003
Interlaboratory study of a liquid chromatography method for erythromycin: determination of uncertaintyP Dehouck, Y Vander Heyden, J Smeyers-Verbeke, et al.
Human Genomics|March 1, 2023
Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritanceValerie Jacquemin, Nassim Versbraegen, Sarah Duerinckx, et al.
Human Mutation|November 8, 2019
Digenic inheritance of human primary microcephaly delineates centrosomal and non-centrosomal pathwaysSarah Duerinckx, Valérie Jacquemin, Séverine Drunat, et al.
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