Celia Menendez-Lopez
Madrid, MD 28029, Spain
Last Updated: 09/26/2026
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Found 11 publications
Kidins220-deficient hydrocephalus mice exhibit altered glial phenotypes and AQP4 differential regulation in the retina and optic nerve, with preserved retinal ganglion cell survival.
Journal: Fluids and barriers of the CNS
Published: September 11, 2024
Refining the phenotype of SINO syndrome: A comprehensive cohort report of 14 novel cases.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 12, 2024
Correction: Lysyl Oxidase-like Protein LOXL2 Promotes Lung Metastasis of Breast Cancer.
Journal: Cancer research
Published: March 15, 2023
Kidins220 sets the threshold for survival of neural stem cells and progenitors to sustain adult neurogenesis.
Journal: Cell death & disease
Published: September 29, 2022
E2A Modulates Stemness, Metastasis, and Therapeutic Resistance of Breast Cancer.
Journal: Cancer research
Published: August 10, 2020
Kidins220 deficiency causes ventriculomegaly via SNX27-retromer-dependent AQP4 degradation.
Journal: Molecular psychiatry
Published: July 14, 2020
Excitotoxic targeting of Kidins220 to the Golgi apparatus precedes calpain cleavage of Rap1-activation complexes.
Journal: Cell death & disease
Published: December 19, 2018
Lysyl Oxidase-like Protein LOXL2 Promotes Lung Metastasis of Breast Cancer.
Journal: Cancer research
Published: November 18, 2016
Development of a neuroprotective peptide that preserves survival pathways by preventing Kidins220/ARMS calpain processing induced by excitotoxicity.
Journal: Cell death & disease
Published: June 03, 2015
Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalance.
Journal: Human molecular genetics
Published: November 03, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026