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Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis | Translational Psychiatry
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance
Precision medicine for the rescue of specific impairments in social behavior associated with the A350V Iqsec2 mutation | bioRxiv
IQSEC2 Research and Advocacy Foundation Research Grant Program 2023 — Orphan Disease Center
IJMS | Free Full-Text | Molecular Insights into IQSEC2 Disease
IQSEC2 - Research and Advocacy Foundation
Ca2+-induced release of IQSEC2/BRAG1 autoinhibition under physiological and pathological conditions | Journal of Cell Biology | Rockefeller University Press
Grant Opportunities — Orphan Disease Center
PDF) IQSEC2 Deficiency Results in Abnormal Social Behaviors Relevant to Autism by Affecting Functions of Neural Circuits in the Medial Prefrontal Cortex
AMA.LE PER LA DISABILITÀ | Reale Foundation
AMA.LE PER LA DISABILITÀ | Reale Foundation
RCSB PDB - 6FAE: The Sec7 domain of IQSEC2 (Brag1) in complex with the small GTPase Arf1
Children | Free Full-Text | Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey
IQSEC2 - Research and Advocacy Foundation
tigercece – Associazione AMA.le IQSEC2
Alba ama AMA.le: missione compiuta! – Associazione AMA.le IQSEC2
IQSEC2 - Research and Advocacy Foundation
Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis | Translational Psychiatry
Deep phenotyping of 14 new patients with IQSEC2 variants, including monozygotic twins of discordant phenotype - Radley - 2019 - Clinical Genetics - Wiley Online Library
Fundraiser for Associazione AMA.le by Danila Borio : IQSEC2: DONA UN SOSTEGNO ALLA RICERCA
Structural and Functional Brain-wide Alterations in A350V IQSEC2 Mutant Mice Displaying Autistic-like Behavior | bioRxiv
Kasr Al Ainy Faculty of Medicine International Affairs | Cairo
Si raccolgono fondi per un camp inclusivo per bambini disabili e normodotati
PDF) Natural Course of IQSEC2-Related Encephalopathy: An Italian National Structured Survey
Fighting Rare Iqsec2 & VWMD Axel & Aria
IQSEC2 - Research and Advocacy Foundation
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females | Life Science Alliance