Fingerprint
- 1 Similar Profiles
Collaborations and top research areas from the last five years
Projects
- 1 Finished
-
Structure: Structure-function analysis of glutamate receptor activity
Eibl, C. (PI)
18.01.2021 → 17.01.2022
Project: Other Research
Research output
-
A biallelic mutation in CACNA2D2 associated with developmental and epileptic encephalopathy affects channel dependent as well as synaptic functions of α2δ-2
Haddad, S., Obermair, G., Stanika, R., Hessenberger, M., Ablinger, C., Eibl, C., Tuluc, P., Campiglio, M. & Ortner, N., Feb 2025.Research output: Contribution to conference › Oral presentation at a conference
-
Consequences of neurological disorder-associated mutations of α2δ subunits on calcium channel trafficking and synaptic composition
Haddad, S., Obermair, G., Hessenberger, M., Stanika, R., Eibl, C., Ablinger, C., Ortner, N., Campiglio, M. & Tuluc, P., May 2025.Research output: Contribution to conference › Oral presentation at a conference
-
Involvement of CACNA2D2 in developmental and epileptic encephalopathy through disruption of calcium channel functionality and synaptic function
Essid, M. (Presenter), Haddad, S., Fraize, J., Jallouli, O., Alvi, J., Bakhtiari, S., Ben Hafsa, M., Benrhouma, H., Bouchaala, W., Burger, R., Cai, E., Chand, P., Chatron, N., Darvish, H., Efthymiou, S., Galaz Montoya, C., Haider, S., Houlden, H., Jelani, M. & Khan, H. & 18 others, , 03 Sept 2025.Research output: Contribution to conference › Oral presentation at a conference
-
Involvement of CACNA2D2 in developmental and epileptic encephalopathy through disruption of calcium channel functionality and synaptic function
Essid, M. (Presenter), Haddad, S., Fraize, J., Jallouli, O., Alvi, J., Bakhtiari, S., Ben Hafsa, M., Benrhouma, H., Bouchaala, W., Burger, R., Cai, E., Chand, P., Chatron, N., Darvish, H., Efthymiou, S., Galaz Montoya, C., Haider, S., Houlden, H., Jelani, M. & Khan, H. & 18 others, , 24 May 2025.Research output: Contribution to conference › Poster at a conference
-
Pathophysiological mechanisms of the R788C mutation in α2δ-2 associated with early infantile epileptic encephalopathy
Lindner, S. (Presenter), Sikora, A., Essid, M., Schulreich, S.-M., Haddad, S., Eibl, C., Stanika, R., Hessenberger, M., Lesca, G. & Obermair, G., 08 Sept 2025.Research output: Contribution to conference › Poster at a conference
Activities
- 39 Organising an event (Science to science)
-
From genetics to revelation: discovering molecular mechanisms from the social life of a worm.
de Bono, M. (Speaker), Eibl, C. (Organiser) & Witalisz-Siepracka, A. (Organiser)
18 Dec 2024Activity: Participating in/organising an event › Organising an event (Science to science)
-
Phosphoinositide switches in lysosome homeostasis and damage control
Ebner, M. (Speaker), Eibl, C. (Organiser) & Witalisz-Siepracka, A. (Organiser)
11 Dec 2024Activity: Participating in/organising an event › Organising an event (Science to science)
-
Dissecting tumor and immune heterogeneity in breast cancer metastasis
Winkler, J. (Speaker), Eibl, C. (Organiser) & Witalisz-Siepracka, A. (Organiser)
04 Dec 2024Activity: Participating in/organising an event › Organising an event (Science to science)
-
Modeling clonal hematopoiesis and leukemogenesis in primary human hematopoietic stem and progenitor cells
Reinisch, A. (Speaker), Eibl, C. (Organiser) & Witalisz-Siepracka, A. (Organiser)
20 Nov 2024Activity: Participating in/organising an event › Organising an event (Science to science)
-
A full, dynamic view of neural stem cell quiescence
Urban, N. (Speaker), Eibl, C. (Organiser) & Witalisz-Siepracka, A. (Organiser)
13 Nov 2024Activity: Participating in/organising an event › Organising an event (Science to science)