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Debora Tibbe

Showing results (1-10 of 10) with videos related to

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Plos One|June 16, 2021
Functional analysis of CASK transcript variants expressed in human brainDebora Tibbe, Yingzhou Edward Pan, Carsten Reißner, et al.
Molecular Neurobiology|September 1, 2023
The Shank/ProSAP N-Terminal (SPN) Domain of Shank3 Regulates Targeting to Postsynaptic Sites and Postsynaptic SignalingDaniel Woike, Debora Tibbe, Fatemeh Hassani Nia, et al.
Life Science Alliance|September 22, 2022
Regulation of Liprin-α phase separation by CASK is disrupted by a mutation in its CaM kinase domainDebora Tibbe, Pia Ferle, Christoph Krisp, et al.
Journal of Neurochemistry|December 1, 2025
Patient-Derived Variants Define Constraints for Ligand Binding at the PDZ Domain of CASKDebora Tibbe, Hans-Hinrich Hönck, Neha Bhatia, et al.
Nucleic Acids Research|October 16, 2025
Dysregulation of AGO2-miRNA dynamics underlies the AGO2-associated Lessel-Kreienkamp syndromeTingYu M Liu, Debora Tibbe, Jan Broder Engler, et al.
Scientific Reports|January 19, 2022
Mutations affecting the N-terminal domains of SHANK3 point to different pathomechanisms in neurodevelopmental disordersDaniel Woike, Emily Wang, Debora Tibbe, et al.
Journal of Neurochemistry|October 22, 2020
Missense mutations in CASK, coding for the calcium-/calmodulin-dependent serine protein kinase, interfere with neurexin binding and neurexin-induced oligomerizationYingzhou Edward Pan, Debora Tibbe, Frederike Leonie Harms, et al.
Molecular Psychiatry|November 30, 2022
Structural deficits in key domains of Shank2 lead to alterations in postsynaptic nanoclusters and to a neurodevelopmental disorder in humansFatemeh Hassani Nia, Daniel Woike, Isabel Bento, et al.
American Journal of Human Genetics|April 10, 2026
Bi-allelic WDHD1 variants cause microcephalic primordial dwarfismDebora Tibbe, Marie Ronja Vogt, Tess Holling, et al.
Nature Communications|September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviorsJana Willim, Daniel Woike, Daniel Greene, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Plos One|June 16, 2021
Functional analysis of CASK transcript variants expressed in human brainDebora Tibbe, Yingzhou Edward Pan, Carsten Reißner, et al.
Molecular Neurobiology|September 1, 2023
The Shank/ProSAP N-Terminal (SPN) Domain of Shank3 Regulates Targeting to Postsynaptic Sites and Postsynaptic SignalingDaniel Woike, Debora Tibbe, Fatemeh Hassani Nia, et al.
Life Science Alliance|September 22, 2022
Regulation of Liprin-α phase separation by CASK is disrupted by a mutation in its CaM kinase domainDebora Tibbe, Pia Ferle, Christoph Krisp, et al.
Journal of Neurochemistry|December 1, 2025
Patient-Derived Variants Define Constraints for Ligand Binding at the PDZ Domain of CASKDebora Tibbe, Hans-Hinrich Hönck, Neha Bhatia, et al.
Nucleic Acids Research|October 16, 2025
Dysregulation of AGO2-miRNA dynamics underlies the AGO2-associated Lessel-Kreienkamp syndromeTingYu M Liu, Debora Tibbe, Jan Broder Engler, et al.
Scientific Reports|January 19, 2022
Mutations affecting the N-terminal domains of SHANK3 point to different pathomechanisms in neurodevelopmental disordersDaniel Woike, Emily Wang, Debora Tibbe, et al.
Journal of Neurochemistry|October 22, 2020
Missense mutations in CASK, coding for the calcium-/calmodulin-dependent serine protein kinase, interfere with neurexin binding and neurexin-induced oligomerizationYingzhou Edward Pan, Debora Tibbe, Frederike Leonie Harms, et al.
Molecular Psychiatry|November 30, 2022
Structural deficits in key domains of Shank2 lead to alterations in postsynaptic nanoclusters and to a neurodevelopmental disorder in humansFatemeh Hassani Nia, Daniel Woike, Isabel Bento, et al.
American Journal of Human Genetics|April 10, 2026
Bi-allelic WDHD1 variants cause microcephalic primordial dwarfismDebora Tibbe, Marie Ronja Vogt, Tess Holling, et al.
Nature Communications|September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviorsJana Willim, Daniel Woike, Daniel Greene, et al.
Pageof 1