A single amino acid residue regulates PTEN-binding and stability of the spinal muscular atrophy protein SMN
Spinal Muscular Atrophy (SMA) is a neuromuscular disease caused by decreased levels of the survival of motoneuron (SMN) protein. Post-translational mechanisms for regulation of its stability are still elusive. Thus, we aimed to identify regulatory phosphorylation sites that modulate function and sta...
Hlavní autoři: | Rademacher, S, Detering, NT, Schüning, T, Lindner, R, Santonicola, P, Wefel, I-M, Dehus, J, Walter, LM, Brinkmann, H, Niewienda, A, Janek, K, Varela, MA, Bowerman, M, Di Schiavi, E, Claus, P |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
MDPI
2020
|
Podobné jednotky
-
A Single Amino Acid Residue Regulates PTEN-Binding and Stability of the Spinal Muscular Atrophy Protein SMN
Autor: Sebastian Rademacher, a další
Vydáno: (2020-11-01) -
What could be the function of the spinal muscular atrophy-causing protein SMN in macrophages?
Autor: Ines Tapken, a další
Vydáno: (2024-05-01) -
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
Autor: Bowerman, M, a další
Vydáno: (2017) -
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
Autor: Bowerman, M, a další
Vydáno: (2017) -
Therapeutic strategies for spinal muscular atrophy: SMN and beyond
Autor: Melissa Bowerman, a další
Vydáno: (2017-08-01)