Molecular mechanisms of cytoskeletal dysregulations in Spinal Muscular Atrophy (SMA)
- Weitere Titel
-
Molekulare Mechanismen der Dysregulation des Zytoskeletts in der Spinalen Muskelatrophie (SMA)
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Ereignis
-
Veröffentlichung
- (wo)
-
Hannover
- (wer)
-
Stiftung Tierärztliche Hochschule Hannover
- (wann)
-
2023
- Urheber
- Beteiligte Personen und Organisationen
- URN
-
urn:nbn:de:gbv:95-119041
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:43 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Schüning, Tobias
- Claus, Peter
- Ponimaskin, Evgeni
- Tipold, Andrea
- Stiftung Tierärztliche Hochschule Hannover
Entstanden
- 2023
Ähnliche Objekte (12)
Cytoskeletal dysregulation in the motoneuron disease Spinal Muscular Atrophy (SMA)
Spinal muscular atrophy
Development of antisense oligonucleotide combinatorial therapies for spinal muscular atrophy (SMA)
Pattern of pareses in 5q-spinal muscular atrophy
Disease burden of spinal muscular atrophy in Germany
Choosing Life with Spinal Muscular Atrophy Type 1
Therapeutic advances in 5q-linked spinal muscular atrophy
Routine cerebrospinal fluid (CSF) parameters in patients with spinal muscular atrophy (SMA) treated with nusinersen
Dynamics and regulation of the actin cytoskeleton in the motoneuron disease Spinal Muscular Atrophy (SMA)
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy
T-plastin, a cytoskeletal protein with important function in axonal growth, acts as a modifier of spinal muscular atrophy
T-plastin, a cytoskeletal protein with important function in axonal growth, acts as a modifier of spinal muscular atrophy
Cytoskeletal dysregulation in the motoneuron disease Spinal Muscular Atrophy (SMA)
Spinal muscular atrophy
Development of antisense oligonucleotide combinatorial therapies for spinal muscular atrophy (SMA)
Pattern of pareses in 5q-spinal muscular atrophy
Disease burden of spinal muscular atrophy in Germany
Choosing Life with Spinal Muscular Atrophy Type 1
Therapeutic advances in 5q-linked spinal muscular atrophy
Routine cerebrospinal fluid (CSF) parameters in patients with spinal muscular atrophy (SMA) treated with nusinersen
Dynamics and regulation of the actin cytoskeleton in the motoneuron disease Spinal Muscular Atrophy (SMA)
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy
T-plastin, a cytoskeletal protein with important function in axonal growth, acts as a modifier of spinal muscular atrophy
T-plastin, a cytoskeletal protein with important function in axonal growth, acts as a modifier of spinal muscular atrophy
Cytoskeletal dysregulation in the motoneuron disease Spinal Muscular Atrophy (SMA)
Spinal muscular atrophy
Development of antisense oligonucleotide combinatorial therapies for spinal muscular atrophy (SMA)
Pattern of pareses in 5q-spinal muscular atrophy
Disease burden of spinal muscular atrophy in Germany
Choosing Life with Spinal Muscular Atrophy Type 1
Therapeutic advances in 5q-linked spinal muscular atrophy
Routine cerebrospinal fluid (CSF) parameters in patients with spinal muscular atrophy (SMA) treated with nusinersen
Dynamics and regulation of the actin cytoskeleton in the motoneuron disease Spinal Muscular Atrophy (SMA)
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy
T-plastin, a cytoskeletal protein with important function in axonal growth, acts as a modifier of spinal muscular atrophy