Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Julia A. Thayer"'
Autor:
Robert A. Brown, Antanina Voit, Manasa P. Srikanth, Julia A. Thayer, Tami J. Kingsbury, Marlene A. Jacobson, Marta M. Lipinski, Ricardo A. Feldman, Ola Awad
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 10 (2019)
Bi-allelic GBA1 mutations cause Gaucher's disease (GD), the most common lysosomal storage disorder. Neuronopathic manifestations in GD include neurodegeneration, which can be severe and rapidly progressive. GBA1 mutations are also the most frequent g
Externí odkaz:
https://doaj.org/article/071ad8f2001a470988d9369dd1d74923
Autor:
Derek P. Narendra, Julia A. Thayer
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 37(7)
Autor:
Julia A. Thayer, Chinmoy Sarkar, Henok Tesfay, Ricardo A. Feldman, Nivedita Hegdekar, Xianmin Zeng, Cameran I. Burt, Marta M. Lipinski, Ola Awad
Publikováno v:
Autophagy. 16:140-153
Recent studies indicate a causative relationship between defects in autophagy and dopaminergic neuron degeneration in Parkinson disease (PD). However, it is not fully understood how autophagy is regulated in the context of PD. Here we identify USP24
Autor:
Julia A. Thayer, Marlene A. Jacobson, Marta M. Lipinski, Ola Awad, Robert A. Brown, Antanina Voit, Ricardo A. Feldman, Manasa P Srikanth, Tami J. Kingsbury
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 10 (2019)
Disease Models & Mechanisms
Disease Models & Mechanisms
Bi-allelic GBA1 mutations cause Gaucher's disease (GD), the most common lysosomal storage disorder. Neuronopathic manifestations in GD include neurodegeneration, which can be severe and rapidly progressive. GBA1 mutations are also the most frequent g
Autor:
Nivedita Hegdekar, Maureen A. Kane, Alan I. Faden, Jace W. Jones, Alok Kumar, Chinmoy Sarkar, Julia A. Thayer, Marta M. Lipinski
Publikováno v:
Autophagy
Lysosomal membrane permeabilization (LMP) is observed under many pathological conditions, leading to cellular dysfunction and death. However, the mechanisms by which lysosomal membranes become leaky in vivo are not clear. Our data demonstrate that LM
Autor:
Julia A, Thayer, Ola, Awad, Nivedita, Hegdekar, Chinmoy, Sarkar, Henok, Tesfay, Cameran, Burt, Xianmin, Zeng, Ricardo A, Feldman, Marta M, Lipinski
Publikováno v:
Autophagy
Recent studies indicate a causative relationship between defects in autophagy and dopaminergic neuron degeneration in Parkinson disease (PD). However, it is not fully understood how autophagy is regulated in the context of PD. Here we identify USP24