检索结果 - Vincent Timmerman
- Showing 1 - 20 results of 66
- Go to Next Page
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
-
10
-
11
-
12
-
13
-
14
-
15
-
16
-
17
Increased Monomerization of Mutant HSPB1 Leads to Protein Hyperactivity in Charcot-Marie-Tooth Neuropathy 由 Leonardo Almeida‐Souza, Sofie Goethals, Vicky De Winter, Ines Dierick, Rodrigo Gallardo, Joost Van Durme, Joy Irobi, Jan Gettemans, Frédéric Rousseau, Joost Schymkowitz, Vincent Timmerman, Sophie Janssens
出版 2010Artigo -
18
Screening for mutations in the peripheral myelin genesPMP22,MPZ andCx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients 由 Irina Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Е. Л. Дадали, В. П. Федотов, Eva Nelis, Ann L�fgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov
出版 2000Artigo -
19
The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype 由 Peter De Jonghe, Vincent Timmerman, C. Ceuterick, Eva Nelis, Els De Vriendt, A. Löfgren, Anina Vercruyssen, Christine Verellen, Lionel Van Maldergem, J. J. Martin, Christine Van Broeckhoven
出版 1999Artigo -
20
HSPB1 facilitates ERK-mediated phosphorylation and degradation of BIM to attenuate endoplasmic reticulum stress-induced apoptosis 由 Donna Kennedy, Katarzyna Mnich, Deepu Oommen, Reka Chakravarthy, Leonardo Almeida‐Souza, Michiel Krols, Svetlana Saveljeva, Karen Doyle, Sanjeev Gupta, Vincent Timmerman, Sophie Janssens, Adrienne M. Gorman, Afshin Samali
出版 2017Artigo
相关主题
Biology
Gene
Genetics
Medicine
Cell biology
Mutation
Pathology
Neuroscience
Phenotype
Disease
Biochemistry
Missense mutation
Mutant
Heat shock protein
Bioinformatics
Apoptosis
Immunology
Anatomy
Central nervous system
Chaperone (clinical)
Computational biology
Genetic heterogeneity
Autophagy
Cell
Chemistry
Endocrinology
Hsp70
In vitro
Internal medicine
Protein aggregation