E-LIB Suche - Ergebnisse für: Melchionda, Laura

1

Role of the small protein Mco6 in the mitochondrial sorting..:

Busto, Jon V. ; Ganesan, Iniyan ; Mathar, Hannah...
Cell Reports. 43 (2024) 3 - p. 113805 , 2024

2

Quantitative high-confidence human mitochondrial proteome a..:

Morgenstern, Marcel ; Peikert, Christian D. ; Lübbert, Philipp...
Cell Metabolism. 33 (2021) 12 - p. 2464-2483.e18 , 2021

Link: https://doi.org/10.1016/..

3

Structural Basis of Membrane Protein Chaperoning through th..:

Weinhäupl, Katharina ; Lindau, Caroline ; Hessel, Audrey...
Cell. 175 (2018) 5 - p. 1365-1379.e25 , 2018

Link: https://doi.org/10.1016/..

4

Mutations inTIMM50compromise cell survival in OxPhos‐depend..:

Reyes, Aurelio ; Melchionda, Laura ; Burlina, Alberto...
EMBO Molecular Medicine. 10 (2018) 10 - p. , 2018

Link: https://doi.org/10.15252..

5

A novel mutation in TTC19 associated with isolated complex ..:

Melchionda, Laura ; Damseh, Nadirah S. ; Abu Libdeh, Bassam Y....
Frontiers in Genetics. 5 (2014) - p. , 2014

Link: https://doi.org/10.3389/..

6

VARS2andTARS2Mutations in Patients with Mitochondrial Encep..:

Diodato, Daria ; Melchionda, Laura ; Haack, Tobias B....
Human Mutation. 35 (2014) 8 - p. 983-989 , 2014

Link: https://doi.org/10.1002/..

7

Reduced expression of the chaperone-mediated autophagy carr..:

Sala, Gessica ; Stefanoni, Giovanni ; Arosio, Alessandro...
Brain Research. 1546 (2014) - p. 46-52 , 2014

Link: https://doi.org/10.1016/..

8

Mutations in APOPT1, Encoding a Mitochondrial Protein, Caus..:

Melchionda, Laura ; Haack, Tobias B. ; Hardy, Steven...
The American Journal of Human Genetics. 95 (2014) 3 - p. 315-325 , 2014

Link: https://doi.org/10.1016/..

9

Novel (ovario) leukodystrophy related toAARS2mutations:

Dallabona, Cristina ; Diodato, Daria ; Kevelam, Sietske H....
Neurology. 82 (2014) 23 - p. 2063-2071 , 2014

Link: https://doi.org/10.1212/..

10

Rotenone Upregulates Alpha-Synuclein and Myocyte Enhancer F..:

Sala, Gessica ; Arosio, Alessandro ; Stefanoni, Giovanni...
BioMed Research International. 2013 (2013) - p. 1-10 , 2013

Link: https://doi.org/10.1155/..

11

Adult-onset Alexander disease, associated with a mutation i..:

Melchionda, Laura ; Fang, Mingyan ; Wang, Hairong...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013

Link: https://doi.org/10.1186/..

12

SURF1 deficiency causes demyelinating Charcot-Marie-Tooth d..:

Echaniz-Laguna, Andoni ; Ghezzi, Daniele ; Chassagne, Maïté...
Neurology. 81 (2013) 17 - p. 1523-1530 , 2013

Link: https://doi.org/10.1212/..

13

MTO1 Mutations are Associated with Hypertrophic Cardiomyopa..:

Baruffini, Enrico ; Dallabona, Cristina ; Invernizzi, Federica...
Human Mutation. 34 (2013) 11 - p. 1501-1509 , 2013

Link: https://doi.org/10.1002/..

14

Mutations of the Mitochondrial-tRNA Modifier MTO1 Cause Hyp..:

Ghezzi, Daniele ; Baruffini, Enrico ; Haack, Tobias B....
The American Journal of Human Genetics. 90 (2012) 6 - p. 1079-1087 , 2012

Link: https://doi.org/10.1016/..

15

Quantitative high-confidence human mitochondrial proteome a..:

Morgenstern, Marcel ; Peikert, Christian D ; Lübbert, Philipp...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8664129/. , 2021

Link: http://www.ncbi.nlm.nih...