E-LIB Suche - Ergebnisse für: Iuso, Arcangela

1

A spatiotemporal proteomic map of human adipogenesis:

Klingelhuber, Felix ; Frendo-Cumbo, Scott ; Omar-Hmeadi, Muhmmad...
Nature Metabolism. 6 (2024) 5 - p. 861-879 , 2024

2

Emerging variants, unique phenotypes, and transcriptomic si..:

Cavestro, Chiara ; Morra, Francesca ; Legati, Andrea...
Annals of Clinical and Translational Neurology. 11 (2024) 6 - p. 1615-1629 , 2024

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

3

A burning question from the first international BPAN sympos..:

Mollereau, Bertrand ; Hayflick, Susan J ; Escalante, Ricardo...
Autophagy. 19 (2023) 12 - p. 3234-3239 , 2023

Link: https://doi.org/10.1080/..

4

Generation of two human iPSC lines, HMGUi004-A and FINCBi00..:

Zanuttigh, Enrica ; Rusha, Ejona ; Peron, Camille...
Stem Cell Research. 72 (2023) - p. 103197 , 2023

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

5

Identification of Autophagy as a Functional Target Suitable..:

Zanuttigh, Enrica ; Derderian, Kevork ; Güra, Miriam A....
Pharmaceutics. 15 (2023) 1 - p. 267 , 2023

Link: https://doi.org/10.3390/..

6

Novel phosphopantothenoylcysteine synthetase (PPCS) mutatio..:

Lok, Aishin ; Fernandez‐Garcia, Miguel A. ; Taylor, Robert W....
American Journal of Medical Genetics Part A. 188 (2022) 9 - p. 2783-2789 , 2022

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

7

Generation of two human iPSC lines, HMGUi003-A and MRIi028-..:

Iuso, Arcangela ; Zhang, Fangfang ; Rusha, Ejona...
Stem Cell Research. 61 (2022) - p. 102773 , 2022

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

8

A comprehensive phenotypic characterization of a whole-body..:

Biagosch, Caroline A. ; Vidali, Silvia ; Faerberboeck, Michael...
Mammalian Genome. 32 (2021) 5 - p. 332-349 , 2021

Link: https://doi.org/10.1007/..

9

Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and V..:

Steel, Dora ; Zech, Michael ; Zhao, Chen...
Annals of Neurology. 88 (2020) 5 - p. 867-877 , 2020

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

10

Arabidopsis thaliana alternative dehydrogenases: a potentia..:

Catania, Alessia ; Iuso, Arcangela ; Bouchereau, Juliette...
Orphanet Journal of Rare Diseases. 14 (2019) 1 - p. , 2019

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

11

OCR-Stats: Robust estimation and statistical testing of mit..:

Yépez, Vicente A. ; Kremer, Laura S. ; Iuso, Arcangela...
PLOS ONE. 13 (2018) 7 - p. e0199938 , 2018

Link: https://doi.org/10.1371/..

12

A Homozygous Splice Site Mutation in SLC25A42, Encoding the..:

, In: JIMD Reports; JIMD Reports, Volume 44,

Iuso, Arcangela ; Alhaddad, Bader ; Weigel, Corina... - p. 1-7 , 2018

Link: https://doi.org/10.1007/..

13

Genetic diagnosis of Mendelian disorders via RNA sequencing:

Kremer, Laura S. ; Bader, Daniel M. ; Mertes, Christian...
Nature Communications. 8 (2017) 1 - p. , 2017

Link: https://doi.org/10.1038/..

14

Characterization of a Leber's hereditary optic neuropathy (..:

Catarino, Claudia B. ; Ahting, Uwe ; Gusic, Mirjana...
Mitochondrion. 36 (2017) - p. 15-20 , 2017

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

15

Rare causes of early-onset dystonia-parkinsonism with cogni..:

Carecchio, Miryam ; Picillo, Marina ; Valletta, Lorella...
neurogenetics. 18 (2017) 3 - p. 175-178 , 2017

Link: https://doi.org/10.1007/..