E-LIB Suche - Ergebnisse für: Çoku, Jorida

1

Reduced ER–mitochondria connectivity promotes neuroblastoma..:

Çoku, Jorida ; Booth, David M ; Skoda, Jan...
The EMBO Journal. 41 (2022) 8 - p. , 2022

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

2

Systematic, network-based characterization of therapeutic t..:

Shen, Yao ; Alvarez, Mariano J. ; Bisikirska, Brygida...
PLOS Computational Biology. 13 (2017) 10 - p. e1005599 , 2017

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

3

A De Novo Mutation in MTND6 Causes Generalized Dystonia in ..:

Kurt, Yasemin Gulcan ; Çoku, Jorida ; Akman, H. Orhan...
Child Neurology Open. 3 (2016) - p. 2329048X1562793 , 2016

Link: https://doi.org/10.1177/..

4

An exon trap with proper poly-A site in the GBE1 is the com..:

Akman, Orhan H. ; Kakhlon, Or ; Coku, Jorida...
Neurology. 84 (2015) 14_supplement - p. , 2015

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

5

Decreased hippocampal expression of calbindin D28K and cogn..:

Emmanuele, Valentina ; Garcia-Cazorla, Angels ; Huang, Hua-Bin...
Journal of the Neurological Sciences. 317 (2012) 1-2 - p. 29-34 , 2012

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

6

Reactive oxygen species, oxidative stress, and cell death c..:

Quinzii, Catarina M. ; Lopez, Luis C. ; Gilkerson, Robert W....
The FASEB Journal. 24 (2010) 10 - p. 3733-3743 , 2010

Link: https://doi.org/10.1096/..

7

Slowly progressive encephalopathy with hearing loss due to ..:

Çoku, Jorida ; Shanske, Sara ; Mehrazin, Mahsa...
Journal of the Neurological Sciences. 290 (2010) 1-2 - p. 166-168 , 2010

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

8

Extensive screening system using suspension array technolog..:

Nishigaki, Yutaka ; Ueno, Hitomi ; Coku, Jorida...
Mitochondrion. 10 (2010) 3 - p. 300-308 , 2010

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

9

A novel mutation in the tRNAIle gene (MTTI) affecting the v..:

Berardo, Andres ; Çoku, Jorida ; Kurt, Bulent..
Neuromuscular Disorders. 20 (2010) 3 - p. 204-206 , 2010

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

10

The m.3244G>A mutation in mtDNA is another cause of progres..:

Sotiriou, Evangelia ; Çoku, Jorida ; Tanji, Kurenai...
Neuromuscular Disorders. 19 (2009) 4 - p. 297-299 , 2009

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

11

Longitudinal changes of mtDNA A3243G mutation load and leve..:

Mehrazin, Mahsa ; Shanske, Sara ; Kaufmann, Petra...
American Journal of Medical Genetics Part A. 149A (2009) 4 - p. 584-587 , 2009

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

12

Mitochondrial DNA depletion syndrome due to mutations in th..:

Bornstein, Belén ; Area, Estela ; Flanigan, Kevin M....
Neuromuscular Disorders. 18 (2008) 6 - p. 453-459 , 2008

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

13

Mitochondrial myopathy associated with a novel mutation in ..:

Pancrudo, Jacklyn ; Shanske, Sara ; Coku, Jorida...
Neuromuscular Disorders. 17 (2007) 8 - p. 651-654 , 2007

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

14

Kearns-Sayre Syndrome Presenting as Complete Heart Block:

Chawla, Sanjay ; Coku, Jorida ; Forbes, Thomas.
Pediatric Cardiology. 29 (2007) 3 - p. 659-662 , 2007

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

15

Reduced ER-mitochondria connectivity promotes neuroblastoma..:

Çoku, Jorida ; Booth, David M ; Skoda, Jan...
https://jdc.jefferson.edu/pacbfp/364. , 2022

Link: https://jdc.jefferson.ed..