E-LIB Suche - Ergebnisse für: Atieh Eslahi - Sprache DE

Personensuche X

Sortierung: Relevanz

Sortierung: Jahr

1

Identification of a novel mutation of Platelet-Derived Grow..:

Rahnama, Maryam ; Movahedi, Tahereh ; Eslahi, Atieh...
Gene. 910 (2024) - p. 148335 , 2024

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

2

Characterizing Homozygous Variants in Bardet-Biedl Syndrome..:

Feizabadi, Masoumeh Heidari ; Alerasool, Masoome ; Eslahi, Atieh...
Biochemical Genetics. , 2024

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

3

Lunapark deficiency leads to an autosomal recessive neurode..:

Accogli, Andrea ; Zaki, Maha S ; Al-Owain, Mohammed...
Brain Communications. , 2023

Link: https://doi.org/10.1093/..

4

Broadening the phenotypic and molecular spectrum of FINCA s..:

Sczakiel, Henrike L. ; Zhao, Max ; Wollert-Wulf, Brigitte...
European Journal of Human Genetics. 31 (2023) 8 - p. 905-917 , 2023

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

5

New advancements in CRISPR based gene therapy of Duchenne m..:

Eslahi, Atieh ; Alizadeh, Farzaneh ; Avan, Amir...
Gene. 867 (2023) - p. 147358 , 2023

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

6

Production of Duchenne muscular dystrophy cellular model us..:

Alizadeh, Farzaneh ; Abraghan, Yousef Jafari ; Farrokhi, Shima...
Molecular and Cellular Biochemistry. 479 (2023) 5 - p. 1027-1040 , 2023

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

7

TMEM218 dysfunction causes ciliopathies, including Joubert ..:

Van De Weghe, Julie C. ; Giordano, Jessica L. ; Mathijssen, Inge B....
Human Genetics and Genomics Advances. 2 (2021) 1 - p. 100016 , 2021

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

8

TMEM263: a novel candidate gene implicated in human autosom..:

Mohajeri, Mahsa Sadat Asl ; Eslahi, Atieh ; Khazaii, Zeinab...
Human Genomics. 15 (2021) 1 - p. , 2021

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

9

Investigating the association of Lamotrigine and Phenytoin‐..:

Sabourirad, Sara ; Mortezaee, Reza ; Mojarad, Majid...
Experimental Dermatology. 30 (2020) 2 - p. 284-287 , 2020

Link: https://doi.org/10.1111/..

10

Early-infantile onset epilepsy and developmental delay caus..:

Neuray, Caroline ; Maroofian, Reza ; Scala, Marcello...
Brain. 143 (2020) 8 - p. 2388-2397 , 2020

Link: https://doi.org/10.1093/..

11

Loss of UGP2 in brain leads to a severe epileptic encephalo..:

Perenthaler, Elena ; Nikoncuk, Anita ; Yousefi, Soheil...
Acta Neuropathologica. 139 (2019) 3 - p. 415-442 , 2019

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

12

PRUNE is crucial for normal brain development and mutated i..:

Zollo, Massimo ; Ahmed, Mustafa ; Ferrucci, Veronica...
Brain. 140 (2017) 4 - p. 940-952 , 2017

Link: https://doi.org/10.1093/..

13

microRNA-124 overexpression in associated with lymph node m..:

Eslahi, Atieh ; Daliri Ghouchan Atigh, Mahdieh ; Tabatabaee, Abbas..
Journal of Cellular Immunotherapy. 1 (2015) 1-2 - p. 35-36 , 2015

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

14

The overexpression of miRNA137 in metastatic breast cancer ..:

Ghouchan Atigh, Mahdieh Daliri ; Eslahi, Atieh ; Abbas Tabatabayi Yazdi, Seyed...
Journal of Cellular Immunotherapy. 1 (2015) 1-2 - p. 33 , 2015

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

15

PLA2G6 gene mutation and infantile neuroaxonal degeneration..:

Reza Jafarzadeh Esfehani ; Atieh Eslahi ; Mehran Beiraghi Toosi...
https://ijbms.mums.ac.ir/article_18639_365afe462dbce6db8d1599de4978cea4.pdf. , 2021

Link: https://doi.org/10.22038..

1-15