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Tlili, Abdelaziz
102
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Online (102)
Mediatypes
Articles (Online) (50)
OpenAccess-fulltext (52)
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1
Silicon/Silver nanocomposite-based surface-enhanced Raman s..:
Safadi, Arwa Al
;
Ramachandran, Krithikadevi
;
Tlili, Abdelaziz
.
Journal of Physics: Conference Series. 2751 (2024) 1 - p. 012007 , 2024
Link:
https://doi.org/10.1088/..
?
2
Mitochondrial genes modulate the phenotypic expression of c..:
Alila-Fersi, Olfa
;
Tej, Amel
;
Maalej, Marwa
...
Gene. 914 (2024) - p. 148388 , 2024
Link:
https://doi.org/10.1016/..
?
3
Highly efficient, label free, ultrafast plasmonic SERS bios..:
A. I. AlSafadi, Arwa
;
Ramachandran, Krithikadevi
;
Columbus, Soumya
...
International Journal of Biological Macromolecules. 259 (2024) - p. 129381 , 2024
Link:
https://doi.org/10.1016/..
?
4
Expanding the genetic and phenotypic spectrum of TRAPPC9 an..:
Kharrat, Marwa
;
Triki, Chahnez
;
ben isaa, Abir
...
Journal of Human Genetics. , 2024
Link:
https://doi.org/10.1038/..
?
5
The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian D..:
Tlili, Abdelaziz
;
Mutery, Abdullah Al
;
Chouchen, Jihen
Genes. 15 (2024) 5 - p. 588 , 2024
Link:
https://doi.org/10.3390/..
?
6
Congenital anomalies of the kidney and urinary tract:
Mahmoud, Anfal Hussain
;
Talaat, Iman M.
;
Tlili, Abdelaziz
.
Frontiers in Medicine. 11 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
?
7
Genetic analysis of 106 sporadic cases with hearing loss in..:
Tlili, Abdelaziz
;
Mahfood, Mona
;
Al Mutery, Abdullah
.
Human Genomics. 18 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
8
Molecular and in silico investigation of a novel ECHS1 gene..:
Maalej, Marwa
;
Sfaihi, Lamia
;
Fersi, Olfa-Alila
...
Metabolic Brain Disease. 39 (2024) 4 - p. 611-623 , 2024
Link:
https://doi.org/10.1007/..
?
9
A novel homozygous PIGO mutation associated with severe inf..:
Aguech, Ameni
;
Sfaihi, Lamia
;
Alila-Fersi, Olfa
...
Metabolic Brain Disease. , 2023
Link:
https://doi.org/10.1007/..
?
10
Functional consequences of Genetics variant in TMC1 and TMC..:
Al Mutery, Abdullah
;
Kamal Eldin Mohamed, Walaa
;
Mahfood, Mona
..
Saudi Journal of Biological Sciences. 30 (2023) 2 - p. 103520 , 2023
Link:
https://doi.org/10.1016/..
?
11
Case report: Functional analysis of the p.Arg507Trp variant..:
Ben Ayed, Ikhlas
;
Jallouli, Olfa
;
Murakami, Yoshiko
...
Frontiers in Neurology. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
12
A Novel Mutation in the MAP7D3 Gene in Two Siblings with Se..:
Kharrat, Marwa
;
Issa, Abir Ben
;
Tlili, Abdelaziz
...
Journal of Molecular Neuroscience. 73 (2023) 9-10 - p. 853-864 , 2023
Link:
https://doi.org/10.1007/..
?
13
Loss-of-function mutations in MYO15A and OTOF cause non-syn..:
Asaad, Maria
;
Mahfood, Mona
;
Al Mutery, Abdullah
.
Human Genomics. 17 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1186/..
?
14
miR-623 Targets Metalloproteinase-1 and Attenuates Extravas..:
Hammash, Dua
;
Mahfood, Mona
;
Khoder, Ghalia
...
Breast Cancer: Targets and Therapy. 14 (2022) - p. 187-198 , 2022
Link:
https://doi.org/10.2147/..
?
15
Identification of a novel homozygous mutation in NAXE gene ..:
Maalej, Marwa
;
Sfaihi, Lamia
;
Ammar, Marwa
...
neurogenetics. 23 (2022) 4 - p. 257-270 , 2022
Link:
https://doi.org/10.1007/..
1-15