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Tlili, Abdelaziz
102  results:
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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