E-LIB Suche - Ergebnisse für: Elkhattabi, Lamiae

1

Insights from the SNP analysis of TYMP gene linking MNGIE:

Laboratory of Genomics and Human Genetics, Institut Pasteur du Maroc, Casablanca, Morocco ; Sifeddine, Najat ; Elkhattabi, Lamiae...
Bioinformation. 20 (2024) 3 - p. 261-270 , 2024

Link: https://doi.org/10.6026/..

2

Molecular docking analysis of PPARγ with phytochemicals fro..:

Laboratory of Biology and Health, Faculty of Sciences Ben M'Sik, Hassan II University ofCasablanca, Morocco ; Elkhattabi, Lamiae
Bioinformation. 19 (2023) 7 - p. 795-805 , 2023

Link: https://doi.org/10.6026/..

3

Computational screening of potential drugs against COVID-19..:

Charoute, Hicham ; Elkarhat, Zouhair ; Elkhattabi, Lamiae...
VirusDisease. 33 (2022) 1 - p. 23-31 , 2022

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

4

Omenn syndrome caused by a novel homozygous mutation in rec..:

Benhsaien, Ibtihal ; Essadssi, Soukaina ; Elkhattabi, Lamiae...
Immunobiology. 226 (2021) 3 - p. 152090 , 2021

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

5

Association of c.56C > G (rs3135506) Apolipoprotein A5 Gene..:

Morjane, Imane ; Charoute, Hicham ; Ouatou, Sanaa...
Cardiology Research and Practice. 2020 (2020) - p. 1-8 , 2020

Link: https://doi.org/10.1155/..

6

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafn..:

Elrharchi, Soukaina ; Riahi, Zied ; Salime, Sara...
Human Heredity. 85 (2020) 1 - p. 35-39 , 2020

Link: https://doi.org/10.1159/..

7

Potential inhibitors of SARS-cov-2 RNA dependent RNA polyme..:

Elkarhat, Zouhair ; Charoute, Hicham ; Elkhattabi, Lamiae..
Journal of Biomolecular Structure and Dynamics. 40 (2020) 1 - p. 361-374 , 2020

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

8

Novel Mutation in AIFM1 Gene Associated with X-Linked Deafn..:

Elrharchi, Soukaina ; Riahi, Zied ; Salime, Sara...
Human Heredity. 85 (2020) 1 - p. 35-39 , 2020

Link: https://www.jstor.org/st..

9

Computational Analysis of nsSNPs of ADA Gene in Severe Comb..:

Essadssi, Soukaina ; Krami, Al Mehdi ; Elkhattabi, Lamiae...
Journal of Immunology Research. 2019 (2019) - p. 1-14 , 2019

Link: https://doi.org/10.1155/..

10

Further Evidence for the Implication of the MET Gene in Non..:

Bousfiha, Amale ; Riahi, Zied ; Elkhattabi, Lamiae...
Human Heredity. 84 (2019) 3 - p. 109-116 , 2019

Link: https://doi.org/10.1159/..

11

In Silico Analysis of Coding/Noncoding SNPs of Human RETN G..:

Elkhattabi, Lamiae ; Morjane, Imane ; Charoute, Hicham...
Journal of Diabetes Research. 2019 (2019) - p. 1-9 , 2019

Link: https://doi.org/10.1155/..

12

Further Evidence for the Implication of the MET Gene in Non..:

Bousfiha, Amale ; Riahi, Zied ; Elkhattabi, Lamiae...
Human Heredity. 84 (2019) 3 - p. 109-116 , 2019

Link: https://www.jstor.org/st..

13

A novel mutation in SLITRK6 causes deafness and myopia in a..:

Salime, Sara ; Riahi, Zied ; Elrharchi, Soukaina...
Gene. 659 (2018) - p. 89-92 , 2018

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

14

Chromosomal Abnormalities in Patients with Intellectual Dis..:

Belkady, Boutaina ; Elkhattabi, Lamiae ; Elkarhat, Zouhair...
Human Heredity. 83 (2018) 5 - p. 274-282 , 2018

Link: https://doi.org/10.1159/..

15

Chromosomal Abnormalities in Patients with Intellectual Dis..:

Belkady, Boutaina ; Elkhattabi, Lamiae ; Elkarhat, Zouhair...
Human Heredity. 83 (2017) 5 - p. 274-282 , 2017

Link: https://www.jstor.org/st..