Detalhe da pesquisa
1.
Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.
Mol Biol Rep
; 49(5): 3949-3954, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35301649
2.
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.
Hum Mol Genet
; 27(7): 1228-1240, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29373757
3.
Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21-year single-center experience.
Am J Med Genet A
; 179(8): 1516-1524, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31207162
4.
Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.
Hum Hered
; 83(5): 274-282, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-31064002
5.
Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review.
J Assist Reprod Genet
; 36(3): 499-507, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30470960
6.
Novel compound heterozygous mutations in the GPR98 (USH2C) gene identified by whole exome sequencing in a Moroccan deaf family.
Mol Biol Rep
; 44(5): 429-434, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28951997
7.
Mediterranean Founder Mutation Database (MFMD): Taking Advantage from Founder Mutations in Genetics Diagnosis, Genetic Diversity and Migration History of the Mediterranean Population.
Hum Mutat
; 36(11): E2441-53, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26173767
8.
Chromosomal abnormalities and Y chromosome microdeletions in infertile men from Morocco.
BMC Urol
; 15: 95, 2015 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-26385215
9.
TNF A -308G>A polymorphism in Moroccan patients with type 2 diabetes mellitus: a case-control study and meta-analysis.
Mol Biol Rep
; 41(9): 5805-11, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24952604
10.
Phylogeography of E1b1b1b-M81 haplogroup and analysis of its subclades in Morocco.
Hum Biol
; 86(2): 105-12, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25397701
11.
Association of APOA5 rs662799 and rs3135506 polymorphisms with arterial hypertension in Moroccan patients.
Lipids Health Dis
; 13: 60, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24684850
12.
Association analysis of IGF2BP2, KCNJ11, and CDKAL1 polymorphisms with type 2 diabetes mellitus in a Moroccan population: a case-control study and meta-analysis.
Biochem Genet
; 52(9-10): 430-42, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24898818
13.
Human male infertility associated with mutations in NR5A1 encoding steroidogenic factor 1.
Am J Hum Genet
; 87(4): 505-12, 2010 Oct 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-20887963
14.
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
Indian J Hum Genet
; 19(3): 331-6, 2013 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24339547
15.
Computational study of the potential impact of AURKC missense SNPs on AURKC-INCENP interaction and their correlation to macrozoospermia.
J Biomol Struct Dyn
; 41(19): 9503-9522, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36326488
16.
In silico exploration and molecular dynamics of deleterious SNPs on the human TERF1 protein triggering male infertility.
J Biomol Struct Dyn
; 41(24): 14665-14688, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36995171
17.
Exploring the impact of CYP11A1's missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study.
Comput Biol Chem
; 106: 107937, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37552904
18.
Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.
Biochem Biophys Res Commun
; 419(4): 643-7, 2012 Mar 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-22382023
19.
The c.242G>A mutation in LRTOMT gene is responsible for a high prevalence of deafness in the Moroccan population.
Mol Biol Rep
; 39(12): 11011-6, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23053991
20.
Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses.
J Biomol Struct Dyn
; 40(1): 361-374, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32873176