Detalhe da pesquisa
1.
The Impact of Recent Demography on Functional Genetic Variation in North African Human Groups.
Mol Biol Evol
; 41(1)2024 Jan 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38152862
2.
Genetic diversity of 15 autosomal STRs in a sample of Berbers from Aurès region in the Northeast of Algeria and genetic relationships with other neighbouring samples.
Ann Hum Biol
; 47(3): 284-293, 2020 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32183545
3.
Paternal lineage of the Berbers from Aurès in Algeria: estimate of their genetic variation.
Ann Hum Biol
; 46(2): 160-168, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30939942
4.
Ankylosing spondylitis: analysis of gene-gene interactions between IL-12ß, JAK2, and STAT3 in Han Chinese and Algerian cohorts.
Cent Eur J Immunol
; 44(1): 65-74, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31114439
5.
Purification and characterization of a platelet aggregation inhibitor and anticoagulant Cc 5_NTase, CD 73-like, from Cerastes cerastes venom.
J Biochem Mol Toxicol
; 31(5)2017 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-27925690
6.
The complex translocation (9;14;14) involving IGH and CEBPE genes suggests a new subgroup in B-lineage acute lymphoblastic leukemia.
Genet Mol Biol
; 39(1): 7-13, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-27007892
7.
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
BMC Med Genet
; 16: 36, 2015 Jun 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-26068213
8.
Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives.
Sci Rep
; 14(1): 9979, 2024 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38693301
9.
Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2.
Nat Genet
; 36(3): 225-7, 2004 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-14770181
10.
Whole mitogenomes reveal that NW Africa has acted both as a source and a destination for multiple human movements.
Sci Rep
; 13(1): 10395, 2023 06 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37369751
11.
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
Hum Mol Genet
; 19(10): 1998-2004, 2010 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20197411
12.
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency.
Am J Hum Genet
; 82(3): 661-72, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18319074
13.
Interaction of an IHF-like protein with the Rhizobium etli nifA promoter.
FEMS Microbiol Lett
; 271(1): 20-6, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17403047
14.
Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases.
J Neurol
; 263(7): 1314-22, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27142713
15.
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes.
Neuromuscul Disord
; 21(8): 543-50, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21741241
16.
LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort.
Parkinsonism Relat Disord
; 16(10): 676-9, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20933457