Detalhe da pesquisa
1.
A novel splice site mutation in the SDCCAG8 gene in an Iranian family with Bardet-Biedl syndrome.
Int Ophthalmol
; 41(2): 389-397, 2021 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-32926352
2.
Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.
Int Ophthalmol
; 41(10): 3269-3276, 2021 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-34019190
3.
Features, genetics and their correlation in Jalili syndrome: a systematic review.
J Med Genet
; 56(6): 358-369, 2019 06.
Artigo
Inglês
| MEDLINE | ID: mdl-30705057
4.
MicroRNAs association with azoospermia, oligospermia, asthenozoospermia, and teratozoospermia: a systematic review.
J Assist Reprod Genet
; 37(4): 763-775, 2020 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-32189180
5.
RIT2: responsible and susceptible gene for neurological and psychiatric disorders.
Mol Genet Genomics
; 293(4): 785-792, 2018 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-29860660
6.
A novel mutation in the ALS2 gene in an iranian kurdish family with juvenile amyotrophic lateral sclerosis.
Amyotroph Lateral Scler Frontotemporal Degener
; 24(1-2): 148-151, 2023 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-35852402
7.
Homozygous mutation in CSF1R causes brain abnormalities, neurodegeneration, and dysosteosclerosis (BANDDOS).
Bioimpacts
; 13(3): 183-190, 2023.
Artigo
Inglês
| MEDLINE | ID: mdl-37431483
8.
An updated overview and classification of bioinformatics tools for MicroRNA analysis, which one to choose?
Comput Biol Med
; 134: 104544, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34119921
9.
Molecular Insight Into the Therapeutic Potential of Long Non-coding RNA-Associated Competing Endogenous RNA Axes in Alzheimer's Disease: A Systematic Scoping Review.
Front Aging Neurosci
; 13: 742242, 2021.
Artigo
Inglês
| MEDLINE | ID: mdl-34899268
10.
Long non-coding RNA-associated competing endogenous RNA axes in the olfactory epithelium in schizophrenia: a bioinformatics analysis.
Sci Rep
; 11(1): 24497, 2021 12 30.
Artigo
Inglês
| MEDLINE | ID: mdl-34969953
11.
LRP8 (rs5177) and CEP85L (rs11756438) are contributed to schizophrenia susceptibility in Iranian population.
Psychiatr Genet
; 30(6): 162-165, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33079740
12.
A new report of autoinflammation and PLCG2-associated antibody deficiency and immune dysregulation (APLAID) with a homozygous pattern from Iran.
Immunol Lett
; 221: 27-32, 2020 05.
Artigo
Inglês
| MEDLINE | ID: mdl-32014489
13.
Novel ABCD1 gene mutations in Iranian pedigrees with X-linked adrenoleukodystrophy.
J Pediatr Endocrinol Metab
; 32(11): 1207-1215, 2019 Nov 26.
Artigo
Inglês
| MEDLINE | ID: mdl-31665121