Detalhe da pesquisa
1.
Scoring Algorithm-Based Genomic Testing in Dystonia: A Prospective Validation Study.
Mov Disord
; 36(8): 1959-1964, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949708
2.
Circulating and tissue microRNAs as a potential diagnostic biomarker in patients with thrombotic events.
J Cell Physiol
; 235(10): 6393-6403, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32198752
3.
Association of the genetic polymorphisms in immunoinflammatory microRNAs with risk of ischemic stroke and subtypes in an Iranian population.
J Cell Physiol
; 234(4): 3874-3886, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30229913
4.
ADAMTS7 and ZC3HC1 Share Genetic Predisposition to Coronary Artery Disease and Large Artery Ischemic Stroke.
Crit Rev Eukaryot Gene Expr
; 29(4): 351-361, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31679296
5.
Assessment of an APOBEC3B truncating mutation, c.783delG, in patients with breast cancer.
Breast Cancer Res Treat
; 162(1): 31-37, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-28062980
6.
Effects of streptozotocin-induced type 1 maternal diabetes on PI3K/AKT signaling pathway in the hippocampus of rat neonates.
J Recept Signal Transduct Res
; 36(3): 254-60, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26479041
7.
Analysis of novel mutations in BRCA1 in Iranian families with breast cancer.
Hereditas
; 151(2-3): 38-42, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25041116
8.
Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease.
Heliyon
; 9(4): e15393, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37095917
9.
Evaluation of COVID-19 Trend in Iran; Population Response to the Recent Pandemic Overtime.
Int J Prev Med
; 13: 6, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35281986
10.
Cell-based Treatment of Cerebral Palsy: Still a Long Way Ahead.
Curr Stem Cell Res Ther
; 17(8): 741-749, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-34727864
11.
Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever.
Case Rep Rheumatol
; 2022: 8334375, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35178266
12.
Exome sequencing identifies RASSF1 and KLK3 germline variants in an Iranian multiple-case breast cancer family.
Eur J Med Genet
; 65(3): 104425, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35032689
13.
Whole-Exome Sequencing Study of Consanguineous Parkinson's Disease Families and Related Phenotypes: Report of Twelve Novel Variants.
J Mol Neurosci
; 72(12): 2486-2496, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36520381
14.
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism.
Parkinsonism Relat Disord
; 97: 52-56, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35306330
15.
Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-ß signaling pathway in colon carcinogenesis.
Iran J Basic Med Sci
; 24(4): 444-450, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-34094025
16.
Developmental regulation and lateralization of N-methyl-d-aspartate (NMDA) receptors in the rat hippocampus.
Neuropeptides
; 89: 102183, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34333368
17.
PLA2G6 gene mutation and infantile neuroaxonal degeneration; report of three cases from Iran.
Iran J Basic Med Sci
; 24(9): 1190-1195, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35083005
18.
Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.
Parkinsonism Relat Disord
; 84: 129-134, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33611074
19.
Genetic variants of the phenylalanine hydroxylase gene in patients with phenylketonuria in the northeast of Iran.
J Pediatr Endocrinol Metab
; 33(3): 355-359, 2020 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32069237
20.
Developmental regulation and lateralisation of the α7 and α4 subunits of nicotinic acetylcholine receptors in developing rat hippocampus.
Int J Dev Neurosci
; 80(4): 303-318, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32198948