Detalhe da pesquisa
1.
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling.
Am J Hum Genet
; 108(1): 115-133, 2021 01 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33308444
2.
The LncRNA MIAT is identified as a regulator of stemness-associated transcript in glioma.
Mol Biol Rep
; 50(1): 517-530, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36352177
3.
A novel compound-primed multiplex ARMS-PCR (CPMAP) for simultaneous detection of common PAH gene mutations.
Metab Brain Dis
; 33(4): 1165-1173, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29616438
4.
Identification of ITPR1 gene as a novel target for hsa-miR-34b-5p in non-obstructive azoospermia: a Ca2+/apoptosis pathway cross-talk.
Sci Rep
; 13(1): 21873, 2023 12 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38072953
5.
Exome sequencing identifies novel variants associated with non-syndromic hearing loss in the Iranian population.
PLoS One
; 18(8): e0289247, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37561809
6.
Phylogenetic relationship analysis of Iranians and other world populations using allele frequencies at 12 polymorphic markers.
Mol Biol Rep
; 39(12): 11187-99, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23065267
7.
LncRNA LOC100507144 acts as a novel regulator of CD44/Nanog/Sox2/miR-302/miR-21 axis in colorectal cancer.
Biofactors
; 48(1): 164-180, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34882869
8.
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
9.
BanI/D13S141/D13S175 represents a novel informative haplotype at the GJB2 gene region in the Iranian population.
Cell Mol Neurobiol
; 31(5): 749-54, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21484343
10.
An artifact band frequently associated with variable number of tandem repeat marker at phenylalanine hydroxylase gene: application in carrier detection and prenatal diagnosis of phenylketonuria.
Mol Biol Rep
; 38(5): 3395-9, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21107727
11.
Meta-analysis of gene signatures and key pathways indicates suppression of JNK pathway as a regulator of chemo-resistance in AML.
Sci Rep
; 11(1): 12485, 2021 06 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-34127725
12.
Significant Association of miR-605 rs2043556 with Susceptibility to Breast Cancer.
Microrna
; 9(2): 133-141, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-31556863
13.
hsa-miR-423 rs6505162 Is Associated with The Increased Risk of Breast Cancer in Isfahan Central Province of Iran.
Cell J
; 22(Suppl 1): 110-116, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32779440
14.
CG/CA genotypes represent novel markers in the NPHS2 gene region associated with nephrotic syndrome.
J Genet
; 992020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32482922
15.
CD24 gene polymorphism is associated with the disease progression and susceptibility to multiple sclerosis in the Iranian population.
Psychiatry Res
; 170(2-3): 271-2, 2009 Dec 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-19896210
16.
A comprehensive study of phenylalanine hydroxylase gene mutations in the Iranian phenylketonuria patients.
Eur J Med Genet
; 62(9): 103559, 2019 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-30389586
17.
Author Correction: Identification of ITPR1 gene as a novel target for hsa-miR-34b-5p in non-obstructive azoospermia: a Ca2+/apoptosis pathway cross-talk.
Sci Rep
; 14(1): 3722, 2024 Feb 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-38355618
18.
UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population.
Iran J Basic Med Sci
; 20(8): 880-885, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-29085579
19.
Association of rs1738074 polymorphism of TAGAP gene with susceptibility to multiple sclerosis in the Iranian population.
Neurosci Lett
; 648: 66-69, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28356229
20.
Comparative genomics of human stem cell factor (SCF).
Mol Biol Res Commun
; 6(1): 1-11, 2017 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-28447043