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1.
Silencing of α-N-acetylgalactosaminidase in the gastric cancer cells amplified cell death and attenuated migration, while the multidrug resistance remained unchanged.
Cell Biol Int
; 46(2): 255-264, 2022 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-34816536
2.
Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
BMC Med Genet
; 21(1): 226, 2020 11 18.
Artículo
en Inglés
| MEDLINE | ID: mdl-33208113
3.
In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane.
Cell Biol Int
; 44(2): 671-683, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-31769568
4.
A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a DFNB12 Nonsyndromic Phenotype of CDH23.
Audiol Neurootol
; 25(5): 258-262, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-32485727
5.
Differentiation of dental pulp stem cells into neuron-like cells.
Int J Neurosci
; 130(2): 107-116, 2020 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-31599165
6.
A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family.
Genomics
; 111(4): 840-848, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-29752989
7.
Update of spectrum c.35delG and c.-23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss.
Ann Hum Genet
; 83(1): 1-10, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30175840
8.
A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.
Audiol Neurootol
; 24(5): 258-263, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31661684
9.
Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
Audiol Neurootol
; 24(1): 25-31, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30943474
10.
A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family.
Int J Audiol
; 58(10): 628-634, 2019 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-31187663
11.
A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.
Am J Otolaryngol
; 39(6): 719-725, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-30077349
12.
cag Pathogenicity island-dependent upregulation of matrix metalloproteinase-7 in infected patients with Helicobacter pylori.
J Immunoassay Immunochem
; 38(6): 595-607, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28699830
13.
MicroRNAs: effective elements in ear-related diseases and hearing loss.
Eur Arch Otorhinolaryngol
; 274(6): 2373-2380, 2017 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-28224282
14.
In Vitro Differentiation of Human Bone Marrow Mesenchymal Stem Cells to Hair Cells Using Growth Factors.
Int Tinnitus J
; 21(2): 179-184, 2017 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29336137
15.
A Review of Medicinal Plants for the Treatment of Earache and Tinnitus in Iran.
Int Tinnitus J
; 21(1): 44-49, 2017 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28723601
16.
Ginkgo biloba in the treatment of tinnitus: An updated literature review.
Int Tinnitus J
; 21(1): 58-62, 2017 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28723603
17.
Comparison of Three Types of Mesenchymal Stem Cells (Bone Marrow, Adipose Tissue, and Umbilical Cord-Derived) as Potential Sources for Inner Ear Regeneration.
Int Tinnitus J
; 21(2): 122-127, 2017 Dec 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29336130
18.
Altered Th17 Cytokine Expression in Helicobacter pylori Patients with TLR4 (D299G) Polymorphism.
Immunol Invest
; 45(2): 161-71, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26853914
19.
Frequency of virulence factors in Helicobacter pylori-infected patients with gastritis.
Microb Pathog
; 80: 67-72, 2015 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-25656240
20.
A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran.
Indian J Med Res
; 142(1): 46-52, 2015 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-26261166