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عنوان
نگارندگان
عنوان مجله
سال انتشار
نوع انتشار
نوع مقاله
1
Role of GJB2 and GJB6 in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature Reviews
مقاله کامل
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2
Association of genetic variations in the mitochondrial DNA control region with presbycusis.
چکیده مقاله
پژوهشي اصيل
3
Abberant Lymphocytes Rate after Gamma-Irradiationn as a Biomarker of Breast Cancer
چکیده مقاله
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4
Alginate/chitosan hydrogel containing olfactory ectomesenchymal stem cells for sciatic nerve tissue engineering
چکیده مقاله
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5
Differentiation of human mesenchymal stem cells (MSC) to dopaminergic neurons: A comparison between Wharton's Jelly and olfactory mucosa as sources of MSCs
چکیده مقاله
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6
Human olfactory stem cells: As a promising source of dopaminergic neuron-like cells for treatment of Parkinson's disease
چکیده مقاله
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7
Differentiation of neural crest stem cells from nasal mucosa into motor neuron-like cells
چکیده مقاله
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8
The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis
چکیده مقاله
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9
Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment
چکیده مقاله
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10
Presbycusis: From Current Knowledge to Future Treatment Prospects
چکیده مقاله
مقالات مروري
11
Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss
چکیده مقاله
پژوهشي اصيل
12
Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.
مقاله کامل
پژوهشي اصيل
13
The anticipation and inheritance pattern of c.487A>G mutation in GJB2 gene.
مقاله کامل
پژوهشي اصيل
14
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
مقاله کامل
پژوهشي اصيل
15
Profile of Iranian GJB2 mutation in young population with novel mutation.
مقاله کامل
پژوهشي اصيل
16
Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages.
مقاله کامل
پژوهشي اصيل
17
A novel nonsense mutation in TUSC3 is responsible for non‐syndromic autosomal recessive mental retardation in a consanguineous Iranian family.
مقاله کامل
پژوهشي اصيل
18
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 novel loci and several mutation hotspots.
مقاله کامل
پژوهشي اصيل
19
A clinical and molecular genetics study of 112 Iranian families with primary microcephaly.
مقاله کامل
پژوهشي اصيل
20
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci.
مقاله کامل
پژوهشي اصيل
21
Identification of a critical novel mutation in the exon 1 of androgen receptor gene in two brothers with complete androgen insensitivity syndrome.
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پژوهشي اصيل