Isfahan University of Medical Sciences

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Faculty Members have conducted research related to the Upregulation of Mtor, Rps6kb1, and Eif4ebp1 in the Whole Blood Samples of Iranian Patients With Multiple Sclerosis Compared to Healthy Controls
Mohammad Amin Tabatabaiefar
Mohammad Amin Tabatabaiefar

Professor of Medical Genetics

Department of Genetics and Molecular Biology, School of Medicine

Pediatric Inherited Diseases Research Center

Research Institute for Primordial Prevention of Non-communicable Disease

Isfahan University of Medical Sciences

All Documents
1. Ataxia With Vitamin E Deficiency: Case Series, Vitamin E Therapy Response, Founder Effect, and in Silico Analysis, Clinical Genetics (2025)
2. Correction To: Decellularized Skin Pretreatment by Monophosphoryl Lipid a and Lactobacillus Casei Supernatant Accelerate Skin Recellularization (Molecular Biology Reports, (2024), 51, 1, (675), 10.1007/S11033-024-09599-Y), Molecular Biology Reports (2025)
3. Correction To: Whole Exome Sequencing Revealed Variants in Four Genes Underlying X-Linked Intellectual Disability in Four Iranian Families: Novel Deleterious Variants and Clinical Features With the Review of Literature (Bmc Medical Genomics, (2023), 16, 1, (239), 10.1186/S12920-023-01680-Y), BMC Medical Genomics (2025)
4. Evaluation of Pathogenic Variant in Wfs1 in a Patient With Wolfram Syndrome, Egyptian Journal of Medical Human Genetics (2025)
5. Filaggrinopathies—Flg/Flg2: Diagnostic Complexities and Immunotherapy, Journal of Investigative Dermatology (2025)
6. Sero-Molecular Prevalence of Toxoplasmosis in Hemodialysis and Peritoneal Dialysis Patients in Markazi Province, Iran, Tropical Medicine and Health (2025)
7. A Novel De Novo Frameshift Variant in the Chd2 Gene Related to Intellectual and Developmental Disability, Seizures and Speech Problems, Molecular Genetics and Genomic Medicine (2024)
8. A Novel Homozygote Pathogenic Variant in the Diaph1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (Scbms): Report of a Family and Literature Review, Molecular Genetics and Genomic Medicine (2024)
9. Clinical Characterizations and Molecular Genetic Study of Two Co-Segregating Variants in Pdzd7 and Pde6c Genes Leading Simultaneously to Non-Syndromic Hearing Loss and Achromatopsia, BMC Medical Genomics (2024)
10. Decellularized Skin Pretreatment by Monophosphoryl Lipid a and Lactobacillus Casei Supernatant Accelerate Skin Recellularization, Molecular Biology Reports (2024)
11. Familial Nonmedullary Thyroid Cancer: A Case Series in Iranian Patients With a Meta-Review of Case Series, Lab Medicine (2024)
12. Identification of Novel Likely Pathogenic Variant in Cdh23 Causing Non-Syndromic Hearing Loss, and a Novel Variant in Otogl in an Extended Iranian Family, Egyptian Journal of Medical Human Genetics (2024)
13. Molecular and Phenotypical Findings of a Novel De Novo Syngap1 Gene Variant in an 11-Year-Old Iranian Boy With Intellectual Disability, Lab Medicine (2024)
14. Monogenic Etiologies of Persistent Human Papillomavirus Infections: A Comprehensive Systematic Review, Genetics in Medicine (2024)
15. Qualitative and Quantitative Optimization of Foxe1 Gene Polymerase Chain Reaction Product As a Gc-Rich Gene, Journal of Isfahan Medical School (2024)
16. Rars1-Related Hypomyelinating Leukodystrophy-9 (Hld-9) in Two Distinct Iranian Families: Case Report and Literature Review, Molecular Genetics and Genomic Medicine (2024)
17. A Deleterious Frameshift Insertion Mutation in the Znf142 Gene Leads to Intellectual Developmental Disorder With Impaired Speech in Three Affected Siblings: Clinical Features and Literature Review, Molecular Genetics and Genomic Medicine (2023)
18. A Homozygous Nonsense Variant in Uvssa Causes Uv‑Sensitive Syndrome From Very Large Kindred: The First Report From Iran, Advanced Biomedical Research (2023)
19. A Novel Heterozygous Truncating Variant in the Ago1 Gene in an Iranian Family With Schizophrenia As an Unreported Symptom, Annals of Human Genetics (2023)
20. A Novel Homozygous Pathogenic Variant in Cyp11b1 in a Female Iranian Patient With 11B Hydroxylase Deficiency, Lab Medicine (2023)
21. A Novel Mettl5 Variant Disrupting a Donor Splice Site Leads to Primary Microcephaly-Related Intellectual Disability in an Iranian Family: Clinical Features and Literature Review, Journal of Genetics (2023)
22. Characterization of a Novel Androgen Receptor Gene Variant Identified in an Iranian Family With Complete Androgen Insensitivity Syndrome (Cais): A Molecular Dynamics Simulation Study, Journal of Biomolecular Structure and Dynamics (2023)
23. Griscelli Syndrome Type 1: A Novel Pathogenic Variant, and Review of Literature, Molecular Genetics and Genomics (2023)
24. Griscelli Syndrome Type 1: A Novel Pathogenic Variant, and Review of Literature, Molecular Genetics and Genomics (2023)
25. Lynch-Like Syndrome and Its Molecular Approaches: A Brief Report and Literature Review, Middle East Journal of Cancer (2023)
26. New Molecular Insights Into the A218v Variant Impact on the Steroidogenic Acute Regulatory Protein (Star) Associated With 46, Xy Disorders of Sexual Development, Molecular Genetics and Genomics (2023)
27. Novel In-Frame Duplication Variant Characterization in Late Infantile Metachromatic Leukodystrophy Using Whole-Exome Sequencing and Molecular Dynamics Simulation, PLoS ONE (2023)
28. The Introduction of Basic Fibroblast Growth Factor Promotes Quadriceps Muscle Regeneration After Damage in Mice, Journal of Sciences# Islamic Republic of Iran (2023)
29. The Introduction of Basic Fibroblast Growth Factor Promotes Quadriceps Muscle Regeneration After Damage in Mice, Journal of Sciences, Islamic Republic of Iran (2023)
30. Two Distinct Deleterious Causative Variants in a Family With Multiple Cancer-Affected Patients, Advanced Biomedical Research (2023)
31. Whole Exome Sequencing Revealed Variants in Four Genes Underlying X-Linked Intellectual Disability in Four Iranian Families: Novel Deleterious Variants and Clinical Features With the Review of Literature, BMC Medical Genomics (2023)
32. A Simplified Protocol for Microsatellite Instability Evaluation in Iranian Patients at Risk for Lynch Syndrome, Lab Medicine (2022)
33. A Versatile Biomimic Nanotemplating Fluidic Assay for Multiplex Quantitative Monitoring of Viral Respiratory Infections and Immune Responses in Saliva and Blood, Advanced Science (2022)
34. Bat25, Acvr2, and Tgfbr2 Mononucleotide Str Markers: A Triplex Panel for Microsatellite Instability Testing in Colorectal Tumors, Advanced Biomedical Research (2022)
35. Clinical Evaluation Followed by Molecular Diagnosis in a Multiplex Pedigree of Angelman Syndrome: A Case Report, Journal of Sciences, Islamic Republic of Iran (2022)
36. Next-Generation Sequencing Reveals a Novel Pathogenic Variant in the Atm Gene, International Journal of Neuroscience (2022)
37. The Importance of Snps at Mirna Binding Sites As Biomarkers of Gastric and Colorectal Cancers: A Systematic Review, Journal of Personalized Medicine (2022)
38. Using Classification and K-Means Methods to Predict Breast Cancer Recurrence in Gene Expression Data, Journal of Medical Signals and Sensors (2022)
39. Whole Exome Sequencing Identified a Novel Lama2 Frameshift Variant Causing Merosin-Deficient Congenital Muscular Dystrophy in a Patient With Cardiomyopathy, and Autism-Like Behavior, Neuromuscular Disorders (2022)
40. Whole-Exome Sequencing Identifies a Recurrent Small In-Frame Deletion in Myo15a Causing Autosomal Recessive Nonsyndromic Hearing Loss in 3 Iranian Pedigrees, Lab Medicine (2022)
41. X-Linked Mental Retardation-Hypotonic Facies Syndrome: Exome Sequencing Identifies Novel Clinical Characteristics Associated With C.5182G>C Mutation in the Atrx Gene, Molecular Genetics and Genomic Medicine (2022)
42. A Computational Framework to Infer Prostate Cancer-Associated Long Noncoding Rnas and Analyses for Identifying a Competing Endogenous Rna Network, Genetic Testing and Molecular Biomarkers (2021)
43. A Computational Framework to Infer Prostate Cancer-Associated Long Noncoding Rnas and Analyses for Identifying a Competing Endogenous Rna Network, Genetic Testing and Molecular Biomarkers (2021)
44. Bisulfite Treatment of Cg-Rich Track of Trinucleotide Repeat Expansion Disorder: Make the Sequence Less Cg Rich, Advanced Biomedical Research (2021)
45. Genetic Variant Effect Prediction by Supervised Nonnegative Matrix Tri-Factorization, Molecular Omics (2021)
46. Homozygous Tfg Gene Variants Expanding the Mutational and Clinical Spectrum of Hereditary Spastic Paraplegia 57 and a Review of Literature, Journal of Human Genetics (2021)
47. Jpx and Linc00641 Ncrnas Expression in Prostate Tissue: A Case-Control Study, Research in Pharmaceutical Sciences (2021)
48. Jpx and Linc00641 Ncrnas Expression in Prostate Tissue: A Case-Control Study, Research in Pharmaceutical Sciences (2021)
49. Molecular Diagnosis of Slc26a4-Related Hereditary Hearing Loss in a Group of Patients From Two Provinces of Iran, Intractable and Rare Diseases Research (2021)
50. Predicting Deleterious Missense Genetic Variants Via Integrative Supervised Nonnegative Matrix Tri-Factorization, Scientific Reports (2021)
51. Selection of Optimal Bioinformatic Tools and Proper Reference for Reducing the Alignment Error in Targeted Sequencing Data, Journal of Medical Signals and Sensors (2021)
52. Wrn Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family, Frontiers in Oncology (2021)
53. A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a Dfnb12 Nonsyndromic Phenotype of Cdh23, Audiology and Neurotology (2020)
54. A Novel Cadherin 23 Variant for Hereditary Hearing Loss Reveals Additional Support for a Dfnb12 Nonsyndromic Phenotype of Cdh23, Audiology and Neurotology (2020)
55. A Novel Pathogenic Variant in the Lrtomt Gene Causes Autosomal Recessive Non-Syndromic Hearing Loss in an Iranian Family, BMC Medical Genetics (2020)
56. A Novel Pathogenic Variant in the Lrtomt Gene Causes Autosomal Recessive Non-Syndromic Hearing Loss in an Iranian Family, BMC Medical Genetics (2020)
57. A Pathogenic Variant in the Transforming Growth Factor Beta I (Tgfbi) in Four Iranian Extended Families Segregating Granular Corneal Dystrophy Type Ii: A Literature Review, Iranian Journal of Basic Medical Sciences (2020)
58. Clinical and Genetic Analysis of Two Wolfram Syndrome Families With High Occurrence of Wolfram Syndrome and Diabetes Type Ii: A Case Report, BMC Medical Genetics (2020)
59. Clinical and Genetic Analysis of Two Wolfram Syndrome Families With High Occurrence of Wolfram Syndrome and Diabetes Type Ii: A Case Report, BMC Medical Genetics (2020)
60. Erratum: Clinical and Genetic Analysis of Two Wolfram Syndrome Families With High Occurrence of Wolfram Syndrome and Diabetes Type Ii: A Case Report (Bmc Medical Genetics (2020) 21 (13) Doi: 10.1186/S12881-020-0950-4), BMC Medical Genetics (2020)
61. Erratum: Clinical and Genetic Analysis of Two Wolfram Syndrome Families With High Occurrence of Wolfram Syndrome and Diabetes Type Ii: A Case Report (Bmc Medical Genetics (2020) 21 (13) Doi: 10.1186/S12881-020-0950-4), BMC Medical Genetics (2020)
62. Evaluation of Antitumor Effects of Aspirin and Lgk974 Drugs on Cellular Signaling Pathways, Cell Cycle and Apoptosis in Colorectal Cancer Cell Lines Compared to Oxaliplatin Drug, Fundamental and Clinical Pharmacology (2020)
63. Genetic Polymorphisms of Y-Chromosome Short Tandem Repeats (Y-Strs) in a Male Population From Golestan Province, Iran, Molecular Biology Research Communications (2020)
64. Homozygosity Mapping and Direct Sequencing Identify a Novel Pathogenic Variant in the Cisd2 Gene in an Iranian Wolfram Syndrome Family, Acta Diabetologica (2020)
65. Homozygosity Mapping and Direct Sequencing Identify a Novel Pathogenic Variant in the Cisd2 Gene in an Iranian Wolfram Syndrome Family, Acta Diabetologica (2020)
66. Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the Cel Gene, Advanced Biomedical Research (2020)
67. Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the Cel Gene, Advanced Biomedical Research (2020)
68. New Variants in the Cdh1 Gene in Iranian Families With Hereditary Diffuse Gastric Cancer, Middle East Journal of Cancer (2020)
69. Upregulation of Mtor, Rps6kb1, and Eif4ebp1 in the Whole Blood Samples of Iranian Patients With Multiple Sclerosis Compared to Healthy Controls, Metabolic Brain Disease (2020)
70. Upregulation of Mtor, Rps6kb1, and Eif4ebp1 in the Whole Blood Samples of Iranian Patients With Multiple Sclerosis Compared to Healthy Controls, Metabolic Brain Disease (2020)
71. Whole Exome Sequencing Identifies Novel Compound Heterozygous Pathogenic Variants in the Myo15a Gene Leading to Autosomal Recessive Non-Syndromic Hearing Loss, Molecular Biology Reports (2020)
72. A Novel Pathogenic Variant in the Cabp2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family, Audiology and Neurotology (2019)
73. A Novel Pathogenic Variant in the Cabp2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family, Audiology and Neurotology (2019)
74. A Novel Pathogenic Variant in the Marveld2 Gene Causes Autosomal Recessive Non-Syndromic Hearing Loss in an Iranian Family, Genomics (2019)
75. A Pathogenic Variant in Slc26a4 Is Associated With Pendred Syndrome in a Consanguineous Iranian Family, International Journal of Audiology (2019)
76. Clinical and Molecular Assessment of 13 Iranian Families With Wolfram Syndrome, Endocrine (2019)
77. Clinical and Molecular Assessment of 13 Iranian Families With Wolfram Syndrome, Endocrine (2019)
78. Engineered Zinc-Finger Nuclease to Generate Site-Directed Modification in the Klf1 Gene for Fetal Hemoglobin Induction, Journal of Cellular Biochemistry (2019)
79. Engineered Zinc-Finger Nuclease to Generate Site-Directed Modification in the Klf1 Gene for Fetal Hemoglobin Induction, Journal of Cellular Biochemistry (2019)
80. Epigenetics and Common Non Communicable Disease, Advances in Experimental Medicine and Biology (2019)
81. Evidence for Expression of Promoterless Gfp Cassette: Is Gfp an Ideal Reporter Gene in Biotechnology Science?, Research in Pharmaceutical Sciences (2019)
82. Evidence for Expression of Promoterless Gfp Cassette: Is Gfp an Ideal Reporter Gene in Biotechnology Science?, Research in Pharmaceutical Sciences (2019)
83. Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran, Advanced Biomedical Research (2019)
84. Identification and Clinical Implications of a Novel Myo15a Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing, Audiology and Neurotology (2019)
85. Molecular Genetic Study of Glutaric Aciduria, Type I: Identification of a Novel Mutation, Journal of Cellular Biochemistry (2019)
86. Molecular Genetic Study of Glutaric Aciduria, Type I: Identification of a Novel Mutation, Journal of Cellular Biochemistry (2019)
87. Mutation Analysis of Gjb2 and Gjb6 Genes and Screening of Nine Common Dfnb Loci in Iranian Pedigrees With Autosomal Recessive Nonsyndromic Hearing Loss, Indian Journal of Otology (2019)
88. Mutation Analysis of Gjb2 and Gjb6 Genes and Screening of Nine Common Dfnb Loci in Iranian Pedigrees With Autosomal Recessive Nonsyndromic Hearing Loss, Indian Journal of Otology (2019)
89. Mutations in Gjb2 As Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300Delat Mutation in Kurdish Population of Iran, Journal of Audiology and Otology (2019)
90. Mutations in Gjb2 As Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of C.299-300Delat Mutation in Kurdish Population of Iran, Journal of Audiology and Otology (2019)
91. Next-Generation Sequencing Reveals a Novel Pathological Mutation in the Tmc1 Gene Causing Autosomal Recessive Non-Syndromic Hearing Loss in an Iranian Kindred, International Journal of Pediatric Otorhinolaryngology (2019)
92. Novel Variants and Copy Number Variation in Cdh1 Gene in Iranian Patients With Sporadic Diffuse Gastric Cancer, Journal of Gastrointestinal Cancer (2019)
93. Profiling of 17 Y-Str Loci in Mazandaran and Gilan Provinces of Ira, Turkish Journal of Medical Sciences (2019)
94. The First Report of a Patient With Trisomy 4P and Monosomy 10Q, Archives of Iranian Medicine (2019)
95. A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type Ii in a Set of Iranian Patients, International Journal of Molecular and Cellular Medicine (2018)
96. A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type Ii in a Set of Iranian Patients, International Journal of Molecular and Cellular Medicine (2018)
97. A Novel Missense Mutation in Gipc3 Causes Sensorineural Hearing Loss in an Iranian Family Revealed by Targeted Next-Generation Sequencing, International Journal of Pediatric Otorhinolaryngology (2018)
98. A Novel Pathologic Variant in Otof in an Iranian Family Segregating Hereditary Hearing Loss, Otolaryngology - Head and Neck Surgery (United States) (2018)
99. A Novel Variant of Slc26a4 and First Report of the C.716T>A Variant in Iranian Pedigrees With Non-Syndromic Sensorineural Hearing Loss, American Journal of Otolaryngology - Head and Neck Medicine and Surgery (2018)
100. A Novel Variant of Slc26a4 and First Report of the C.716T>A Variant in Iranian Pedigrees With Non-Syndromic Sensorineural Hearing Loss, American Journal of Otolaryngology - Head and Neck Medicine and Surgery (2018)
101. Frequency of Gjb2 Mutations in Families With Autosomal Recessive Non-Syndromic Hearing Loss in Khuzestan Province, Genetika (2018)
102. Genetic Study of the Braf Gene Reveals New Variants and High Frequency of the V600e Mutation Among Iranian Ameloblastoma Patients, Journal of Oral Pathology and Medicine (2018)
103. Gjb2 Mutations Causing Autosomal Recessive Non-Syndromic Hearing Loss (Arnshl) in Two Iranian Populations: Report of Two Novel Variants, International Journal of Pediatric Otorhinolaryngology (2018)
104. Gjb2 Mutations Causing Autosomal Recessive Non-Syndromic Hearing Loss (Arnshl) in Two Iranian Populations: Report of Two Novel Variants, International Journal of Pediatric Otorhinolaryngology (2018)
105. Inducing Indel Mutation in the Sox6 Gene by Zinc Finger Nuclease for Gamma Reactivation: An Approach Towards Gene Therapy of Beta Thalassemia, Journal of Cellular Biochemistry (2018)
106. Investigating of Four Main Carbapenem-Resistance Mechanisms in High-Level Carbapenem Resistant Pseudomonas Aeruginosa Isolated From Burn Patients, Journal of the Chinese Medical Association (2018)
107. A Novel Pathogenic Variant in an Iranian Ataxia Telangiectasia Family Revealed by Next-Generation Sequencing Followed by in Silico Analysis, Journal of the Neurological Sciences (2017)
108. A Novel Pathogenic Variant in the Fzd6 Gene Causes Recessive Nail Dysplasia in a Large Iranian Kindred, Journal of Dermatological Science (2017)
109. A Novel Pathogenic Variant in the Fzd6 Gene Causes Recessive Nail Dysplasia in a Large Iranian Kindred, Journal of Dermatological Science (2017)
110. A Novel Pathogenic Variant in the Mitf Gene Segregating With a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred, Molecular Syndromology (2017)
111. A Novel Pathogenic Variant in the Mitf Gene Segregating With a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred, Molecular Syndromology (2017)
112. A Novel Tecta Mutation Causes Arnshl, International Journal of Pediatric Otorhinolaryngology (2017)
113. A Novel Tecta Mutation Causes Arnshl, International Journal of Pediatric Otorhinolaryngology (2017)
114. A Pcr-Based Molecular Detection of Strongyloides Stercoralisin Human Stool Samples From Tabriz City, Iran, Scientia Pharmaceutica (2017)
115. Cancers of the Endocrine System, Cancer Genetics and Psychotherapy (2017)
116. Comparative Study on Mutations in Cdh1 Gene in Iranian Patients With Hereditary Diffuse Gastric Cancer (Hdgc) and Sporadic Diffuse Gastric Cancer (Sdgc), Journal of Isfahan Medical School (2017)
117. Gastrointestinal Cancers, Cancer Genetics and Psychotherapy (2017)
118. Screening of Myo7a Mutations in Iranian Patients With Autosomal Recessive Hearing Loss From West of Iran, Iranian Journal of Public Health (2017)
119. Screening of Myo7a Mutations in Iranian Patients With Autosomal Recessive Hearing Loss From West of Iran, Iranian Journal of Public Health (2017)
120. Sox10 Mutation Causes Waardenburg Syndrome Associated With Distinctive Phenotypic Features in an Iranian Family: A Clue for Phenotype-Directed Genetic Analysis, International Journal of Pediatric Otorhinolaryngology (2017)
121. Sox10 Mutation Causes Waardenburg Syndrome Associated With Distinctive Phenotypic Features in an Iranian Family: A Clue for Phenotype-Directed Genetic Analysis, International Journal of Pediatric Otorhinolaryngology (2017)
122. The Lack of Correlation Between Tp53 Mutations and Gastric Cancer: A Report From a Province of Iran, Genetika (2017)
123. The Silencing Effect of Mir-30A on Itga4 Gene Expression in Vitro: An Approach for Gene Therapy, Research in Pharmaceutical Sciences (2017)
124. The Silencing Effect of Mir-30A on Itga4 Gene Expression in Vitro: An Approach for Gene Therapy, Research in Pharmaceutical Sciences (2017)
125. Characterization of Oxacillinase and Metallo-Β-Lactamas Genes and Molecular Typing of Clinical Isolates of Acinetobacter Baumannii in Ahvaz, South-West of Iran, Jundishapur Journal of Microbiology (2016)
126. Comparison of Different Methods for Erythroid Differentiation in the K562 Cell Line, Biotechnology Letters (2016)
127. Comparison of Different Methods for Erythroid Differentiation in the K562 Cell Line, Biotechnology Letters (2016)
128. Damage Intensity of Carvacrol on Prostatic Cancer Cells Linedu145 and Molecular Dynamic Simulation of It Effect on Apoptotic Factors, International Journal of PharmTech Research (2016)
129. Genetic Disruption of the Klf1 Gene to Overexpress the Γ-Globin Gene Using the Crispr/Cas9 System, Journal of Gene Medicine (2016)
130. Genetic Disruption of the Klf1 Gene to Overexpress the Γ-Globin Gene Using the Crispr/Cas9 System, Journal of Gene Medicine (2016)
131. Genetic Linkage Analysis of Dfnb40 and Dfnb48 Loci in Families With Autosomal Recessive Non-Syndromic Hearing Loss (Arnshl) From Western Provinces of Iran, Journal of Isfahan Medical School (2016)
132. Mutation in Second Exon of Myo15a Gene Cause of Nonsyndromic Hearing Loss and Its Association in the Arab Population in Iran, Genetika (2016)
133. Mutation in Second Exon of Myo15a Gene Cause of Nonsyndromic Hearing Loss and Its Association in the Arab Population in Iran, Genetika (2016)
134. Screening of Dfnb3 in Iranian Families With Autosomal Recessive Non-Syndromic Hearing Loss Reveals a Novel Pathogenic Mutation in the Myth4 Domain of the Myo15a Gene in a Linked Family, Iranian Journal of Basic Medical Sciences (2016)
135. Using Intron Splicing Trick for Preferential Gene Expression in Transduced Cells: An Approach for Suicide Gene Therapy, Cancer Gene Therapy (2016)
136. Using Intron Splicing Trick for Preferential Gene Expression in Transduced Cells: An Approach for Suicide Gene Therapy, Cancer Gene Therapy (2016)
137. A Lentiviral Vector Expressing Desired Gene Only in Transduced Cells: An Approach for Suicide Gene Therapy, Molecular Biotechnology (2015)
138. A Lentiviral Vector Expressing Desired Gene Only in Transduced Cells: An Approach for Suicide Gene Therapy, Molecular Biotechnology (2015)
139. A Novel Mutation in the Pax3 Gene Causes Waardenburg Syndrome Type I in an Iranian Family, International Journal of Pediatric Otorhinolaryngology (2015)
140. A Novel Mutation in the Pax3 Gene Causes Waardenburg Syndrome Type I in an Iranian Family, International Journal of Pediatric Otorhinolaryngology (2015)
141. Association of Interleukin-1 Gene Cluster Polymorphisms and Haplotypes With Multiple Sclerosis in an Iranian Population, Journal of Neuroimmunology (2015)
142. Correlation Between Mucosal Il-6 Mrna Expression Level and Virulence Factors of Helicobacter Pylori in Iranian Adult Patients With Chronic Gastritis, Jundishapur Journal of Microbiology (2015)
143. Correlation Between Mucosal Il-6 Mrna Expression Level and Virulence Factors of Helicobacter Pylori in Iranian Adult Patients With Chronic Gastritis, Jundishapur Journal of Microbiology (2015)
144. Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and Sparc Genes in Vascular Smooth Muscle Cells, Iranian Biomedical Journal (2015)
145. Genetic Linkage Analysis of the Dfnb63 Locus in Families With Autosomal Recessive Nonsyndromic Hearing Loss From Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran, Journal of Isfahan Medical School (2015)
146. Interleukin-1 Β Gene Polymorphisms in Iranian Patients With Uterine Fibroid, a Case-Control Study, Biosciences Biotechnology Research Asia (2015)
147. Molecular and Clinical Characterization of Waardenburg Syndrome Type I in an Iranian Cohort With Two Novel Pax3 Mutations, Gene (2015)
148. Molecular and Clinical Characterization of Waardenburg Syndrome Type I in an Iranian Cohort With Two Novel Pax3 Mutations, Gene (2015)
149. Staphylococcus Aureus Isolates Carrying Panton-Valentine Leucocidin Genes: Their Frequency, Antimicrobial Patterns, and Association With Infectious Disease in Shahrekord City, Southwest Iran, Jundishapur Journal of Microbiology (2015)
150. Staphylococcus Aureus Isolates Carrying Panton-Valentine Leucocidin Genes: Their Frequency, Antimicrobial Patterns, and Association With Infectious Disease in Shahrekord City, Southwest Iran, Jundishapur Journal of Microbiology (2015)
151. The Role and Spectrum of Slc26a4 Mutations in Iranian Patients With Autosomal Recessive Hereditary Deafness, International Journal of Audiology (2015)
152. The Role and Spectrum of Slc26a4 Mutations in Iranian Patients With Autosomal Recessive Hereditary Deafness, International Journal of Audiology (2015)
153. Detection of Metallo-Beta Lactamases Among Carbapenem-Resistant Pseudomonas Aeruginosa, Jundishapur Journal of Microbiology (2014)
154. Lack of Association Between Esr1 and Cyp1a1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent, Cell Journal (2014)
155. Significant Expressivity of Wolfram Syndrome: Phenotypic Assessment of Two Known and One Novel Mutation in the Wfs1 Gene in Three Iranian Families, Molecular Biology Reports (2014)