Code

Feb 21,2018     Morning

HN10100290007

VDR, CYP24A1, CYP27B1 gene expression analysis in schizophrenia patients

HN10102630259

Investigation of the role of apoptosis, necroptosis and DNA damage signaling pathways in multiple sclerosis

HN10102650275

Relationship between COMT polymorphism and opioid addiction in zabol (Iran)

HN10102570240

Association analysis between interleukin 1 beta locus -511 gene polymorphism and bipolar I disorder,a case control study in an Iranian population

HN10101160063

Hydroalcoholic extract of Anchusa italica injection protects against global cerebral ischemia–reperfusion injury via nitric oxide mechanism in rats

HN10102290193

Whole Exome Sequencing reveals de novo mutations in POGZ and KMT2D genes of Iranian individuals with NDD

HN10102340270

The first world report of a homozygous mutation in inositol monophosphatase 1 (IMPA1) gene two boy with autismin an Iranian family

HN10100650071

Role of epigenetics factor (miRNA) in diagnose and treatment of depression

HN10100490057

A Systematic review of vitamin D pathway genetic variation and Risk of Breast Cancer

HN10101940169

Blood assessment of the expression levels of matrix metalloproteinase 9 (MMP9) and its natural inhibitor,TIMP1 genes in Iranian schizophrenic patients

HN10101110059

The Study of association between polymorphism Ser311Cys in DRD2 in patients with Schizophrenia reffred to a spechialized psychiatric hospital in Yazd

HN10100530243

Computational neurogenetics models : integration of gene regulatory networks and artificial neural networks

HN10102050187

MicroRNAs mediate regulatory effects on cerebral ischemia process

HN10102890321

Bioinformatic prediction of Long-Non Coding RNAs as Regulatory Candidates of ADRB2 Gene Expression

HN10100780177

Gene expression and methylation analysis on MBP, TCF4, EGR1 genes in the blood of patients with schizophrenia and its psychopathology, intelligence and cognitive impairments

HN10101140084

The Study of association between Val158Met polymorphism in COMT gene and deleting polymorphism of Glutathione S-transferasesM1 gene in patient with Schizophrenia reffered to a specialized psychiatric hospital in Yazd

HN10102020168

Evaluation of CXCL8 gene expression in patients with bipolar disorder

HN10101180067

A novel candidate gene, SNRK, causes Bardet-Biedl Syndrome in an Iranian Family

HN10100350010

Novel mechanisms mediated by FMRP in Fragile X syndrome (FXS)

HN10100540022

Genetic landscape of Non-syndromic Intellectual disability

HN10101540147

Epigenetic reprogramming and regulation of neural cell fate using small molecules to cure neurological disorders: Is it possible?

HN10102620256

Investigation of association between coagulation factor v, factor II, methylenetetrahydrofolate reductase, tumor necrosis factor alpha and plasminogen activator inhibitor genetic variations and stroke: a case-control study in an Iranian population with high incidence rate of stroke

HN10102620255

The association of miR-221 rs113054794, miR-146a rs2910164 and miR-34a rs369892834 polymorphisms with stroke risk

HN10102620254

Association Study on SNPs of PPAP2B, ZC3HC1 and ADAMTS7 genes with Stroke and Myocardial infarction

HN10102620252

Analysis of polymorphisms of paraoxonase, coagulation factor 13, platelet glycoprotein IIb, β2 adrenergic receptor and angiotensin II receptor genes in patients with stroke problem

HN10102620251

The association of AGT, PDE4D and IL10 gene polymorphisms and stroke risk

HN10102620250

The association study of APOE Ɛ2 Ɛ3 Ɛ4, IL-6-572GC, IL6-174GC, ACE InsertionDeletion, and eNOS4b4a Polymorphisms in Iranian Stroke patients

HN10102620249

Association between mir-125a and mir-30c gene polymorphisms and ischemic stroke; a case control study

HN10102620248

Association of the miR-499 and miR-608 Polymorphisms With ischemic stroke in northeast Iran Population

HN10102620247

Therapeutic approaches for Facioscapulohumeral Muscular Dystrophy(FSHD)

HN10102620246

Review and case series on the genetic and epigenetic alteration in Facioscapulohumeral muscular dystrophy

HN10100880045

A Study of CAG repeat instability of HTT gene following spermatogenesis,by single sperm analysis

HN10100180004

Radiological Survey in intraventricular Cavernomas

HN10100440020

Epigenetic mechanisms of Central nervous system (CNS) disorders is the key in pharmacoepigenomics development

HN10101230226

Expression of influence BKN2A and PTEN In Glioblastoma Multiforme

HN10101960160

Polymorphisms at activated protein C cleavage sites of factor V: Are they important in the absence of factor V Leiden?

HN10102360198

Genotoxicity and cytotoxicity of mineral trioxide aggregate and calcium enriched mixture cements on L929 mouse fibroblast cells

HN10102370199

Evaluation of in vitro toxicity of peptide (N-acetyl-Leu-Gly-Leu-COOH)-substituted-β- cyclodextrin derivative, a novel drug carrier, in PC-12 cells

HN10101560305

genotype-phenotype correlationin in Iranian patients with Kennedy disease

HN10100790069

Evaluation the possibility of induction of neurogenic differentiation of mesenchymal stem cells using Butylated hydroxyl anisol and curcumin

HN10101510152

Multiple Sclerosis and mitochondrial gene variation: A systematic review

HN10102380203

Molecular Analysis of SNP (rs16147) polymorphism of Neuropeptide Y gene in the autism spectrum disorders ‎

HN10102760298

Detection of MFSD8 gene Mutation in Neuronal ceroid lipofuscinosis (type 7): A Case Report

HN10101790141

Regulation of Gene Expression in Neural Stem Cell Differentiation and Self-Renewal

HN10101950154

Case Report: Limb-girdle Muscular Dystrophy with New Mutation in SGCB gene

HN10102550228

Detection of PANK2 Gene Mutation in PKAN: A Case Report

HN10102670282

Case report: members of a family with ADHD and t (2; 7) (q33; q31.2) karyotype

Code

Feb 21,2018     Afternoon

HN10101160065

Application of whole exome sequencing to Genetic Diagnosis in Families with Autosomal Recessive Non-syndromic Hearing Loss

HN10101340215

A case study on Hereditary Pheochromocytoma and Paraganglioma, and Alzheimer’s disease

HN10102170185

The frequency Distribution of HLA-DRB1*1501,-DQA1*0102,-DQB1*0602,-DRB5*01,-A*0301 alleles and haplotypes in normal population of Khuzestan

HN10102170184

Distribution Analysis of two,three and four allelic HLA haplotypes in normal population of Khuzestan

HN10101010066

Association of HLA-DRB1*1501 allele with Multiple Sclerosis in North East and West of Iran.

HN10102040167

Therapeutic Effect of Transplanted Human Wharton’s Jelly Stem Cell-Derived Oligodendrocyte Progenitor Cells in an Animal Model of Multiple Sclerosis

HN10102100172

Genetic Linkage of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations

HN10100490018

MTHFR 677C>T Polymorphism and Male Infertility Risk: A Meta-Analysis

HN10101130213

Sorting nexin expression involved in endosomal trafficking is decreased in high EDSS of multiple sclerosis

HN10101000049

Expression of apoptosis-regulatory genes in the hippocampus of rat neonates born to mothers with diabetes

HN10101050140

Parkinson"s disease and reliable biomarkers for early detection

HN10100990119

Amyloid plaques and Alzheimer’s disease

HN10101670171

Association of HLA-DQA1*0102,-DQB1*0602,-DRB5*01,-A*0301 haplotypes in different genders of Khuzestan

HN10101670170

Analysis of two allelic HLA haplotypes in different ethnicities of Khuzestan Province

HN10102850318

A model for Brain tumor growth

HN10102580242

Intensive speech and language disorders treatment of hydrocephalic children - a case study

HN10101420116

Expression analysis of protein inhibitor of activated STAT (PIAS) genes in multiple sclerosis patients

HN10102190192

Genetic screening in two Iranian families with early-onset Alzheimer’s disease identified a novel PSEN1 mutation

HN10102690288

Isocitrate dehydrogenase (IDH1 and IDH2) Mutations in brain tomur

HN10102690287

Analysis of Cancer testis antigens in Glioblastoma

HN10101360099

Potentiating effects of Perovskia abrotanoides Karel. on pentobarbital-induced sleep

HN10102280222

Effects of CB1 antagonist rimonabant on passive avoidance memory in harmaline induced tremor

HN10100900244

Supranuclear Gaze Palsy, Mechanism, Disorders and Case Report

HN10100960056

Synesthesia: The privilege of genetic mutations

HN10101530130

Role of Glucocorticoid- receptor gene polymorphisms in multiple sclerosis pathogenesis

HN10101250085

Multiple sclerosis during pregnancy and maternal, fetal, neonatal outcomes: A systematic review study

HN10101890195

Genetic basis of Autism a neurogenetic complex disease.

HN10100590133

Autosomal Recessive Cerebellar Ataxia,NGS,Classification,Diagnosis Algorithm,50 cases.

HN10102770295

Genetics of Parkinson

HN10101440100

Ecotropic Viral Integration Site 5 (EVI5) variants are associated with multiple sclerosis in Iranian population

HN10100210092

Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism

HN10102750309

Genetic Background Influences Immunity-Related Genes in two Iranian Ethnical Multiple Sclerosis Groups

HN10101550122

Dysregulated serum concentration of lipid fractions and its association with the risk of Parkinson"s disease

Code

Feb 22,2018         Morning

HN10100570031

Novel deletion mutation in GAA in Iranian glycogen storage disease type II patients

HN10102330197

Study of causes of 1-59 year old children with genetic causes in the external department of Tabriz University of Medical Sciences in 2016

HN10100420016

Association study between ACE gene polymorphisms and migraine

HN10102340299

Continuous limb tremors can create due to del18

HN10102210256

Evaluation of HLA class I & II frequency in MS patients from Khuzeatan province.

HN10101740135

The study of miR-202-3p gene expression in Multiple Sclerosis patients

HN10100710029

A Novel Mutation in the Choline Kinase Beta Gene in an Iranian Kindred

HN10100570023

Pompe disease: Genetics aspects of diagnosis and treatment

HN10102110173

The study of relationship of rs1800872 polymorphism in IL-10 gene promoter in Iranian patients with coronary artery disease

HN10100560080

The Identification of Nucleotide Variations in Mitochondrial tRNA of Serine, Asparagine, Aspartic acid, Cysteine and Tyrosine Genes in Non-Dystrophic Myotonia Patients

HN10101610127

The genetic basis and gene therapy of duchenne muscular dystrophy (DMD)

HN10102150175

Distribution Analysis of HLA-DQA1*0102,-DQB1*0602,-DRB5*01,-A*0301 alleles and haplotypes in normal population of Khuzestan Province

HN10102840325

Associated SNPs with MS : Bioinformatics analysis of MS associated genes,long non - coding RNAs and their SNPs

HN10102610317

Multiple sclerosis genetics

HN10100870044

Role of the MTHFR C677T and 2572G>T polymorphisms in genetic susceptibility of migraine in Iranian population

HN10102320304

Protective effects of chamomile extract against harmaline induced essential tremor

HN10101600292

neuromuscular disorders patients referring to Kashmar Genetic Counseling Center

HN10102740302

Genetic basis of myasthenia gravis , A Review.

HN10100730030

Association between polymorphisms of NOS2 and NOS3 genes and multiple sclerosis

HN10101320087

In silico characterization and analysis of transcriptional inhibition of PDGF in glioblastoma tumor cells by CRISPR-C13a technique

HN10100360089

exosome and spinal cord injury

HN10101170279

An overview of gene therapy for lumbar disc disease Take on animal and human studies

HN10101170276

Viral gene therapy in paikinson"s disease

HN10100750032

Correlation of miR-622 downregulation with development of multiple¬ sclerosis

HN10100970148

The role of vitamin D in Multiple Sclerosis disease

HN10100770224

Spinal-Muscular Atrophy gene therapy: From ASOs to CRISPR/Cas9

HN10100770047

production of CRISPR/Cas9 based gene editing vector in order to correction of dystrophin gene

HN10102590235

Gene Therapy in Duchenne Muscular Dystrophy

HN10101310088

In silico characterization and analysis of transcriptional inhibition of EGFR in childhood brain stem glioma tumor cells by CRISPR-C13a technique

HN10101370091

The Effect and Therapeutic Potential Role of microRNAs in Alzheimer’s Disease

HN10102480271

Current Developments in Stem Cell Therapy for Amyotrophic Lateral Sclerosis

HN10102480261

Precise Correction of Disease Mutations: an Emerging therapy in Limb Girdle Muscular Dystrophy

HN10102330194

A survey on the evolution of 12-month-old children in Tabriz University of medical sciences during the first nine months of the year1396

HN10101390105

Determining the Relationship between Hypermethylation of Apoptotic Genes with Clinical and Therapeutic Characteristics of Patients with Gastric Cancer under Chemotherapy

HN10101950156

Prevalence and molecular pathway in limb girdle muscular dystrophies: a review

HN10102140221

Protective effects of Fennel extract against harmaline essential tremor rat model

HN10101350090

Duchenne Muscular Dystrophy (DMD): An updated review of common available therapies

HN10101470112

A Novel mutation of WNK1 gene causes hereditary sensory and autonomic neuropathy type II

HN10101470111

A Novel mutation of SMN1 Gene causes Spinal Muscular Atrophy type 1

HN10102230217

Effects of chamomile extract on stride pattern in harmaline Essential tremor Rat model

HN10100580038

The evaluation of NDM29 non-coding RNA in plasma of patients with Alzheimer"s disease

HN10100590118

CRISPR in Neurology and Neuroscience

HN10102180180

Theranostic value of MicroRNAs in Bipolar disorder

HN10102180179

The versatile role of MicroRNA in Huntington disease

HN10100810058

Rare Variants, a way of personalized medicine in neurological disorders

HN10100810039

Next Generation Sequencing Diagnosis in Neurological Disorders

HN10102420225

HbF induction by Simvastatin and Romidepsin

Code

Feb 22,2018          Afternoon

HN10102560232

Rescue of dystrophin protein expression by using of U7 snRNA-Mediated Exon skipping

HN10101780142

Neurogenetic and Maternal Occupational Exposures

HN10102500253

Expression of motor neuron markers in endometrial stem cell derived neurons differentiated with purmorphamin small molecule

HN10101930300

Aequorin mutations Asn 28 and Lys 30 enhance Ca2+ capture activity - A possibility for neurodegenerative disease treatment

HN10100860210

Genetic basis of Type I Interferon excessive production in Neuropsychiatric Systemic Lupus Erythematosus

HN10100910138

Detection of PLEKHG2 Mutation in Microcephaly: A Case Report

HN10100910137

Detection of GAN gene Mutation in Leukodystrophy: A Case Report

HN10100840284

Cytokine profile in autistic patients

HN10102200196

Assessment of miRNA Expression data from human postmortem putamen samples in Parkinson’s disease

HN10102050189

Prognostic value and regulatory effect of MicroRNAs in Encephalitis

HN10101480125

Maternal Pesticide Exposure and Neural Tube Defects: A systematic review

HN10101480124

Vitamin D status in children with cerebral palsy: A systematic review

HN10101120062

The Study of Inbreeding Levels of 3 and 4 in Infertile Couples and Their Parents

HN10100940273

The effects of ω-3 fatty acids and Nano-curcumin supplementation on vascular cell Adhesion Molecule-1 (VCAM-1) gene expression and serum level in migraine patients

HN10100940048

Molecular mechanism and affected gene by omega 3 fatty acids in migraine headache

HN10101850238

Interferon-beta Gene Therapy in Multiple Sclerosis; Prospective and Challenges

HN10102610241

Genetic Role in Migraine

HN10102640280

Recent therapeutic advances for spinal muscular atrophy: SMN and beyond.

HN10102000263

Potential therapeutic application of CRISPR-Cas9 in Huntington"s disease

HN10102690285

Analysis of HORMAD1, FTHL17 and ADAM29 Cancer/testis specific genes expression in Glioblastoma

HN10100460161

Micro RNA Therapeutics in Multiple Sclerosis: New Era of Myelin Repair Drugs

HN10102680296

Current development of Duchenne muscular dystrophy therapies

HN10101410098

A Study on Role of Neurogenetics in NBIC Convergent Technologies Network

HN10101290083

Zinc Deficiency in Pregnancy and fetal Neurobehavioral Development

HN10101380095

cloning the coding region of ODNaTx8 gene from Odonthobuthus doriae in E. coli

HN10102390201

New approaches to treatment in Glioblastoma multiform.

HN10102430214

Gene editing as a new therapeutic era for SMA

HN10100630164

microRNA- based Novel Therapeutic Approach in Epilepsy;

HN10101250086

The Role of Acupuncture in Treatment of Cerebral Palsy: A systematic review

HN10100410037

The relationship between hypermethylation of BAX gene and gastric carcinoma

HN10100070003

Stem Cell and Gene therapy as new therapeutic platforms for Alzheimer therapy

HN10101240078

novel mutations in SH3TC2 in a young Iranian boy with Charcot-Marie-Tooth disease type 4C.

HN10100470015

Anxiety leads to up-regulation of CD36 on the monocytes of chronic hepatitis B-infected patients

HN10102900324

Inductive and Inhibitory Pathways in Oligodendrocyte Precursor Cells Differentiation

HN10100550019

Ataxia-Telangiectasia with novel splice site mutation in the ATM gene

HN10101070077

Title: Investigating the frequency distribution of febrile seizure in pediatric patients admitted to Shariati Hospital in Isfahan in the years 1377-1376

HN10101270126

A case of Frank-Ter Haar syndrome with a c.127C>T (p.Arg43Trp) mutation in SH3PXD2B gene

HN10101990163

CRISPR-CAS9 Application for Treating Neurological Diseases

HN10102710289

“Modifier Genes” Influenced Phenotype in Spinal Muscular Atrophy (SMA) Disease as Future Therapeutic

HN10100210005

An update of common autosomal recessive non-syndromic hearing loss genes in Iranian population

HN10100690026

Efficacy of modified ketogenic diet on frequency of seizure in patients (2-6 year) with refractory epilepsy

HN10102880323

Neurotoxicity and Breast Cancer Therapy

HN10101030055

A novel missense mutation in the POMGNT1 gene in an Iranian patient with muscle eye brain disease

HN10101030053

A missense mutation in the OCRL gene in an Iranian family with three affected boys