Lista de obras -

A Novel Regulatory Function of Long Non-coding RNAs at Different Levels of Gene Expression in Multiple Sclerosis

artículo científico publicado en 2019

Aberrant Expression of Long Non-coding RNAs in Peripheral Blood of Autistic Patients

scientific article published on 18 December 2018

Assessment of Protein Prenylation Pathway in Multiple Sclerosis Patients

artículo científico publicado en 2018

Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders

scientific article published on 01 April 2019

Association Study of VMAT1 Polymorphisms and Suicide Behavior

artículo científico publicado en 2018

Association of ANRIL gene polymorphisms with prostate cancer and benign prostatic hyperplasia in an Iranian population

artículo científico publicado en 2017

Association of HLA alleles with autism

artículo científico publicado en 2018

Association study of a single nucleotide polymorphism in brain cytoplasmic 200 long-noncoding RNA and psychiatric disorders

artículo científico publicado en 2020

Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population.

artículo científico publicado en 2017

Associations Between Two Single-Nucleotide Polymorphisms in NINJ2 Gene and Risk of Psychiatric Disorders

artículo científico publicado en 2019

Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism

artículo científico publicado en 2018

Determination of cytokine levels in multiple sclerosis patients and their relevance with patients' response to Cinnovex.

artículo científico publicado en 2017

Dysregulation of long non-coding RNA profile in peripheral blood of multiple sclerosis patients

scientific article published on 01 August 2018

Ecotropic Viral Integration Site 5 (EVI5) expression analysis in multiple sclerosis patients.

artículo científico publicado en 2017

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

artículo científico publicado en 2017

Erratum: Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients [Corrigendum]

article

Expression Analysis of Long Non-coding RNAs in the Blood of Multiple Sclerosis Patients

artículo científico publicado en 2017

Expression Analysis of Vitamin D Signaling Pathway Genes in Epileptic Patients

artículo científico publicado en 2018

Expression Analysis of lncRNAs in Refractory and Non-Refractory Epileptic Patients

scientific article published on 03 January 2020

Expression analysis of beta-secretase 1 (BACE1) and its naturally occurring antisense (BACE1-AS) in blood of epileptic patients

artículo científico publicado en 2018

Expression analysis of cytokine coding genes in epileptic patients

artículo científico publicado en 2018

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

article

FOXP3 gene variations and susceptibility to autism: A case-control study.

artículo científico publicado en 2016

HOTAIR genetic variants are associated with prostate cancer and benign prostate hyperplasia in an Iranian population

artículo científico publicado en 2017

Interleukin (IL)-8 polymorphisms contribute in suicide behavior

artículo científico publicado en 2018

Myxovirus resistance protein A (MxA) polymorphism is associated with IFNβ response in Iranian multiple sclerosis patients.

artículo científico publicado en 2017

Peripheral expression of long non-coding RNAs in bipolar patients

artículo científico publicado en 2019

Phospholipase D1 expression analysis in relapsing-remitting multiple sclerosis patients.

artículo científico publicado en 2017

Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.

artículo científico publicado en 2017

Retinoic acid-related orphan receptor alpha (RORA) variants and risk of breast cancer.

artículo científico publicado en 2017

Retinoic acid-related orphan receptor alpha (RORA) variants are associated with autism spectrum disorder.

artículo científico publicado en 2017

STAT5a and STAT6 gene expression levels in multiple sclerosis patients

artículo científico publicado en 2017

The Growth Arrest-Specific Transcript 5 (GAS5) and Nuclear Receptor Subfamily 3 Group C Member 1 (NR3C1): Novel Markers Involved in Multiple Sclerosis

artículo científico publicado en 2018

Upregulation of VEGF-A and correlation between VEGF-A and FLT-1 expressions in Iranian multiple sclerosis patients

scientific article published on 11 January 2020

Vaccinia Related Kinase 2 (VRK2) expression in neurological disorders: schizophrenia, epilepsy and multiple sclerosis

artículo científico publicado en 2017

Lista de obras de

A Novel Regulatory Function of Long Non-coding RNAs at Different Levels of Gene Expression in Multiple Sclerosis

Aberrant Expression of Long Non-coding RNAs in Peripheral Blood of Autistic Patients

Assessment of Protein Prenylation Pathway in Multiple Sclerosis Patients

Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders

Association Study of VMAT1 Polymorphisms and Suicide Behavior

Association of ANRIL gene polymorphisms with prostate cancer and benign prostatic hyperplasia in an Iranian population

Association of HLA alleles with autism

Association study of a single nucleotide polymorphism in brain cytoplasmic 200 long-noncoding RNA and psychiatric disorders

Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population.

Associations Between Two Single-Nucleotide Polymorphisms in NINJ2 Gene and Risk of Psychiatric Disorders

Cytoplasmic FMRP interacting protein 1/2 (CYFIP1/2) expression analysis in autism

Determination of cytokine levels in multiple sclerosis patients and their relevance with patients' response to Cinnovex.

Dysregulation of long non-coding RNA profile in peripheral blood of multiple sclerosis patients

Ecotropic Viral Integration Site 5 (EVI5) expression analysis in multiple sclerosis patients.

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

Erratum: Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients [Corrigendum]

Expression Analysis of Long Non-coding RNAs in the Blood of Multiple Sclerosis Patients

Expression Analysis of Vitamin D Signaling Pathway Genes in Epileptic Patients

Expression Analysis of lncRNAs in Refractory and Non-Refractory Epileptic Patients

Expression analysis of beta-secretase 1 (BACE1) and its naturally occurring antisense (BACE1-AS) in blood of epileptic patients

Expression analysis of cytokine coding genes in epileptic patients

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

FOXP3 gene variations and susceptibility to autism: A case-control study.

HOTAIR genetic variants are associated with prostate cancer and benign prostate hyperplasia in an Iranian population

Interleukin (IL)-8 polymorphisms contribute in suicide behavior

Myxovirus resistance protein A (MxA) polymorphism is associated with IFNβ response in Iranian multiple sclerosis patients.

Peripheral expression of long non-coding RNAs in bipolar patients

Phospholipase D1 expression analysis in relapsing-remitting multiple sclerosis patients.

Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder.

Retinoic acid-related orphan receptor alpha (RORA) variants and risk of breast cancer.

Retinoic acid-related orphan receptor alpha (RORA) variants are associated with autism spectrum disorder.

STAT5a and STAT6 gene expression levels in multiple sclerosis patients

The Growth Arrest-Specific Transcript 5 (GAS5) and Nuclear Receptor Subfamily 3 Group C Member 1 (NR3C1): Novel Markers Involved in Multiple Sclerosis

Upregulation of VEGF-A and correlation between VEGF-A and FLT-1 expressions in Iranian multiple sclerosis patients

Vaccinia Related Kinase 2 (VRK2) expression in neurological disorders: schizophrenia, epilepsy and multiple sclerosis