Lista de obras - Mohammad Mehdi Heidari - Dominio Público Uruguay

A novel heteroplasmic mutation in mitochondrial tRNA gene associated with non-dystrophic myotonias

article

A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's ataxia

scientific article published on 19 September 2008

Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?

artículo científico publicado en 2009

Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.

artículo científico publicado en 2008

Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia.

artículo científico publicado en 2009

Detection of novel mitochondrial mutations in cytochrome C oxidase subunit 1 (COX1) in patients with familial adenomatous polyposis (FAP)

scientific article published on 24 September 2019

Electrochemical detection of the MT-ND6 gene and its enzymatic digestion: application in human genomic sample

artículo científico publicado en 2014

Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis

artículo científico publicado en 2017

Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism.

artículo científico publicado en 2017

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

artículo científico publicado en 2021

Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease

artículo científico publicado en 2020

Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease

article

Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients

artículo científico publicado en 2019

Quantum-dot biosensor for hybridization and detection of R3500Q mutation of apolipoprotein B-100 gene.

artículo científico publicado en 2015

Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis

artículo científico publicado en 2020

Sex determination based on amelogenin DNA by modified electrode with gold nanoparticle.

artículo científico publicado en 2013

Simple and label-free detection of DNA hybridization on a modified graphene nanosheets electrode.

artículo científico publicado en 2015

Simple and label-free electrochemical impedance Amelogenin gene hybridization biosensing based on reduced graphene oxide.

artículo científico publicado en 2014

Synthesis, structure characterization, DNA binding, and cleavage properties of mononuclear and tetranuclear cluster of copper(II) complexes

artículo científico publicado en 2015

The association of renin-angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss.

artículo científico publicado en 2017

Upregulation of miR-222 in both Helicobacter pylori- infected and noninfected gastric cancer patients.

artículo científico publicado en 2016

Lista de obras de Mohammad Mehdi Heidari

A novel heteroplasmic mutation in mitochondrial tRNA gene associated with non-dystrophic myotonias

A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's ataxia

Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?

Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.

Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia.

Detection of novel mitochondrial mutations in cytochrome C oxidase subunit 1 (COX1) in patients with familial adenomatous polyposis (FAP)

Electrochemical detection of the MT-ND6 gene and its enzymatic digestion: application in human genomic sample

Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis

Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism.

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease

Novel Point Mutations in the Gene in Pediatric Patients with Non-Familial Congenital Heart Disease

Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients

Quantum-dot biosensor for hybridization and detection of R3500Q mutation of apolipoprotein B-100 gene.

Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis

Sex determination based on amelogenin DNA by modified electrode with gold nanoparticle.

Simple and label-free detection of DNA hybridization on a modified graphene nanosheets electrode.

Simple and label-free electrochemical impedance Amelogenin gene hybridization biosensing based on reduced graphene oxide.

Synthesis, structure characterization, DNA binding, and cleavage properties of mononuclear and tetranuclear cluster of copper(II) complexes

The association of renin-angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss.

Upregulation of miR-222 in both Helicobacter pylori- infected and noninfected gastric cancer patients.