Lista de obras - Mohammad Hossein Sanati - Dominio Público Uruguay

3-Hydrogenkwadaphnin targets inosine 5'-monophosphate dehydrogenase and triggers post-G1 arrest apoptosis in human leukemia cell lines.

artículo científico publicado en 2005

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family.

artículo científico publicado en 2008

A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran

artículo científico publicado en 2007

A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

artículo científico publicado en 2008

Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians

artículo científico publicado en 2012

BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia.

artículo científico publicado en 2009

C77G mutation in protein tyrosine phosphatase CD45 gene and autoimmune hepatitis.

artículo científico publicado en 2005

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

artículo científico publicado en 2007

Cloning and Expression of Iranian Turkmen-thoroughbred Horse Follicle Stimulating Hormone in Pichia pastoris

artículo científico publicado en 2015

Colorimetric Assay for Exon 7 SMN1/SMN2 Single Nucleotide Polymorphism Using Gold Nanoprobes

artículo científico publicado en 2013

Colourimetric-based method for the diagnosis of spinal muscular atrophy using gold nanoprobes

artículo científico publicado en 2015

Designing A Transgenic Chicken: Applying New Approaches toward A Promising Bioreactor

scientific article published on 14 October 2019

Differential expression of mRNA for T-bet and GATA-3 transcription factors in peripheral blood mononuclear cells of patients with vitiligo.

artículo científico publicado en 2015

Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus

artículo científico publicado en 2012

Effect of flavonoids rich extract of Capparis spinosa on inflammatory involved genes in amyloid-beta peptide injected rat model of Alzheimer's disease.

artículo científico publicado en 2016

Effect of tertiary-butyl hydroperoxide (TBHP)-induced oxidative stress on mice sperm quality and testis histopathology.

artículo científico publicado en 2012

Effects of calcium binding on the structure and stability of human growth hormone.

artículo científico publicado en 2005

Expression patterns of Th1/Th2 transcription factors in patients with guttate psoriasis.

artículo científico publicado en 2013

Functional SNP in stem of mir-146a affects Her2 status and breast cancer survival.

artículo científico publicado en 2016

Granisetron adjunct to fluvoxamine for moderate to severe obsessive-compulsive disorder: a randomized, double-blind, placebo-controlled trial

scientific article published on 01 October 2012

Heat-induced production of human growth hormone by high cell density cultivation of recombinant Escherichia coli

artículo científico publicado en 2004

Identification of peptides specific for antibodies in vitiligo using a phage library.

artículo científico publicado en 2005

IgG subclasses pattern and high-avidity antibody to the C-terminal region of merozoite surface protein 1 of Plasmodium vivax in an unstable hypoendemic region in Iran

artículo científico publicado en 2009

Inhibitor IκBα promoter functional polymorphisms in patients with multiple sclerosis

artículo científico publicado en 2013

Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.

artículo científico publicado en 2003

Lack of association between interferon-gamma receptor-1 polymorphism and pulmonary TB in Iranian population sample.

artículo científico publicado en 2005

MiRNA-375 promotes beta pancreatic differentiation in human induced pluripotent stem (hiPS) cells.

artículo científico publicado en 2014

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

artículo científico publicado en 2006

Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia

artículo científico publicado en 2012

Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations

artículo científico publicado en 2008

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

artículo científico publicado en 2008

On the computation of the tertiary structure of globular proteins. III. Inter-residue distances and computed structures.

artículo científico publicado en 1982

Origin and spread of human mitochondrial DNA haplogroup U7.

artículo científico publicado en 2017

Pancreatic Endoderm-Derived From Diabetic Patient-Specific Induced Pluripotent Stem Cell Generates Glucose-Responsive Insulin-Secreting Cells

artículo científico publicado en 2016

Pancreatic islet differentiation of human embryonic stem cells by microRNA overexpression.

artículo científico publicado en 2013

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.

artículo científico publicado en 2005

Proteome analysis of post-transplantation recovery mechanisms of an EAE model of multiple sclerosis treated with embryonic stem cell-derived neural precursors.

artículo científico publicado en 2013

Psychiatry and psychoanalysis in Iran.

artículo científico publicado en 2006

Role of Th1/Th2 cells and related cytokines in autoimmune hepatitis

artículo científico publicado en 2017

Role of orexin-A in experimental autoimmune encephalomyelitis.

artículo científico publicado en 2016

Study of Th1/Th2 balance in peripheral blood mononuclear cells of patients with alopecia areata.

artículo científico publicado en 2015

TBHP-induced oxidative stress alters microRNAs expression in mouse testis

artículo científico publicado en 2014

The analysis of correlation between IL-1B gene expression and genotyping in multiple sclerosis patients.

artículo científico publicado en 2014

The influence of uric acid treatments on liver glutathione system prevent oxidative damages in experimental autoimmune encephalomyelitis mice.

artículo científico publicado en 2008

The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer.

artículo científico publicado en 2013

Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patients.

artículo científico publicado en 2007

Utility of Myelin Basic Protein as an Early Prognostic Biomarker in Multiple Sclerosis

Vector and Cell Line Engineering Technologies Toward Recombinant Protein Expression in Mammalian Cell Lines

artículo científico publicado en 2018

Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.

artículo científico publicado en 2016

Y chromosome diversity among the Iranian religious groups: A reservoir of genetic variation

artículo científico publicado en 2011

Lista de obras de Mohammad Hossein Sanati

3-Hydrogenkwadaphnin targets inosine 5'-monophosphate dehydrogenase and triggers post-G1 arrest apoptosis in human leukemia cell lines.

A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family.

A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran

A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

Ancient migratory events in the Middle East: new clues from the Y-chromosome variation of modern Iranians

BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia.

C77G mutation in protein tyrosine phosphatase CD45 gene and autoimmune hepatitis.

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.

Cloning and Expression of Iranian Turkmen-thoroughbred Horse Follicle Stimulating Hormone in Pichia pastoris

Colorimetric Assay for Exon 7 SMN1/SMN2 Single Nucleotide Polymorphism Using Gold Nanoprobes

Colourimetric-based method for the diagnosis of spinal muscular atrophy using gold nanoprobes

Designing A Transgenic Chicken: Applying New Approaches toward A Promising Bioreactor

Differential expression of mRNA for T-bet and GATA-3 transcription factors in peripheral blood mononuclear cells of patients with vitiligo.

Distinguishing the co-ancestries of haplogroup G Y-chromosomes in the populations of Europe and the Caucasus

Effect of flavonoids rich extract of Capparis spinosa on inflammatory involved genes in amyloid-beta peptide injected rat model of Alzheimer's disease.

Effect of tertiary-butyl hydroperoxide (TBHP)-induced oxidative stress on mice sperm quality and testis histopathology.

Effects of calcium binding on the structure and stability of human growth hormone.

Expression patterns of Th1/Th2 transcription factors in patients with guttate psoriasis.

Functional SNP in stem of mir-146a affects Her2 status and breast cancer survival.

Granisetron adjunct to fluvoxamine for moderate to severe obsessive-compulsive disorder: a randomized, double-blind, placebo-controlled trial

Heat-induced production of human growth hormone by high cell density cultivation of recombinant Escherichia coli

Identification of peptides specific for antibodies in vitiligo using a phage library.

IgG subclasses pattern and high-avidity antibody to the C-terminal region of merozoite surface protein 1 of Plasmodium vivax in an unstable hypoendemic region in Iran

Inhibitor IκBα promoter functional polymorphisms in patients with multiple sclerosis

Lack of association between Leber's hereditary optic neuropathy primary point mutations and multiple sclerosis in Iran.

Lack of association between interferon-gamma receptor-1 polymorphism and pulmonary TB in Iranian population sample.

MiRNA-375 promotes beta pancreatic differentiation in human induced pluripotent stem (hiPS) cells.

Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!

Mitochondrial DNA signals of late glacial recolonization of Europe from near eastern refugia

Mitochondrial mutation in Iranian patients with multiple sclerosis, correlation between haplogroups H, A and clinical manifestations

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

On the computation of the tertiary structure of globular proteins. III. Inter-residue distances and computed structures.

Origin and spread of human mitochondrial DNA haplogroup U7.

Pancreatic Endoderm-Derived From Diabetic Patient-Specific Induced Pluripotent Stem Cell Generates Glucose-Responsive Insulin-Secreting Cells

Pancreatic islet differentiation of human embryonic stem cells by microRNA overexpression.

Population screening for association of mitochondrial haplogroups BM, J, K and M with multiple sclerosis: interrelation between haplogroup J and MS in Persian patients.

Proteome analysis of post-transplantation recovery mechanisms of an EAE model of multiple sclerosis treated with embryonic stem cell-derived neural precursors.

Psychiatry and psychoanalysis in Iran.

Role of Th1/Th2 cells and related cytokines in autoimmune hepatitis

Role of orexin-A in experimental autoimmune encephalomyelitis.

Study of Th1/Th2 balance in peripheral blood mononuclear cells of patients with alopecia areata.

TBHP-induced oxidative stress alters microRNAs expression in mouse testis

The analysis of correlation between IL-1B gene expression and genotyping in multiple sclerosis patients.

The influence of uric acid treatments on liver glutathione system prevent oxidative damages in experimental autoimmune encephalomyelitis mice.

The mitochondrial C16069T polymorphism, not mitochondrial D310 (D-loop) mononucleotide sequence variations, is associated with bladder cancer.

Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patients.

Utility of Myelin Basic Protein as an Early Prognostic Biomarker in Multiple Sclerosis

Vector and Cell Line Engineering Technologies Toward Recombinant Protein Expression in Mammalian Cell Lines

Whole-exome sequencing of familial cases of multiple morphological abnormalities of the sperm flagella (MMAF) reveals new DNAH1 mutations.

Y chromosome diversity among the Iranian religious groups: A reservoir of genetic variation