Lista de obras - Mahsa M. Amoli - Dominio Público Uruguay

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Patients with Neonatal Diabetes.

artículo científico publicado en 2017

A new frameshift MEN1 gene mutation associated with familial malignant insulinomas

artículo científico publicado en 2011

A novel missense mutation in oncostatin M receptor beta causing primary localized cutaneous amyloidosis

artículo científico publicado en 2014

A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations

artículo científico publicado en 2014

Absence of kl-vs variant of klotho gene in Iranian cardiac patients (comparison to the world populations).

artículo científico publicado en 2011

Acarbose versus trans-chalcone: comparing the effect of two glycosidase inhibitors on obese mice.

artículo científico publicado en 2015

Adenosine deaminase gene polymorphism is associated with obesity in Iranian population

artículo científico publicado en 2007

Adiponectin gene variants and abdominal obesity in an Iranian population

article

An in silico approach to identify and prioritize miRNAs target sites polymorphisms in colorectal cancer and obesity

scientific article published on 18 October 2020

Apolipoprotein E gene polymorphism and its effect on anthropometric measures in normoglycemic subjects and type 2 diabetes

artículo científico publicado en 2012

Apolipoprotein E gene polymorphism and total serum cholesterol level in Iranian population

artículos científicos

Association Between the Polymorphism of Glu298Asp in Exon 7 of the eNOS Gene With Foot Ulcer and Oxidative Stress in Adult Patients With Type 2 Diabetes

artículo científico publicado en 2017

Association between 318C/T polymorphism of the CTLA-4 gene and systemic lupus erythematosus in Iranian patients

artículo científico publicado en 2014

Association between Genetic Variants and Diabetes Mellitus in Iranian Populations: A Systematic Review of Observational Studies.

artículo científico publicado en 2015

Association between MIF gene variation and Meniere's disease.

artículo científico publicado en 2013

Association between vitamin D receptor gene polymorphisms (Fok1 and Bsm1) and osteoporosis: a systematic review

artículo científico publicado en 2014

Association of interleukin-6 polymorphisms with obesity: A systematic review and meta-analysis

artículo científico publicado en 2019

Association of miRNA targetome variants in LAMC1 and GNB3 genes with colorectal cancer and obesity

Association of survivin gene polymorphism with endometrial cancer.

artículo científico publicado en 2012

Association of vascular endothelial growth factor (VEGF) Gene polymorphisms and expression with the risk of endometriosis: a case-control study

scientific article published on 22 April 2019

Association of vitamin D receptor gene polymorphism with the occurrence of low bone density, osteopenia, and osteoporosis in patients with type 2 diabetes

CDH1 and DDR1 common variants confer risk to vitiligo and autoimmune comorbidities

scientific article published on 16 March 2019

Comments on "Association between miR-499 rs3746444 polymorphism and coronary heart disease susceptibility: An evidence-based meta-analysis of 5063 cases and 4603 controls"

scientific article published on 04 May 2019

Curcumin inhibits in vitro MCP-1 release from mouse pancreatic islets.

artículo científico publicado en 2006

Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation

article

Effect of adiponectin gene polymorphisms on waist circumference in patients with diabetes.

artículo científico publicado en 2012

Effects of extremely low frequency electromagnetic fields on paraoxonase serum activity and lipid peroxidation metabolites in rat

artículo científico publicado en 2014

Endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism association with type 2 diabetes and its chronic complications

scientific article published on 21 January 2011

Epistatic interaction between adiponectin and survivin gene polymorphisms in endometrial carcinoma

artículo científico publicado en 2014

Establishing a cGMP pancreatic islet processing facility: the first experience in Iran.

artículo científico publicado en 2011

Evaluation of the presence of Epstein-Barr virus (EBV) in Iranian patients with thyroid papillary carcinoma

artículo científico publicado en 2017

Genetic markers of disease susceptibility and severity in giant cell arteritis and polymyalgia rheumatica.

artículo científico publicado en 2003

IL-23 gene expression in PBMCs of patients with coronary artery disease

scientific article published on January 2012

Inducible but not endothelial nitric oxide synthase polymorphism is associated with susceptibility to rheumatoid arthritis in northwest Spain.

artículo científico publicado en 2004

Inflammation related miRNAs as an important player between obesity and cancers

scientific article published on 26 November 2019

Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

scientific article published on 29 May 2018

Is DNA methylation responsible for immune system dysfunction in schizophrenia?

artículo científico publicado en 2011

Liver alpha-amylase gene expression as an early obesity biomarker

artículo científico publicado en 2016

Macrophage migration inhibitory factor gene polymorphism is not associated with pemphigus vulgaris in Iranian patients.

artículo científico publicado en 2012

Methylomics of breast cancer: Seeking epimarkers in peripheral blood of young subjects.

artículo científico publicado en 2017

MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis ⬇️

artículo científico publicado en 2019

Mutation screening of RET proto-oncogene in a family with medullary thyroid carcinoma, marfanoid habitus and pheochromocytoma; from clinically MEN2B to genetically MEN2A syndrome

scientific article published on 31 January 2012

Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease

artículo científico publicado en 2009

No evidence of association between CTLA-4 polymorphisms and systemic lupus erythematosus in Iranian patients

artículo científico publicado en 2013

Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Polymorphism (rs4821481) is Associated with Urinary Albumin Excretion in Iranian Diabetic Patients

article

Novel mutations of wolframin: a report with a look at the protein structure

artículo científico publicado en 2011

Polymorphism in the STAT6 gene encodes risk for nut allergy

artículo científico publicado en 2002

RANTES gene mRNA expression and its -403 G/A promoter polymorphism in coronary artery disease

artículo científico publicado en 2011

Rapid detection of intercellular adhesion molecule 1 (G241R and K469E) polymorphisms by a novel PCR-SSP assay.

artículo científico publicado en 2007

SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuria.

artículo científico publicado en 2012

Sex-specific association of RANTES gene -403 variant in Meniere's disease.

artículo científico publicado en 2014

Survivin gene polymorphism association with papillary thyroid carcinoma

artículo científico publicado en 2012

Survivin gene polymorphism association with tongue squamous cell carcinoma

scientific article published on 23 November 2012

TGF-β and IL-23 gene expression in unstimulated PBMCs of patients with diabetes

artículo científico publicado en 2011

TNF-α and IFN-γ gene variation and genetic susceptibility to type 1 diabetes and its microangiopathic complications

artículo científico publicado en 2014

The antioxidants dilemma: are they potentially immunosuppressants and carcinogens?

artículo científico publicado en 2014

VEGF gene mRNA expression in patients with coronary artery disease

artículo científico publicado en 2012

VEGF gene polymorphism association with diabetic foot ulcer

scientific article published on 18 May 2011

VEGF gene polymorphism association with diabetic neuropathy

artículo científico publicado en 2010

Vitamin D receptor gene FokI variant in diabetic foot ulcer and its relation with oxidative stress

artículo científico publicado en 2016

Would blockage of cytokines improve the outcome of pancreatic islet transplantation?

scientific article published on 08 November 2005

eNOS gene polymorphism association with retinopathy in type 1 diabetes

artículo científico publicado en 2010

Lista de obras de Mahsa M. Amoli

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Patients with Neonatal Diabetes.

A new frameshift MEN1 gene mutation associated with familial malignant insulinomas

A novel missense mutation in oncostatin M receptor beta causing primary localized cutaneous amyloidosis

A patient with features of albright hereditory osteodystrophy and unusual neuropsychiatric findings without coding Gsalpha mutations

Absence of kl-vs variant of klotho gene in Iranian cardiac patients (comparison to the world populations).

Acarbose versus trans-chalcone: comparing the effect of two glycosidase inhibitors on obese mice.

Adenosine deaminase gene polymorphism is associated with obesity in Iranian population

Adiponectin gene variants and abdominal obesity in an Iranian population

An in silico approach to identify and prioritize miRNAs target sites polymorphisms in colorectal cancer and obesity

Apolipoprotein E gene polymorphism and its effect on anthropometric measures in normoglycemic subjects and type 2 diabetes

Apolipoprotein E gene polymorphism and total serum cholesterol level in Iranian population

Association Between the Polymorphism of Glu298Asp in Exon 7 of the eNOS Gene With Foot Ulcer and Oxidative Stress in Adult Patients With Type 2 Diabetes

Association between 318C/T polymorphism of the CTLA-4 gene and systemic lupus erythematosus in Iranian patients

Association between Genetic Variants and Diabetes Mellitus in Iranian Populations: A Systematic Review of Observational Studies.

Association between MIF gene variation and Meniere's disease.

Association between vitamin D receptor gene polymorphisms (Fok1 and Bsm1) and osteoporosis: a systematic review

Association of interleukin-6 polymorphisms with obesity: A systematic review and meta-analysis

Association of miRNA targetome variants in LAMC1 and GNB3 genes with colorectal cancer and obesity

Association of survivin gene polymorphism with endometrial cancer.

Association of vascular endothelial growth factor (VEGF) Gene polymorphisms and expression with the risk of endometriosis: a case-control study

Association of vitamin D receptor gene polymorphism with the occurrence of low bone density, osteopenia, and osteoporosis in patients with type 2 diabetes

CDH1 and DDR1 common variants confer risk to vitiligo and autoimmune comorbidities

Comments on "Association between miR-499 rs3746444 polymorphism and coronary heart disease susceptibility: An evidence-based meta-analysis of 5063 cases and 4603 controls"

Curcumin inhibits in vitro MCP-1 release from mouse pancreatic islets.

Ectopic Cushing syndrome associated with thymic carcinoid tumor as the first presentation of MEN1 syndrome-report of a family with MEN1 gene mutation

Effect of adiponectin gene polymorphisms on waist circumference in patients with diabetes.

Effects of extremely low frequency electromagnetic fields on paraoxonase serum activity and lipid peroxidation metabolites in rat

Endothelial nitric oxide synthase VNTR (intron 4 a/b) polymorphism association with type 2 diabetes and its chronic complications

Epistatic interaction between adiponectin and survivin gene polymorphisms in endometrial carcinoma

Establishing a cGMP pancreatic islet processing facility: the first experience in Iran.

Evaluation of the presence of Epstein-Barr virus (EBV) in Iranian patients with thyroid papillary carcinoma

Genetic markers of disease susceptibility and severity in giant cell arteritis and polymyalgia rheumatica.

IL-23 gene expression in PBMCs of patients with coronary artery disease

Inducible but not endothelial nitric oxide synthase polymorphism is associated with susceptibility to rheumatoid arthritis in northwest Spain.

Inflammation related miRNAs as an important player between obesity and cancers

Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria

Is DNA methylation responsible for immune system dysfunction in schizophrenia?

Liver alpha-amylase gene expression as an early obesity biomarker

Macrophage migration inhibitory factor gene polymorphism is not associated with pemphigus vulgaris in Iranian patients.

Methylomics of breast cancer: Seeking epimarkers in peripheral blood of young subjects.

MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis ⬇️

Mutation screening of RET proto-oncogene in a family with medullary thyroid carcinoma, marfanoid habitus and pheochromocytoma; from clinically MEN2B to genetically MEN2A syndrome

Mutation screening of VHL gene in a family with malignant bilateral pheochromocytoma: from isolated familial pheochromocytoma to von Hippel-Lindau disease

No evidence of association between CTLA-4 polymorphisms and systemic lupus erythematosus in Iranian patients

Non-Muscle Myosin Heavy Chain 9 Gene (MYH9) Polymorphism (rs4821481) is Associated with Urinary Albumin Excretion in Iranian Diabetic Patients

Novel mutations of wolframin: a report with a look at the protein structure

Polymorphism in the STAT6 gene encodes risk for nut allergy

RANTES gene mRNA expression and its -403 G/A promoter polymorphism in coronary artery disease

Rapid detection of intercellular adhesion molecule 1 (G241R and K469E) polymorphisms by a novel PCR-SSP assay.

SLC34A3 intronic deletion in a new kindred with hereditary hypophosphatemic rickets with hypercalciuria.

Sex-specific association of RANTES gene -403 variant in Meniere's disease.

Survivin gene polymorphism association with papillary thyroid carcinoma

Survivin gene polymorphism association with tongue squamous cell carcinoma

TGF-β and IL-23 gene expression in unstimulated PBMCs of patients with diabetes

TNF-α and IFN-γ gene variation and genetic susceptibility to type 1 diabetes and its microangiopathic complications

The antioxidants dilemma: are they potentially immunosuppressants and carcinogens?

VEGF gene mRNA expression in patients with coronary artery disease

VEGF gene polymorphism association with diabetic foot ulcer

VEGF gene polymorphism association with diabetic neuropathy

Vitamin D receptor gene FokI variant in diabetic foot ulcer and its relation with oxidative stress

Would blockage of cytokines improve the outcome of pancreatic islet transplantation?

eNOS gene polymorphism association with retinopathy in type 1 diabetes