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Analysis of Polymorphism and Expression Profile of ASIC1 and IL-6 Genes in Patients with Gastric Cancer

Asian Pacific Journal of Cancer Prevention, 2018-12, Vol.19 (12), p.3451-3455

2018

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Contribution of LATS1 and LATS2 promoter methylation in OSCC development

Journal of cell communication and signaling, 2017-03, Vol.11 (1), p.49-55

2017

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Strategies for whole-exome sequencing analysis in a case series study of familial male infertility

International journal of reproductive biomedicine (Yazd, Iran), 2020-05, Vol.18 (5), p.375-384

2020

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Association of Genetic Polymorphisms in GSTP1, GSTM1 , and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran

Iranian journal of public health, 2020-07, Vol.49 (7), p.1364-1371

2020

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Impact of methylenetetrahydrofolate reductase (MTHFR) codon (677) and methionine synthase (MS) codon (2756) on risk of cervical carcinogenesis in North Indian population

Archives of gynecology and obstetrics, 2008-12, Vol.278 (6), p.517-524

2008

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Different Effects of Low-Level Laser Therapy on the Proliferation of HT29 Cells in Culture and Xenograft Models

Journal of lasers in medical sciences, 2023-08, Vol.14, p.e31-e31

2023

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Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia

Disease and diagnosis, 2022-12, Vol.11 (4), p.142-146

2022

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Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

Orphanet journal of rare diseases, 2019-02, Vol.14 (1), p.41-41, Article 41

2019

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Association between promoter methylation and expression of thyroid hormone receptor beta (THRβ) gene in patients with gastric cancer in an Iranian population

Journal of gastroenterology and hepatology, 2015-03, Vol.30 (3), p.485-489

2015

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Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update

Journal of clinical medicine, 2022-10, Vol.11 (21), p.6415

2022

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Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients

European Journal of Biological Research, 2022-11, Vol.12 (4), p.294-306

2022

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Impact of polymorphism in IL-1RA gene on the risk of cervical cancer

Archives of gynecology and obstetrics, 2008-06, Vol.277 (6), p.527-533

2008

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Association of interleukin-18 gene promoter polymorphism on the risk of cervix carcinogenesis in north Indian population

Oncology research, 2008-01, Vol.17 (4), p.159-166

2008

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Evaluation of LATS1 and LATS2 Promoter Methylation with the Risk of Pterygium Formation

Journal of Ophthalmology, 2016-01, Vol.2016 (2016), p.1-5

2016

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Expression of Long Non-Coding RNAs in Placentas of Intrauterine Growth Restriction (IUGR) Pregnancies

Reports of biochemistry and molecular biology, 2019-04, Vol.8 (1), p.25-31

2019

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Epigenetic Inactivation of Protocadherin 10 by Methylation in Colorectal Cancer

Acta medica Iranica, 2019, Vol.57 (8), p.472

2019

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Analysis of methylation and mRNA expression status of FADD and FAS genes in patients with oral squamous cell carcinoma

Medicina oral, patología oral y cirugía bucal, 2014-11, Vol.19 (6), p.e562-e568

2014

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Association of CTLA-4 gene polymorphisms −318C/T and +49A/G and Hashimoto's thyroidits in Zahedan, Iran

Biomedical reports, 2017-01, Vol.6 (1), p.108-112

2017

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Association between paraoxonase-1 gene polymorphisms and risk of metabolic syndrome

Molecular biology reports, 2012-02, Vol.39 (2), p.937-943

2012

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Serum paraoxonase and arylesterase activities in metabolic syndrome in Zahedan, southeast Iran

European journal of endocrinology, 2011-02, Vol.164 (2), p.219-222

2011

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Interleukin-12 gene polymorphism and cervical cancer risk

American journal of clinical oncology, 2009-10, Vol.32 (5), p.524-528

2009

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Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer

International journal of reproductive biomedicine (Yazd, Iran), 2016-04, Vol.14 (4), p.271-274

2016

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A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

Frontiers in pediatrics, 2019-03, Vol.7, p.89-89

2019

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Lack of association of GSTT1 and GSTP1 genes methylation and their expression profiles with risk of NAFLD in a sample of Iranian patients

Clinics and research in hepatology and gastroenterology, 2011-05, Vol.35 (5), p.387-392

2011

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Analysis of hypermethylation and expression profiles of APC and ATM genes in patients with oral squamous cell carcinoma

Clinical epigenetics, 2011-11, Vol.3 (1), p.6-6, Article 6

2011

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Analysis of Polymorphism and Expression Profile of ASIC1 and IL-6 Genes in Patients with Gastric Cancer

Contribution of LATS1 and LATS2 promoter methylation in OSCC development

Strategies for whole-exome sequencing analysis in a case series study of familial male infertility

Association of Genetic Polymorphisms in GSTP1, GSTM1 , and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran

Impact of methylenetetrahydrofolate reductase (MTHFR) codon (677) and methionine synthase (MS) codon (2756) on risk of cervical carcinogenesis in North Indian population

Different Effects of Low-Level Laser Therapy on the Proliferation of HT29 Cells in Culture and Xenograft Models

Novel WDR62 and MTR Variants in a Patient With Autosomal Recessive Primary Microcephaly-2 With Polymicrogyria and Homocystinuria-Megaloblastic Anemia

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

Association between promoter methylation and expression of thyroid hormone receptor beta (THRβ) gene in patients with gastric cancer in an Iranian population

Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update

Novel mutations of PCCA and PCCB genes found by whole-exome sequencing related to propionic acidemia patients

Impact of polymorphism in IL-1RA gene on the risk of cervical cancer

Association of interleukin-18 gene promoter polymorphism on the risk of cervix carcinogenesis in north Indian population

Evaluation of LATS1 and LATS2 Promoter Methylation with the Risk of Pterygium Formation

Expression of Long Non-Coding RNAs in Placentas of Intrauterine Growth Restriction (IUGR) Pregnancies

Epigenetic Inactivation of Protocadherin 10 by Methylation in Colorectal Cancer

Analysis of methylation and mRNA expression status of FADD and FAS genes in patients with oral squamous cell carcinoma

Association of CTLA-4 gene polymorphisms −318C/T and +49A/G and Hashimoto's thyroidits in Zahedan, Iran

Association between paraoxonase-1 gene polymorphisms and risk of metabolic syndrome

Serum paraoxonase and arylesterase activities in metabolic syndrome in Zahedan, southeast Iran

Interleukin-12 gene polymorphism and cervical cancer risk

Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer

A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

Lack of association of GSTT1 and GSTP1 genes methylation and their expression profiles with risk of NAFLD in a sample of Iranian patients

Analysis of hypermethylation and expression profiles of APC and ATM genes in patients with oral squamous cell carcinoma

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