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The effect of N-acetyl cysteine consumption on men with abnormal sperm parameters due to positive history of COVID-19 in the last three months

Archivio italiano di urologia, andrologia, 2021-12, Vol.93 (4), p.465

2021

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Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1

Human genome variation, 2021-10, Vol.8 (1), p.39-39, Article 39

2021

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The effects of melatonin and metformin on histological characteristics of the ovary and uterus in letrozole-induced polycystic ovarian syndrome mice: A stereological study

International journal of reproductive biomedicine (Yazd, Iran), 2022-11, Vol.20 (11), p.973-988

2022

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Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS

Journal of genetics, 2021, Vol.100 (2), Article 68

2021

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EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review

Human genome variation, 2023-01, Vol.10 (1), p.1-1, Article 1

2023

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A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report

Human genome variation, 2021-08, Vol.8 (1), p.33-33, Article 33

2021

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Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report

Human genome variation, 2021-11, Vol.8 (1), p.42-42, Article 42

2021

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Exosome as a target for cancer treatment

Journal of Investigative Medicine, 2022-06, Vol.70 (5), p.1212-1218

2022

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Creating cell and animal models of human disease by genome editing using CRISPR/Cas9

The journal of gene medicine, 2019-04, Vol.21 (4), p.e3082-n/a

2019

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MicroRNA-126: Dual Role in Angiogenesis Dependent Diseases

Current pharmaceutical design, 2020-01, Vol.26 (38), p.4883

2020

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A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness

Annals of human genetics, 2023-07, Vol.87 (4), p.147-157

2023

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Comparative analysis of mouse bone marrow and adipose tissue mesenchymal stem cells for critical limb ischemia cell therapy

Stem cell research & therapy, 2021-01, Vol.12 (1), p.58-58, Article 58

2021

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Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature

Annals of human genetics, 2022-01, Vol.86 (1), p.52-62

2022

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Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1

European journal of medical genetics, 2022-03, Vol.65 (3), p.104449-104449, Article 104449

2022

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A combination of two novels homozygous FCSK variants cause disorder of glycosylation with defective fucosylation: New patient and literature review

European journal of medical genetics, 2022-08, Vol.65 (8), p.104535-104535, Article 104535

2022

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Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder

Journal of genetics, 2023-02, Vol.102 (1), Article 24

2023

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Phenotype of ST3GAL3 deficient patients: A case and review of the literature

European journal of medical genetics, 2021-08, Vol.64 (8), p.104250-104250, Article 104250

2021

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The Role of Circular RNAs in Male Infertility and Reproductive Cancers: A Narrative Review

Iranian journal of medical sciences, 2023-11, Vol.48 (6), p.527-541

2023

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Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review

Journal of dermatology, 2023-10, Vol.50 (10), p.1357-1362

2023

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Alteration in IFN-γ and CCL2 serum levels at first trimester of pregnancy contribute to development of preeclampsia and fetal growth restriction

Taiwanese journal of obstetrics & gynecology, 2023-01, Vol.62 (1), p.71-76

2023

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Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report

BMC medical genetics, 2018-05, Vol.19 (1), p.86-86, Article 86

2018

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Severe phenotype of an Iranian patient with methemoglobinemia type II due to a novel mutation in the CYB5R3 gene

Iranian journal of pediatric hematology and oncology, 2021-09

2021

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Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

Frontiers in pediatrics, 2021-09, Vol.9, p.734946-734946

2021

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Effects of N-acetylcysteine and metformin treatment on the stereopathological characteristics of uterus and ovary

European journal of translational myology, 2022-05, Vol.32 (2)

2022

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A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction

ARYA atherosclerosis, 2020-11, Vol.16 (6), p.301-305

2020

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The effect of N-acetyl cysteine consumption on men with abnormal sperm parameters due to positive history of COVID-19 in the last three months

Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1

The effects of melatonin and metformin on histological characteristics of the ovary and uterus in letrozole-induced polycystic ovarian syndrome mice: A stereological study

Exome sequencing identified a de novo frameshift pathogenic variant of CTBP1 in an extremely rare case of HADDTS

EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review

A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report

Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report

Exosome as a target for cancer treatment

Creating cell and animal models of human disease by genome editing using CRISPR/Cas9

MicroRNA-126: Dual Role in Angiogenesis Dependent Diseases

A novel nonsense variant in the ATL3 gene is associated with disturbed pain sensitivity, numbness of distal limbs and muscle weakness

Comparative analysis of mouse bone marrow and adipose tissue mesenchymal stem cells for critical limb ischemia cell therapy

Clinical features of patients with Yin Yang 1 deficiency causing Gabriele‐de Vries syndrome: A new case and review of the literature

Phenotypic spectrum of autosomal recessive Keratitis-Ichthyosis-Deafness Syndrome (KIDAR) due to mutations in AP1B1

A combination of two novels homozygous FCSK variants cause disorder of glycosylation with defective fucosylation: New patient and literature review

Intronic OTOF mutation causes an atypical splicing defect resulting in auditory neuropathy spectrum disorder

Phenotype of ST3GAL3 deficient patients: A case and review of the literature

The Role of Circular RNAs in Male Infertility and Reproductive Cancers: A Narrative Review

Novel insight into the ectodermal dysplasia 11A: Splicing variant of the EDARADD gene in a family with clinical variability and literature review

Alteration in IFN-γ and CCL2 serum levels at first trimester of pregnancy contribute to development of preeclampsia and fetal growth restriction

Splicing defect in FKBP10 gene causes autosomal recessive osteogenesis imperfecta disease: a case report

Severe phenotype of an Iranian patient with methemoglobinemia type II due to a novel mutation in the CYB5R3 gene

Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran

Effects of N-acetylcysteine and metformin treatment on the stereopathological characteristics of uterus and ovary

A substitution mutation in LRP8 gene is significantly associated with susceptibility to familial myocardial infarction

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