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The Role of Tissue Factor In Signaling Pathways of Pathological Conditions and Angiogenesis

Current molecular medicine, 2024-01, Vol.24 (9), p.1135-1151

2024

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Understanding the prion-like behavior of mutant p53 proteins in triple-negative breast cancer pathogenesis: The current therapeutic strategies and future directions

Heliyon, 2024-02, Vol.10 (4), p.e26260, Article e26260

2024

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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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Harnessing the Power of CAR-NK Cells: A Promising Off-the-Shelf Therapeutic Strategy for CD38-Positive Malignancies

Iranian journal of immunology, 2023-12, Vol.20 (4), p.410-426

2023

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Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature

Taiwanese journal of obstetrics & gynecology, 2018-02, Vol.57 (1), p.1-6

2018

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Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

Iranian journal of medical sciences, 2020-03, Vol.45 (2), p.118-124

2020

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Identifying a Novel Pathogenic Mutation in Exon 3 of ARID1A Gene in Colon Cancer

Middle East journal of cancer, 2020-04, Vol.11 (2), p.225-229

2020

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Novel insight into FCSK‐congenital disorder of glycosylation through a CRISPR‐generated cell model

Molecular genetics & genomic medicine, 2024-05, Vol.12 (5), p.e2445-n/a

2024

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Impact of Various Parameters as Predictors of The Success Rate of In Vitro Fertilization

International journal of fertility & sterility, 2022-04, Vol.16 (2), p.76-84

2022

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A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure

International journal of fertility & sterility, 2019-07, Vol.13 (2), p.135-138

2019

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Exploring the anti-cancer potential of SGLT2 inhibitors in breast cancer treatment in pre-clinical and clinical studies

European journal of pharmacology, 2024-09, Vol.978, p.176803, Article 176803

2024

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Using small molecules as a new challenge to redirect metabolic pathway

3 Biotech, 2014-10, Vol.4 (5), p.513-522

2014

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A Review on Advanced CRISPR-Based Genome-Editing Tools: Base Editing and Prime Editing

Molecular biotechnology, 2023-06, Vol.65 (6), p.849-860

2023

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PyComp: A Versatile Tool for Efficient Data Extraction, Conversion, and Management in High-throughput Virtual Drug Screening

Current computer-aided drug design, 2024-01, Vol.20

2024

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Overview of clinical, molecular, and therapeutic features of Niemann–Pick disease (types A, B, and C): Focus on therapeutic approaches

Cell biochemistry and function, 2024-06, Vol.42 (4), p.e4028-n/a

2024

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Recent advances and applications of peptide–agent conjugates for targeting tumor cells

Journal of cancer research and clinical oncology, 2023-11, Vol.149 (16), p.15249-15273

2023

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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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Gene therapy approaches for GM1 gangliosidosis: Focus on animal and cellular studies

Cell biochemistry and function, 2023-12, Vol.41 (8), p.1093-1105

2023

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An Investigation into Cell-Free DNA in Different Common Cancers

Molecular biotechnology, 2023-12

2023

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Functional mechanisms of miR‐192 family in cancer

Genes chromosomes & cancer, 2020-12, Vol.59 (12), p.722-735

2020

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Partial Reprogramming as a Method for Regenerating Neural Tissues in Aged Organisms

Cellular reprogramming, 2024-02, Vol.26 (1), p.10-23

2024

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CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 gene

The journal of gene medicine, 2020-11, Vol.22 (11), p.e3258-n/a

2020

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Angiogenesis in diabetic mouse model with critical limb ischemia; cell and gene therapy

Microvascular research, 2022-05, Vol.141, p.104339-104339, Article 104339

2022

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Creation of an in vitro model of GM1 gangliosidosis by CRISPR/Cas9 knocking‐out the GLB1 gene in SH‐SY5Y human neuronal cell line

Cell biochemistry and function, 2024-08, Vol.42 (6), p.e4102-n/a

2024

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Gene-edited cells: novel allogeneic gene/cell therapy for epidermolysis bullosa

Journal of applied genetics, 2024-03

2024

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The Role of Tissue Factor In Signaling Pathways of Pathological Conditions and Angiogenesis

Understanding the prion-like behavior of mutant p53 proteins in triple-negative breast cancer pathogenesis: The current therapeutic strategies and future directions

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

Harnessing the Power of CAR-NK Cells: A Promising Off-the-Shelf Therapeutic Strategy for CD38-Positive Malignancies

Clinical and genetic-epignetic aspects of recurrent hydatidiform mole: A review of literature

Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles

Identifying a Novel Pathogenic Mutation in Exon 3 of ARID1A Gene in Colon Cancer

Novel insight into FCSK‐congenital disorder of glycosylation through a CRISPR‐generated cell model

Impact of Various Parameters as Predictors of The Success Rate of In Vitro Fertilization

A Novel Mutation in NLRP7 Related to Recurrent Hydatidiform Mole and Reproductive Failure

Exploring the anti-cancer potential of SGLT2 inhibitors in breast cancer treatment in pre-clinical and clinical studies

Using small molecules as a new challenge to redirect metabolic pathway

A Review on Advanced CRISPR-Based Genome-Editing Tools: Base Editing and Prime Editing

PyComp: A Versatile Tool for Efficient Data Extraction, Conversion, and Management in High-throughput Virtual Drug Screening

Overview of clinical, molecular, and therapeutic features of Niemann–Pick disease (types A, B, and C): Focus on therapeutic approaches

Recent advances and applications of peptide–agent conjugates for targeting tumor cells

Exosome as a target for cancer treatment

Gene therapy approaches for GM1 gangliosidosis: Focus on animal and cellular studies

An Investigation into Cell-Free DNA in Different Common Cancers

Functional mechanisms of miR‐192 family in cancer

Partial Reprogramming as a Method for Regenerating Neural Tissues in Aged Organisms

CRISPR/Cas9 knock‐in toward creating a Rett syndrome cell model with a synonymous mutation in the MECP2 gene

Angiogenesis in diabetic mouse model with critical limb ischemia; cell and gene therapy

Creation of an in vitro model of GM1 gangliosidosis by CRISPR/Cas9 knocking‐out the GLB1 gene in SH‐SY5Y human neuronal cell line

Gene-edited cells: novel allogeneic gene/cell therapy for epidermolysis bullosa

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