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Inconsistency in the expression pattern of a five-lncRNA signature as a potential diagnostic biomarker for gastric cancer patients in bioinformatics and in vitro.
Published in:
Iranian Journal of Basic Medical Sciences, 2022, v. 25, n. 6, p. 704, doi. 10.22038/IJBMS.2022.62181.13762
By:
- Ghanei, Mahmoud;
- Poursheikhani, Arash;
- Aarabi, Azadeh;
- Taghechian, Negin;
- Abbaszadegan, Mohammad Reza
Publication type:
Article
Genetic evaluation of hyperphenylalaninemia patients with tetrahydrobiopterin deficiency in Iranian population: Identification of four novel disease‐causing variants.
Published in:
Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 12, p. 1, doi. 10.1002/mgg3.2081
By:
- Sadat Fatemi, Seyedeh Helia;
- Eshraghi, Peyman;
- Ghanei, Mahmoud;
- Hamzehloei, Tayebeh
Publication type:
Article
A novel mutation in the cathepsin C (CTSC) gene in Iranian family with Papillon‐Lefevre syndrome.
Published in:
Clinical & Experimental Dental Research, 2021, v. 7, n. 4, p. 568, doi. 10.1002/cre2.387
By:
- Ghanei, Mahmoud;
- Abbaszadegan, Mohammad R.;
- Forghanifard, Mohammad M.;
- Aarabi, Azadeh;
- Arab, Hamidreza
Publication type:
Article
Association of Genotypes of ANGPTL3 with Vitamin D and Calcium Concentration in Cardiovascular Disease.
Published in:
Biochemical Genetics, 2024, v. 62, n. 4, p. 2482, doi. 10.1007/s10528-023-10533-3
By:
- Aghasizadeh, Malihe;
- Ghanei, Mahmoud;
- Ghoflchi, Sahar;
- Asadian-sohan, Parisa;
- Haghani, Mohammad;
- Kazemi, Tooba;
- Esmaily, Habibollah;
- Avan, Amir;
- Ferns, Gordon A.;
- Miri-Moghaddam, Ebrahim;
- Ghayour-Mobarhan, Majid
Publication type:
Article
Homozygous deletion of exon 7 in SMN1 gene without phenotypic features of spinal muscular atrophy.
Published in:
Neurology Asia, 2022, v. 27, n. 4, p. 955, doi. 10.54029/2022jdc
By:
- Ghanei, Mahmoud;
- Sadat Fatemi, Seyedeh Helia;
- Soudyab, Mohammad;
- Esfehani, Reza Jafarzadeh
Publication type:
Article
Current insights into the metastasis of epithelial ovarian cancer - hopes and hurdles.
Published in:
Cellular Oncology (2211-3428), 2020, v. 43, n. 4, p. 515, doi. 10.1007/s13402-020-00513-9
By:
- Yousefi, Meysam;
- Dehghani, Sadegh;
- Nosrati, Rahim;
- Ghanei, Mahmoud;
- Salmaninejad, Arash;
- Rajaie, Sara;
- Hasanzadeh, Malihe;
- Pasdar, Alireza
Publication type:
Article
An Update on the Application of CRISPR Technology in Clinical Practice.
Published in:
Molecular Biotechnology, 2024, v. 66, n. 2, p. 179, doi. 10.1007/s12033-023-00724-z
By:
- Morshedzadeh, Firouzeh;
- Ghanei, Mahmoud;
- Lotfi, Malihe;
- Ghasemi, Morteza;
- Ahmadi, Mohsen;
- Najari-Hanjani, Parisa;
- Sharif, Samaneh;
- Mozaffari-Jovin, Sina;
- Peymani, Maryam;
- Abbaszadegan, Mohammad Reza
Publication type:
Article
A Comprehensive Study of Disease-Causing Variants in PAH, QDPR, PTS, and PCD Genes in Iranian Patients with Hyperphenylalaninemia: A Systematic Review.
Published in:
Human Heredity, 2023, v. 88, n. 1, p. 8, doi. 10.1159/000529037
By:
- Ghanei, Mahmoud;
- Sadat Fatemi, Seyedeh Helia;
- Hamzehlouei, Tayebeh
Publication type:
Article

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