Seyed Mohammad Bagher Tabei
Overview
Explore the profile of Seyed Mohammad Bagher Tabei including associated specialties, affiliations and a list of published articles.
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52
Citations
181
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Recent Articles
1.
Nammian P, Asadi-Yousefabad S, Daneshi S, Fallahi J, Khajeh S, Tabei S, et al.
Microrna
. 2025 Feb;
PMID: 39945266
Background: Critical limb ischemia (CLI) is considered the most severe form of peripheral artery disease (PAD). Nowadays, using stem cells such as mesenchymal stem cells (MSCs) to induce angiogenesis seems...
2.
Heidari Z, Fallahi J, Sisakht M, Safari F, Hosseini K, Bahmanimehr A, et al.
Cell Biochem Funct
. 2024 Dec;
42(8):e70021.
PMID: 39660566
Multipotent mesenchymal stromal/stem cells (MSCs) refer to a population of stem cells that exhibit distinct progenitor cell characteristics including the potential for differentiation into a wide range of cell types....
3.
Derakhshan Z, Bahmanpour S, Nasr-Esfahani M, Masjedi F, Mirani M, Dara M, et al.
Iran J Med Sci
. 2024 Aug;
49(8):515-527.
PMID: 39205823
Background: Ovarian granulosa cells (GCs) are essential for follicular development. Ovarian advanced glycation end-products (AGEs) accumulation is related to GCs dysfunction. Alpha-lipoic acid (ALA) illustrates therapeutic capabilities for infertility-related disorders....
4.
Hosseini K, Fallahi J, Aligholi H, Heidari Z, Nadimi E, Safari F, et al.
Cell Biochem Funct
. 2024 Jul;
42(6):e4102.
PMID: 39076066
GM1 gangliosidosis is one type of hereditary error of metabolism that occurs due to the absence or reduction of β-galactosidase enzyme content in the lysosome of cells, including neurons. In...
5.
Manoochehri J, Shiri A, Khoddam S, Aghasipour M, Kamal N, Jafari Khamirani H, et al.
Eur J Med Genet
. 2024 Jun;
70:104953.
PMID: 38852771
Jaberi-Elahi syndrome is an extremely rare genetic disease caused by pathogenic variants in GTPBP2. The core symptoms of this disease are intellectual disability, motor development delay, abnormal reflexes, skeletal abnormalities,...
6.
Fazelzadeh Haghighi M, Jafari Khamirani H, Fallahi J, Arabi Monfared A, Ashrafi Dehkordi K, Tabei S
Mol Genet Genomic Med
. 2024 May;
12(5):e2445.
PMID: 38722107
Background: FCSK-congenital disorder of glycosylation (FCSK-CDG) is a recently discovered rare autosomal recessive genetic disorder with defective fucosylation due to mutations in the fucokinase encoding gene, FCSK. Despite the essential...
7.
Khoddam S, Kamal N, Shiri A, Jafari Khamirani H, Manoochehri J, Dianatpour M, et al.
Eur J Med Genet
. 2024 Feb;
68:104928.
PMID: 38423277
The PEX11β gene contains four exons and encodes peroxisomal membrane protein 11β, which is involved in peroxisome proliferation and division. Pathogenic variants in this gene result in a rare genetic...
8.
Derakhshan Z, Bahmanpour S, Alaee S, Fallahi J, Tabei S
Iran J Med Sci
. 2023 Dec;
48(6):527-541.
PMID: 38094281
Infertility is a global health problem affecting about 15% of all couples, of which 50% are due to male infertility. Although the etiology of infertility is known in most infertile...
9.
Shiri A, Jafari Khamirani H, Kamal N, Manoochehri J, Dianatpour M, Tabei S, et al.
Eur J Med Genet
. 2023 Sep;
66(10):104846.
PMID: 37734708
COPB2 gene encodes the Coatomer Protein Complex Subunit Beta-2 that plays a crucial role in the cellular vesicle transport system and it is essential for brain development during embryogenesis. Mutations...
10.
Mirani M, Bahmanpour S, Masjedi F, Derakhshan Z, Dara M, Nasr-Esfahani M, et al.
Mol Biol Rep
. 2023 Aug;
50(10):8537-8549.
PMID: 37642758
Background: Ovarian advanced glycation end-products (AGEs) accumulation is associated with ovarian granulosa cells (GCs) dysfunction. Vitamin B6 derivatives positively affected reproduction. The current study was conducted to elucidate the AGEs...