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Genetics-Molecular genetics-Biochemistry
Iran

Activities

Employment (1)

Shiraz University of Medical Sciences: Shiraz, Fars, IR

1995-03-18 to present
Employment
Source: Self-asserted source
Seyed Mohammad Bagher Tabei

Education and qualifications (1)

Shiraz University of Medical Sciences: Shiraz, Fars, IR

1995-03-18 to present
Education
Source: Self-asserted source
Seyed Mohammad Bagher Tabei

Works (50 of 210)

Items per page:
Page 1 of 5

Impact of Tissue Factor Gene Knockout on Coagulation Properties of Umbilical Cord‐Derived Multipotent Mesenchymal Stromal/Stem Cells

Cell Biochemistry and Function
2024-12 | Journal article
Contributors: Zahra Heidari; Jafar Fallahi; Mohsen Sisakht; Fatemeh Safari; Kamran Hosseini; Ardeshir Bahmanimehr; Amir Savardashtaki; Sahar Khajeh; Seyed Mohammad Bagher Tabei; Vahid Razban
Source: check_circle
Crossref

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 | Journal article
Contributors: Kamran Hosseini; Jafar Fallahi; Hadi Aligholi; Zahra Heidari; Elham Nadimi; Fatemeh Safari; Mohsen Sisakht; Amir Atapour; Sahar Khajeh; Seyed Mohammad Bagher Tabei et al.
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Crossref

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

Molecular Genetics & Genomic Medicine
2024-05 | Journal article
Contributors: Maryam Fazelzadeh Haghighi; Hossein Jafari Khamirani; Jafar Fallahi; Ali Arabi Monfared; Korosh Ashrafi Dehkordi; Seyed Mohammad Bagher Tabei
Source: check_circle
Crossref

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 | Journal article
EID:

2-s2.0-85149385836

Part of ISSN: 14691809 00034800
Contributors: Mohammadi, S.; Jafari Khamirani, H.; Baneshi, M.; Kamal, N.; Manoocheri, J.; Saffar, M.; Dianatpour, M.; Tabei, S.M.B.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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 and Gynecology
2023 | Journal article
EID:

2-s2.0-85144961212

Part of ISSN: 18756263 10284559
Contributors: Vafaei, H.; Faraji, S.; Ahmadi, M.; Tabei, S.M.B.; Fereidoni, S.; Shiravani, Z.; Hosseini, S.N.; Asadi, N.; Kasraeian, M.; Faraji, A. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Human Genome Variation
2023 | Journal article
EID:

2-s2.0-85146329612

Part of ISSN: 2054345X
Contributors: Abbasi, Z.; Jafari Khamirani, H.; Tabei, S.M.B.; Manoochehri, J.; Dianatpour, M.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Journal of Genetics
2023 | Journal article
EID:

2-s2.0-85150418234

Part of ISSN: 09737731 00221333
Contributors: Mohammadi, S.; Jafari Khamirani, H.; Zoghi, S.; Dastgheib, S.A.; Tabei, S.M.B.; Talebzadeh, M.; Adibi, M.H.; Dianatpour, M.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

The third patient of ACACA-related acetyl-CoA carboxylase deficiency with seizure and literature review

European Journal of Medical Genetics
2023 | Journal article
EID:

2-s2.0-85147650572

Part of ISSN: 18780849 17697212
Contributors: Shafieipour, N.; Jafari Khamirani, H.; Kamal, N.; Tabei, S.M.B.; Dianatpour, M.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Thymoquinone improves folliculogenesis, sexual hormones, gene expression of apoptotic markers and antioxidant enzymes in polycystic ovary syndrome rat model

Veterinary Medicine and Science
2023 | Journal article
EID:

2-s2.0-85137943970

Part of ISSN: 20531095
Contributors: Alaee, S.; Mirani, M.; Derakhshan, Z.; Koohpeyma, F.; Bakhtari, A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Cell Biochemistry and Function
2023-12 | Journal article
Contributors: Kamran Hosseini; Jafar Fallahi; Seyed M. B. Tabei; Vahid Razban
Source: check_circle
Crossref

Novel insight into the phenotype of microcephaly 19 in the patient with missense COPB2 mutation.

European journal of medical genetics
2023-09 | Journal article
Contributors: Shiri A; Jafari Khamirani H; Kamal N; Manoochehri J; Dianatpour M; Tabei SMB; Dastgheib SA
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Europe PubMed Central

Pyridoxamine protects human granulosa cells against advanced glycation end-products-induced steroidogenesis disturbances.

Molecular biology reports
2023-08 | Journal article
Contributors: Mirani M; Bahmanpour S; Masjedi F; Derakhshan Z; Dara M; Nasr-Esfahani MH; Tabei SMB
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Europe PubMed Central
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Preferred source (of 2)‎

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

The Journal of dermatology
2023-06 | Journal article
Contributors: Fazelzadeh Haghighi N; Kamal N; Jafari Khamirani H; Fazelzadeh Haghighi M; Dastgheib SA; Dianatpour M; Tabei SMB
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Europe PubMed Central
grade
Preferred source (of 2)‎

Protooncogenic Role of ARHGAP11A and ARHGAP11B in Invasive Ductal Carcinoma: Two Promising Breast Cancer Biomarkers

BioMed Research International
2023-01 | Journal article
Contributors: Y. Naeimzadeh; S. Ilbeigi; H. Dastsooz; M. Rafiee Monjezi; Y. Mansoori; S. M. B. Tabei; Yuan Li
Source: check_circle
Crossref

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 | Journal article
EID:

2-s2.0-85132515167

Part of ISSN: 18780849 17697212
Contributors: Manoochehri, J.; Kamal, N.; Khamirani, H.J.; Zoghi, S.; Haghighi, M.F.; Goodarzi, H.R.; Bagher Tabei, S.M.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Microvascular Research
2022 | Journal article
EID:

2-s2.0-85124492234

Part of ISSN: 10959319 00262862
Contributors: Asadi-Yousefabad, S.-L.; Nammian, P.; Tabei, S.M.B.; Daneshi, S.; Fallahi, J.; Razban, V.; Sheikhha, M.H.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Clinical Features of Okur-Chung Neurodevelopmental Syndrome: Case Report and Literature Review

Molecular Syndromology
2022 | Journal article
EID:

2-s2.0-85129044370

Part of ISSN: 16618777 16618769
Contributors: Jafari Khamirani, H.; Zoghi, S.; Motealleh, A.; Dianatpour, M.; Tabei, S.M.B.; Mohammadi, S.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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 | Journal article
EID:

2-s2.0-85118486436

Part of ISSN: 14691809 00034800
Contributors: Khamirani, H.J.; Zoghi, S.; Namdar, Z.M.; Kamal, N.; Dianatpour, M.; Tabei, S.M.B.; Mohammadi, S.; Dehghanian, F.; Farbod, Z.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Comparative study of mouse adipose- and bone marrow mesenchymal stem cells in diabetic model with critical limb ischemia

Cell and Tissue Banking
2022 | Journal article
EID:

2-s2.0-85130462098

Part of ISSN: 15736814 13899333
Contributors: Asadi-Yousefabad, S.-L.; Nammian, P.; Sheikhha, M.H.; Tabei, S.M.B.; Daneshi, S.; Nikukar, H.; Lotfi, M.; Razban, V.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

European Journal of Translational Myology
2022 | Journal article
EID:

2-s2.0-85134542389

Part of ISSN: 20377460 20377452
Contributors: Rafiee, B.; Karbalay-Doust, S.; Tabei, S.M.B.; Azarpira, N.; Alaee, S.; Lohrasbi, P.; Bahmanpour, S.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

EXOSC9 mutation causes pontocerebellar hypoplasia type 1D (PCH1D): Refining the phenotype and literature review

Gene Reports
2022 | Journal article
EID:

2-s2.0-85125442337

Part of ISSN: 24520144
Contributors: Khamirani, H.J.; Sichani, A.S.; Panahandeh, S.M.; Zoghi, S.; Tabei, S.S.; Darayee, M.; Talebzadeh, M.; Dianatpour, M.; Dastgheib, S.A.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Exosome as a target for cancer treatment

Journal of Investigative Medicine
2022 | Journal article
EID:

2-s2.0-85133101019

Part of ISSN: 17088267 10815589
Contributors: Nafar, S.; Nouri, N.; Alipour, M.; Fallahi, J.; Zare, F.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Exploring the dysregulated mRNAs–miRNAs–lncRNAs interactions associated to idiopathic non-obstructive azoospermia

Journal of Biomolecular Structure and Dynamics
2022 | Journal article
EID:

2-s2.0-85099809141

Part of ISSN: 15380254 07391102
Contributors: Sabetian, S.; Zarei, M.; Jahromi, B.N.; Morowvat, M.H.; Tabei, S.M.B.; Cava, C.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier
grade
Preferred source (of 2)‎

Expression Levels of LINC01296 and LINC00152 in Breast Cancer Tissue: Association with the Use of Oral Contraceptives

Eurasian Journal of Medicine and Oncology
2022 | Journal article
EID:

2-s2.0-85127137694

Part of ISSN: 2587196X 25872400
Contributors: Davoodabadi-Farahani, M.; Mansoori, Y.; Ilbeigi, S.; Barahman, M.; Mazloomrezaei, M.; Khani, P.; Tabei, S.M.; Dastgheib, S.A.; Neamatzadeh, H.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Genotypic and phenotypic spectrum of Myofibrillar Myopathy 7 as a result of Kyphoscoliosis Peptidase deficiency: The first description of a missense mutation in KY and literature review

European Journal of Medical Genetics
2022 | Journal article
EID:

2-s2.0-85133653191

Part of ISSN: 18780849 17697212
Contributors: Ehsani, E.; Khamirani, H.J.; Abbasi, Z.; Gohari, M.; Zoghi, S.; Mohammadi, S.; Dianatpour, M.; Tabei, S.M.B.; Mohamadjani, O.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

MCM2 mutation causes autosomal dominant nonsyndromic hearing loss (DFNA70): novel variant in the second family

Journal of Genetics
2022 | Journal article
EID:

2-s2.0-85128455379

Part of ISSN: 09737731 00221333
Contributors: Zeraatpisheh, Z.; Sichani, A.S.; Kamal, N.; Khamirani, H.J.; Zoghi, S.; Ehsani, E.; Mohammadi, S.; Tabei, S.S.; Dastgheib, S.A.; Tabei, S.M.B. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

European Journal of Medical Genetics
2022 | Journal article
EID:

2-s2.0-85124293765

Part of ISSN: 18780849 17697212
Contributors: Faghihi, F.; Khamirani, H.J.; Zoghi, S.; Kamal, N.; Yeganeh, B.S.; Dianatpour, M.; Bagher Tabei, S.M.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Pontocerebellar Hypoplasia Type 3: Report of Five Novel PCLO Variants and Literature Review

SSRN
2022 | Other
EID:

2-s2.0-85137083050

Part of ISSN: 15565068
Contributors: Mohammadi, S.; Baneshi, M.; Zoghi, S.; Dastgheib, S.A.; Dianatpour, M.; Manoochehri, J.; Mohammadi, S.; Farbod, Z.; Tabei, S.M.B.; Khamirani, H.J.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Recurrent Infections and Immunodeficiency Caused by Severe Pancytopenia Associated with a Novel Life-Threatening Mutation in Hypoxia-Upregulated Protein 1

Immunological Investigations
2022 | Journal article
EID:

2-s2.0-85130327023

Part of ISSN: 15324311 08820139
Contributors: Jafari Khamirani, H.; Dianatpour, M.; Zoghi, S.; Mohammadi, S.; Habib, A.; Dastgheib, S.A.; Tabei, S.M.B.; Molayemat, M.; Shirazi Yeganeh, B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Spastic paraplegia 51: phenotypic spectrum related to novel homozygous AP4E1 mutation

Journal of Genetics
2022 | Journal article
EID:

2-s2.0-85137987833

Part of ISSN: 09737731 00221333
Contributors: Manoochehri, J.; Goodarzi, H.R.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Suggesting Tissue-Specific MSMB Gene Promoter as a Novel Approach for Prostate Targeted Gene Therapy

Asian Pacific Journal of Cancer Prevention
2022 | Journal article
EID:

2-s2.0-85133106869

Part of ISSN: 2476762X 15137368
Contributors: Darayee, M.; Geramizadeh, B.; Tabei, S.M.B.; Rezvani, A.; Soleimanian, S.; Rahimi, A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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
2022 | Journal article
EID:

2-s2.0-85143080503

Part of ISSN: 24763772 24764108
Contributors: Lohrasbi, P.; Karbalay-Doust, S.; Tabei, S.M.B.; Azarpira, N.; Alaee, S.; Rafiee, B.; Bahmanpour, S.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

ZNF142 mutation causes neurodevelopmental disorder with speech impairment and seizures: Novel variants and literature review

European Journal of Medical Genetics
2022 | Journal article
EID:

2-s2.0-85131372718

Part of ISSN: 18780849 17697212
Contributors: Kamal, N.; Khamirani, H.J.; Mohammadi, S.; Dastgheib, S.A.; Dianatpour, M.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Two Novel Mutations in <i>LAMC2</i> Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa.

Reports of biochemistry & molecular biology
2022-01 | Journal article
Contributors: Taghdiri M; Naeimi S; Fardaei M; Tabei SMB
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Europe PubMed Central

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

Human Genome Variation
2021 | Journal article
EID:

2-s2.0-85112683691

Part of ISSN: 2054345X
Contributors: Manoochehri, J.; Dastgheib, S.A.; Khamirani, H.J.; Mollaie, M.; Sharifi, Z.; Zoghi, S.; Tabei, S.M.B.; Mohammadi, S.; Dehghanian, F.; Farbod, Z. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Clinical values of two estrogen receptor signaling targeted lncRNAs in invasive ductal breast carcinoma,Klinické hodnoty dvou lncRNA signální dráhy estrogenového receptoru u invazivního duktálního karcinomu prsu

Klinicka Onkologie
2021 | Journal article
EID:

2-s2.0-85120929349

Part of ISSN: 18025307 0862495X
Contributors: Ilbeigi, S.; Naeimzadeh, Y.; Davoodabadi, F.M.; Rafiee, M.M.; Dastsooz, H.; Daraei, A.; Farahani, F.; Dastgheib, A.; Mansoori, Y.; Bagher Tabei, S.M.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Stem Cell Research and Therapy
2021 | Journal article
EID:

2-s2.0-85099254734

Part of ISSN: 17576512
Contributors: Nammian, P.; Asadi-Yousefabad, S.-L.; Daneshi, S.; Sheikhha, M.H.; Tabei, S.M.B.; Razban, V.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report (Human Genome Variation, (2021), 8, 1, (33), 10.1038/s41439-021-00164-8)

Human Genome Variation
2021 | Journal article
EID:

2-s2.0-85119703155

Part of ISSN: 2054345X
Contributors: Manoochehri, J.; Dastgheib, S.A.; Khamirani, H.J.; Mollaie, M.; Sharifi, Z.; Zoghi, S.; Tabei, S.M.B.; Mohammadi, S.; Dehghanian, F.; Farbod, Z. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Journal of Genetics
2021 | Journal article
EID:

2-s2.0-85115669410

Part of ISSN: 09737731 00221333
Contributors: Khamirani, H.J.; Zoghi, S.; Sichani, A.S.; Dianatpour, M.; Mohammadi, S.; Tabei, S.M.B.; Dastgheib, S.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Expression signature of lncRNA APTR in clinicopathology of breast cancer: Its potential oncogenic function in dysregulation of ErbB signaling pathway

Gene Reports
2021 | Journal article
EID:

2-s2.0-85104080505

Part of ISSN: 24520144
Contributors: Mansoori, H.; Darbeheshti, F.; Daraei, A.; Mokhtari, M.; Tabei, M.B.; Abdollahzadeh, R.; Dastsooz, H.; Bastami, M.; Nariman-Saleh-Fam, Z.; Salmani, H. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Frontiers in Pediatrics
2021 | Journal article
EID:

2-s2.0-85115177835

Part of ISSN: 22962360
Contributors: Nejabat, M.; Inaloo, S.; Sheshdeh, A.T.; Bahramjahan, S.; Sarvestani, F.M.; Katibeh, P.; Nemati, H.; Tabei, S.M.B.; Faghihi, M.A.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Genetically modified bone marrow mesenchymal stem cells and dental pulp mesenchymal stem cells by HIF-1alpha overexpression, differs in survival and angiogenic effects after in animal model of hind limb ischemia

Gene Reports
2021 | Journal article
EID:

2-s2.0-85109168937

Part of ISSN: 24520144
Contributors: Moradi, S.; Fallahi, J.; Tanideh, N.; Dara, M.; Aliabadi, B.E.; Nafar, S.; Asadi-Yousefabad, S.-L.; Tabei, S.M.B.; Razban, V.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

European Journal of Medical Genetics
2021 | Journal article
EID:

2-s2.0-85106664588

Part of ISSN: 18780849 17697212
Contributors: Khamirani, H.J.; Zoghi, S.; Faghihi, F.; Dastgheib, S.A.; Hassanipour, H.; Bagher Tabei, S.M.; Mohammadi, S.; Masoudi, M.; Poorang, S.; Ehsani, E. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Preclinical Evaluation of Bone Marrow Mesenchymal Stem Cells Overexpressing MicroRNA-126 to Treat Critical Limb Ischemia

Research Square
2021 | Other
EID:

2-s2.0-85168032742

Contributors: Nammian, P.; Asadi-Yousefabad, S.-L.; Daneshi, S.; Fallahi, J.; Bagher Tabei, S.M.; Razban, V.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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 e Andrologia
2021 | Journal article
EID:

2-s2.0-85122344875

Part of ISSN: 22824197 11243562
Contributors: Rafiee, B.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa

Reports of Biochemistry and Molecular Biology
2021 | Journal article
EID:

2-s2.0-85123532794

Part of ISSN: 23223480
Contributors: Taghdiri, M.; Naeimi, S.; Fardaei, M.; Tabei, S.M.B.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

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

Human Genome Variation
2021 | Journal article
EID:

2-s2.0-85118276225

Part of ISSN: 2054345X
Contributors: Alavi, O.; Khamirani, H.J.; Zoghi, S.; Feili, A.; Dastgheib, S.A.; Tabei, S.M.B.; Manoochehri, J.; Panahandeh, S.M.; Kamali, M.; Dianatpour, M.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

A substitution mutation in lrp8 gene is significantly associated with susceptibility to familial myocardial infarction

ARYA Atherosclerosis
2020 | Journal article
EID:

2-s2.0-85097289358

Part of ISSN: 22516638 17353955
Contributors: Ghorbani, M.J.; Razmi, N.; Tabei, S.M.B.; Zibaeenezhad, M.J.; Goodarzi, H.R.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Clinical and Para Clinical Findings in Children with Progressive Familial Intrahepatic Cholestasis in Iran; A Referral Center Report

Research Square
2020 | Other
EID:

2-s2.0-85166721386

Contributors: Zarenezhad, M.; Dehghani, S.M.; Ejtehadi, F.; Fattahi, M.R.; Kaboodkhani, R.; Bagher Tabei, S.M.; Doroudchi, A.; Forouzesh, M.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier

Efficacy of insulin targeted gene therapy for type 1 diabetes mellitus: A systematic review and meta-analysis of rodent studies

Iranian Journal of Basic Medical Sciences
2020 | Journal article
EID:

2-s2.0-85087436931

Part of ISSN: 20083874 20083866
Contributors: Ghiasi, M.R.; Mohammadi, H.; Symonds, M.E.; Tabei, S.M.B.; Salehi, A.R.; Jafarpour, S.; Barough, L.N.; Rahimi, E.; Amirkhani, Z.; Miraghajani, M. et al.
Source: Self-asserted source
Seyed Mohammad Bagher Tabei via Scopus - Elsevier
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