Kaoru Tabei

Shiraz University — IR

Medicine · Health Sciences

32h-index4.1kcitations326works1.22yr avg
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Research Topics

Dialysis and Renal Disease Management(46), Ion Transport and Channel Regulation(21), Hemodynamic Monitoring and Therapy(15), Blood Pressure and Hypertension Studies(13), Acute Ischemic Stroke Management(12)

Publications320 total

Retraction: Effects of N-acetylcysteine and metformin treatment on the stereopathological characteristics of uterus and ovary
European Journal of Translational Myology·2025Open Access
miR-153 Overexpression and BCL2 Targeting Induce Apoptosis and Autophagy in HepG2 Cells
Indian Journal of Clinical Biochemistry·2025Open Access
Concurrent inheritance of achromatopsia and MMAT syndrome in a pedigree: Genetic and clinical insights
European Journal of Medical Genetics·2025Open Access
Novel Insights into Pontocerebellar Hypoplasia Type 3: Discovery of a New Disease-causing PCLO Variant and Development of a CRISPR-generated Cell Model
Galen Medical Journal·2025Open Access
Unraveling the role of NOG gene in hereditary sensory neuropathy type 1F through CRISPR/Cas9-mediated ATL3 knockout
Egyptian Journal of Medical Human Genetics·2025· 1 citedOpen Access
Bone Marrow Mesenchymal Stem Cells Overexpressing MicroRNA-126 to Treat Critical Limb Ischemia
MicroRNA·2025· 1 cited
Association between psoas muscle mass index and bone mineral density in patients undergoing hemodialysis
Scientific Reports·2025· 1 citedOpen Access
Impact of Tissue Factor Gene Knockout on Coagulation Properties of Umbilical Cord‐Derived Multipotent Mesenchymal Stromal/Stem Cells
Cell Biochemistry and Function·2024· 4 citedOpen Access
Alpha-Lipoic Acid Ameliorates Impaired Steroidogenesis in Human Granulosa Cells Induced by Advanced Glycation End-Products.
PubMed·2024· 1 citedOpen Access
Creation of an in vitro model of GM1 gangliosidosis by CRISPR/Cas9 knocking‐out the <i>GLB1</i> gene in SH‐SY5Y human neuronal cell line
Cell Biochemistry and Function·2024Open Access
Jaberi-Elahi syndrome: Exploring a novel GTPBP2 mutation and a literature review
European Journal of Medical Genetics·2024· 1 citedOpen Access
Novel insight into <i>FCSK</i>‐congenital disorder of glycosylation through a <scp>CRISPR</scp>‐generated cell model
Molecular Genetics & Genomic Medicine·2024· 1 citedOpen Access
Two siblings with PEX11B-related peroxisome biogenesis disorder
European Journal of Medical Genetics·2024· 4 citedOpen Access
ST3GAL3 deficiency with autistic behavior: First description of frameshift variant and literature review
Gene Reports·2024· 1 cited
siRNA-mediated downregulation of BATF3 diminished proliferation and induced apoptosis through downregulating c-Myc expression in chronic myelogenous leukemia cells
Molecular Biology Reports·2024· 3 cited
Gene therapy approaches for GM1 gangliosidosis: Focus on animal and cellular studies
Cell Biochemistry and Function·2023· 7 citedOpen Access
The Role of Circular RNAs in Male Infertility and Reproductive Cancers: A Narrative Review.
PubMed·2023· 5 citedOpen Access
Novel insight into the phenotype of microcephaly 19 in the patient with missense COPB2 mutation
European Journal of Medical Genetics·2023· 2 cited
Pyridoxamine protects human granulosa cells against advanced glycation end-products-induced steroidogenesis disturbances
Molecular Biology Reports·2023· 4 cited
Novel insight into the ectodermal dysplasia <scp>11A</scp>: Splicing variant of the <scp><i>EDARADD</i></scp> gene in a family with clinical variability and literature review
The Journal of Dermatology·2023
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Frequent Co-authors

Susumu Ookawara(9), Yasushi Asano(7), Kiyonori Ito(7), Takashi Akiba(6), Kunitoshi Iseki(5), Shigeru Nakai(5), Ikuto Masakane(5), Honami Mori(5), Haruhisa Miyazawa(5), Yoshiyuki Morishita(5), Yoshihide Asano(4), Izumi Yoshida(4), Masashi Imai(4), Kiyohide Fushimi(4), Kenjiro Kikuchi(4), Yuichiro Ueda(4), Yoshio Kaku(4), Keiji Hirai(4), Taro Hoshino(4), Kazuo Kubo(3)