Search Results - "Visuttijai, Kittichate"
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Potential Natural Products Regulation of Molecular Signaling Pathway in Dermal Papilla Stem Cells
Published in Molecules (Basel, Switzerland) (19-07-2023)“…Stem cells have demonstrated significant potential for tissue engineering and repair, anti-aging, and rejuvenation. Hair follicle stem cells can be found in…”
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Chitooligosaccharide prevents vascular endothelial cell apoptosis by attenuation of endoplasmic reticulum stress via suppression of oxidative stress through Nrf2-SOD1 up-regulation
Published in Pharmaceutical biology (31-12-2022)“…Endoplasmic reticulum (ER) stress contributes to endothelium pathological conditions. Chitooligosaccharides (COS) have health benefits, but their effect on…”
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Histopathological Evaluation of Somatostatin Receptor 2 Expression in Myocarditis—Rationale for the Diagnostic Use of Somatostatin Receptor Imaging
Published in Diagnostics (Basel) (24-10-2024)“…Background/Objectives: Myocarditis is an inflammatory disease of the myocardium and remains to this day a challenging diagnosis. A promising novel imaging…”
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Structural modification of resveratrol analogue exhibits anticancer activity against lung cancer stem cells via suppression of Akt signaling pathway
Published in BMC complementary and alternative medicine (03-06-2023)“…Compound with cancer stem cell (CSC)-suppressing activity is promising for the improvement of lung cancer clinical outcomes. Toward this goal, we discovered…”
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Lowered Expression of Tumor Suppressor Candidate MYO1C Stimulates Cell Proliferation, Suppresses Cell Adhesion and Activates AKT
Published in PloS one (07-10-2016)“…Myosin-1C (MYO1C) is a tumor suppressor candidate located in a region of recurrent losses distal to TP53. Myo1c can tightly and specifically bind to PIP2, the…”
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Shrimp Lipid Prevents Endoplasmic Reticulum-Mediated Endothelial Cell Damage
Published in Foods (01-10-2022)“…Shrimp contains a fat that benefits cardiovascular function and may help in the prevention of diseases. The stress of essential cellular organelle endoplasmic…”
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Abnormal expression of myosin heavy chains in early postnatal stages of spinal muscular atrophy type I at single fibre level
Published in Acta myologica (01-09-2024)“…We investigated myosin heavy chain (MyHC) isoform expression at early postnatal stages of clinically and genetically confirmed spinal muscular atrophy type 1…”
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Ribonuclease inhibitor 1 (RNH1) deficiency cause congenital cataracts and global developmental delay with infection-induced psychomotor regression and anemia
Published in European journal of human genetics : EJHG (01-08-2023)“…Ribonuclease inhibitor 1, also known as angiogenin inhibitor 1, encoded by RNH1, is a ubiquitously expressed leucine-rich repeat protein, which is highly…”
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Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing
Published in Brain pathology (Zurich, Switzerland) (01-05-2021)“…Muscle pathology in inclusion body myositis (IBM) typically includes inflammatory cell infiltration, muscle fibers with rimmed vacuoles and cytochrome c…”
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Respiratory chain dysfunction in perifascicular muscle fibres in patients with dermatomyositis is associated with mitochondrial DNA depletion
Published in Neuropathology and applied neurobiology (01-12-2022)“…Aims Patients with dermatomyositis (DM) suffer from reduced aerobic metabolism contributing to impaired muscle function, which has been linked to cytochrome c…”
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Abstract 2166: Analyses of protein expression of PI 3-kinase/AKT signaling in response to altered expression of motor protein MYO1C
Published in Cancer research (Chicago, Ill.) (01-08-2015)“…In the previous work, a minimal region of recurrent deletion distal to the Tp53 gene was identified in BDII rat model for endometrial adenocarcinoma and the…”
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Proteomic profiling of polyglucosan bodies associated with glycogenin‐1 deficiency in skeletal muscle
Published in Neuropathology and applied neurobiology (01-06-2024)“…Aims Polyglucosan storage disorders represent an emerging field within neurodegenerative and neuromuscular conditions, including Lafora disease (EPM2A, EPM2B),…”
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Long-term follow-up and characteristic pathological findings in severe nemaline myopathy due to LMOD3 mutations
Published in Neuromuscular disorders : NMD (01-02-2019)“…•Novel mutation in Leiomodin 3 (LMOD3) gene leading to loss of LMOD3 transcripts and protein.•Characteristic histopathological appearance of the nemaline…”
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Glycogenin is Dispensable for Glycogen Synthesis in Human Muscle, and Glycogenin Deficiency Causes Polyglucosan Storage
Published in The journal of clinical endocrinology and metabolism (01-02-2020)“…Abstract Context Glycogenin is considered to be an essential primer for glycogen biosynthesis. Nevertheless, patients with glycogenin-1 deficiency due to…”
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Progressive external ophthalmoplegia associated with novelMT-TNmutations
Published in Acta neurologica Scandinavica (2021)“…Objectives To describe two patients with progressive external ophthalmoplegia (PEO) and mitochondrial myopathy associated with mutations in mitochondrial DNA,…”
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Progressive external ophthalmoplegia associated with novel MT‐TN mutations
Published in Acta neurologica Scandinavica (01-01-2021)“…Objectives To describe two patients with progressive external ophthalmoplegia (PEO) and mitochondrial myopathy associated with mutations in mitochondrial DNA,…”
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Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variant
Published in Brain pathology (Zurich, Switzerland) (01-07-2022)“…Two homoplasmic variants in tRNAGlu (m.14674T>C/G) are associated with reversible infantile respiratory chain deficiency. This study sought to further…”
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Cardiomyopathy with lethal arrhythmias associated with inactivation of KLHL24
Published in Human molecular genetics (01-06-2019)“…Abstract Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiovascular disorder, yet the genetic cause of up to 50% of cases remains unknown…”
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Loss of supervillin causes myopathy with myofibrillar disorganization and autophagic vacuoles
Published in Brain (London, England : 1878) (01-08-2020)“…The muscle specific isoform of the supervillin protein (SV2), encoded by the SVIL gene, is a large sarcolemmal myosin II- and F-actin-binding protein…”
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