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significantly impaired » significantly improved (Expand Search), significantly improve (Expand Search), significantly improves (Expand Search)
impaired decrease » marked decrease (Expand Search)
smaller decrease » small decrease (Expand Search), marked decrease (Expand Search), larger decrease (Expand Search)
smaller areas » small area (Expand Search)
significantly impaired » significantly improved (Expand Search), significantly improve (Expand Search), significantly improves (Expand Search)
impaired decrease » marked decrease (Expand Search)
smaller decrease » small decrease (Expand Search), marked decrease (Expand Search), larger decrease (Expand Search)
smaller areas » small area (Expand Search)
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7761
Data_Sheet_1_Profiling morphologic MRI features of motor neuron disease caused by TARDBP mutations.docx
Published 2022“…VBM analysis showed significant atrophy of the right lateral parietal cortex in TARDBP patients, compared with controls. …”
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7762
Supplementary Material for: Pulmonary Recovery 12 Months after Non-Severe and Severe COVID-19: The Prospective Swiss COVID-19 Lung Study
Published 2022“…The difference for forced vital capacity (91.6% vs. 96.3% predicted, <i>p</i> = 0.082) was not statistically significant. Between 3 and 12 months, lung function improved in both groups and differences in DLCO between non-severe and severe COVID-19 patients decreased. …”
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7763
Image_2_Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss.TIF
Published 2022“…Moreover, 26 loci in the TNFSF11 gene were in linkage disequilibrium with rs1021188, revealing relative similarities between different populations. Significant differences in both DNA methylation and unmethylation status were detected with 4.53- and 4.83-fold decreases in the global DNA methylation levels in female and male OTSC groups, respectively. …”
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7764
Image_1_Seizures regulate the cation-Cl− cotransporter NKCC1 in a hamster model of epilepsy: implications for GABA neurotransmission.JPEG
Published 2023“…Mounting evidence suggests that the impairment of GABAergic inhibitory neurotransmission plays a crucial role in the pathophysiology of epilepsy, both in patients and animal models. …”
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7765
Table 1_Dietary quercetagetin attenuates H2O2-induced oxidative damage and preserves meat quality in broilers by modulating redox status and Nrf2/ferroptosis signaling pathway.docx
Published 2025“…Meanwhile, the addition of QG to the diet increased the mRNA expressions of Nrf2 and TFR1, showing no significant difference from those of the control group. …”
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7766
Image_1_Genetic Association of rs1021188 and DNA Methylation Signatures of TNFSF11 in the Risk of Conductive Hearing Loss.TIF
Published 2022“…Moreover, 26 loci in the TNFSF11 gene were in linkage disequilibrium with rs1021188, revealing relative similarities between different populations. Significant differences in both DNA methylation and unmethylation status were detected with 4.53- and 4.83-fold decreases in the global DNA methylation levels in female and male OTSC groups, respectively. …”
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7767
Data_Sheet_1_Early Brassica Crops Responses to Salinity Stress: A Comparative Analysis Between Chinese Cabbage, White Cabbage, and Kale.xlsx
Published 2019“…In parallel with the photosynthetic impairments, the Na<sup>+</sup>/K<sup>+</sup> ratio was highest in Chinese cabbage leaves and lowest in kale leaves while kale root is able to keep high Na<sup>+</sup>/K<sup>+</sup> ratio without a significant increase in MDA. …”
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7768
Image_1_Seizures regulate the cation-Cl− cotransporter NKCC1 in a hamster model of epilepsy: implications for GABA neurotransmission.JPEG
Published 2023“…Mounting evidence suggests that the impairment of GABAergic inhibitory neurotransmission plays a crucial role in the pathophysiology of epilepsy, both in patients and animal models. …”
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7769
DataSheet1_Synthesis, Characterization, and in vivo Evaluation of a Novel Potent Autotaxin-Inhibitor.docx
Published 2022“…Taken together, these results provide evidence that the dysregulation of the ATX-LPA axis in the aqueous humor of glaucoma patients, in addition to the postulated outflow impairment, might also contribute to RGC loss. The observation that ATX-inhibitor treatment in both glaucoma models did not result in significant IOP increases or decreases after oral treatment indicates that protection from RGC loss due to inhibition of the ATX-LPA axis is independent of an IOP lowering effect.…”
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7770
DataSheet1_Molecular dynamics study of tropical calcific pancreatitis (TCP) associated calcium-sensing receptor single nucleotide variation.docx
Published 2022“…The results of molecular dynamic simulations showed that the mutations P163R, I427S, D433H, and V477A caused conformational changes and decreased the stability of protein structures. This study also demonstrates the significance of TCP associated mutations. …”
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7771
Table_1_NADPH and Mito-Apocynin Treatment Protects Against KA-Induced Excitotoxic Injury Through Autophagy Pathway.pdf
Published 2021“…Compared with NADPH, the combination showed more significant neuroprotective effects, presenting more neurons survive and better motor function recovery. …”
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7772
Image_2_Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson’s disease reveal upregulation of oxidative phosphorylation-related genes associated with...
Published 2024“…In contrast, C57- En1<sup>+/−</sup> mice had no significant increase in axonal swellings or cell loss in SNpc at 16 weeks. …”
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7773
Image_1_Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson’s disease reveal upregulation of oxidative phosphorylation-related genes associated with...
Published 2024“…In contrast, C57- En1<sup>+/−</sup> mice had no significant increase in axonal swellings or cell loss in SNpc at 16 weeks. …”
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7774
Table_1_Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson’s disease reveal upregulation of oxidative phosphorylation-related genes associated with...
Published 2024“…In contrast, C57- En1<sup>+/−</sup> mice had no significant increase in axonal swellings or cell loss in SNpc at 16 weeks. …”
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7775
Table_2_Nigral transcriptomic profiles in Engrailed-1 hemizygous mouse models of Parkinson’s disease reveal upregulation of oxidative phosphorylation-related genes associated with...
Published 2024“…In contrast, C57- En1<sup>+/−</sup> mice had no significant increase in axonal swellings or cell loss in SNpc at 16 weeks. …”
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7776
DataSheet1_Quanduzhong capsules for the treatment of grade 1 hypertension patients with low-to-moderate risk: A multicenter, randomized, double-blind, placebo-controlled clinical t...
Published 2023“…After 4 weeks of treatment, there were no significant differences between the groups in terms of safety indicators (p > .05). …”
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7777
Supporting data for “Androgen receptor modulates chemotherapy response in breast cancer”
Published 2025“…For palbociclib, a CDK4/6 inhibitor, AR activation induced RB1 polyubiquitination and degradation, diminishing RB1 levels—a key downstream target of CDK4/6—and thus impairing palbociclib efficacy. Chromatin immunoprecipitation (ChIP) sequencing identified 1,209 AR-regulated genes, with gene ontology (GO) analysis highlighting significant enrichment of ubiquitin-related genes. qPCR validation pinpointed TRIM37, an AR-regulated E3 ligase, as a mediator of RB1 degradation. …”
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7778
Image2_Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family.JPEG
Published 2024“…Keratoconus (KC) is a kind of genetically predisposed eye disease that causes blindness characterized by a dilated thinning of the central or paracentral cornea conically projected forward, highly irregular astigmatism, and severe visual impairment. Klinefelter syndrome is caused by an extra X chromosome in the cells of male patients, and the main phenotype is tall stature and dysplasia with secondary sex characteristics. …”
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7779
Image1_Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family.JPEG
Published 2024“…Keratoconus (KC) is a kind of genetically predisposed eye disease that causes blindness characterized by a dilated thinning of the central or paracentral cornea conically projected forward, highly irregular astigmatism, and severe visual impairment. Klinefelter syndrome is caused by an extra X chromosome in the cells of male patients, and the main phenotype is tall stature and dysplasia with secondary sex characteristics. …”
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7780
Ciliary pattern of paramecia depleted for TZ proteins.
Published 2020“…DNAH2<sup>RNAi</sup> cells present a percentage of short cilia slightly higher than the controls. Impairing ciliary beating of TMEM216<sup>RNAi</sup> cells by DNAH2 decreases this percentage. …”