يعرض 1 - 20 نتائج من 55 نتيجة بحث عن '(( 5 y descrease ) OR ((((( _ mt increase ) OR ( y de decrease ))) OR ( _ rare decrease ))))*', وقت الاستعلام: 0.14s تنقيح النتائج
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    EndMT Regulation by Small RNAs in Diabetes-Associated Fibrotic Conditions: Potential Link With Oxidative Stress حسب Roberta Giordo (299595)

    منشور في 2021
    "…Recent evidence suggests that small RNAs, in particular microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), are crucial mediators of EndMT. Furthermore, EndMT and miRNAs are both affected by oxidative stress, another key player in the pathophysiology of diabetic fibrotic complications. …"
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    Pleiotropic functions of the tumor- and metastasis-suppressing matrix metalloproteinase-8 in mammary cancer in MMTV-PyMT transgenic mice حسب Julie Decock (44558)

    منشور في 2015
    "…Likewise, lung metastasis dramatically increased in the MMTV-PyMT; Mmp8-null mice. Immunohistochemistry revealed that tumors in wild-type, Mmp8-heterozygotes and -null animals had similar vascular density at 8 weeks, but at 10 weeks Mmp8-wild-type tumors had a lower vascularity than their heterozygote and null counterparts. …"
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    Resveratrol-Elicited PKC Inhibition Counteracts NOX-Mediated Endothelial to Mesenchymal Transition in Human Retinal Endothelial Cells Exposed to High Glucose حسب Roberta Giordo (299595)

    منشور في 2021
    "…Here, we investigate whether EndMT is implicated in the diabetic retinopathy fibrotic process and evaluate the possibility that resveratrol could counteract EndMT by inhibiting high glucose (HG)-induced increases in ROS. …"
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    Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls حسب Daniel Erskine (3471959)

    منشور في 2019
    "…<p dir="ltr">Mitochondrial diseases arise due to defects in mitochondrial DNA (mtDNA) or nuclear mitochondrial genes (nDNA), leading to impaired mitochondrial oxidative phosphorylation and dysfunction of organs with particularly high energy requirements. …"
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    Inhibitory synapse dysfunction and epileptic susceptibility associated with KIF2A deletion in cortical interneurons حسب Nuria Ruiz-Reig (14434026)

    منشور في 2023
    "…Mutations in genes encoding microtubules (MT) and MT-associated proteins are one of the most frequent causes of MCD in humans. …"
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    Inhibition of cytochrome P450 epoxygenase promotes endothelium-to-mesenchymal transition and exacerbates doxorubicin-induced cardiovascular toxicity حسب Hevna Dhulkifle (14724821)

    منشور في 2024
    "…Furthermore, we also show that MSPPOH increased cardiac edema, lowered vascular blood flow velocity, and worsened the expression of EndMT and cardiac injury markers in our zebrafish model of DOX-induced cardiotoxicity.…"
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    Geospatial assessment of the carbon footprint of water and electricity consumption in residential buildings in Doha, Qatar حسب Ammar, Abulibdeh

    منشور في 2024
    "…Concurrently, the annual average water CF in residential buildings is around 0.06 MtCO2 equivalent, predominantly attributed to villas. …"
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    NMT verb rendering: A cognitive approach to informing Arabic-into-English post-editing حسب Ali Almanna (14585162)

    منشور في 2022
    "…However, despite professional translators increasingly considering PE as a valid stage in their translation workflow, little has been done to investigate MT output for the purpose of informing training in PE. …"
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    Removal of Methylene Blue from Water Using Magnetic GTL-Derived Biosolids: Study of Adsorption Isotherms and Kinetic Models حسب Shifa Zuhara (14150862)

    منشور في 2023
    "…<p dir="ltr">Global waste production is significantly rising with the increase in population. Efforts are being made to utilize waste in meaningful ways and increase its economic value. …"
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    Simultaneous Bilateral Neck of Femur Fracture in a Young Adult with Underlying Metabolic Disturbances حسب Eslam Alkaramani (14570439)

    منشور في 2020
    "…Simultaneous bilateral fractures of the femoral neck are considered very rare injuries. Few cases were reported in the literature. …"
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    Genomic architecture of autism spectrum disorder in Qatar: The BARAKA-Qatar Study حسب Mona Abdi (10196665)

    منشور في 2023
    "…Dominant variants, including de novo and inherited, contributed to 15 (55.6%) of these families, consisting of SNVs/indels (66.7%), CNVs (13.3%), TREs (13.3%), and mtDNA variants (6.7%). Moreover, homozygous variants were found in 7 families (25.9%), with a sixfold increase in homozygous burden in consanguineous versus non-consanguineous families (13.6% and 1.8%, respectively). …"
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    Investigating the moderating role of Export PromotionProgrammes using evidence from North-Africa حسب Yacine Haddoud, Mohamed

    منشور في 2017
    "…Originality/value– This study offers a rare focus on the moderating role of EPPs in the relationship between export barriers andexport propensity, within thesetting of a North-African country.…"
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