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  1. 112821
    Total Sesquiterpene Glycosides from Loquat Leaves Ameliorate HFD-Induced Insulin Resistance by Modulating IRS-1/GLUT4, TRPV1, and SIRT6/Nrf2 Signaling Pathways
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  2. 112822
    Ghrelin Ameliorates Diabetic Retinal Injury: Potential Therapeutic Avenues for Diabetic Retinopathy
    por Jie Bai, Fan Yang, Ruiqi Wang, Qinghui Yan
    Publicado 2021
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  3. 112823
    Lifestyle-Induced Redox-Sensitive Alterations: Cross-Talk among the RAAS, Antioxidant/Inflammatory Status, and Hypertension
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  4. 112824
    Genetic testing and clinical relevance of patients with thoracic aortic aneurysm and dissection in northwestern China
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  5. 112825
    A novel mutation of AMHR2 in two brothers with persistent Müllerian duct syndrome and their intracytoplasmic sperm injection outcome
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  6. 112826
    Beckwith–Wiedemann syndrome: Clinical, histopathological and molecular study of two Tunisian patients and review of literature
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  7. 112827
    Assessing the association of common genetic variants in EPHB4 and RASA1 with phenotype severity in familial cerebral cavernous malformation
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  8. 112828
    A two‐year prospective study assessing the performance of fetal chromosomal microarray analysis and next‐generation sequencing in high‐risk pregnancies
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  9. 112829
    Acupuncture With deqi Modulates the Hemodynamic Response and Functional Connectivity of the Prefrontal-Motor Cortical Network
    “... of complementary and alternative therapy to Western medicine. Despite acupuncture’s long history and public...”
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  10. 112830
    Allelic and genotypic frequencies of NAT2, CYP2E1, and AADAC genes in a cohort of Peruvian tuberculosis patients
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  11. 112831
    Identification of a novel COL10A1: c.1952 G>T variant in a family with Schmid metaphyseal chondrodysplasia and development of a noninvasive prenatal testing method
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  12. 112832
    Detection of TSC1/TSC2 mosaic variants in patients with cardiac rhabdomyoma and tuberous sclerosis complex by hybrid‐capture next‐generation sequencing
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  13. 112833
    Usher syndrome type 2A complicated with glycogen storage disease type 3 due to paternal uniparental isodisomy of chromosome 1 in a sporadic patient
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  14. 112834
    Mid-infrared all-fiber gain-switched pulsed laser at 3 μm
    “..., spectroscopy, chemical detection and medicine. So far, these MIR lasers largely required bulk optical elements...”
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  15. 112835
    Amputation for chronic pain and/or functional impairment of a limb
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  16. 112836
    Three de novo variants in KMT2A (MLL) identified by whole exome sequencing in patients with Wiedemann–Steiner syndrome
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  17. 112837
    Clinicoradiographic and genetic features of cerebral small vessel disease indicate variability in mode of inheritance for monoallelic HTRA1 variants
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  18. 112838
    Genetic and clinical heterogeneity in Korean patients with Rubinstein–Taybi syndrome
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  19. 112839
    Current practice of thoracic anaesthesia in Europe – a survey by the European Society of Anaesthesiology Part I – airway management and regional anaesthesia techniques
    “...” of the German Society of Anaesthesiology and Intensive Care Medicine (DGAI) has performed an online survey...”
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  20. 112840
    Real Time Pain Detection Using Facial Action Units in Telehealth System
    por dalya abdullah anwar
    Publicado 2021
    “... of the patient to be able to prescribe the correct medicine and diagnose the disease proficiently. In this paper...”
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