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Mostrando 61 - 80 Resultados de 121 Para Buscar '"Aladin"', tiempo de consulta: 0.44s Limitar resultados
  1. 61
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    Dipolar-stabilized first and second-order antiskyrmions in ferrimagnetic multilayers
  2. 62
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    Mitochondria supply sub-lethal signals for cytokine secretion and DNA-damage in H. pylori infection
  3. 63
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    Correction to: Mitochondria supply sub-lethal signals for cytokine secretion and DNA-damage in H. pylori infection
  4. 64
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    Thickness dependence of the triplet spin-valve effect in superconductor–ferromagnet–ferromagnet heterostructures
  5. 65
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    Investigation of IL-23 (p19, p40) and IL-23R identifies nuclear expression of IL-23 p19 as a favorable prognostic factor in colorectal cancer: a retrospective multicenter study of 675 patients
  6. 66
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    Spontaneous activity of the mitochondrial apoptosis pathway drives chromosomal defects, the appearance of micronuclei and cancer metastasis through the Caspase-Activated DNAse
  7. 67
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    Experimental demonstration of a skyrmion-enhanced strain-mediated physical reservoir computing system
  8. 68
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    Clinical Characteristics and Prognostic Impact of Short Physical Performance Battery in Hospitalized Patients with Acute Heart Failure—Results of the PROFUND-IC Registry †
  9. 69
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    Pectoralis muscle area and mortality in smokers without airflow obstruction
  10. 70
    “…ALADIN is a component of the nuclear pore complex in higher eukaryotes. …”
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    Decreased Expression of a Gene Caused by a T-DNA Insertion in an Adjacent Gene in Arabidopsis
  11. 71
    “…RESULTS: In the current study, we present that proliferation is decreased when ALADIN, PGRMC1 or PGRMC2 are over-expressed. Furthermore, we find that depletion of ALADIN results in mislocalization of Aurora kinase A and PGRMC1 in metaphase cells. …”
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    Triple A patient cells suffering from mitotic defects fail to localize PGRMC1 to mitotic kinetochore fibers
  12. 72
    “…BACKGROUND: Achalasia‐addisonianism‐alacrima syndrome, frequently referred to as Allgrove syndrome or Triple A syndrome, is a multisystem disorder resulting from homozygous or compound heterozygous pathogenic variants in the gene encoding aladin (AAAS). Aladin is a member of the WD‐repeat family of proteins and is a component of the nuclear pore complex. …”
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    Functional validation of a novel AAAS variant in an atypical presentation of Allgrove syndrome
  13. 73
    “…Allgrove disease is due to recessive mutations in the AAAS gene, which encodes for the nucleoporin Aladin, implicated in the nucleocytoplasmic transport. …”
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    SCARB1 downregulation in adrenal insufficiency with Allgrove syndrome
  14. 74
    “…The Aladin cassette is integrated with Datex Ohmeda S/5 ADU and GE Aisys anaesthesia machines. …”
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    Advances in vaporisation: A narrative review
  15. 75
    “…The overall results of ALADIN showed a significant increase in well-being from the baseline final testing with the new adaptive lighting system. …”
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    Ambient Assistive Technologies (AAT): socio-technology as a powerful tool for facing the inevitable sociodemographic challenges?
  16. 76
    “…RESULTS: The current appraisal summarizes data from 1160 participants in the ALADIN, SYDNEY, ORPIL, SYDNEY 2, and ALADIN III trials. …”
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    Critical appraisal of the use of alpha lipoic acid (thioctic acid) in the treatment of symptomatic diabetic polyneuropathy
  17. 77
    “…METHODS: Clinical data from the observational studies HEROIC (cardiology and hematology; n=1,727), EMIR (cardiology; n=1,493), BRONCE-AP (primary care; n=133), SILVER-AP (primary care; n=457), ALADIN (internal medicine and neurology; n=249), and ESPARTA (internal medicine; n=110) of patients taking rivaroxaban were analyzed. …”
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    Clinical profile and management of rivaroxaban in patients with atrial fibrillation in routine practice in Spain: data from six nationwide studies
  18. 78
    “…For further interpretation and discussion please refer to the research article “Left ventricular dysfunction in ADPKD and effects of Octreotide-LAR: a cross-sectional and longitudinal sub study of the ALADIN trial” (Spinelli et al., 2018) [1].…”
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    Data on the assessment of LV mechanics by speckle tracking echocardiography in ADPKD patients
  19. 79
    “…We present a case of a 16-year-old male presenting with the classic triad and a homozygous mutation in the Aladin WD Repeat Nucleoporin (AAAS gene). Genetic analysis and detection of AAAS gene mutation is the cornerstone of diagnosis. …”
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    Triple A Multisystem Disorder: Allgrove Syndrome
  20. 80
    “…The disease features include variable degrees of neurological and neuro-ophthalmic manifestations. Protein ALADIN encoded by the AAAS gene is found to be defective in Triple A Syndrome. …”
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    Spectral Domain – Optical Coherence Tomography findings in Triple-A Syndrome – A case series from Pakistan
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