Search Results - "Moin, A"

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  1. 1

    Molecular stratification of idiopathic nephrotic syndrome by Saleem, Moin A.

    Published in Nature reviews. Nephrology (01-12-2019)
    “…Idiopathic nephrotic syndrome (INS) describes a group of pathologies of the renal glomerulus that result in the classic triad of heavy proteinuria, oedema and…”
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    Long-Term Outcomes in IgA Nephropathy by Pitcher, David, Braddon, Fiona, Hendry, Bruce, Mercer, Alex, Osmaston, Kate, Saleem, Moin A, Steenkamp, Retha, Wong, Katie, Turner, A Neil, Wang, Kaijun, Gale, Daniel P, Barratt, Jonathan

    “…IgA nephropathy can progress to kidney failure, and risk assessment soon after diagnosis has advantages both for clinical management and the development of new…”
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    What is circulating factor disease and how is it currently explained? by Hayward, Samantha, Parmesar, Kevon, Saleem, Moin A.

    Published in Pediatric nephrology (Berlin, West) (01-11-2023)
    “…Nephrotic syndrome (NS) consists of the clinical triad of hypoalbuminaemia, high levels of proteinuria and oedema, and describes a heterogeneous group of…”
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    β-Aminoisobutyric acid (L-BAIBA) is a novel regulator of mitochondrial biogenesis and respiratory function in human podocytes by Audzeyenka, Irena, Szrejder, Maria, Rogacka, Dorota, Angielski, Stefan, Saleem, Moin A., Piwkowska, Agnieszka

    Published in Scientific reports (14-01-2023)
    “…Podocytes constitute an external layer of the glomerular filtration barrier, injury to which is a hallmark of renal disease. Mitochondrial dysfunction often…”
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    One hundred ways to kill a podocyte by Saleem, Moin A

    Published in Nephrology, dialysis, transplantation (01-08-2015)
    “…The podocyte is a highly specialized cell, forming within the developing glomerulus from a mesenchymal origin, acquiring some but not complete features of an…”
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    What is the Role of Soluble Urokinase-Type Plasminogen Activator in Renal Disease? by Saleem, Moin A

    Published in Nephron (2015) (01-01-2018)
    “…Soluble urokinase-type plasminogen activator -(suPAR) is an inflammatory signal with pleiotropic biological effects depending on context and post-translational…”
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    Deriving and understanding the risk of post-transplant recurrence of nephrotic syndrome in the light of current molecular and genetic advances by Bierzynska, Agnieszka, Saleem, Moin A.

    Published in Pediatric nephrology (Berlin, West) (01-11-2018)
    “…After renal transplantation, recurrence of the original disease is the second most common cause of graft loss, after rejection. The most dramatic manifestation…”
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    Insulin induces bioenergetic changes and alters mitochondrial dynamics in podocytes by Audzeyenka, Irena, Rachubik, Patrycja, Rogacka, Dorota, Saleem, Moin A, Piwkowska, Agnieszka

    Published in Journal of endocrinology (01-06-2024)
    “…Diabetic nephropathy (DN) is one of the most frequent complications of diabetes. Early stages of DN are associated with hyperinsulinemia and progressive…”
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    The podocyte cytoskeleton—key to a functioning glomerulus in health and disease by Welsh, Gavin I., Saleem, Moin A.

    Published in Nature reviews. Nephrology (01-01-2012)
    “…An understanding of the intricacies of cytoskeletal dynamics and regulation in podocytes is essential to facilitate investigation and treatment of patients…”
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    New developments in steroid-resistant nephrotic syndrome by Saleem, Moin A.

    Published in Pediatric nephrology (Berlin, West) (01-05-2013)
    “…Nephrotic syndrome is a disorder of the glomerular filtration barrier, a highly specialised tri-layer structure with unique functional properties. Recent…”
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    Nephrin--signature molecule of the glomerular podocyte by Welsh, Gavin I, Saleem, Moin A

    Published in The Journal of pathology (01-02-2010)
    “…In recent years there has been an explosion of interest in the glomerular podocyte, which plays a central role in control of glomerular filtration. A host of…”
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    Dysregulated autophagy contributes to podocyte damage in Fabry's disease by Liebau, Max C, Braun, Fabian, Höpker, Katja, Weitbrecht, Claudia, Bartels, Valerie, Müller, Roman-Ulrich, Brodesser, Susanne, Saleem, Moin A, Benzing, Thomas, Schermer, Bernhard, Cybulla, Markus, Kurschat, Christine E

    Published in PloS one (17-05-2013)
    “…Fabry's disease results from an inborn error of glycosphingolipid metabolism that is due to deficiency of the lysosomal hydrolase α-galactosidase A. This…”
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