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The anti-PLA2R antibody in membranous nephropathy: what we know and what remains a decade after its discovery.

Immune system-mediated cellular and molecular mechanisms in idiopathic membranous nephropathy pathogenesis and possible therapeutic targets.

Protein uptake at glomerular level: is it just the work of podocytes?

The inability of podocytes to proliferate: cause, consequences and origin.

Mitochondrial pyruvate carrier 2 mediates mitochondrial dysfunction and apoptosis in high glucose-treated podocytes.

TGF-β1 inhibits the autophagy of podocytes by activating mTORC1 in IgA nephropathy.

Intrinsic disorder and amino acid specificity modulate binding of the WW2 domain in kidney and brain protein (KIBRA) to synaptopodin.

Expression of Urokinase-type Plasminogen Activator Receptor and its Soluble Form in Type 2 Diabetic Kidney Disease.

Coexistence of Fabry disease with IgM nephropathy: A case report.

Cre recombinase toxicity in podocytes, a novel genetic model for FSGS in adolescent mice.

Gastric duplication cyst in an infant with Finnish-type congenital nephrotic syndrome: concurrence or coincidence?

The impact of steroids on the injured podocytes in nephrotic syndrome.

Arctigenin attenuates diabetic kidney disease through the activation of PP2A in podocytes.

Identification of glomerular and podocyte-specific genes and pathways activated by sera of patients with focal segmental glomerulosclerosis.

Kidney organoids: accurate models or fortunate accidents.

Calpain-10 drives podocyte apoptosis and renal injury in diabetic nephropathy.

Exosomal microRNA-16-5p from human urine-derived stem cells ameliorates diabetic nephropathy through protection of podocyte.

Renal globotriaosylceramide deposits for Fabry disease linked to uncertain pathogenicity gene variant c.352C>T/p.Arg118Cys: A family study.

Combined inhibition of CCR2 and ACE provides added protection against progression of diabetic nephropathy in deficient mice.

A Simple and Highly Purified Glomeruli Isolation from the Mouse Kidney.

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