Translating genetic findings in hereditary nephrotic syndrome: the missing loops (Q28088653)

Rasheed A. Gbadegesin

series ordinal

2

1 reference

language of work or name

1 reference

1 July 2015

1 reference

American Journal of Physiology - Renal Physiology

published in

1 reference

volume

309

1 reference

page(s)

F24-8

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issue

1

1 reference

Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS

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Alpha-actinin-4-mediated FSGS: an inherited kidney disease caused by an aggregated and rapidly degraded cytoskeletal protein

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Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

20 March 2017

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NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

20 March 2017

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Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis

20 March 2017

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HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

20 March 2017

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Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

29 September 2017

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A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS.

29 September 2017

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Phosphodiesterase 5 inhibition ameliorates angiontensin II-induced podocyte dysmotility via the protein kinase G-mediated downregulation of TRPC6 activity

29 September 2017

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Genetic testing in nephrotic syndrome--challenges and opportunities

29 September 2017

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The glomerular filtration barrier: components and crosstalk

29 September 2017

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Educational paper: the podocytopathies

29 September 2017

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Rituximab targets podocytes in recurrent focal segmental glomerulosclerosis

29 September 2017

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Generation of induced pluripotent stem cells from human kidney mesangial cells

29 September 2017

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Podocyte-secreted angiopoietin-like-4 mediates proteinuria in glucocorticoid-sensitive nephrotic syndrome

29 September 2017

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Pathogenesis and therapy of focal segmental glomerulosclerosis: an update

29 September 2017

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Effect of cyclosporin A on proteinuria in the course of glomerulopathy associated with WT1 mutations

29 September 2017

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A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9

29 September 2017

1 reference

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Conditionally immortalized human podocyte cell lines established from urine

29 September 2017

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Cellular origins of type IV collagen networks in developing glomeruli.

29 September 2017

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Familial forms of nephrotic syndrome.

29 September 2017

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The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A.

29 September 2017

1 reference

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The zebrafish pronephros: a model to study nephron segmentation

29 September 2017

1 reference

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TRPC6 and FSGS: the latest TRP channelopathy

29 September 2017

1 reference

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Podocytes in culture: past, present, and future

29 September 2017

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Glucocorticoids protect and enhance recovery of cultured murine podocytes via actin filament stabilization

29 September 2017

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A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

29 September 2017

1 reference

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The fine structure of the renal glomerulus of the mouse

29 September 2017

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Nephrotic syndrome in childhood.

29 September 2017

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Cell biology of the glomerular podocyte

29 September 2017

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Precise and efficient genome editing in zebrafish using the CRISPR/Cas9 system

29 September 2017

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Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis

2 June 2018

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Non-immunologic mechanisms of calcineurin inhibitors explain its antiproteinuric effects in genetic glomerulopathies

2 June 2018

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Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.

21 January 2018

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Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

21 January 2018

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Congenital nephrotic syndrome in mice lacking CD2-associated protein

21 January 2018

1 reference

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AKT2 is essential to maintain podocyte viability and function during chronic kidney disease

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/25810439

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A familial childhood-onset relapsing nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/25810439