(Q37569711)

21 August 2017

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title

Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier (English)

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21 August 2017

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Corinne Antignac

3

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Martin Zenker

series ordinal

1

object named as

Martin Zenker

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21 August 2017

Eduardo Machuca

2

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21 August 2017

language of work or name

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1 August 2009

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Journal of Molecular Medicine

21 August 2017

published in

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21 August 2017

volume

87

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21 August 2017

issue

9

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21 August 2017

page(s)

849-857

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https://scigraph.springernature.com/pub.10.1007/s00109-009-0505-9

21 August 2017

exact match

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cites work

Genetic models: clues for understanding the pathogenesis of idiopathic nephrotic syndrome

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-009-0505-9

Nephrin strands contribute to a porous slit diaphragm scaffold as revealed by electron tomography

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-009-0505-9

Identification and functional analysis of a novel TRPC6 mutation associated with late onset familial focal segmental glomerulosclerosis in Chinese patients

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00109-009-0505-9

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

21 January 2018

1 reference

12 December 2020

2007 Young Investigator Award: TRP'ing into a new era for glomerular disease.

1 reference

12 December 2020

Integrin beta1-mediated matrix assembly and signaling are critical for the normal development and function of the kidney glomerulus

1 reference

12 December 2020

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

1 reference

12 December 2020

CD151, the first member of the tetraspanin (TM4) superfamily detected on erythrocytes, is essential for the correct assembly of human basement membranes in kidney and skin.

1 reference

12 December 2020

Variable phenotype of Pierson syndrome

1 reference

12 December 2020

Phosphorylation of Nephrin Triggers Ca2+ Signaling by Recruitment and Activation of Phospholipase C-{gamma}1.

1 reference

12 December 2020

Interaction with podocin facilitates nephrin signaling

1 reference

12 December 2020

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

1 reference

12 December 2020

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

1 reference

12 December 2020

Neph-Nephrin proteins bind the Par3-Par6-atypical protein kinase C (aPKC) complex to regulate podocyte cell polarity

1 reference

12 December 2020

Podocin participates in the assembly of tight junctions between foot processes in nephrotic podocytes

1 reference

12 December 2020

Laminins: structure and genetic regulation

1 reference

12 December 2020

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome

1 reference

12 December 2020

Identification of BRAF as a new interactor of PLCepsilon1, the protein mutated in nephrotic syndrome type 3.

1 reference

12 December 2020

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Connecting the interpodocyte slit diaphragm and actin dynamics: Emerging role for the nephrin signaling complex

1 reference

12 December 2020

Kidney failure in mice lacking the tetraspanin CD151.

1 reference

12 December 2020

The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1

1 reference

12 December 2020

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12 December 2020

Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes

1 reference

12 December 2020

Nephrotic syndrome in childhood.

1 reference

12 December 2020

A milder variant of Pierson syndrome.

1 reference

12 December 2020

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

1 reference

12 December 2020

Induction of TRPC6 channel in acquired forms of proteinuric kidney disease

1 reference

12 December 2020

TRPC6 mutations associated with focal segmental glomerulosclerosis cause constitutive activation of NFAT-dependent transcription.

1 reference

12 December 2020

Update on the glomerular filtration barrier

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12 December 2020

Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

1 reference

12 December 2020

Nephrin mediates actin reorganization via phosphoinositide 3-kinase in podocytes.

1 reference

12 December 2020

Characterization of the interactions of the nephrin intracellular domain.

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12 December 2020

The slit diaphragm: a signaling platform to regulate podocyte function

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12 December 2020

Synaptopodin regulates the actin-bundling activity of alpha-actinin in an isoform-specific manner

1 reference

12 December 2020

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

1 reference

12 December 2020

Neph1 cooperates with nephrin to transduce a signal that induces actin polymerization

1 reference

12 December 2020

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

1 reference

12 December 2020

Nephrin--a unique structural and signaling protein of the kidney filter

1 reference

12 December 2020

A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2

1 reference

12 December 2020

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

1 reference

12 December 2020

Podocin organizes ion channel-lipid supercomplexes: implications for mechanosensation at the slit diaphragm.

1 reference

12 December 2020

Loss of podocyte aPKClambda/iota causes polarity defects and nephrotic syndrome

1 reference

12 December 2020

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

1 reference

12 December 2020

Podocyte-specific deletion of integrin-linked kinase results in severe glomerular basement membrane alterations and progressive glomerulosclerosis.

1 reference

12 December 2020

Sensitizing the Slit Diaphragm with TRPC6 ion channels.

1 reference

12 December 2020

Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis

1 reference

12 December 2020

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

1 reference

12 December 2020

1 reference

12 December 2020

PLC-epsilon: a shared effector protein in Ras-, Rho-, and G alpha beta gamma-mediated signaling

1 reference

12 December 2020

Laminin functions in tissue morphogenesis.

1 reference

12 December 2020

Downregulation of TRPC6 protein expression by high glucose, a possible mechanism for the impaired Ca2+ signaling in glomerular mesangial cells in diabetes

1 reference

12 December 2020

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12 December 2020

Regulation of TRPC6 channel activity by tyrosine phosphorylation

1 reference

12 December 2020

A common mechanism underlies stretch activation and receptor activation of TRPC6 channels

1 reference

12 December 2020

Molecular architecture of the glomerular slit diaphragm: lessons learnt for a better understanding of disease pathogenesis

1 reference

12 December 2020

Basement membrane assembly, stability and activities observed through a developmental lens.

1 reference

12 December 2020

Nephrin ectodomain engagement results in Src kinase activation, nephrin phosphorylation, Nck recruitment, and actin polymerization

1 reference

12 December 2020

SRC-family kinase Fyn phosphorylates the cytoplasmic domain of nephrin and modulates its interaction with podocin

1 reference

12 December 2020

Proteinuria precedes podocyte abnormalities inLamb2-/- mice, implicating the glomerular basement membrane as an albumin barrier

1 reference

12 December 2020

Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton

1 reference

12 December 2020

Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

1 reference

12 December 2020

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

1 reference

12 December 2020

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

1 reference

12 December 2020

Nephrin and CD2AP associate with phosphoinositide 3-OH kinase and stimulate AKT-dependent signaling

1 reference

12 December 2020

10.1007/S00109-009-0505-9

Identifiers

DOI

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21 August 2017

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