(Q40066555)

17 September 2017

title

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

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17 September 2017

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Roger C Wiggins

5

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author name string

Hassan Chaib

1

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17 September 2017

Bethan E Hoskins

2

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17 September 2017

Shazia Ashraf

3

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17 September 2017

Meera Goyal

4

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17 September 2017

Friedhelm Hildebrandt

6

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17 September 2017

publication date

17 October 2007

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American Journal of Physiology - Renal Physiology

17 September 2017

published in

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17 September 2017

volume

294

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17 September 2017

issue

1

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17 September 2017

page(s)

F93-9

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

17 September 2017

cites work

1 reference

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Extracellular signals and reversible protein phosphorylation: what to Mek of it all.

21 January 2018

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Mutations of the BRAF gene in human cancer

21 January 2018

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New insight into BRAF mutations in cancer

21 January 2018

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Nephrotic syndrome in the 1st year of life

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

B-raf, a new member of the raf family, is activated by DNA rearrangement

21 January 2018

1 reference

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The mitogen-activated protein kinase cascade is activated by B-Raf in response to nerve growth factor through interaction with p21ras

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

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

21 January 2018

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https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

Phospholipase C(epsilon): a novel Ras effector

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

Identification and characterization of podocalyxin--the major sialoprotein of the renal glomerular epithelial cell

21 January 2018

1 reference

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Molecular cloning, expression, and characterization of podocalyxin-like protein 1 from rabbit as a transmembrane protein of glomerular podocytes and vascular endothelium

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

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

21 January 2018

1 reference

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Cell junction-associated proteins IQGAP1, MAGI-2, CASK, spectrins, and alpha-actinin are components of the nephrin multiprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

Association of MEK1 with p21ras.GMPPNP is dependent on B-Raf

21 January 2018

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Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

21 January 2018

1 reference

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Post-translational modification of H-Ras is required for activation of, but not for association with, B-Raf

21 January 2018

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

21 January 2018

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IQGAP1 modulates activation of B-Raf

21 January 2018

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IQGAP1 binds ERK2 and modulates its activity

21 January 2018

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IQGAP1 is a scaffold for mitogen-activated protein kinase signaling

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

Identification of PLC210, a Caenorhabditis elegans phospholipase C, as a putative effector of Ras.

21 January 2018

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Hereditary proteinuria syndromes and mechanisms of proteinuria

21 January 2018

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B-Raf-dependent regulation of the MEK-1/mitogen-activated protein kinase pathway in PC12 cells and regulation by cyclic AMP.

21 January 2018

1 reference

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Podocyte depletion causes glomerulosclerosis: diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

Genome-wide prediction of C. elegans genetic interactions

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

21 January 2018

A signal chain of events

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00345.2007

10.1152/AJPRENAL.00345.2007

21 January 2018

Identifiers

DOI

1 reference

17 September 2017

1 reference