Lista de obras -

APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases.

artículo científico publicado en 2015

Antagonistic Regulation of Actin Dynamics and Cell Motility by TRPC5 and TRPC6 Channels ⬇️

artículo científico publicado el 26 de octubre de 2010

Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development

artículo científico publicado en 1996

Cosmc-dependent mucin-type O-linked glycosylation is essential for podocyte function

artículo científico publicado en 2020

Electrolyte abnormalities and progressive renal failure in a cancer patient

artículo científico publicado en 2007

Evidence for a role of a tumor necrosis factor-alpha (TNF-alpha)-converting enzyme-like protease in shedding of TRANCE, a TNF family member involved in osteoclastogenesis and dendritic cell survival

artículo científico publicado en 1999

Evidence for an interaction of the metalloprotease-disintegrin tumour necrosis factor alpha convertase (TACE) with mitotic arrest deficient 2 (MAD2), and of the metalloprotease-disintegrin MDC9 with a novel MAD2-related protein, MAD2beta

artículo científico publicado en 1999

Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1

artículo científico publicado en 2002

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis.

artículo científico publicado en 2013

Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS).

artículo científico publicado en 2007

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

artículo científico publicado en 2012

Gain-of-function mutations in transient receptor potential C6 (TRPC6) activate extracellular signal-regulated kinases 1/2 (ERK1/2)

artículo científico publicado en 2013

How many Achilles' heels does a podocyte have? An update on podocyte biology.

artículo científico

Intracellular maturation and localization of the tumour necrosis factor alpha convertase (TACE)

artículo científico publicado en 2000

Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling.

artículo científico publicado en 2013

Metalloprotease-disintegrins: modular proteins capable of promoting cell-cell interactions and triggering signals by protein-ectodomain shedding.

artículo científico publicado en 1999

Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury

artículo científico publicado en 2016

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

artículo científico publicado en 2010

Nephrin AKTs on actin: The slit diaphragm-actin cytoskeleton signaling network expands.

artículo científico publicado en 2008

Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)

artículo científico publicado en 2011

SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity

artículo científico publicado en 2012

Six members of the mouse forkhead gene family are developmentally regulated ⬇️

artículo científico publicado el 15 de agosto de 1993

Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy

artículo científico publicado en 2019

TRPC6 and kidney disease: sclerosing more than just glomeruli?

artículo científico publicado en 2017

TRPC6 in glomerular health and disease: what we know and what we believe

artículo científico publicado en 2006

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

artículo científico publicado en 2009

The Glomerular Disease Study and Trial Consortium: A Grassroots Initiative to Foster Collaboration and Innovation.

artículo científico publicado en 2018

Transmembrane insertases and N-glycosylation critically determine synthesis, trafficking, and activity of the nonselective cation channel TRPC6

scientific article published on 02 July 2019

Lista de obras de

APOL1 kidney disease risk variants cause cytotoxicity by depleting cellular potassium and inducing stress-activated protein kinases.

Antagonistic Regulation of Actin Dynamics and Cell Motility by TRPC5 and TRPC6 Channels ⬇️

Clustered arrangement of winged helix genes fkh-6 and MFH-1: possible implications for mesoderm development

Cosmc-dependent mucin-type O-linked glycosylation is essential for podocyte function

Electrolyte abnormalities and progressive renal failure in a cancer patient

Evidence for a role of a tumor necrosis factor-alpha (TNF-alpha)-converting enzyme-like protease in shedding of TRANCE, a TNF family member involved in osteoclastogenesis and dendritic cell survival

Evidence for an interaction of the metalloprotease-disintegrin tumour necrosis factor alpha convertase (TACE) with mitotic arrest deficient 2 (MAD2), and of the metalloprotease-disintegrin MDC9 with a novel MAD2-related protein, MAD2beta

Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1

Exome sequencing and in vitro studies identified podocalyxin as a candidate gene for focal and segmental glomerulosclerosis.

Functional genetic variation in aminopeptidase A (ENPEP): lack of clear association with focal and segmental glomerulosclerosis (FSGS).

GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.

Gain-of-function mutations in transient receptor potential C6 (TRPC6) activate extracellular signal-regulated kinases 1/2 (ERK1/2)

How many Achilles' heels does a podocyte have? An update on podocyte biology.

Intracellular maturation and localization of the tumour necrosis factor alpha convertase (TACE)

Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling.

Metalloprotease-disintegrins: modular proteins capable of promoting cell-cell interactions and triggering signals by protein-ectodomain shedding.

Mice with mutant Inf2 show impaired podocyte and slit diaphragm integrity in response to protamine-induced kidney injury

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

Nephrin AKTs on actin: The slit diaphragm-actin cytoskeleton signaling network expands.

Rho activation of mDia formins is modulated by an interaction with inverted formin 2 (INF2)

SNF8, a member of the ESCRT-II complex, interacts with TRPC6 and enhances its channel activity

Six members of the mouse forkhead gene family are developmentally regulated ⬇️

Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy

TRPC6 and kidney disease: sclerosing more than just glomeruli?

TRPC6 in glomerular health and disease: what we know and what we believe

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

The Glomerular Disease Study and Trial Consortium: A Grassroots Initiative to Foster Collaboration and Innovation.

Transmembrane insertases and N-glycosylation critically determine synthesis, trafficking, and activity of the nonselective cation channel TRPC6