TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype. - Wikidata - wikimedia - TriplyDB

TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.

TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.

http://www.wikidata.org/entity/Q54360965

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Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice The renal channelopathies Genetic causes of proteinuria and nephrotic syndrome: impact on podocyte pathobiology.A novel TRPC6 mutation in a family with podocytopathy and clinical variability.Resolvin D1 protects podocytes in adriamycin-induced nephropathy through modulation of 14-3-3β acetylation Gq signaling causes glomerular injury by activating TRPC6.Rituximab in children with resistant idiopathic nephrotic syndrome.The Genetics of Nephrotic Syndrome.Educational paper: the podocytopathies.Genetics of steroid-resistant nephrotic syndrome: a review of mutation spectrum and suggested approach for genetic testing.Steroid-resistant nephrotic syndrome: impact of genetic testing.Molecular and genetic basis of inherited nephrotic syndrome Canonical Transient Receptor Potential 6 Channel: A New Target of Reactive Oxygen Species in Renal Physiology and Pathology.Renoprotection: focus on TRPV1, TRPV4, TRPC6 and TRPM2.Pharmacological inhibition of FSGS-related TRPC6 gain of function mutants by semisynthetic larixol-derived compounds.TRPC6 G757D Loss-of-Function Mutation Associates with FSGS.New TRPC6 gain-of-function mutation in a non-consanguineous Dutch family with late-onset focal segmental glomerulosclerosis.254C>G: a TRPC6 promoter variation associated with enhanced transcription and steroid-resistant nephrotic syndrome in Chinese children.Steroid-resistant nephrotic syndrome: past and current perspectives.A molecular genetic analysis of childhood nephrotic syndrome in a cohort of Saudi Arabian families.TRPC6 gene promoter polymorphisms in steroid resistant nephrotic syndrome children.Podocyte-associated gene mutation screening in a heterogeneous cohort of patients with sporadic focal segmental glomerulosclerosis.Monogenic Causes of Proteinuria in Children.Genetic Interactions Between TRPC6 and NPHS1 Variants Affect Posttransplant Risk of Recurrent Focal Segmental Glomerulosclerosis.Focal segmental glomerulosclerosis and end-stage kidney disease in children.Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy Mutational screening of inverted formin 2 in adult-onset focal segmental glomerulosclerosis or minimal change patients from the Czech Republic

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TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype.

http://www.wikidata.org/entity/Q54360965

description

2011 nî lūn-bûn

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2011年の論文

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年学术文章

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2011年學術文章

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2011年學術文章

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2011年學術文章

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name

TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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type

label

TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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prefLabel

TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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Clinical Journal of the American Society of Nephrology

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TRPC6 mutations in children wi ...... ndrome and atypical phenotype.

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Annalisa Schirinzi

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Elena Ranieri

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Eustacchio Montemurno

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Filippo Aucella

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Francesco Emma

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Giovanni Messina

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Giuseppina Cerullo

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Laura Massella

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Maria d'Apolito

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Tommaso De Palo

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1626-1634

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scholarly article

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10.2215/CJN.07830910

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7

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Gian Marco Ghiggeri

Gianluca Caridi

Maddalena Gigante

Loreto Gesualdo

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2011-07-01T00:00:00Z

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21734084

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