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A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

Journal of the American Society of Nephrology(2021)10.1681/asn.2020081234Source: DataRank Database

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS is a research paper published in Journal of the American Society of Nephrology (2021). On theSindex it has a DataRank of 0. It has been cited 7 times.

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Open Access7 citations

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Enrichment:Funding (31 grants)OA: bronzeTopics (14)IDs (PubMed, PMC)Annotations (1)SDGs (2)

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (26)

Susan Murray ORCID,Katherine A. Benson ORCID,Agnieszka Bierżyńska ORCID,Megan Chryst-Stangl,Liming Wang ORCID

Live enrichment

PubMed:33863784 PMC:PMC8425665

National Institute of Diabetes and Digestive and Kidney Diseases

Grant: 5R01DK098135

National Institute of Diabetes and Digestive and Kidney Diseases

Grant: 5R01DK094987

National Institute of Diabetes and Digestive and Kidney Diseases

Grant: U54‐DK‐083912

National Institute of Diabetes and Digestive and Kidney Diseases

Grant: T32-DK007731

Doris Duke Charitable Foundation

Grant: 2009033

Canadian Institutes of Health Research

Grant: 432980

McLaughlin Accelerator Award

Grant: 2019

NephCure Kidney International–NEPTUNE

Grant: Ancillary Studies Grant

Physicians Services Incorporated

Grant: Health Research Grant 14-04

National Institutes of Health

Grant: R01-DK108805

National Institutes of Health

Grant: R01-DK119380

NIDDK NIH HHS

Grant: R01 DK076683

NIDDK NIH HHS

Grant: T32 DK007731

NIDDK NIH HHS

Grant: RC2 DK122397

NIDDK NIH HHS

Grant: R01 DK119380

NIDDK NIH HHS

Grant: R01 DK098135

NIDDK NIH HHS

Grant: R01 DK108805

Medical Research Council

Grant: MR/R013942/1

Kidney Research UK

Grant: PDF_005_20171124

NIDDK NIH HHS

Grant: R01 DK094987

Canadian Institutes of Health Research

Grant: unidentified

unidentified

Borden Scholars Award

Toronto General Hospital Foundation

National Center for Advancing Translational Sciences

NephCure Kidney International

Duke Health Scholars Award

Halpin Foundation

University of Michigan

Kidney Research UK

Office of Rare Diseases Research

Can-SOLVE CKD Network

bronze

publisherhttps://jasn.asnjournals.org/content/jnephrol/32/7/1682.full.pdf

publisherhttps://www.ovid.com/10.1681/ASN.2020081234

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/8425665

https://doi.org/10.1681/asn.2020081234

https://pubmed.ncbi.nlm.nih.gov/33863784

Fields of Study

0301 basic medicine0303 health sciences03 medical and health sciences

Keywords

CalcineurinNephrotic syndromePodocyteChronic Kidney DiseaseCalcineurin InhibitorsTacrolimusFocal Segmental GlomerulosclerosisGlomerular DiseaseGenetic Renal Disease570610

Sustainable Development Goals

SDG 2: 2. Zero hungerSDG 3: 3. Good health

A Rare Autosomal Dominant Variant in Regulator of Calcineurin Type 1 (RCAN1) Gene Confers Enhanced Calcineurin Activity and May Cause FSGS

FAIR Checklist

Authors (26)

Funding (31 grants)

Open Access

Topics

Annotations (Europe PMC)