A new locus for familial FSGS on chromosome 2p (Q34124184)

31 July 2017

A new locus for familial FSGS on chromosome 2p (English)

1 reference

31 July 2017

Rasheed Gbadegesin

1

1 reference

31 July 2017

Peter Lavin

2

1 reference

31 July 2017

Louis Janssens

3

1 reference

31 July 2017

Bartlomiej Bartkowiak

4

1 reference

31 July 2017

Alison Homstad

5

1 reference

31 July 2017

Guanghong Wu

6

1 reference

31 July 2017

Brandy Bowling

7

1 reference

31 July 2017

Jason Eckel

8

1 reference

31 July 2017

Chris Potocky

9

1 reference

31 July 2017

Diana Abbott

10

1 reference

31 July 2017

Peter Conlon

11

1 reference

31 July 2017

William K Scott

12

1 reference

31 July 2017

David Howell

13

1 reference

31 July 2017

Elizabeth Hauser

14

1 reference

31 July 2017

Michelle P Winn

15

1 reference

31 July 2017

8 July 2010

1 reference

Journal of the American Society of Nephrology

31 July 2017

1 reference

31 July 2017

21

1 reference

31 July 2017

8

1 reference

31 July 2017

1390-1397

1 reference

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

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Modulation of renal cell injury by heat shock proteins: lessons learned from the immature kidney

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Differential proteomic analysis of proteins induced by glucocorticoids in cultured murine podocytes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Twenty-one-year trend in ESRD due to focal segmental glomerulosclerosis in the United States

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Trends in the epidemiology of focal segmental glomerulosclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Hsp27 regulates podocyte cytoskeletal changes in an in vitro model of podocyte process retraction

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Cytosolic chaperonin-containing t-complex polypeptide 1 changes the content of a particular subunit species concomitant with substrate binding and folding activities during the cell cycle

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Molecular chaperones in the kidney: distribution, putative roles, and regulation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

The racial prevalence of glomerular lesions in nephrotic adults

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Pathology of the nephrotic syndrome in children: a report for the International Study of Kidney Disease in Children.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Pathogenesis of lipoid nephrosis: a disorder of T-cell function

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Estimating the power of a proposed linkage study: a practical computer simulation approach

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Recurrence of nephrotic syndrome after transplantation in CNF is due to autoantibodies to nephrin.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2938593

Circulating factor associated with increased glomerular permeability to albumin in recurrent focal segmental glomerulosclerosis

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20616172

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20616172

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1681/ASN.2009101046

1 reference

31 July 2017

1 reference

31 July 2017

1 reference