(Q37774243)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

review article

1 reference

title

Glomerular diseases: genetic causes and future therapeutics (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

author name string

Reiko Inagi

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

language of work or name

English

0 references

publication date

20 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

Nature Reviews Nephrology

8 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

volume

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

539-554

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nrneph.2010.103

8 February 2020

exact match

0 references

cites work

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The enigmatic parietal epithelial cell is finally getting noticed: a review

21 January 2018

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The mesangial cell revisited: no cell is an island

21 January 2018

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"Treasure your exceptions": recent advances in molecular genetics of glomerular disease

21 January 2018

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Therapeutic targets in focal and segmental glomerulosclerosis

21 January 2018

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New insights into the role of podocytes in proteinuria

21 January 2018

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Hereditary proteinuria syndromes and mechanisms of proteinuria

21 January 2018

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

21 January 2018

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Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

21 January 2018

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Nephrin is specifically located at the slit diaphragm of glomerular podocytes

21 January 2018

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Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for Finnish congenital nephrosis (NPHS1) in 19q13.1.

21 January 2018

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Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

21 January 2018

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Nephrin localizes to the slit pore of the glomerular epithelial cell

21 January 2018

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Clustering-induced tyrosine phosphorylation of nephrin by Src family kinases

21 January 2018

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Fyn binds to and phosphorylates the kidney slit diaphragm component Nephrin

21 January 2018

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SRC-family kinase Fyn phosphorylates the cytoplasmic domain of nephrin and modulates its interaction with podocin

21 January 2018

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Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

21 January 2018

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

21 January 2018

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Podocin localizes in the kidney to the slit diaphragm area

21 January 2018

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Early glomerular filtration defect and severe renal disease in podocin-deficient mice

21 January 2018

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Slit diaphragms contain tight junction proteins

21 January 2018

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Direct activation of human TRPC6 and TRPC3 channels by diacylglycerol

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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Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

21 January 2018

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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

21 January 2018

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Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

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/10.1038%2FNRNEPH.2010.103

Molecular cloning and expression of phospholipase C epsilon 1 in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain

21 January 2018

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A novel adaptor protein orchestrates receptor patterning and cytoskeletal polarity in T-cell contacts

21 January 2018

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CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

21 January 2018

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CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).

21 January 2018

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Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis

21 January 2018

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Actinin-4, a novel actin-bundling protein associated with cell motility and cancer invasion

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Disease-associated mutant alpha-actinin-4 reveals a mechanism for regulating its F-actin-binding affinity

21 January 2018

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The role of transient receptor potential channels in kidney disease

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

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

21 January 2018

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Increased vascular smooth muscle contractility in TRPC6-/- mice

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

A common mechanism underlies stretch activation and receptor activation of TRPC6 channels

21 January 2018

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Genetics of nephrotic syndrome: new insights into molecules acting at the glomerular filtration barrier

21 January 2018

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Hereditary macrothrombocytopathia, nephritis and deafness

21 January 2018

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Human nonmuscle myosin heavy chain mRNA: generation of diversity through alternative polyadenylylation

21 January 2018

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Fechtner syndrome: clinical and genetic aspects

21 January 2018

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MYH9 is associated with nondiabetic end-stage renal disease in African Americans

21 January 2018

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MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

21 January 2018

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Targeted disruption of mouse ortholog of the human MYH9 responsible for macrothrombocytopenia with different organ involvement: hematological, nephrological, and otological studies of heterozygous KO mice

21 January 2018

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An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor

21 January 2018

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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

21 January 2018

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New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes

21 January 2018

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Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

21 January 2018

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Cloning and characterization of HARP/SMARCAL1: a prokaryotic HepA-related SNF2 helicase protein from human and mouse

21 January 2018

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Inherited diseases of the glomerular basement membrane

21 January 2018

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Glomerular filtration is normal in the absence of both agrin and perlecan-heparan sulfate from the glomerular basement membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Alport's syndrome, Goodpasture's syndrome, and type IV collagen.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Identification of mutations in the COL4A5 collagen gene in Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Identification of a distinct type IV collagen alpha chain with restricted kidney distribution and assignment of its gene to the locus of X chromosome-linked Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The renal lesions of Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Deletion of the paired alpha 5(IV) and alpha 6(IV) collagen genes in inherited smooth muscle tumors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Identification of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autosomal recessive Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mutations in the type IV collagen alpha 3 (COL4A3) gene in autosomal recessive Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Thin basement membrane nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Colocalization of the genes for the alpha 3(IV) and alpha 4(IV) chains of type IV collagen to chromosome 2 bands q35-q37

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

21 January 2018

12 December 2020

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

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The renal glomerulus of mice lacking s-laminin/laminin beta 2: nephrosis despite molecular compensation by laminin beta 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genotype-phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The podocyte-specific inactivation of Lmx1b, Ldb1 and E2a yields new insight into a transcriptional network in podocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Glomerular disease: sugars and immune complex formation in IgA nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22-23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genetic heterogeneity in Italian families with IgA nephropathy: suggestive linkage for two novel IgA nephropathy loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

ADAMTS13 gene deletion aggravates ischemic brain damage: a possible neuroprotective role of ADAMTS13 by ameliorating postischemic hypoperfusion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

von Willebrand factor-cleaving protease ADAMTS13 reduces ischemic brain injury in experimental stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Familial haemolytic uraemic syndrome and an MCP mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genetics of HUS: the impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Familial hypocomplementemic hemolytic uremic syndrome with HLA-A3,B7 haplotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mutations in complement C3 predispose to development of atypical hemolytic uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Thrombomodulin mutations in atypical hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Atypical hemolytic-uremic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genetic variation at the SLC12A3 locus is unlikely to explain risk for advanced diabetic nephropathy in Caucasians with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Confirmation of genetic associations at ELMO1 in the GoKinD collection supports its role as a susceptibility gene in diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Molecular cloning and characterization of the protein 4.1O gene, a novel member of the protein 4.1 family with focal expression in ovary

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Distinct distribution of specific members of protein 4.1 gene family in the mouse nephron.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The role of aminoacyl-tRNA synthetases in genetic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Lipoprotein glomerulopathy: glomerular lipoprotein thrombi in a patient with hyperlipoproteinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Lipoprotein glomerulopathy induced by ApoE-Sendai is different from glomerular lesions in aged apoE-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Impact of lipoprotein glomerulopathy on the relationship between lipids and renal diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Guidelines to diagnosis and monitoring of Fabry disease and review of treatment experiences

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Differential phenotypic expression by three mutant alleles in familial lecithin:cholesterol acyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mutations in the glucose-6-phosphatase gene that cause glycogen storage disease type 1a

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Glycogen storage disease in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Angiotensin mediates renal fibrosis in the nephropathy of glycogen storage disease type Ia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Leigh syndrome with nephropathy and CoQ10 deficiency due to decaprenyl diphosphate synthase subunit 2 (PDSS2) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Coenzyme Q10 supplementation rescues renal disease in Pdss2kd/kd mice with mutations in prenyl diphosphate synthase subunit 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The genetics of systemic lupus erythematosus stratified by renal disease: linkage at 10q22.3 (SLEN1), 2q34-35 (SLEN2), and 11p15.6 (SLEN3).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Genetics of human lupus nephritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

New genomic region for Wegener's granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Focal segmental glomerulosclerosis in patients with mandibuloacral dysplasia owing to ZMPSTE24 deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

A nonsense mutation in the LIMP-2 gene associated with progressive myoclonic epilepsy and nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Changing trends in pediatric transplantation: 2001 Annual Report of the North American Pediatric Renal Transplant Cooperative Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Cyclosporine a slows the progressive renal disease of alport syndrome (X-linked hereditary nephritis): results from a canine model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Antifibrotic, nephroprotective potential of ACE inhibitor vs AT1 antagonist in a murine model of renal fibrosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Treatment of X-linked hereditary nephritis in Samoyed dogs with angiotensin converting enzyme (ACE) inhibitor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Preemptive ramipril therapy delays renal failure and reduces renal fibrosis in COL4A3-knockout mice with Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Delayed chemokine receptor 1 blockade prolongs survival in collagen 4A3-deficient mice with Alport disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Irradiation prolongs survival of Alport mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Stem cell therapies benefit Alport syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Stem cell therapy for Alport syndrome: the hope beyond the hype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Enzyme replacement therapy in Fabry disease: a randomized controlled trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Endoplasmic reticulum stress--a double edged sword for Z alpha-1 antitrypsin deficiency hepatoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Endoplasmic reticulum stress as a progression factor for kidney injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Defective trafficking of nephrin missense mutants rescued by a chemical chaperone

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The genetics of IgA nephropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Association analysis of podocyte slit diaphragm genes as candidates for diabetic nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Stem Cell-Based Therapy for Glomerular Diseases: An Evolving Concept

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

The fine structure of the renal glomerulus of the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Congenital nephrotic syndrome in mice lacking CD2-associated protein

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Focal segmental glomerulosclerosis in a patient homozygous for a CD2AP mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Induction of TRPC6 channel in acquired forms of proteinuric kidney disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Chronic renal failure and shortened lifespan in COL4A3+/- mice: an animal model for thin basement membrane nephropathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

A clinical study of hereditary interstitial pyelonephritis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Congenital nephrosis, mesangial sclerosis, and distinct eye abnormalities with microcoria: an autosomal recessive syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Transcriptional induction of slit diaphragm genes by Lmx1b is required in podocyte differentiation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Multiple calvarial defects in lmx1b mutant mice.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

ELMO1 increases expression of extracellular matrix proteins and inhibits cell adhesion to ECMs

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Neonatal presentation of coenzyme Q10 deficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Congenital focal segmental glomerulosclerosis associated with beta4 integrin mutation and epidermolysis bullosa

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Renin-angiotensin axis blockade reduces proteinuria in presymptomatic patients with familial FSGS

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Plasma exchange and retransplantation in recurrent nephrosis of patients with congenital nephrotic syndrome of the Finnish type (NPHS1)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Long-term effects of cyclosporine A in Alport's syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Cell therapy for Alport syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2010.103

Glomerular morphometry in biopsy evaluation of minimal change disease, membranous glomerulonephritis, thin basement membrane disease and Alport's syndrome

31 March 2020

1 reference

12 December 2020

Hereditary and acquired complement dysregulation in membranoproliferative glomerulonephritis

1 reference

12 December 2020

Alport syndrome and thin glomerular basement membrane nephropathy: a practical approach to diagnosis

1 reference

12 December 2020

O-linked oligosaccharide on IgA1 hinge region in IgA nephropathy. Fundamental study for precise structure and possible role

1 reference

12 December 2020

Genetic studies into inherited and sporadic hemolytic uremic syndrome

1 reference

12 December 2020

[Lipoprotein glomerulopathy]

1 reference

12 December 2020

Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.

1 reference

12 December 2020

Fechtner syndrome--a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia

1 reference

12 December 2020

Nephrotic syndrome in newborn and young infants

1 reference

12 December 2020

The Genetics of Angiokeratoma Corporis Diffusum (Fabry's Disease) and Its Linkage Relations with the Xg Locus

1 reference

12 December 2020

Aberrantly glycosylated IgA1 in IgA nephropathy patients is recognized by IgG antibodies with restricted heterogeneity

1 reference

12 December 2020

WT1: a novel tumor suppressor gene inactivated in Wilms' tumor

1 reference

12 December 2020

Familial lecithin-cholesterol acyltransferase deficiency.

1 reference

12 December 2020

Molecular cloning of alpha 5(IV) collagen and assignment of the gene to the region of the X chromosome containing the Alport syndrome locus

1 reference

12 December 2020

Association of asialo-galactosyl beta 1-3N-acetylgalactosamine on the hinge with a conformational instability of Jacalin-reactive immunoglobulin A1 in immunoglobulin A nephropathy

1 reference

12 December 2020

Genetic impact of pathogenesis and prognosis of ANCA-associated vasculitides.

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEPH.2010.103

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20644582%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference