(Q28215959)

English

Insight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes

scientific article (publication date: May 2002)

In more languages

Statements

scholarly article

0 references

1 reference

Europe PubMed Central

Insight into podocyte differentiation from the study of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes (English)

0 references

nail-patella syndrome

1 reference

based on heuristic

inferred from title

genetic disease

1 reference

based on heuristic

inferred from title

author name string

Roy Morello

1

0 references

Brendan Lee

2

0 references

language of work or name

0 references

publication date

May 2002

0 references

Pediatric Research

0 references

51

0 references

5

0 references

551-8

0 references

The molecular basis of embryonic kidney development

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Inductive tissue interactions, cell signaling, and the control of kidney organogenesis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Kidney morphogenesis: cellular and molecular regulation

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Kidney development branches out.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Regulatory molecules in kidney development

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

The malformed kidney: disruption of glomerular and tubular development

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Collagen IV alpha 3, alpha 4, and alpha 5 chains in rodent basal laminae: sequence, distribution, association with laminins, and developmental switches

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

The laminin alpha chains: expression, developmental transitions, and chromosomal locations of alpha1-5, identification of heterotrimeric laminins 8-11, and cloning of a novel alpha3 isoform

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Organization and expression of basement membrane collagen IV genes and their roles in human disorders

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Insertional mutation of the collagen genes Col4a3 and Col4a4 in a mouse model of Alport syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Molecular and functional defects in kidneys of mice lacking collagen alpha 3(IV): implications for Alport syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Kidney development: regulatory molecules crucial to both mice and men.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Regulation of podocyte structure during the development of nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Glomerular podocytes and adhesive interaction with glomerular basement membrane.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Cell cycle regulation and differentiation in the human podocyte lineage

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

The role of the podocyte in glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Nephrin is specifically located at the slit diaphragm of glomerular podocytes

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Role of nephrin in cell junction formation in human nephrogenesis

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

The murine nephrin gene is specifically expressed in kidney, brain and pancreas: inactivation of the gene leads to massive proteinuria and neonatal death

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Stomatin, a MEC-2 like protein, is expressed by mammalian sensory neurons

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Synaptopodin: an actin-associated protein in telencephalic dendrites and renal podocytes

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Altered podocyte structure in GLEPP1 (Ptpro)-deficient mice associated with hypertension and low glomerular filtration rate

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Molecular cloning of cDNAs encoding human GLEPP1, a membrane protein tyrosine phosphatase: characterization of the GLEPP1 protein distribution in human kidney and assignment of the GLEPP1 gene to human chromosome 12p12-p13

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Nail-patella syndrome in a spontaneously aborted 18-week fetus: ultrastructural and immunofluorescent study of the kidneys

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Mutation analysis of LMX1B gene in nail-patella syndrome patients

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Restricted distribution of loss-of-function mutations within the LMX1B genes of nail-patella syndrome patients.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

LIM domains: multiple roles as adapters and functional modifiers in protein interactions

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

The LIM domain: regulation by association

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Functions of LIM-homeobox genes.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Induction of the LIM homeobox gene Lmx1 by WNT6a establishes dorsoventral pattern in the vertebrate limb

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

LMX1B transactivation and expression in nail-patella syndrome

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Two genes, COL4A3 and COL4A4 coding for the human alpha3(IV) and alpha4(IV) collagen chains are arranged head-to-head on chromosome 2q36.

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Transcriptional synergy between LIM-homeodomain proteins and basic helix-loop-helix proteins: the LIM2 domain determines specificity

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Pod-1, a mesoderm-specific basic-helix-loop-helix protein expressed in mesenchymal and glomerular epithelial cells in the developing kidney

1 reference

https://api.crossref.org/works/10.1203%2F00006450-200205000-00002

21 January 2018

Identifiers

10.1203/00006450-200205000-00002

0 references

Dimensions Publication ID

0 references

PubMed publication ID

0 references

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28215959&oldid=2177515686"