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

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About: Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity Goto Sponge NotDistinct Permalink

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rdf:type	Item
description	article (en) հոդված (hy) wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 1999 (uk) im Juni 1999 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57624029-0544967A-9C28-488A-841A-AFD4F474F458
publication date	1999-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57624029-05389946-E478-4614-BEB8-9B4362B1174C wds:Q57624029-329D3A16-4267-403A-906E-A1AF4CF6771B wds:Q57624029-3D586F1F-867F-488E-8359-8DE69BA33A55 wds:Q57624029-3EC71BF2-EDE2-455E-A293-01B4BE0C1BA9 wds:Q57624029-882B3CE5-0E76-48AD-9EC4-A55E8E770D69 wds:Q57624029-9CE3579E-DAAC-406A-BA59-1F41EF81B046 wds:Q57624029-A5354664-A1ED-4C6A-8F0A-9C471756AF5F wds:Q57624029-BEB9AC62-9083-40A5-9220-874B9940575D wds:Q57624029-FAE64ABB-AAD8-4E4C-8050-01B806FA5F22
author name string	M A Pericak-Vance A H Smith P J Conlon M Bembe D N Howell F L Graham K L Lynn B D Slotterbeck M P Winn
rdfs:label	Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (en) Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (nl)
skos:prefLabel	Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (en) Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (nl)
name	Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (en) Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity (nl)
author	wds:Q57624029-4C4142C5-D0E3-40DA-9982-AA4950D797A7 wds:Q57624029-99FCA524-8976-4DB5-8418-7B47A453D5CE
author	Jeffery M. Vance L. Darryl Quarles
title	wds:Q57624029-69377775-7DEF-4A0E-AE4A-087B286604A7
title	Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity (en)
page(s)	wds:Q57624029-AC11F8F3-7E74-4F4C-ABAF-F01AB37CDD4F
page(s)	113-120
instance of	wds:Q57624029-CD38A4B0-476E-4BCB-8F37-BCED11A0C048
instance of	scholarly article
main subject	wds:Q57624029-36F7009B-3F51-4812-A459-ED9BAFA38167 wds:Q57624029-ACAAFC03-045A-4600-B937-83A71595FFCF
main subject	focal segmental glomerulosclerosis heterogeneity
PubMed ID	wds:Q57624029-AC0151E2-7BF7-418C-BA23-4ACEB7519A06
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10368108
PubMed ID	10368108
published in	wds:Q57624029-ACE0BC2E-C815-42A8-948E-35D269F93DAF
published in	Genomics
issue	wds:Q57624029-CECB5B52-562D-4AFB-9787-3EBAED3FA06C
volume	wds:Q57624029-362A7B4B-FE4E-4AF0-BD94-22988591854E
issue	2
volume	58
DOI	wds:Q57624029-73E02BCB-1DD7-4E70-9DF2-2E05AF361475
DOI	http://dx.doi.org/10.1006/GENO.1999.5828
DOI	10.1006/GENO.1999.5828
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57624029
is cites work of	Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis A new locus for familial FSGS on chromosome 2p Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis The pediatric nephrotic syndrome spectrum: clinical homogeneity and molecular heterogeneity NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome Familial forms of nephrotic syndrome. NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele An investigation of genome-wide associations of hypertension with microsatellite markers in the family blood pressure program (FBPP) Respiratory chain deficiency presenting as congenital nephrotic syndrome. Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS Exclusion of homozygous PLCE1 (NPHS3) mutations in 69 families with idiopathic and hereditary FSGS. NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome FVB mouse genotype confers susceptibility to OVE26 diabetic albuminuria Inverted formin 2 mutations with variable expression in patients with sporadic and hereditary focal and segmental glomerulosclerosis Unraveling the genetics of chronic kidney disease using animal models A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21. Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis. Slit or pore? A mutation of the ion channel TRPC6 causes FSGS. End-stage renal failure in African Americans: insights in kidney disease susceptibility The genetic basis of FSGS and steroid-resistant nephrosis A novel missense mutation of Wilms' Tumor 1 causes autosomal dominant FSGS. Educational paper: the podocytopathies Second Messenger-Operated Calcium Entry Through TRPC6. Recent Progress in the Pathogenesis of Nephrotic Proteinuria Permeability factors in focal segmental glomerulosclerosis Analysis of mutations in alpha-actinin 4 and podocin genes of patients with chronic renal failure due to sporadic focal segmental glomerulosclerosis African American hypertensive nephropathy maps to a new locus on chromosome 9q31-q32. Annotated chromosome maps for renal disease Familial steroid-resistant nephrotic syndromes: recent advances Pathobiochemistry of nephrotic syndrome TRPC Channels in Proteinuric Kidney Diseases A novel mutation of NPHS2 identified in a Chinese family
is cites work of	wds:Q34577537-3A09794D-9E04-4287-AC7D-B6038FF7579F wds:Q37344693-ED0740FD-1224-440E-AFB9-54268B9D87F1 wds:Q28145757-C50E7F9D-885A-402B-9A26-1B87D8CC5102 wds:Q34149617-C753E85C-760C-4FAD-9150-A27C0D60FBE6 wds:Q34142642-7588138A-8454-48C4-B7FB-2011DD9C80DE wds:Q77550183-E86455DD-5330-44A8-8B38-17D409EA831B wds:Q35110850-D45AA633-D4FE-4650-863F-B9F534C40663 wds:Q34181272-1C9F4ABC-25A0-41FB-A6D5-C1DA6B366171 wds:Q28116208-95936D24-9FF1-4949-A04B-2ADB97DF3364

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