(Q79537574)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

title

Do mutations in COL4A1 or COL4A2 cause thin basement membrane nephropathy (TBMN)? (English)

1 reference

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24 December 2019

6

1 reference

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24 December 2019

author name string

Ke Wei Zhang

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Stephen Tonna

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Yan Yan Wang

3

1 reference

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24 December 2019

Kesha Rana

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

Smitha Padavarat

5

1 reference

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24 December 2019

publication date

10 January 2007

1 reference

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24 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

volume

22

1 reference

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24 December 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17216253%20AND%20SRC:MED&resulttype=core&format=json

24 December 2019

page(s)

645-651

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00467-006-0391-0

24 December 2019

exact match

0 references

cites work

Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly.

1 reference

12 December 2020

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

1 reference

12 December 2020

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

12 December 2020

Absence of basement membranes after targeting the LAMC1 gene results in embryonic lethality due to failure of endoderm differentiation

1 reference

12 December 2020

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

1 reference

12 December 2020

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

1 reference

12 December 2020

Persistent familial hematuria in children and the locus for thin basement membrane nephropathy

1 reference

12 December 2020

Mutations in the COL4A4 gene in thin basement membrane disease

1 reference

12 December 2020

The genetics of thin basement membrane nephropathy

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Thin membrane nephropathy: a clinico-pathological study

1 reference

12 December 2020

Segregation of hematuria in thin basement membrane disease with haplotypes at the loci for Alport syndrome

1 reference

12 December 2020

Hematuria: a simple method for identifying glomerular bleeding.

1 reference

12 December 2020

Thin basement membrane nephropathy

1 reference

12 December 2020

Split and extremely thin glomerular basement membranes in hereditary nephropathy (Alport's syndrome).

1 reference

12 December 2020

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

1 reference

12 December 2020