(Q62644413)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

title

Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1

1 reference

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17 January 2020

Jane Gibson

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Andrew Collins

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Karen Temple

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

9

William J Tapper

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

12

Newton E Morton

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

author name string

Esta Cross

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Beverley Dell

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Claire L S Turner

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Paul S Bass

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Mushfequr R Haq

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

David J Bunyan

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

Juliet C Needell

10

1 reference

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17 January 2020

David O Robinson

14

1 reference

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17 January 2020

language of work or name

English

0 references

publication date

26 November 2008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

volume

75

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

17 January 2020

page(s)

415-419

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19037252%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/ki.2008.573

17 January 2020

exact match

0 references

cites work

Respiratory chain deficiency presenting as congenital nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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/10.1038%2FKI.2008.573

7 January 2021

Spectrum of early onset nephrotic syndrome associated with WT1 missense mutations

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Centiles for adult head circumference

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Identification of BRAF as a new interactor of PLCepsilon1, the protein mutated in nephrotic syndrome type 3.

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Phospholipase C epsilon modulates beta-adrenergic receptor-dependent cardiac contraction and inhibits cardiac hypertrophy

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Exploiting large scale computing to construct high resolution linkage disequilibrium maps of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://api.crossref.org/works/10.1038%2FKI.2008.573

7 January 2021