Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients (Q62937781)

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scientific article published on 30 June 2006

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Language	Label	Description	Also known as
English	Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients	scientific article published on 30 June 2006

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

title

Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

main subject

nephrotic syndrome

1 reference

based on heuristic

inferred from title

author

Selçuk Yüksel

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Mustafa Tekin

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

author name string

Nermin Uncu

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Banu Acar

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Mesiha Ekim

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Z Birsin Ozçakar

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

F Başak Cengiz

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Nilgün Cakar

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Nazli Kara

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Fatoş Yalçinkaya

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

publication date

30 June 2006

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

published in

Pediatric Nephrology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

volume

21

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

issue

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

page(s)

1093-1096

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

cites work

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three siblings with steroid-resistant nephrotic syndrome: new NPHS2 mutations in a Turkish family.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetic basis of FSGS and steroid-resistant nephrosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Broadening the spectrum of diseases related to podocin mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16810518

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00467-006-0116-4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

Dimensions Publication ID

1042918748

0 references

PubMed publication ID

16810518

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16810518

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

retrieved

26 December 2019

 

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