Mutations in DSTYK and dominant urinary tract malformations (Q24309178)

positive regulation of ERK1 and ERK2 cascade

1 reference

Dual serine/threonine and tyrosine protein kinase

1 reference

Dual serine/threonine and tyrosine protein kinase

1 reference

16

G Caridi

0 references

Francesca Lugani

F Lugani

13

0 references

Neal Paragas

N Paragas

15

0 references

Maddalena Gigante

M Gigante

27

0 references

Qais Al-awqati

Q Al-Awqati

42

0 references

Loreto Gesualdo

L Gesualdo

29

0 references

Anna Latos-Bieleńska

36

A Latos-Bielenska

0 references

Anna Materna-Kiryluk

19

A Materna-Kiryluk

0 references

author name string

S Sanna-Cherchi

1

0 references

R V Sampogna

2

0 references

N Papeta

3

0 references

K E Burgess

4

0 references

S N Nees

5

0 references

B J Perry

6

0 references

M Choi

7

0 references

M Bodria

8

0 references

Y Liu

9

0 references

P L Weng

10

0 references

V J Lozanovski

11

0 references

M Verbitsky

12

0 references

R Sterken

14

0 references

A Carrea

17

0 references

M Dagnino

18

0 references

G Santamaria

20

0 references

C Murtas

21

0 references

N Ristoska-Bojkovska

22

0 references

C Izzi

23

0 references

N Kacak

24

0 references

B Bianco

25

0 references

S Giberti

26

0 references

G Piaggio

28

0 references

D Kosuljandic Vukic

30

0 references

K Vukojevic

31

0 references

M Saraga-Babic

32

0 references

M Saraga

33

0 references

Z Gucev

34

0 references

L Allegri

35

0 references

D Casu

37

0 references

M State

38

0 references

F Scolari

39

0 references

R Ravazzolo

40

0 references

K Kiryluk

41

0 references

V D D'Agati

43

0 references

I A Drummond

44

0 references

V Tasic

45

0 references

R P Lifton

46

0 references

G M Ghiggeri

47

0 references

A G Gharavi

The New England Journal of Medicine

48

0 references

language of work or name

English

0 references

publication date

15 August 2013

0 references

published in

0 references

volume

369

0 references

issue

7

0 references

page(s)

621-9

0 references

cites work

Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study

1 reference

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Role of fibroblast growth factor receptors 1 and 2 in the metanephric mesenchyme

19 March 2017

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RIP5 is a RIP-homologous inducer of cell death

19 March 2017

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Spatial and temporal patterns of ERK signaling during mouse embryogenesis

19 March 2017

1 reference

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Copy-number disorders are a common cause of congenital kidney malformations

19 March 2017

1 reference

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FGF9 and FGF20 maintain the stemness of nephron progenitors in mice and man.

27 September 2017

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Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

27 September 2017

1 reference

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From cradle to grave: the multiple roles of fibroblast growth factors in neural development

27 September 2017

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Paper 4: EUROCAT statistical monitoring: identification and investigation of ten year trends of congenital anomalies in Europe

27 September 2017

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HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

A recessive gene for primary vesicoureteral reflux maps to chromosome 12p11-q13.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Renal abnormalities and their developmental origin

27 September 2017

1 reference

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Genetic approaches to human renal agenesis/hypoplasia and dysplasia

27 September 2017

1 reference

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Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Cre/lox-regulated transgenic zebrafish model with conditional myc-induced T cell acute lymphoblastic leukemia.

27 September 2017

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Role of fibroblast growth factor receptors 1 and 2 in the ureteric bud.

27 September 2017

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Epidemiology of chronic renal failure in children: data from the ItalKid project

27 September 2017

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Molecular mechanisms of human embryogenesis: developmental pathogenesis of renal tract malformations

27 September 2017

1 reference

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Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Renal outcome in patients with congenital anomalies of the kidney and urinary tract.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Function of FGF signaling in the developmental process of the median fin fold in zebrafish.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Interplay between FGF, one-eyed pinhead, and T-box transcription factors during zebrafish posterior development

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Zebrafish foxi one modulates cellular responses to Fgf signaling required for the integrity of ear and jaw patterning

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3846391

Role of fibroblast growth factor receptor signaling in kidney development

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23862974

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Birth Defects Monitoring Program (BDMP)/Commission on Professional and Hospital Activities (CPHA) surveillance data, 1988-1991

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23862974