(Q51789312)

English

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations.

scientific article published on 3 March 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Absence of mutations in the HOXA11 and HOXD11 genes in children with congenital renal malformations. (English)

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

author name string

Ioanna Bouba

1

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Ekaterini Siomou

2

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Constantinos J Stefanidis

3

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Anastasia Emmanouilidou

4

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Anna Galidi

5

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Elissavet Hatzi

6

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Sofia Markoula

7

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Andromachi Mitsioni

8

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Antigoni Siamopoulou

9

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Ioannis Georgiou

10

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

publication date

3 March 2009

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

24

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

8

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

1569-1572

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

https://scigraph.springernature.com/pub.10.1007/s00467-009-1140-y

0 references

Mutation of HOXA13 in hand-foot-genital syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct roles and regulations for HoxD genes in metanephric kidney development

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How to find all those mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hoxa11 and Hoxd11 regulate branching morphogenesis of the ureteric bud in the developing kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homeobox genes in embryogenesis and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinoids and nephron mass control

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of hoxd-11

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homeotic transformations and limb defects in Hox A11 mutant mice.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atlas of Hox gene expression in the developing kidney

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PCR-SSCP: a simple and sensitive method for detection of mutations in the genomic DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of radius and ulna in mice lacking hoxa-11 andhoxd-11

1 reference

https://pubmed.ncbi.nlm.nih.gov/19255789

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-009-1140-Y

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 April 2018

http://europepmc.org/abstract/MED/19255789

ResearchGate publication ID

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