(Q28587212)

GOA release 2020-03-11

author name string

P. X. Xu

1

1 reference

31 January 2017

J. Adams

2

1 reference

31 January 2017

H. Peters

3

1 reference

31 January 2017

M. C. Brown

4

1 reference

31 January 2017

S. Heaney

5

1 reference

31 January 2017

R. Maas

A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family

6

1 reference

31 January 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

31 January 2017

1 reference

31 January 2017

23

1 reference

31 January 2017

113–117

1 reference

31 January 2017

1

1 reference

31 January 2017

1 reference

7 January 2021

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1

1 reference

7 January 2021

GDNF signalling through the Ret receptor tyrosine kinase

1 reference

7 January 2021

Glial cell line-derived neurotrophic factor activates the receptor tyrosine kinase RET and promotes kidney morphogenesis

1 reference

7 January 2021

Glial cell line-derived neurotrophic factor-dependent RET activation can be mediated by two different cell-surface accessory proteins

1 reference

7 January 2021

Functional receptor for GDNF encoded by the c-ret proto-oncogene

1 reference

7 January 2021

The eye-specification proteins So and Eya form a complex and regulate multiple steps in Drosophila eye development

1 reference

7 January 2021

Frequency of the branchio-oto-renal (BOR) syndrome in children with profound hearing loss.

1 reference

7 January 2021

Phenotypic manifestations of branchio-oto-renal syndrome.

1 reference

7 January 2021

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred

1 reference

7 January 2021

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus

1 reference

7 January 2021

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

1 reference

7 January 2021

The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidney

1 reference

7 January 2021

Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.

1 reference

7 January 2021

WT-1 is required for early kidney development

1 reference

7 January 2021

Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret

1 reference

7 January 2021

Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome

1 reference

7 January 2021