(Q45345154)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471491%20AND%20SRC:MED&resulttype=core&format=json

12 December 2019

title

Frequent activating mutations of FGFR3 in human bladder and cervix carcinomas (English)

1 reference

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12 December 2019

6

1 reference

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12 December 2019

François Radvanyi

9

1 reference

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12 December 2019

author name string

Cappellen D

1

1 reference

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12 December 2019

De Oliveira C

2

1 reference

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12 December 2019

Ricol D

3

1 reference

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12 December 2019

de Medina S

4

1 reference

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12 December 2019

Bourdin J

5

1 reference

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12 December 2019

Chopin D

7

1 reference

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12 December 2019

Thiery JP

8

1 reference

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12 December 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

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12 December 2019

1 reference

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12 December 2019

volume

23

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12 December 2019

page(s)

18-20

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12 December 2019

issue

1

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https://scigraph.springernature.com/pub.10.1038/12615

12 December 2019

exact match

0 references

cites work

FGFR activation in skeletal disorders: too much of a good thing

1 reference

7 January 2021

A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene

1 reference

7 January 2021

Graded activation of fibroblast growth factor receptor 3 by mutations causing achondroplasia and thanatophoric dysplasia

1 reference

7 January 2021

A Lys644Glu substitution in fibroblast growth factor receptor 3 (FGFR3) causes dwarfism in mice by activation of STATs and ink4 cell cycle inhibitors

1 reference

7 January 2021

A mouse model for achondroplasia produced by targeting fibroblast growth factor receptor 3.

1 reference

7 January 2021

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3.

1 reference

7 January 2021

Fibroblast growth factor receptor 3 is a negative regulator of bone growth

1 reference

7 January 2021

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

1 reference

7 January 2021

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

1 reference

7 January 2021

Decreased expression of keratinocyte growth factor receptor in a subset of human transitional cell bladder carcinomas

1 reference

7 January 2021

Abnormal FGFR 3 expression in cartilage of thanatophoric dysplasia fetuses

1 reference

7 January 2021

Identifiers

DOI

10.1038/12615

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10471491%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

12 December 2019

0 references

1 reference