The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor (Q74410676)

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10 November 2019

title

The medaka rs-3 locus required for scale development encodes ectodysplasin-A receptor (English)

1 reference

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10 November 2019

author name string

S Kondo

1

1 reference

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10 November 2019

Y Kuwahara

2

1 reference

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10 November 2019

M Kondo

3

1 reference

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10 November 2019

K Naruse

4

1 reference

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10 November 2019

H Mitani

5

1 reference

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10 November 2019

Y Wakamatsu

6

1 reference

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10 November 2019

K Ozato

7

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10 November 2019

S Asakawa

8

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10 November 2019

N Shimizu

9

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10 November 2019

A Shima

10

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10 November 2019

language of work or name

English

0 references

publication date

1 August 2001

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10 November 2019

number of pages

5

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inferred from page(s)

published in

Current Biology

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10 November 2019

volume

11

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10 November 2019

issue

15

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10 November 2019

page(s)

1202-1206

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The syntenic relationship of the zebrafish and human genomes.

10 November 2019

cites work

1 reference

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7 January 2021

Zebrafish comparative genomics and the origins of vertebrate chromosomes

1 reference

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7 January 2021

Involvement of a novel Tnf receptor homologue in hair follicle induction

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900324-4

7 January 2021

Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900324-4

7 January 2021

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900324-4

7 January 2021

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900324-4

7 January 2021

Mutations in the founder of the MIP gene family underlie cataract development in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2801%2900324-4

7 January 2021

Transposon-induced splicing defect in the rat nude gene

1 reference

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7 January 2021

HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo

1 reference

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7 January 2021

10.1016/S0960-9822(01)00324-4

Identifiers

DOI

1 reference

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10 November 2019

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