(Q51812312)

English

A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia.

scientific article published in April 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

A novel missense mutation of the EDA gene in a Mongolian family with congenital hypodontia. (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

0 references

author name string

Ran Tao

1

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Buhe Jin

2

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Shen Zheng Guo

3

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Wei Qing

4

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Guo Yin Feng

5

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

David G Brooks

6

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Lijun Liu

7

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Junfu Xu

8

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Taiwei Li

9

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Yujuan Yan

10

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Lin He

11

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

publication date

1 April 2006

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

51

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

5

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

498-502

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

Identification of a new splice form of the EDA1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Edar/Eda interactions regulate enamel knot formation in tooth morphogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ectodermal dysplasias: a clinical classification and a causal review

1 reference

https://pubmed.ncbi.nlm.nih.gov/16583127

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10038-006-0389-2

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/16583127

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