(Q43729256)

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Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

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Europe PubMed Central

PubMed publication ID

26 November 2017

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

hypotrichosis with juvenile macular dystrophy

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author name string

Sprecher E

1

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Europe PubMed Central

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26 November 2017

Bergman R

2

1 reference

Europe PubMed Central

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26 November 2017

Richard G

3

1 reference

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26 November 2017

Lurie R

4

1 reference

Europe PubMed Central

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26 November 2017

Shalev S

5

1 reference

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26 November 2017

Petronius D

6

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26 November 2017

Shalata A

7

1 reference

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26 November 2017

Anbinder Y

8

1 reference

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26 November 2017

Leibu R

9

1 reference

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26 November 2017

Perlman I

10

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26 November 2017

Cohen N

11

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26 November 2017

Szargel R

12

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26 November 2017

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publication date

1 October 2001

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26 November 2017

Nature Genetics

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26 November 2017

29

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26 November 2017

2

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26 November 2017

134-136

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26 November 2017

Unusual association of juvenile macular dystrophy with congenital hypotrichosis: occurrence in two siblings suggesting autosomal recessive inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

E- and P-cadherin expression during murine hair follicle morphogenesis and cycling.

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Cadherin function is required for axon outgrowth in retinal ganglion cells in vivo.

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Cadherin function is required for human keratinocytes to assemble desmosomes and stratify in response to calcium

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Progesterone regulates beta-catenin mRNA levels in human endometrial stromal cells in vitro

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

Precocious mammary gland development in P-cadherin-deficient mice.

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

beta-Catenin controls hair follicle morphogenesis and stem cell differentiation in the skin

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

De Novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin

1 reference

https://api.crossref.org/works/10.1038%2FNG716

7 January 2021

based on heuristic

inferred from DOI database lookup

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Europe PubMed Central

PubMed publication ID

26 November 2017

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PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 November 2017

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