Developmental mosaicism may explain spontaneous reappearance of the Axin(Fu) mutation in mice. (Q52141074)

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scientific article published in February 2001

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English	Developmental mosaicism may explain spontaneous reappearance of the Axin(Fu) mutation in mice.	scientific article published in February 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

title

Developmental mosaicism may explain spontaneous reappearance of the Axin(Fu) mutation in mice. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

author name string

Ruvinsky A

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

Flood W

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

Costantini F

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

publication date

1 February 2001

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

published in

Genesis

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stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

volume

29

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

page(s)

49-54

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Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

cites work

Genetic analysis of mutations at the fused locus in the mouse

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Revertant mosaicism in epidermolysis bullosa caused by mitotic gene conversion

1 reference

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reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products

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reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Evidence for Cyclophosphamide-Induced Gene Conversion and Mutation in Mouse Germ Cells

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reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

The mouse Fused locus encodes Axin, an inhibitor of the Wnt signaling pathway that regulates embryonic axis formation

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Inheritance of alternative states of the fused gene in mice

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Gene conversion of major histocompatibility complex genes is associated with CpG-rich regions

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Phenotypic expression of the fused (Fu) gene in chimaeric mice

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Unusual inheritance of the AxinFu mutation in mice is associated with widespread rearrangements in the proximal region of chromosome 17

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1002%2F1526-968X%28200102%2929%3A2%3C49%3A%3AAID-GENE1004%3E3.0.CO%3B2-2

retrieved

21 January 2018

Identifiers

DOI

10.1002/1526-968X(200102)29:2<49::AID-GENE1004>3.0.CO;2-2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

PubMed publication ID

11170344

1 reference

stated in

Europe PubMed Central

PubMed publication ID

11170344

retrieved

23 April 2018

reference URL

http://europepmc.org/abstract/MED/11170344

 

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