Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3. (Q45424133)

14 December 2017

title

Characterization of mouse Dactylaplasia mutations: a model for human ectrodactyly SHFM3. (English)

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14 December 2017

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Stilianos Antonarakis

7

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14 December 2017

5

Denis Duboule

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14 December 2017

6

François Spitz

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14 December 2017

Marc Friedli

1

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14 December 2017

Sergey Nikolaev

2

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14 December 2017

Robert Lyle

3

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14 December 2017

Mélanie Arcangeli

4

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14 December 2017

publication date

5 April 2008

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14 December 2017

number of pages

7

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inferred from page(s)

published in

Mammalian Genome

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14 December 2017

volume

19

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14 December 2017

issue

4

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14 December 2017

page(s)

272-278

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Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.

14 December 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-008-9106-0

Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac

21 January 2018

1 reference

12 December 2020

Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype

1 reference

12 December 2020

Long-range control of gene expression: emerging mechanisms and disruption in disease

1 reference

12 December 2020

BLAT—The BLAST-Like Alignment Tool

1 reference

12 December 2020

Side effects of genome structural changes

1 reference

12 December 2020

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant

1 reference

12 December 2020

In vivo enhancer analysis of human conserved non-coding sequences

1 reference

12 December 2020

A genomic rearrangement resulting in a tandem duplication is associated with split hand-split foot malformation 3 (SHFM3) at 10q24.

1 reference

12 December 2020

Patterning mechanisms controlling vertebrate limb development

1 reference

12 December 2020

Undulated short-tail deletion mutation in the mouse ablates Pax1 and leads to ectopic activation of neighboring Nkx2-2 in domains that normally express Pax1.

1 reference

12 December 2020

Insertional polymorphisms of ETn retrotransposons include a disruption of the wiz gene in C57BL/6 mice

1 reference

12 December 2020

Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus

1 reference

12 December 2020

Fgf8 is required for outgrowth and patterning of the limbs

1 reference

12 December 2020

Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line

1 reference

12 December 2020

A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood

1 reference

12 December 2020

Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse

1 reference

12 December 2020

Primer3 on the WWW for general users and for biologist programmers

1 reference

12 December 2020

Dactylaplasia in mice a two-locus model for development anomalies

1 reference

12 December 2020

Split hand foot malformation is associated with a reduced level of Dactylin gene expression

1 reference

12 December 2020

Conserved non-genic sequences - an unexpected feature of mammalian genomes

1 reference

12 December 2020

An active murine transposon family pair: retrotransposition of "master" MusD copies and ETn trans-mobilization

1 reference

12 December 2020

A regulatory SNP causes a human genetic disease by creating a new transcriptional promoter

1 reference

12 December 2020

10.1007/S00335-008-9106-0

Identifiers

DOI

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Dimensions Publication ID

14 December 2017

1008949985

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