Synpolydactyly in mice with a targeted deficiency in the HoxD complex (Q28593833)

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English	Synpolydactyly in mice with a targeted deficiency in the HoxD complex	scientific journal article

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scholarly article

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31 January 2017

Synpolydactyly in mice with a targeted deficiency in the HoxD complex (English)

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31 January 2017

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GOA release 2020-03-11

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GOA release 2020-03-11

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GOA release 2020-03-11

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D. Duboule

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31 January 2017

author name string

J. Zákány

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31 January 2017

language of work or name

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publication date

7 November 1996

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31 January 2017

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31 January 2017

384

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31 January 2017

6604

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31 January 2017

69–71

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31 January 2017

Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs

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Hox gene expression in teleost fins and the origin of vertebrate digits

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Independent control of immunoglobulin switch recombination at individual switch regions evidenced through Cre-loxP-mediated gene targeting

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Chromosome engineering in mice

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A large Turkish kindred with syndactyly type II (synpolydactyly). 2. Homozygous phenotype?

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Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13

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Hox genes in vertebrate development

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Gene transpositions in the HoxD complex reveal a hierarchy of regulatory controls.

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Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice

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Localization of the syndactyly type II (synpolydactyly) locus to 2q31 region and identification of tight linkage to HOXD8 intragenic marker

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Colinearity and functional hierarchy among genes of the homeotic complexes

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Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: evidence for tissue-specific modulation of receptor function

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7 January 2021

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