(Q28506182)

24 January 2017

title

The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements (English)

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24 January 2017

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GOA release 2020-03-11

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3

Sigmar Stricker

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Stefan Mundlos

6

object named as

Stefan Mundlos

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24 January 2017

Annett Böddrich

4

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author name string

Andrea N. Albrecht

1

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24 January 2017

Georg C. Schwabe

2

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24 January 2017

Erich E. Wanker

5

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24 January 2017

publication date

1 March 2002

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Mechanisms of Development

24 January 2017

published in

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24 January 2017

volume

112

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24 January 2017

issue

1-2

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24 January 2017

page(s)

53–67

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HedgehogandBmpGenes Are Coexpressed at Many Diverse Sites of Cell–Cell Interaction in the Mouse Embryo

24 January 2017

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Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

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The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes

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Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton

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Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

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Absence of radius and ulna in mice lacking hoxa-11 andhoxd-11

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

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Vertebrate Hox genes and proliferation: an alternative pathway to homeosis?

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BMP/GDF-signalling interactions during synovial joint development

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CAG tract of MJD-1 may be prone to frameshifts causing polyalanine accumulation

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Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

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Human HOX gene mutations

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Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

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A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly

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Role of parathyroid hormone-related peptide and Indian hedgehog in skeletal development

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A transcriptional repressor obtained by alternative translation of a trinucleotide repeat

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Multigenic control of the localization of the zone of polarizing activity in limb morphogenesis in the mouse.

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Targeted misexpression of Hox-4.6 in the avian limb bud causes apparent homeotic transformations

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Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

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

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Mouse mutant "rib-vertebrae" (rv): a defect in somite polarity.

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Intracellular green fluorescent protein-polyalanine aggregates are associated with cell death

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SH3GL3 associates with the Huntingtin exon 1 protein and promotes the formation of polygln-containing protein aggregates

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Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation

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7 January 2021

GDF5 coordinates bone and joint formation during digit development

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Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily

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Amegakaryocytic thrombocytopenia and radio-ulnar synostosis are associated with HOXA11 mutation

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7 January 2021

Regulation of rate of cartilage differentiation by Indian hedgehog and PTH-related protein

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Accumulation of mutant huntingtin fragments in aggresome-like inclusion bodies as a result of insufficient protein degradation

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Synpolydactyly in mice with a targeted deficiency in the HoxD complex

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Hox genes in digit development and evolution

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Regulation of number and size of digits by posterior Hox genes: A dose-dependent mechanism with potential evolutionary implications

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7 January 2021

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Identifiers

DOI

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