The synpolydactyly homolog (spdh) mutation in the mouse -- a defect in patterning and growth of limb cartilage elements (Q28506182)

24 January 2017

title

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

1 reference

24 January 2017

1 reference

GOA release 2020-03-11

1 reference

1 reference

3

Sigmar Stricker

0 references

Stefan Mundlos

6

object named as

Stefan Mundlos

1 reference

24 January 2017

Annett Böddrich

4

0 references

author name string

Andrea N. Albrecht

1

1 reference

24 January 2017

Georg C. Schwabe

2

1 reference

24 January 2017

Erich E. Wanker

5

1 reference

24 January 2017

publication date

1 March 2002

1 reference

Mechanisms of Development

24 January 2017

published in

1 reference

24 January 2017

volume

112

1 reference

24 January 2017

issue

1-2

1 reference

24 January 2017

page(s)

53–67

1 reference

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

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

BMP/GDF-signalling interactions during synovial joint development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Human HOX gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

A transcriptional repressor obtained by alternative translation of a trinucleotide repeat

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

GDF5 coordinates bone and joint formation during digit development

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Synpolydactyly in mice with a targeted deficiency in the HoxD complex

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

Hox genes in digit development and evolution

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0925-4773%2801%2900639-6

7 January 2021

10.1016/S0925-4773(01)00639-6

Identifiers

DOI

0 references

1 reference