Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation
about
Transcriptome changes affecting Hedgehog and cytokine signalling in the umbilical cord: implications for disease riskExtracellular matrix and developing growth plate.Armet/Manf and Creld2 are components of a specialized ER stress response provoked by inappropriate formation of disulphide bonds: implications for genetic skeletal diseases.Analysis of the cartilage proteome from three different mouse models of genetic skeletal diseases reveals common and discrete disease signatures.
P2860
Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@ast
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@en
type
label
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@ast
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@en
prefLabel
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@ast
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@en
P2093
P2860
P356
P1476
Loss of matrilin 1 does not ex ...... used by a Matn3 V194D mutation
@en
P2093
David J Thornton
Katarzyna A Piróg
Maryline Fresquet
Michael D Briggs
Peter A Bell
Raymond P Boot-Handford
P2860
P304
P356
10.1002/ART.33486
P577
2012-05-01T00:00:00Z