One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
about
The dual role of the novel Wnt receptor tyrosine kinase, ROR2, in human carcinogenesisThe role of Ryk and Ror receptor tyrosine kinases in Wnt signal transductionRor2 receptor requires tyrosine kinase activity to mediate Wnt5A signalingBiallelic mutation of BEST1 causes a distinct retinopathy in humansNaviSE: superenhancer navigator integrating epigenomics signal algebra.Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patientsWnts' fashion statement: from body stature to dysplasia.Novel domains of expression for orphan receptor tyrosine kinase Ror2 in the human and mouse reproductive systemComparative quantification of the surfaceome of human multipotent mesenchymal progenitor cells.Planar cell polarity signaling in craniofacial development.A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN.ROR1 and ROR2 in Human Malignancies: Potentials for Targeted Therapy.Expression of WNT-5a and ROR2 correlates with disease severity in osteosarcomaROR2 is epigenetically inactivated in the early stages of colorectal neoplasia and is associated with proliferation and migrationWnt/planar cell polarity signaling: an important mechanism to coordinate growth and patterning in the limb.Wnt signaling through the Ror receptor in the nervous system.Receptor tyrosine kinase-like orphan receptor 1: a novel target for cancer immunotherapy.Prickle1 stunts limb growth through alteration of cell polarity and gene expressionDisruption of PCP signaling causes limb morphogenesis and skeletal defects and may underlie Robinow syndrome and brachydactyly type B.The receptor tyrosine kinase Ror2 associates with and is activated by casein kinase Iepsilon.A significant association exists between receptor tyrosine kinase-like orphan receptor 2 gene variants and the OPG/RANKL ratio in human plasma.Delineation of an interstitial 9q22 deletion in basal cell nevus syndromeTargeted next-generation sequencing-based molecular diagnosis of congenital hand malformations in Chinese population
P2860
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P2860
One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
description
2003 nî lūn-bûn
@nan
2003年の論文
@ja
2003年学术文章
@wuu
2003年学术文章
@zh-cn
2003年学术文章
@zh-hans
2003年学术文章
@zh-my
2003年学术文章
@zh-sg
2003年學術文章
@yue
2003年學術文章
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2003年學術文章
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name
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@en
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@nl
type
label
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@en
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@nl
prefLabel
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@en
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@nl
P356
P1433
P1476
One gene, two phenotypes: ROR2 ...... dominant brachydactyly type B.
@en
P2093
Ali R Afzal
Steve Jeffery
P356
10.1002/HUMU.10233
P577
2003-07-01T00:00:00Z