Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 226,136,471 papers from all fields of science
Search
Sign In
Create Free Account
ROR2 wt Allele
Known as:
Receptor Tyrosine Kinase-Like Orphan Receptor 2 wt Allele
, BDB1
, BDB
Expand
Human ROR2 wild-type allele is located within 9q22 and is approximately 228 kb in length. This allele, which encodes tyrosine-protein kinase…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
9 relations
9q22
BRACHYDACTYLY, TYPE B1
Cell Proliferation Regulatory Process
Ligand Binding
Expand
Broader (1)
ROR2 gene
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
High-Resolution Ultrasound Findings in the Symptomatic Residual Limbs of Amputees Marian A.R. O'Reilly, FRCR, FRCP, FFR RCSI, FRCR, FFSEM, MSc*; Peter M.R. O'Reilly, BDB, NUI, BSc, PhD, FAGD USA†;
J. Sullivan
,
J. Sheahan
2013
Corpus ID: 74770212
Introduction: Amputations are increasingly prevalent because of medical complications associated with diabetes, meningitis…
Expand
Review
2010
Review
2010
You Shall Not Eat These Abominable Things : An Examination Of Different Interpretations On Deuteronomy
Deuteronomy
2010
Corpus ID: 14071423
AR Archiv fur Religionswissenschaft BAR Biblical Archaeology Review BCOT Biblical Commentary on the Old Testament. 10 vols. C.F…
Expand
2010
2010
Penyakit darah pada pisang :: Infeksi dan keanekaragaman genetika patogen
Hadiwiyono
,
M. S. Subandiyah
2010
Corpus ID: 191132846
Penyakit darah pada pisang yang disebabkan oleh blood disease bacterium (BDB), sequevar 10 phylotype IV dalam kompleks spesies…
Expand
2009
2009
A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.
Wibke Schwarzer
,
Florian Witte
,
A. Rajab
,
S. Mundlos
,
S. Stricker
Human Molecular Genetics
2009
Corpus ID: 24713286
Mutations in ROR2 cause dominant brachydactyly type B (BDB1) or recessive Robinow syndrome (RRS), each characterized by a…
Expand
2008
2008
The mutation ROR2W749X, linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome
R. Raz
,
S. Stricker
,
+14 authors
A. Economides
Development
2008
Corpus ID: 8865495
Mutations in ROR2 result in a spectrum of genetic disorders in humans that are classified, depending on the nature of the…
Expand
2008
2008
Benefits of using biosolid nutrients in Australian agriculture - a national perspective.
M. Mclaughlin
,
M. Bell
,
+7 authors
N. Penney
2008
Corpus ID: 87443215
Increased nutrient levels in inland waterways have led to algal blooms and eutrophication in many agricultural regions. To ensure…
Expand
Review
1995
Review
1995
Wine, women and work: the generic transformation of the Masoretic text of Qohelet 9. 7-10 in the Targum Qohelet and Qohelet Midrash Rabbah
J. Hardy
1995
Corpus ID: 140503269
This thesis seeks to understand the generic changes wrought by targum Qohelet and Qohelet midrash rabbah upon our home-text, the…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE