W. de Lau
Molecular Biology · 2002–2014
A researcher in the Science corpus: 3 papers; trusts 3 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Subfields
- Molecular Biology — 32 citations into it; #16,609 of 17,773 by trust here, #7,980 by citations
- Genetics — 15 citations into it
- Oncology — 15 citations into it
- Surgery — 6 citations into it
Whom W. de Lau trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Hans Clevers
- Toshiro Sato
- Meritxell Huch
- Albert J. Vilella
- Nick Barker
- R. Nusse
- A. Gregorieff
- Hugo J. G. Snippert
Who trusts W. de Lau overall
Papers from W. de Lau's perspective
Ordered by how strongly the researchers W. de Lau trusts endorse each paper. Same corpus, a different order for every researcher.
- Wnt/β-catenin signaling and disease. (Cell)
- R-spondins function as ligands of the orphan receptors LGR4 and LGR5 to regulate Wnt/β-catenin signaling (Proceedings of the National Academy of Sciences of the United States of America)
- Recurrent R-spondin fusions in colon cancer (Nature)
- In vitro expansion of single Lgr5+ liver stem cells induced by Wnt-driven regeneration (Nature)
- Unlimited in vitro expansion of adult bi-potent pancreas progenitors through the Lgr5/R-spondin axis (EMBO Journal)
- EnsemblCompara GeneTrees: Complete, duplication-aware phylogenetic trees in vertebrates. (Genome Research)
- R-spondin1 is essential in sex determination, skin differentiation and malignancy (Nature Genetics)
- Intestinal label-retaining cells are secretory precursors expressing Lgr5 (Nature)
- Lgr5 homologues associate with Wnt receptors and mediate R-spondin signalling (Nature)
- Canonical Wnt signals are essential for homeostasis of the intestinal epithelium. (Genes & Development)
Their papers
- Lgr5 homologues associate with Wnt receptors and mediate R-spondin signalling (2011) — 1,270 citations
- The R-spondin/Lgr5/Rnf43 module: regulator of Wnt signal strength (2014) — 620 citations
- The beta-catenin/TCF-4 complex imposes a crypt progenitor phenotype on colorectal cancer cells. (2002) — 1,063 citations