P. Beales
Genetics · 2001–2011
A researcher in the Science corpus: 5 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 31 citations into it
Whom P. Beales trusts
Their strongest outbound trust, strongest first, inferred from their citations.
- B. Yoder (in Genetics)
Papers from P. Beales's perspective
Ordered by how strongly the researchers P. Beales trusts endorse each paper. Same corpus, a different order for every researcher.
- The gene mutated in autosomal recessive polycystic kidney disease encodes a large, receptor-like protein (Nature Genetics)
- The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. (Journal of the American Society of Nephrology)
- Chlamydomonas IFT88 and Its Mouse Homologue, Polycystic Kidney Disease Gene Tg737, Are Required for Assembly of Cilia and Flagella (Journal of Cell Biology)
- Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination (Nature Genetics)
- Gli2 and Gli3 Localize to Cilia and Require the Intraflagellar Transport Protein Polaris for Processing and Function (PLoS Genetics)
- Cilia and Hedgehog responsiveness in the mouse. (Proceedings of the National Academy of Sciences of the United States of America)
- Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates (Nature Genetics)
- Pilus retraction powers bacterial twitching motility (Nature)
- A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis. (Cell)
- Cell Cycle via Direct Activation of the JAK-STAT Signaling Pathway in a Process Requiring PKD2
Their papers
- Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder (2001) — 675 citations
- The ciliopathies: an emerging class of human genetic disorders. (2006) — 1,198 citations
- Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene. (2004) — 798 citations
- Ciliopathies: an expanding disease spectrum (2011) — 669 citations
- Basal body dysfunction is a likely cause of pleiotropic Bardet–Biedl syndrome (2003) — 714 citations