Rab23 is required for cardiac progenitor cell differentiation and positively-regulates Wnt11/AP-1 signalling in zebrafish

por Jenkins, D, Beales, PL, Wilkie, AOM
Publicado 2012

A novel role for the obesity-associated gene FTO in ciliogenesis and Wnt signalling

por Osborn, DPS, Mukherjee, S, Roccasecca, RM, Barosso, I, Stemple, D, Beales, PL, Christou-Savina, S
Publicado 2012

Heat-shock induces rapid resorption of primary cilia

por Thompson, CL, Prodromou, NV, Osborn, DP, Ashworth, R, Knight, MM, Beales, PL, Chapple, JP
Publicado 2012

A novel 9 kDa phosphoprotein is a component of the primary cilium and interacts with polycystin-1

por Osborn, DPS, Boucher, C, Wilson, P, Gattone, V, Beales, PL, Drummond, I, Sandford, R
Publicado 2012

Bardet-Biedl syndrome proteins control cilia length through regulation of actin polymerisation

por Hernandez, V, Pravincumar, P, Diaz-Font, A, May-Simera, H, Jenkins, D, Knight, M, Beales, PL
Publicado 2012

The Lowe syndrome protein OCRL1 is involved in primary cilia assembly

por Hernandez, V, Coon, BG, Madhivanan, K, Mukherjee, D, Hanna, CB, Barinaga-Rementeria Ramirez, I, Lowe, M, Beales, PL, Aguilar, RC
Publicado 2012

Genetic predictors of cardiovascular morbidity in Bardet–Biedl syndrome

por Forsythe, E, Sparks, K, Hoskins, BE, Bagkeris, E, McGowan, BM, Carroll, PV, Huda, MSB, Mujahid, S, Peters, C, Barrett, T, Mohammed, S, Beales, PL
Publicado 2015

Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongation

por Fu, S., Thompson, C.L., Ali, A., Wang, W., Chapple, J.P., Mitchison, H.M., Beales, P.L., Wann, A.K.T., Knight, M.M.
Publicado 2019

An enzyme-linked immunosorbent assay (ELISA) for quantification of human collectin 11 (CL-11, CL-K1)

por Selman, L., Henriksen, M.L., Brandt, J., Palarasah, Y., Waters, A., Beales, P.L., Holmskov, U., Jørgensen, T.J.D., Nielsen, C., Skjodt, K., Hansen, S.
Publicado 2012

SYSCILIA, “A systems biology approach to dissect cilia function and its disruption in human genetic disease”

por Roepman, R, Ueffing, M, Kremer, H, Huynen, MA, Gibson, TJ, Katsanis, N, Walz, GT, Wolfrum, U, Franco, B, Giles, RH, Beales, PL, Johnson, CA, Blacque, OE, Pontoglio, M, Képès, F, Apic, G, Russell, RB, Omran, H
Publicado 2012

Pitfalls of whole exome-sequencing: hidden DYNC2H1 mutations in patients with Jeune asphyxiating thoracic dystrophy

por Arts, H, Schmidts, M, Bongers, EMHF, Oud, MM, Duijkers, LEM, Yap, Z, Stalker, J, Yntema, JL, Hoischen, A, Gilissen, C, Veltman, JA, Kutkowska-Kaźmierczak, A, Kamsteeg, EJ, Scambler, PJ, Beales, PL, Knoers, NVAM, Roepman, R, Mitchison, HM
Publicado 2012