P. Beales

发表

Erratum to: Adjustable Gastric Banding and Sleeve Gastrectomy in Bardet-Biedl Syndrome

P. Carroll, M. Huda, S. Mujahid, 2015, Obesity Surgery.

Adjustable Gastric Banding and Sleeve Gastrectomy in Bardet-Biedl Syndrome

P. Carroll, M. Huda, S. Mujahid, 2014, Obesity Surgery.

Chromosome 11q13 and atopic asthma

S. R. Lin, C. Adra, T. Shirakawa, 1999, Clinical genetics.

Heat-shock induces rapid resorption of primary cilia

C. Thompson, J. Chapple, M. Knight, 2012, Journal of Cell Science.

Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2019, Nature Communications.

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

M. Knight, H. May-Simera, D. Jenkins, 2012, Cilia.

Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci.

J. Lupski, M. Woods, N. Katsanis, 2001, American journal of human genetics.

Glutaihione protects a human insulinoma cell line from tumor necrosis factors-α-mediated cytotoxicity

P. Pozzilli, M. Cavallo, L. Monetini, 1997 .

Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees.

J. Lupski, M. Leppert, N. Katsanis, 1999, American journal of human genetics.

The Lowe syndrome protein OCRL1 is involved in primary cilia assembly

D. Mukherjee, M. Lowe, Claudia B. Hanna, 2012, Cilia.

Erratum: The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypes

Colin A. Johnson, M. Hubank, E. Stupka, 2016, Journal of Medical Genetics.

Energy metabolism in Bardet–Biedl syndrome

C. Summerbell, S. Jebb, P. Kopelman, 2003, International Journal of Obesity.

Genetic predictors of cardiovascular morbidity in Bardet–Biedl syndrome

Bethan E. Hoskins, B. Hoskins, S. Mohammed, 2014, Clinical genetics.

Glutathione protects a human insulinoma cell line from tumor necrosis factor-alpha-mediated cytotoxicity.

P. Pozzilli, M. Cavallo, L. Monetini, 1997, International journal of clinical & laboratory research.

Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia Syndrome.

T. Strom, H. Williams, H. Brunner, 2017, American journal of human genetics.

Mainzer-Saldino syndrome is a ciliopathy caused by mutations in the IFT140 gene

A. Munnich, S. Hanein, C. Antignac, 2012, Cilia.

Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signalling.

C. Thompson, M. Knight, P. Beales, 2017, European cells & materials.