B. Coull

发表

R. Woodgate, A. Lehmann, D. Zicha, 2013 .

FLCN is a novel regulator of autophagy 1 FLCN , a novel autophagy component , interacts with GABARAP and is regulated by ULK 1 1 phosphorylation 2 3

J. Blenis, S. Wilkinson, A. Tee, 2014 .

A de novoFLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Q. Waisfisz, P. Postmus, E. Thunnissen, 2012, Familial Cancer.

Distinct BRCT domains in Mcph1/Brit1 mediate ionizing radiation-induced focus formation and centrosomal localization

B. Coull, C. Morrison, L. Jeffers, 2008, Oncogene.

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

P. Lockhart, M. Bahlo, D. Amor, 2018, bioRxiv.

A rare missense mutation in GJB3 (Cx31G45E) is associated with a unique cellular phenotype resulting in necrotic cell death

J. Broers, B. Coull, M. V. van Steensel, 2019, Experimental dermatology.

A de novoFLCN mutation in a patient with spontaneous pneumothorax and renal cancer; a clinical and molecular evaluation

Q. Waisfisz, P. Postmus, E. Thunnissen, 2013, Familial Cancer.

FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation

J. Blenis, S. Wilkinson, J. Murray, 2014, Autophagy.

Multifaceted transforming growth factor-beta (TGFβ) signalling in glioblastoma.

G. Inman, N. Syed, B. Coull, 2020, Cellular signalling.

The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation.

Ming Yan, B. Faubert, Russell G. Jones, 2014, The Journal of clinical investigation.

Localization of DNA polymerases η and ι to the replication machinery is tightly co‐ordinated in human cells

R. Woodgate, A. Lehmann, D. Zicha, 2002, The EMBO journal.

Ubiquitin-Binding Domains in Y-Family Polymerases Regulate Translesion Synthesis

G. Wider, M. Peter, K. Hofmann, 2005, Science.

Multicentric osteolytic syndromes represent a phenotypic spectrum defined by defective collagen remodeling

B. Coull, M. V. van Steensel, T. Welting, 2019, American journal of medical genetics. Part A.

FLCN and AMPK Confer Resistance to Hyperosmotic Stress via Remodeling of Glycogen Stores

D. Hall, M. Gingras, A. Pause, 2015, PLoS genetics.

Localization of DNA polymerases eta and iota to the replication machinery is tightly co-ordinated in human cells.

R. Woodgate, A. Lehmann, D. Zicha, 2003, The EMBO journal.

Birt–Hogg–Dubé syndrome and the skin

M. Steensel, B. Coull, M. V. van Steensel, 2013, Familial Cancer.

Birt-Hogg-Dube syndrome is a novel ciliopathy.

A. Tee, R. Giles, J. Broers, 2013, Human molecular genetics.

Birt–Hogg–Dubé syndrome and the skin

M. Steensel, B. Coull, T. Claessens, 2013, Familial Cancer.

What’s new in Birt–Hogg–Dubé syndrome?

M. Steensel, B. Coull, T. Claessens, 2012 .