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

Birch, J. L., Coull, B. J., Spender, L. C., Watt, C., Willison, A., Syed, N., Chalmers, A. J., Hossain-Ibrahim, M. K. & Inman, G. J., 08/2020, In: Cellular Signalling. 72, p. 109638 109638.

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

Easton, J. A., Albuloushi, A. K., Kamps, M. A. F., Brouns, G. H. M. R., Broers, J. L. V., Coull, B. J., Oji, V., van Geel, M., van Steensel, M. A. M. & Martin, P. E., 1/10/2019, In: Experimental Dermatology. 28, 10, p. 1106-1113 8 p.

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

de Vos, I. J. H. M., Wong, A. S. W., Welting, T. J. M., Coull, B. J. & van Steensel, M. A. M., 1/08/2019, In: American Journal of Medical Genetics, Part A. 179, 8, p. 1652-1664 13 p.

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

De Vos, I. J. H. M., Tao, E. Y., Ong, S. L. M., Goggi, J. L., Scerri, T., Wilson, G. R., Low, C. G. M., Wong, A. S. W., Grussu, D., Stegmann, A. P. A., Van Geel, M., Janssen, R., Amor, D. J., Bahlo, M., Dunn, N. R., Carney, T. J., Lockhart, P. J., Coull, B. J. & Van Steensel, M. A. M., 15/08/2018, In: Human Molecular Genetics. 27, 16, p. 2775-2788 14 p.

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

Dunlop, E. A., Seifan, S., Claessens, T., Behrends, C., Kamps, M. A. F., Rozycka, E., Kemp, A. J., Nookala, R. K., Blenis, J., Coull, B. J., Murray, J. T., Van Steensel, M. A. M., Wilkinson, S. & Tee, A. R., 1/10/2014, In: Autophagy. 10, 10, p. 1749-1760 12 p.

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The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation

Yan, M., Gingras, M. C., Dunlop, E. A., Nouët, Y., Dupuy, F., Jalali, Z., Possik, E., Coull, B. J., Kharitidi, D., Dydensborg, A. B., Faubert, B., Kamps, M., Sabourin, S., Preston, R. S., Davies, D. M., Roughead, T., Chotard, L., Van Steensel, M. A. M., Jones, R., Tee, A. R., & 1 othersPause, A., 2/06/2014, In: Journal of Clinical Investigation. 124, 6, p. 2640-2650 11 p.

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Birt-hogg-dubé syndrome is a novel ciliopathy

Luijten, M. N. H., Basten, S. G., Claessens, T., Vernooij, M., Scott, C. L., Janssen, R., Easton, J. A., Kamps, M. A. F., Vreeburg, M., Broers, J. L. V., Geel, M. V., Menko, F. H., Harbottle, R. P., Nookala, R. K., Tee, A. R., Land, S. C., Giles, R. H., Coull, B. J. & van Steensel, M. A. M., 1/11/2013, In: Human Molecular Genetics. 22, 21, p. 4383-4397 15 p.

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

Menko, F. H., Johannesma, P. C., Van Moorselaar, R. J. A., Reinhard, R., Van Waesberghe, J. H., Thunnissen, E., Houweling, A. C., Leter, E. M., Waisfisz, Q., Van Doorn, M. B., Starink, T. M., Postmus, P. E., Coull, B. J., Van Steensel, M. A. M. & Gille, J. J. P., 1/09/2013, In: Familial Cancer. 12, 3, p. 373-379 7 p.

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What's new in Birt-Hogg-Dubé syndrome?

Claessens, T., Vernooij, M., Luijten, M., Coull, B. J. & Van Steensel, M. A., 1/12/2012, In: Expert Review of Dermatology. 7, 6, p. 521-528 8 p.

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Birt-hogg-dubésyndroom is een ciliopathie

Vernooij, M., Luijten, M. N. H., Claessens, T., Coull, B. J. & Van Steensel, M. A. M., 06/2012, In: Nederlands Tijdschrift voor Dermatologie en Venereologie. 22, 6, p. 391-394 4 p.

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

Jeffers, L. J., Coull, B. J., Stack, S. J. & Morrison, C. G., 3/01/2008, In: Oncogene. 27, 1, p. 139-144 6 p.

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Ubiquitin-binding domains in Y-family polymerases regulate translesion synthesis

Bienko, M., Green, C. M., Crosetto, N., Rudolf, F., Zapart, G., Coull, B., Kannouche, P., Wider, G., Peter, M., Lehmann, A. R., Hofmann, K. & Dikic, I., 16/12/2005, In: Science. 310, 5755, p. 1821-4 4 p.

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

Kannouche, P., Fernández de Henestrosa, A. R., Coull, B., Vidal, A. E., Gray, C., Zicha, D., Woodgate, R. & Lehmann, A. R., 3/03/2003, In: EMBO Journal. 21, 22, p. 1223-33 11 p.

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