McGrath, John A.

Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations

Pollard, P. J., Brière, J. J., Alam, N. A., Barwell, J., Barclay, E., Wortham, N. C., Hunt, T., Mitchell, M., Olpin, S., Moat, S. J., et al. (2005) · Human Molecular Genetics

Cancer, Hypoxia, and MetabolismAdrenal and Paraganglionic Tumors

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Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation

Zhong, F. L., Mamaï, O., Sborgi, L., Boussofara, L., Hopkins, R., Robinson, K., Szeverényi, I., Takeichi, T., Balaji, R., Lau, A., et al. (2016) · Cell

Inflammasome and immune disordersGenetic and rare skin diseases.

Cited by 440

Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa

Wagner, J. E., Ishida-Yamamoto, A., McGrath, J. A., Hordinsky, M., Keene, D. R., Woodley, D. T., Chen, M., Riddle, M. J., Osborn, M. J., Lund, T., et al. (2010) · New England Journal of Medicine

Skin and Cellular Biology ResearchHematopoietic Stem Cell Transplantation

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Kindlin-1 controls Wnt and TGF-β availability to regulate cutaneous stem cell proliferation

Rognoni, E., Widmaier, M., Jakobson, M., Ruppert, R., Ussar, S., Katsougkri, D., Böttcher, R. T., Lai-Cheong, J. E., Rifkin, D. B., McGrath, J. A., et al. (2014) · Nature Medicine

Skin and Cellular Biology ResearchCell Adhesion Molecules Research

Cited by 140

A prenatal skin atlas reveals immune regulation of human skin morphogenesis

Gopee, N. H., Winheim, E., Olabi, B., Admane, C., Foster, A. R., Huang, N., Botting, R. A., Torabi, F., Sumanaweera, D., Le, A. P., et al. (2024) · Nature

Hair Growth and DisordersSkin and Cellular Biology Research

Cited by 108

The role of kindlins in cell biology and relevance to human disease

Lai-Cheong, J. E., Parsons, M., & McGrath, J. A. (2010) · The International Journal of Biochemistry & Cell Biology

Cell Adhesion Molecules ResearchCellular Mechanics and Interactions

Cited by 92

WNT10A , dermatology and dentistry

Doolan, B. J., Onoufriadis, A., Kantaputra, P., & McGrath, J. A. (2021) · British Journal of Dermatology

dental development and anomaliesHair Growth and Disorders

Cited by 56

Ectodermal dysplasia–skin fragility syndrome resulting from a new homozygous mutation, 888delC, in the desmosomal protein plakophilin 1

Ersoy-Evans, S., Erkin, G., Fassihi, H., Chan, I., Paller, A. S., Sürücü, S., & McGrath, J. A. (2006) · Journal of the American Academy of Dermatology

Skin and Cellular Biology ResearchGenetic and rare skin diseases.

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