Irreducible representations of space groups/ by Zak, J.

Functional genetics of cancer and congenital disorders by Zak, J

Mechanics of air-inflated 3D distance fabric by Votrubec V., Žák J.

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Cancer genetics may aid diagnostics of developmental disorders by Zak, J, Schuster-Boeckler, B, Bond, G

HTX: a tool for the exploration and visualization of high-throughput image assays by Arteta, C, Lempitsky, V, Zak, J, Lu, X, Noble, JA, Zisserman, A

Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy by O'Donnell-Luria, A, Pais, L, Faundes, V, Lu, X, Taylor, J, Zak, J, al., E

ASPP2 links the apical lateral polarity complex to the regulation of YAP activity in epithelial cells by Royer, C, Koch, S, Qin, X, Zak, J, Buti, L, Dudziec, E, Zhong, S, Ratnayaka, I, Srinivas, S, Lu, X

A code for RanGDP binding in ankyrin repeats defines a nuclear import pathway. by Lu, M, Zak, J, Chen, S, Sanchez-Pulido, L, Severson, D, Endicott, J, Ponting, C, Schofield, C, Lu, X

Tumour suppression by a protein hydroxylase by Zayer, A, Smith, H, Pillai, M, Sekirnik, R, Zak, J, Lu, X, Schofield, C, Bix, M, Ratcliffe, P, Coleman, M

P-030: CRIZANLIZUMAB REDUCES ENDOTHELIAL ADHESION OF RED BLOOD CELLS FROM SCD PATIENTS IN STANDARDIZED MICROFLUIDIC PLATFORM: IN VITRO TECHNOLOGY ASSESSMENT by FEDERICI C., KUCUKAL E., KOCEVAR R., GILKEY L., SERTEL S., MONCHAMP K., WOLFE A., NAYAK L., BRUEDERLE A., ZAK J., GURKAN U.

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TOI-1268b: The youngest hot Saturn-mass transiting exoplanet by Subjak, J, Endl, M, Chaturvedi, P, Karjalainen, R, Cochran, WD, Esposito, M, Gandolfi, D, Lam, KWF, Stassun, K, Zák, J, Lodieu, N, Boffin, HMJ, MacQueen, PJ, Hatzes, A, Guenther, EW, Georgieva, I, Grziwa, S, Schmerling, H, Skarka, M

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ASPP2 controls epithelial plasticity and inhibits metastasis through β-catenin-dependent regulation of ZEB1. by Wang, Y, Bu, F, Royer, C, Serres, S, Larkin, JR, Soto, MS, Sibson, N, Salter, V, Fritzsche, F, Turnquist, C, Koch, S, Zak, J, Zhong, S, Wu, G, Liang, A, Olofsen, P, Moch, H, Hancock, D, Downward, J, Goldin, R, Zhao, J, Tong, X, Guo, Y, Lu, X

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome by Zak, J, Vives, V, Szumska, D, Vernet, A, Schneider, J, Miller, P, Slee, E, Joss, S, Lacassie, Y, Chen, E, Escobar, L, Tucker, M, Aylsworth, A, Dubbs, H, Collins, A, Andrieux, J, Dieux-Coeslier, A, Haberlandt, E, Kotzot, D, Scott, D, Parker, M, Zakaria, Z, Choy, Y, Wieczorek, D, Innes, A, Jun, K, Zinner, S, Prin, F, Lygate, C, Pretorius, P, Rosenfeld, J, Mohun, T, Lu, X