Showing 1 - 20 results of 23 for search 'Almeida, M', query time: 2.34s
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The role of RNA processing in the pathogenesis of motor neuron degeneration. by Bäumer, D, Ansorge, O, Almeida, M, Talbot, K
Published 2010Journal article -
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Estimation of a quantum interaction parameter using weak measurements: Theory and experiment by Hofmann, H, Goggin, M, Almeida, M, Barbieri, M
Published 2012Journal article -
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The role of RNA processing in the pathogenesis of motor neuron degeneration by Bäumer, D, Ansorge, O, Almeida, M, Talbot, K
Published 2010Journal article -
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Xist Repeats B and C, but not Repeat A, mediate de novo recruitment of the Polycomb system in X chromosome inactivation by Wei, G, Almeida, M, Bowness, JS, Nesterova, TB, Brockdorff, N
Published 2021Journal article -
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Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYS. by Santos, H, Almeida, M, Fernandes, H, Wilkie, A, Wilkie, A
Published 2007Journal article -
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Acute depletion of METTL3 implicates N6-methyladenosine in alternative intron/exon inclusion in the nascent transcriptome by Wei, G, Almeida, M, Pintacuda, G, Coker, H, Bowness, J, Ule, J, Brockdorff, N
Published 2021Journal article -
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Towards quantum chemistry on a quantum computer. by Lanyon, B, Whitfield, J, Gillett, G, Goggin, M, Almeida, M, Kassal, I, Biamonte, J, Mohseni, M, Powell, B, Barbieri, M, Aspuru-Guzik, A, White, A
Published 2010Journal article -
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PCGF3/5-PRC1 initiates Polycomb recruitment in X chromosome inactivation by Almeida, M, Pintacuda, G, Masui, O, Koseki, Y, Gdula, M, Cerase, A, Brown, D, Mould, A, Innocent, C, Nakayama, M, Schermelleh, L, Nesterova, T, Koseki, H, Brockdorff, N
Published 2017Journal article -
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Systematic allelic analysis defines the interplay of key pathways in X chromosome inactivation by Nesterova, TB, Wei, G, Coker, H, Pintacuda, G, Bowness, JS, Zhang, T, Almeida, M, Bloechl, B, Moindrot, B, Carter, EJ, Rodrigo, I, Pan, Q, Bi, Y, Song, C-X, Brockdorff, N
Published 2019Journal article -
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A noncoding expansion in EIF4A3 causes Richieri-Costa-Pereira syndrome, a craniofacial disorder associated with limb defects. by Favaro, F, Alvizi, L, Zechi-Ceide, R, Bertola, D, Felix, T, de Souza, J, Raskin, S, Twigg, SR, Weiner, A, Armas, P, Margarit, E, Calcaterra, N, Andersen, G, McGowan, S, Wilkie, A, Richieri-Costa, A, de Almeida, M, Passos-Bueno, MR
Published 2014Journal article -
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Ultraviolet and visible reflectance spectra of Phobos and Deimos as measured by the ExoMars-TGO/Nomad-UVIS spectrometer by Mason, JP, Patel, MR, Pajola, M, Cloutis, ED, Alday, J, Olsen, KS, Marriner, C, Holmes, JA, Sellers, G, Thomas, N, Almeida, M, Read, M, Nakagawa, H, Thomas, IR, Ristic, B, Willame, Y, Depiesse, C, Daerden, F, Vandaele, AC, Lopez-Moreno, JJ, Bellucci, G
Published 2023Journal article