Physical Baryon Resonance Spectroscopy from Lattice QCD

Autor: Morel, D., Crouch, B., Leinweber, D. B., Thomas, A. W.

We complement recent advances in the calculation of the masses of excited baryons in quenched lattice QCD with finite-range regulated chiral effective field theory enabling contact with the physical quark mass region. We examine the P-wave contributi

Externí odkaz: http://arxiv.org/abs/nucl-th/0309044

Temperature driven structural evolution of Ge-rich GeSbTe alloys and role of N-doping.

Autor: Prazakova, L., Nolot, E., Martinez, E., Fillot, F., Rouchon, D., Rochat, N., Bernard, M., Sabbione, C., Morel, D., Bernier, N., Grenier, A., Papon, A.-M., Cyrille, M.-C., Navarro, G.

Publikováno v: Journal of Applied Physics; 12/7/2020, Vol. 128 Issue 21, p1-10, 10p

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Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3

Autor: Schirwani, S., Albaba, S., Carere, D.A., Sacoto, M.J. Guillen, Zamora, F. Milan, Si, Y., Rabin, R., Pappas, J., Renaud, D.L., Hauser, N., Reid, E., Blanchet, P., Foulds, N., Dixit, A., Fisher, R., Armstrong, R., Isidor, B., Cogne, B., Vergano, S. Schrier, Demirdas, S., Dykzeul, N., Cohen, J.S., Grand, K., Morel, D., Slavotinek, A., Albassam, H.F., Naik, S., Dean, J., Ragge, N., Cinzia, C., Tedesco, M.G., Harrison, R.E., Bouman, A., Palen, E., Challman, T.D., Willemsen, M.H., Vogt, J., Cunniff, C., Bergstrom, K., Walia, J.S., Bruel, A.L., Kini, U., Alkuraya, F.S., Slegesky, V., Meeks, N., Girotto, P., Johnson, D., Newbury-Ecob, R., Ockeloen, C.W., Prontera, P., Lynch, S.A., Li, D., Graham, J.M., Balasubramanian, M.

Publikováno v: American Journal of Medical Genetics, Part A, 185(11), 3446-3458. Wiley-Liss Inc.
American Journal of Medical Genetics. Part A, 185, 3446-3458
American Journal of Medical Genetics. Part A, 185, 11, pp. 3446-3458

Item does not contain fulltext The study aimed at widening the clinical and genetic spectrum of ASXL3-related syndrome, a neurodevelopmental disorder, caused by truncating variants in the ASXL3 gene. In this international collaborative study, we have

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::d43c121986c2a547dbd8f85e0da5f2b7
https://doi.org/10.1002/ajmg.a.62465

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