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Results 1-10 of 15 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2020Definition and diagnosis of cerebral palsy in genetic studies: a systematic reviewPham, R.; Mol, B.W.; Gecz, J.; MacLennan, A.H.; MacLennan, S.C.; Corbett, M.A.; van Eyk, C.L.; Webber, D.L.; Palmer, L.J.; Berry, J.G.
2021A framework for high-resolution phenotyping of candidate male infertility mutants: from human to mouseHouston, B.J.; Conrad, D.F.; O'Bryan, M.K.
2020Phenotypic characterization and comparison of Phe508del and cystic fibrosis transmembrane conductance regulator (CFTR) knockout rat models of cystic fibrosis generated by CRISPR/Cas9 gene editingMcCarron, A.; Cmielewski, P.; Reyne, N.; McIntyre, C.; Finnie, J.; Craig, F.; Rout-Pitt, N.; Delhove, J.; Schjenken, J.E.; Chan, H.Y.; Boog, B.; Knight, E.; Gilmore, R.C.; O'Neal, W.K.; Boucher, R.C.; Parsons, D.; Donnelley, M.
2020Dissecting new genetic components of salinity tolerance in two-row spring barley at the vegetative and reproductive stagesSaade, S.; Brien, C.; Pailles, Y.; Berger, B.; Shahid, M.; Russell, J.; Waugh, R.; Negrão, S.; Tester, M.; Li, C.
2021Dire wolves were the last of an ancient New World canid lineagePerri, A.R.; Mitchell, K.J.; Mouton, A.; Álvarez-Carretero, S.; Hulme-Beaman, A.; Haile, J.; Jamieson, A.; Meachen, J.; Lin, A.T.; Schubert, B.W.; Ameen, C.; Antipina, E.E.; Bover, P.; Brace, S.; Carmagnini, A.; Carøe, C.; Samaniego Castruita, J.A.; Chatters, J.C.; Dobney, K.; Dos Reis, M.; et al.
2021Further delineation of BCAP31-linked intellectual disability: description of 17 new families with LoF and missense variantsWhalen, S.; Shaw, M.; Mignot, C.; Héron, D.; Bastaraud, S.C.; Walti, C.C.; Liebelt, J.; Elmslie, F.; Yap, P.; Hurst, J.; Forsythe, E.; Kirmse, B.; Ozmore, J.; Spinelli, A.M.; Calabrese, O.; de Villemeur, T.B.; Tabet, A.C.; Levy, J.; Guet, A.; Kossorotoff, M.; et al.
2021MADS1 maintains barley spike morphology at high ambient temperaturesLi, G.; Kuijer, H.N.J.; Yang, X.; Liu, H.; Shen, C.; Shi, J.; Betts, N.; Tucker, M.R.; Liang, W.; Waugh, R.; Burton, R.A.; Zhang, D.
2020RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AMLBrown, A.L.; Arts, P.; Carmichael, C.L.; Babic, M.; Dobbins, J.; Chong, C.-E.; Schreiber, A.W.; Feng, J.; Phillips, K.; Wang, P.P.S.; Ha, T.; Homan, C.C.; King-Smith, S.L.; Rawlings, L.; Vakulin, C.; Dubowsky, A.; Burdett, J.; Moore, S.; McKavanagh, G.; Henry, D.; et al.
2021RUNX1 mutations in blast-phase chronic myeloid leukemia associate with distinct phenotypes, transcriptional profiles, and drug responsesAdnan Awad, S.; Dufva, O.; Ianevski, A.; Ghimire, B.; Koski, J.; Maliniemi, P.; Thomson, D.; Schreiber, A.; Heckman, C.A.; Koskenvesa, P.; Korhonen, M.; Porkka, K.; Branford, S.; Aittokallio, T.; Kankainen, M.; Mustjoki, S.
2020QTL analysis and fine mapping of a QTL for yield-related traits in wheat grown in dry and hot environmentsTura, H.; Edwards, J.; Gahlaut, V.; Garcia, M.; Sznajder, B.; Baumann, U.; Shahinnia, F.; Reynolds, M.; Langridge, P.; Balyan, H.S.; Gupta, P.K.; Schnurbusch, T.; Fleury, D.