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A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall-Smith Syndrome.
Kooblall KG, Stevenson M, Stewart M, Harris L, Zalucki O, Dewhurst H, Butterfield N, Leng H, Hough TA, Ma D, Siow B, Potter P, Cox RD, Brown SDM, Horwood N, Wright B, Lockstone H, Buck D, Vincent TL, Hannan FM, Bassett JHD, Williams GR, Lines KE, Piper M, Wells S, Teboul L, Hennekam RC, Thakker RV. Kooblall KG, et al. Among authors: ma d. JBMR Plus. 2023 Mar 30;7(6):e10739. doi: 10.1002/jbm4.10739. eCollection 2023 Jun. JBMR Plus. 2023. PMID: 37283649 Free PMC article.
Investigating brain alterations in the Dp1Tyb mouse model of Down syndrome.
Serrano ME, Kim E, Siow B, Ma D, Rojo L, Simmons C, Hayward D, Gibbins D, Singh N, Strydom A, Fisher EMC, Tybulewicz VLJ, Cash D. Serrano ME, et al. Among authors: ma d. Neurobiol Dis. 2023 Nov;188:106336. doi: 10.1016/j.nbd.2023.106336. Neurobiol Dis. 2023. PMID: 38317803 Free PMC article.
Color-map recommendation for MR relaxometry maps.
Fuderer M, Wichtmann B, Crameri F, de Souza NM, Baeßler B, Gulani V, Wang M, Poot D, de Boer R, Cashmore M, Keenan KE, Ma D, Pirkl C, Sollmann N, Weingärtner S, Mandija S, Golay X. Fuderer M, et al. Among authors: ma d. Magn Reson Med. 2024 Oct 16. doi: 10.1002/mrm.30290. Online ahead of print. Magn Reson Med. 2024. PMID: 39415361
9,488 results