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Loss of Frrs1l disrupts synaptic AMPA receptor function, and results in neurodevelopmental, motor, cognitive and electrographical abnormalities.
Stewart M, Lau P, Banks G, Bains RS, Castroflorio E, Oliver PL, Dixon CL, Kruer MC, Kullmann DM, Acevedo-Arozena A, Wells SE, Corrochano S, Nolan PM. Stewart M, et al. Among authors: lau p. Dis Model Mech. 2019 Feb 22;12(2):dmm036806. doi: 10.1242/dmm.036806. Dis Model Mech. 2019. PMID: 30692144 Free PMC article.
A missense mutation in Katnal1 underlies behavioural, neurological and ciliary anomalies.
Banks G, Lassi G, Hoerder-Suabedissen A, Tinarelli F, Simon MM, Wilcox A, Lau P, Lawson TN, Johnson S, Rutman A, Sweeting M, Chesham JE, Barnard AR, Horner N, Westerberg H, Smith LB, Molnár Z, Hastings MH, Hirst RA, Tucci V, Nolan PM. Banks G, et al. Among authors: lau p. Mol Psychiatry. 2018 Mar;23(3):713-722. doi: 10.1038/mp.2017.54. Epub 2017 Apr 4. Mol Psychiatry. 2018. PMID: 28373692 Free PMC article.
Forward genetics identifies a novel sleep mutant with sleep state inertia and REM sleep deficits.
Banks GT, Guillaumin MCC, Heise I, Lau P, Yin M, Bourbia N, Aguilar C, Bowl MR, Esapa C, Brown LA, Hasan S, Tagliatti E, Nicholson E, Bains RS, Wells S, Vyazovskiy VV, Volynski K, Peirson SN, Nolan PM. Banks GT, et al. Among authors: lau p. Sci Adv. 2020 Aug 12;6(33):eabb3567. doi: 10.1126/sciadv.abb3567. eCollection 2020 Aug. Sci Adv. 2020. PMID: 32851175 Free PMC article.
Single-cell analysis of the epigenome and 3D chromatin architecture in the human retina.
Yuan Y, Biswas P, Zemke NR, Dang K, Wu Y, D'Antonio M, Xie Y, Yang Q, Dong K, Lau PK, Li D, Seng C, Bartosik W, Buchanan J, Lin L, Lancione R, Wang K, Lee S, Gibbs Z, Ecker J, Frazer K, Wang T, Preissl S, Wang A, Ayyagari R, Ren B. Yuan Y, et al. Among authors: lau pk. bioRxiv [Preprint]. 2024 Dec 29:2024.12.28.630634. doi: 10.1101/2024.12.28.630634. bioRxiv. 2024. PMID: 39764062 Free PMC article. Preprint.
952 results