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Page 1
A branching model of lineage differentiation underpinning the neurogenic potential of enteric glia.
Laddach A, Chng SH, Lasrado R, Progatzky F, Shapiro M, Erickson A, Sampedro Castaneda M, Artemov AV, Bon-Frauches AC, Amaniti EM, Kleinjung J, Boeing S, Ultanir S, Adameyko I, Pachnis V. Laddach A, et al. Among authors: sampedro castaneda m. Nat Commun. 2023 Sep 22;14(1):5904. doi: 10.1038/s41467-023-41492-3. Nat Commun. 2023. PMID: 37737269 Free PMC article.
Myotonia in a patient with a mutation in an S4 arginine residue associated with hypokalaemic periodic paralysis and a concomitant synonymous CLCN1 mutation.
Thor MG, Vivekanandam V, Sampedro-Castañeda M, Tan SV, Suetterlin K, Sud R, Durran S, Schorge S, Kullmann DM, Hanna MG, Matthews E, Männikkö R. Thor MG, et al. Among authors: sampedro castaneda m. Sci Rep. 2019 Nov 26;9(1):17560. doi: 10.1038/s41598-019-54041-0. Sci Rep. 2019. PMID: 31772215 Free PMC article.
A novel ATP1A2 mutation in a patient with hypokalaemic periodic paralysis and CNS symptoms.
Sampedro Castañeda M, Zanoteli E, Scalco RS, Scaramuzzi V, Marques Caldas V, Conti Reed U, da Silva AMS, O'Callaghan B, Phadke R, Bugiardini E, Sud R, McCall S, Hanna MG, Poulsen H, Männikkö R, Matthews E. Sampedro Castañeda M, et al. Brain. 2018 Dec 1;141(12):3308-3318. doi: 10.1093/brain/awy283. Brain. 2018. PMID: 30423015 Free PMC article.
Spider toxin inhibits gating pore currents underlying periodic paralysis.
Männikkö R, Shenkarev ZO, Thor MG, Berkut AA, Myshkin MY, Paramonov AS, Kulbatskii DS, Kuzmin DA, Sampedro Castañeda M, King L, Wilson ER, Lyukmanova EN, Kirpichnikov MP, Schorge S, Bosmans F, Hanna MG, Kullmann DM, Vassilevski AA. Männikkö R, et al. Among authors: sampedro castaneda m. Proc Natl Acad Sci U S A. 2018 Apr 24;115(17):4495-4500. doi: 10.1073/pnas.1720185115. Epub 2018 Apr 10. Proc Natl Acad Sci U S A. 2018. PMID: 29636418 Free PMC article.