Implementation of a P&E management system for a dual-source EV powered by different batteries.

Autor: Thakre, Mohan P., Tapre, Pawan C., Kadlag, Sunil Somnath, Kadam, Deepak Prakash, Thorat, Jayawant S., Nandeshwar, Rahul N., Gaikwad, Rohit S.

Publikováno v: Bulletin of Electrical Engineering & Informatics; Dec2023, Vol. 12 Issue 6, p3190-3201, 12p

Subdural Haemorrhages in Infants: Population Based Study

Autor: Jayawant, S., Rawlinson, A., Gibbon, F., Price, J., Schulte, J., Sharples, P., Sibert, J. R., Kemp, A. M.

Publikováno v: BMJ: British Medical Journal, 1998 Dec 01. 317(7172), 1558-1561.

Externí odkaz: https://www.jstor.org/stable/25181203

Defective tubulin detyrosination causes structural brain abnormalities with cognitive deficiency in humans and mice

Autor: Pagnamenta, AT, Heemeryck, P, Martin, HC, Bosc, C, Peris, L, Uszynski, I, Gory-Fauré, S, Couly, S, Deshpande, C, Siddiqui, A, Elmonairy, AA, Consortium, WGS500, Consortium, Genomics England Research, Jayawant, S, Murthy, S, Walker, I, Loong, L, Bauer, P, Vossier, F, Denarier, E, Maurice, T, Barbier, EL, Deloulme, J-C, Taylor, JC, Blair, EM, Andrieux, A, Moutin, M-J

Publikováno v: Hum Mol Genet
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2019, ⟨10.1093/hmg/ddz186⟩
Human Molecular Genetics, 2019, ⟨10.1093/hmg/ddz186⟩

Reversible detyrosination of tubulin, the building block of microtubules, is crucial for neuronal physiology. Enzymes responsible for detyrosination were recently identified as complexes of vasohibins (VASHs) one or two with small VASH-binding protei

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7d34fc643d09769823472ee19c051e30
https://pubmed.ncbi.nlm.nih.gov/31363758

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

Autor: Clare Logan, Cossins J, Pm, Rodríguez Cruz, Da, Parry, Maxwell S, Martínez-Martínez P, Riepsaame J, Za, Abdelhamed, Av, Lake, Moran M, Robb S, Chow G, Sewry C, Pm, Hopkins, Sheridan E, Jayawant S, Palace J, Ca, Johnson, Beeson D

Publikováno v: Logan, C V, Cossins, J, Rodríguez Cruz, P M, Parry, D A, Maxwell, S, Martínez-Martínez, P, Riepsaame, J, Abdelhamed, Z A, Lake, A V R, Moran, M, Robb, S, Chow, G, Sewry, C, Hopkins, P M, Sheridan, E, Jayawant, S, Palace, J, Johnson, C A & Beeson, D 2015, ' Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain ', American Journal of Human Genetics, vol. 97, no. 6, pp. 878-885 . https://doi.org/10.1016/j.ajhg.2015.10.017
Europe PubMed Central
American Journal of Human Genetics, 97(6), 878-85. Cell Press

The neuromuscular junction (NMJ) consists of a tripartite synapse with a presynaptic nerve terminal, Schwann cells that ensheathe the terminal bouton, and a highly specialized postsynaptic membrane. Synaptic structural integrity is crucial for effici

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6a3cebcaf6961d1c452f6492c563ca36

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