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1دورية أكاديمية
المؤلفون: Viswanathan, SK, Puckelwartz, MJ, Mehta, A, Ramachandra, CJA, Jagadeesan, A, Fritsche-Danielson, R, Bhat, RV, Wong, P, Kandoi, S, Schwanekamp, JA, Kuffel, G, Pesce, LL, Zilliox, MJ, Durai, UNB, Verma, RS, Molokie, RE, Suresh, DP, Khoury, PR, Thomas, A, Sanagala, T, Tang, HC, Becker, RC, Knoll, R, Shim, W, McNally, EM, Sadayappan, S
المصدر: JAMA cardiology. 3(6):481-488
مصطلحات موضوعية: Medicin och hälsovetenskap
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2دورية أكاديميةDefining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
المؤلفون: Towns, C, Richer, M, Jasaityte, S, Stafford, EJ, Joubert, J, Antar, T, Martinez-Carrasco, A, Makarious, MB, Casey, B, Vitale, D, Levine, K, Leonard, H, Pantazis, CB, Screven, LA, Hernandez, DG, Wegel, CE, Solle, J, Nalls, MA, Blauwendraat, C, Singleton, AB, Tan, MMX, Iwaki, H, Morris, HR, Gatto, EM, Kauffman, M, Khachatryan, S, Tavadyan, Z, Shepherd, CE, Hunter, J, Kumar, K, Ellis, M, Rentería, ME, Koks, S, Zimprich, A, Schumacher-Schuh, AF, Rieder, C, Awad, PS, Tumas, V, Camargos, S, Fon, EA, Monchi, O, Fon, T, Galleguillos, BP, Miranda, M, Bustamante, ML, Olguin, P, Chana, P, Tang, B, Shang, H, Guo, J, Chan, P, Luo, W, Arboleda, G, Orozco, J, del Rio, MJ, Hernandez, A, Salama, M, Kamel, WA, Zewde, YZ, Brice, A, Corvol, J-C, Westenberger, A, Illarionova, A, Mollenhauer, B, Klein, C, Vollstedt, E-J, Hopfner, F, Höglinger, G, Madoev, H, Trinh, J, Junker, J, Lohmann, K, Lange, LM, Sharma, M, Groppa, S, Gasser, T, Fang, Z-H, Akpalu, A, Xiromerisiou, G, Hadjigorgiou, G, Dagklis, I, Tarnanas, I, Stefanis, L, Stamelou, M, Dadiotis, E, Medina, A, Chan, GH-F, Ip, N, Cheung, NY-F, Zhou, X, Kishore, A, KP, D, Pal, P, Kukkle, PL, Rajan, R, Borgohain, R, Salari, M, Quattrone, A, Valente, EM, Parnetti, L, Avenali, M, Schirinzi, T, Funayama, M, Hattori, N, Shiraishi, T, Karimova, A, Kaishibayeva, G, Shambetova, C, Krüger, R, Tan, AH, Ahmad-Annuar, A, Norlinah, MI, Murad, NAA, Azmin, S, Lim, S-Y, Mohamed, W, Tay, YW, Martinez-Ramirez, D, Rodriguez-Violante, M, Reyes-Pérez, P, Tserensodnom, B, Ojha, R, Anderson, TJ, Pitcher, TL, Sanyaolu, A, Okubadejo, N, Ojo, O, Aasly, JO, Pihlstrøm, L, Tan, M, Ur-Rehman, S, Cornejo-Olivas, M, Doquenia, ML, Rosales, R, Vinuela, A, Iakovenko, E, Mubarak, BA, Umair, M, Tan, E-K, Foo, JN, Amod, F, Carr, J, Bardien, S, Jeon, B, Kim, YJ, Cubo, E, Alvarez, I, Hoenicka, J, Beyer, K, Periñan, MT, Pastor, P, El-Sadig, S, Zweier, C, Krack, P, Lin, C-H, Wu, H-C, Kung, P-J, Wu, R-M, Wu, Y, Amouri, R, Sassi, SB, Başak, AN, Genc, G, Çakmak, ÖÖ, Ertan, S, Noyce, A, Schrag, A, Schapira, A, Carroll, C, Bale, C, Grosset, D, Houlden, H, Hardy, J, Mok, KY, Rizig, M, Wood, N, Williams, N, Okunoye, O, Lewis, PA, Kaiyrzhanov, R, Weil, R, Love, S, Stott, S, Jasaitye, S, Dey, S, Obese, V, Espay, A, O’Grady, A, Sobering, AK, Siddiqi, B, Fiske, B, Jonas, C, Cruchaga, C, Comart, C, Wegel, C, Hall, D, Hernandez, D, Shiamim, E, Riley, E, Faghri, F, Serrano, GE, Chen, H, Mata, IF, Sarmiento, IJK, Williamson, J, Kim, JJ, Jankovic, J, Shulman, J, Solle, JC, Murphy, K, Nuytemans, K, Kieburtz, K, Markopoulou, K, Marek, K, Levine, KS, Chahine, LM, Ibanez, L, Screven, L, Ruffrage, L, Shulman, L, Marsili, L, Kuhl, M, Dean, M, Koretsky, M, Puckelwartz, MJ, Inca-Martinez, M, Louie, N, Mencacci, NE, Albin, R, Alcalay, R, Walker, R, Bandres-Ciga, S, Chowdhury, S, Dumanis, S, Lubbe, S, Xie, T, Foroud, T, Beach, T, Sherer, T, Song, Y, Nguyen, D, Nguyen, T, Atadzhanov, M
مصطلحات موضوعية: Global Parkinson’s Genetics Program (GP2)
وصف الملف: 131-; Electronic; application/pdf
العلاقة: E-ISSN:2373-8057; 131; https://pearl.plymouth.ac.uk/handle/10026.1/21810Test
الإتاحة: https://doi.org/10.1038/s41531-023-00533-wTest
https://pearl.plymouth.ac.uk/handle/10026.1/21810Test -
3دورية أكاديمية
المؤلفون: Zhou, C, Li, C, Zhou, B, Sun, H, Koullourou, V, Holt, I, Puckelwartz, MJ, Warren, DT, Hayward, R, Lin, Z, Zhang, L, Morris, GE, McNally, EM, Shackleton, S, Rao, L, Shanahan, CM, Zhang, Q
مصطلحات موضوعية: R Medicine (General)
وصف الملف: text
العلاقة: https://eprints.keele.ac.uk/id/eprint/4871/1/Novel%20nesprin-1%20mutations%20associated%20with%20dilated%20cardiomyopathy%20cause%20nuclear%20envelope%20disruption%20and%20defects%20in%20myogenesis.pdfTest; Zhou, C, Li, C, Zhou, B, Sun, H, Koullourou, V, Holt, I, Puckelwartz, MJ, Warren, DT, Hayward, R, Lin, Z, Zhang, L, Morris, GE, McNally, EM, Shackleton, S, Rao, L, Shanahan, CM and Zhang, Q (2017) Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis. Human Molecular Genetics, 26 (12). 2258 - 2276.
الإتاحة: https://doi.org/10.1093/hmg/ddx116Test
https://eprints.keele.ac.uk/id/eprint/4871Test/
https://eprints.keele.ac.uk/id/eprint/4871/1/Novel%20nesprin-1%20mutations%20associated%20with%20dilated%20cardiomyopathy%20cause%20nuclear%20envelope%20disruption%20and%20defects%20in%20myogenesis.pdfTest
https://academic.oup.com/hmg/article/26/12/2258/3111721#87891230Test