Zobrazeno 1 - 10
of 784
pro vyhledávání: '"Seidman, CE"'
Autor:
Margara, F, Psaras, Y, Wang, ZJ, Schmid, M, Doste, R, Garfinkel, AC, Repetti, GG, Seidman, JG, Seidman, CE, Rodriguez, B, Toepfer, CN, Bueno-Orovio, A
Publikováno v:
Scientific reports. 12(1)
Cardiomyopathies have unresolved genotype–phenotype relationships and lack disease-specific treatments. Here we provide a framework to identify genotype-specific pathomechanisms and therapeutic targets to accelerate the development of precision med
Autor:
Garcia-Pavia, P, Kim, Y, Restrepo-Cordoba, MA, Lunde, IG, Wakimoto, H, Smith, AM, Toepfer, CN, Getz, K, Gorham, J, Patel, P, Ito, K, Willcox, JA, Arany, Z, Li, J, Owens, AT, Govind, R, Nuñez, B, Mazaika, E, Bayes-Genis, A, Walsh, R, Finkelman, B, Lupon, J, Whiffin, N, Serrano, I, Midwinter, W, Wilk, A, Bardaji, A, Ingold, N, Buchan, R, Tayal, U, Pascual-Figal, DA, De Marvao, A, Ahmad, M, Garcia-Pinilla, JM, Pantazis, A, Dominguez, F, John Baksi, A, O'Regan, DP, Rosen, SD, Prasad, SK, Lara-Pezzi, E, Provencio, M, Lyon, AR, Alonso-Pulpon, L, Cook, SA, DePalma, SR, Barton, PJR, Aplenc, R, Seidman, JG, Ky, B, Ware, JS, Seidman, CE
Publikováno v:
Circulation
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Repisalud
Instituto de Salud Carlos III (ISCIII)
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Repisalud
Instituto de Salud Carlos III (ISCIII)
BACKGROUND: Cancer therapy-induced cardiomyopathy (CCM) is associated with cumulative drug exposures and preexisting cardiovascular disorders. These parameters incompletely account for substantial interindividual susceptibility to CCM. We hypothesize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ab94f88417d0f5971f353ebde1cc5ef7
https://hdl.handle.net/10668/13834
https://hdl.handle.net/10668/13834
Autor:
Esslinger, U, Garnier, S, Korniat, A, Proust, C, Kararigas, G, Mueller-Nurasyid, M, Empana, J-P, Morley, MP, Perret, C, Stark, K, Bick, AG, Prasad, SK, Kriebel, J, Li, J, Tiret, L, Strauch, K, O'Regan, DP, Marguiles, KB, Seidman, JG, Boutouyrie, P, Lacolley, P, Jouven, X, Hengstenberg, C, Komajda, M, Hakonarson, H, Isnard, R, Arbustini, E, Grallert, H, Cook, SA, Seidman, CE, Regitz-Zagrosek, V, Cappola, TP, Charron, P, Cambien, F, Villard, E
Publikováno v:
PLoS ONE
PLoS ONE, 2017, 12 (3), pp.e0172995. ⟨10.1371/journal.pone.0172995⟩
PLoS ONE, Vol 12, Iss 3, p e0172995 (2017)
PLoS ONE, 2017, 12 (3), pp.e0172995. ⟨10.1371/journal.pone.0172995⟩
PLoS ONE, Vol 12, Iss 3, p e0172995 (2017)
International audience; Aims: Dilated cardiomyopathy (DCM) is an important cause of heart failure with a strong familial component. We performed an exome-wide array-based association study (EWAS) to assess the contribution of missense variants to spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ee5789f2d5fd36c33788a37843a590e5
https://hal.univ-lorraine.fr/hal-03571195
https://hal.univ-lorraine.fr/hal-03571195
Autor:
Lakdawala, NK, Dellefave, L, Sparks, E, Cirino, A, Depalma, S, Funke, B, Colan, SD, Watkins, H, Robinson, P, Redwood, CS, Seidman, CE, Seidman, JG, McNally, EM, Ho, CY
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cdee92da757dbf64e211b30fa5135286
https://ora.ox.ac.uk/objects/uuid:43b99dcc-014a-4570-b19a-6c83cb04dd57
https://ora.ox.ac.uk/objects/uuid:43b99dcc-014a-4570-b19a-6c83cb04dd57
Autor:
Ware, JS, Li, J, Mazaika, E, Yasso, C, DeSouza, T, Cappola, T, Tsai, EJ, Hilfiker Kleiner, D, Kamiya, CA, Mazzarotto, F, Cook, SA, Halder, I, Prasad, SK, Pisarcik, J, Hanley Yanez, K, Alharethi, R, Damp, J, Hsich, E, Elkayam, U, Sheppard, R, Kealey, A, Alexis, J, Ramani, G, Safirstein, J, Boehmer, J, Pauly, DF, Wittstein, IS, Thohan, V, Zucker, MJ, Liu, P, Gorcsan, J, McNamara, DM, Seidman, CE, Seidman, JG, Arany, Z
Background: Peripartum cardiomyopathy (PPCM) shares some clinical features with idiopathic dilated cardiomyopathy, a disorder caused by mutations in over 40 genes, including TTN, which encodes the sarcomere protein titin. Methods: We sequenced 43 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::bedcdf9745acf993fd6527843a19abc9
http://hdl.handle.net/10044/1/28795
http://hdl.handle.net/10044/1/28795
Autor:
Homsy, J, Zaidi, S, Shen, Y, Ware, JS, Samocha, KE, Wakimoto, H, Gorham, J, Chih Jin, S, Deanfield, J, Giardini, A, Porter Jr., GA, Kim, R, Bilguvar, K, Lopez, F, Tikhonova, I, Mane, S, Romano Adesman, A, Qi, H, Vardarajan, B, Ma, L, Daly, M, Roberts, AE, Russell, MW, Mital, S, Newburger, JW, Gaynor, JW, Breitbart, RE, Iossifov, I, Ronemus, M, Sanders, SJ, Kaltman, JR, Seidman, JG, Brueckner, M, Gelb, BD, Goldmuntz, E, Lifton, RP, Seidman, CE, Chung, WK
Congenital heart disease (CHD) patients have increased prevalence of extra-cardiac congenital anomalies (CA) and risk of neurodevelopmental disabilities (NDD). Exome sequencing of 1,213 CHD parent-offspring trios identified an excess of protein-damag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::09a23ab027e5c648665d8d03fda3636b
http://hdl.handle.net/10044/1/27100
http://hdl.handle.net/10044/1/27100
Publikováno v:
Zou, L, Shen, M, Arad, M, He, H, Løfgren, B, Ingwall, JS, Seidman, CE, Seidman, JG & Tian, R 2005, ' N4881 mutation of the g2-subunit results in increased basal activity of AMPK but reduced respons to stress ', Circulation Research, vol. 97, no. 4, pp. 323-8 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pure_au_____::8373bd0b2a1f6a18833f567e63898666
https://pure.au.dk/portal/da/publications/n4881-mutation-of-the-g2subunit-results-in-increased-basal-activity-of-ampk-but-reduced-respons-to-stress(3eae3e50-a387-11da-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/n4881-mutation-of-the-g2subunit-results-in-increased-basal-activity-of-ampk-but-reduced-respons-to-stress(3eae3e50-a387-11da-bee9-02004c4f4f50).html
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