Zobrazeno 1 - 10
of 262
pro vyhledávání: '"Lie BA"'
Autor:
Kesheng Li, Dandan Chai, Shiyang Ren, Xiaowen Lian, Xiaoling Shi, Yang Xu, Lie Bao, Suisheng Yang, Yurong Liang, Xiaoqin Li, Huifen Du
Publikováno v:
BMC Cancer, Vol 24, Iss 1, Pp 1-14 (2024)
Abstract Background Our previous study demonstrated that β2-microglobulin (β2M) promoted ER+/HER2– breast cancer survival via the SGK1/Bcl-2 signaling pathway. However, the role of β2M has not been investigated in ER–/HER2+ breast cancer. Here
Externí odkaz:
https://doaj.org/article/c9007b550ae04b5b939397f324d7d403
Autor:
Sandling, JK., Rosenberg, L. Hultin, Farias, FHG., Alexsson, A., Leonard, D., Kozyrev, S., Murén, E., Karlsson, Å., Mathioudaki, A., Pucholt, P., Eriksson, D., Pielberg, G., Meadows, J., Nordin, J., Dahlqvist, J., Bianchi, M., Jonsson, R., Omdal, R., Lerang, K., Molberg, Ø., Lie, BA., Massarenti, L., Jacobsen, S., Voss, A., Jakobsen, MA., Lillevang, ST., Troldborg, AM., Steffensen, Rudi, Bengtsson, C., Jönsen, A., Padyukov, L., Eloranta, M-L., Sjöwall, C., Gunnarsson, I., Svenungsson, E., Rantapää-Dahlqvist, S., Bengtsson, AA., Syvänen, A-C., Lindblad-Toh, K., Rönnblom, L.
Publikováno v:
Sandling, JK, Rosenberg, L H, Farias, FHG, Alexsson, A, Leonard, D, Kozyrev, S, Murén, E, Karlsson, Å, Mathioudaki, A, Pucholt, P, Eriksson, D, Pielberg, G, Meadows, J, Nordin, J, Dahlqvist, J, Bianchi, M, The ImmunoArray Development Consortium, Jonsson, R, Omdal, R, Lerang, K, Molberg, Ø, Lie, BA, Massarenti, L, Jacobsen, S, Voss, A, Jakobsen, MA, Lillevang, ST, Troldborg, AM, Steffensen, R, Bengtsson, C, Jönsen, A, Padyukov, L, Eloranta, M-L, Sjöwall, C, Gunnarsson, I, Svenungsson, E, Rantapää-Dahlqvist, S, Bengtsson, AA, Syvänen, A-C, Lindblad-Toh, K, Rönnblom, L & The DISSECT Consortium 2019, ' Targeted next-generation sequencing suggests novel risk loci in juvenile onset systemic lupus erythematosus ', 52nd European Society of Human Genetics Conference (ESHG), Gøteborg, Sweden, 15/06/2019-18/06/2019 .
Sandling, JK, Rosenberg, L H, Farias, FHG, Alexsson, A, Leonard, D, Kozyrev, S, Murén, E, Karlsson, Å, Mathioudaki, A, Pucholt, P, Eriksson, D, Pielberg, G, Meadows, J, Nordin, J, Dahlqvist, J, Bianchi, M, The ImmunoArray Development Consortium, Jonsson, R, Omdal, R, Lerang, K, Molberg, Ø, Lie, BA, Massarenti, L, Jacobsen, S, Voss, A, Jakobsen, MA, Lillevang, ST, Troldborg, AM, Steffensen, R, Bengtsson, C, Jönsen, A, Padyukov, L, Eloranta, M-L, Sjöwall, C, Gunnarsson, I, Svenungsson, E, Rantapää-Dahlqvist, S, Bengtsson, AA, Syvänen, A-C, Lindblad-Toh, K, Rönnblom, L & The DISSECT Consortium 2019, ' Targeted next-generation sequencing suggests novel risk loci in juvenile onset systemic lupus erythematosus ', European Journal of Human Genetics, vol. 27, no. Suppl. 2, P07.28D, pp. 1372 . < https://www.nature.com/articles/s41431-019-0494-2 >
Sandling, JK, Rosenberg, L H, Farias, FHG, Alexsson, A, Leonard, D, Kozyrev, S, Murén, E, Karlsson, Å, Mathioudaki, A, Pucholt, P, Eriksson, D, Pielberg, G, Meadows, J, Nordin, J, Dahlqvist, J, Bianchi, M, The ImmunoArray Development Consortium, Jonsson, R, Omdal, R, Lerang, K, Molberg, Ø, Lie, BA, Massarenti, L, Jacobsen, S, Voss, A, Jakobsen, MA, Lillevang, ST, Troldborg, AM, Steffensen, R, Bengtsson, C, Jönsen, A, Padyukov, L, Eloranta, M-L, Sjöwall, C, Gunnarsson, I, Svenungsson, E, Rantapää-Dahlqvist, S, Bengtsson, AA, Syvänen, A-C, Lindblad-Toh, K, Rönnblom, L & The DISSECT Consortium 2019, ' Targeted next-generation sequencing suggests novel risk loci in juvenile onset systemic lupus erythematosus ', European Journal of Human Genetics, vol. 27, no. Suppl. 2, P07.28D, pp. 1372 . < https://www.nature.com/articles/s41431-019-0494-2 >
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1b4f875fb46c4729b20b6e96782d92b2
https://vbn.aau.dk/da/publications/7188acd0-e0af-4455-bd84-5fd9ff0b8717
https://vbn.aau.dk/da/publications/7188acd0-e0af-4455-bd84-5fd9ff0b8717
Autor:
Henriksen, EKK, Viken, MK, Wittig, M, Holm, K, Folseraas, T, Mucha, S, Melum, E, Hov, JR, Lazaridis, KN, Juran, BD, Chazouillères, O, Färkkilä, M, Gotthardt, DN, Invernizzi, P, Carbone, M, Hirschfield, GM, Rushbrook, SM, Goode, E, UK-PSC Consortium, Ponsioen, CY, Weersma, RK, Eksteen, B, Yimam, KK, Gordon, SC, Goldberg, D, Yu, L, Bowlus, CL, Franke, A, Lie, BA, Karlsen, TH
Publikováno v:
HLA, vol 90, iss 4
Primary sclerosing cholangitis (PSC) is strongly associated with several human leukocyte antigen (HLA) haplotypes. Due to extensive linkage disequilibrium and multiple polymorphic candidate genes in the HLA complex, identifying the alleles responsibl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::8659da7c5aec11bb61dd5bbb2379e241
https://escholarship.org/uc/item/5cr1s258
https://escholarship.org/uc/item/5cr1s258
Autor:
Witoelar, A, Jansen, IE, Wang, Y, Desikan, RS, Gibbs, JR, Blauwendraat, C, Thompson, WK, Hernandez, DG, Djurovic, S, Schork, AJ, Bettella, F, Ellinghaus, D, Franke, A, Lie, BA, McEvoy, LK, Karlsen, T, Lesage, S, Morris, HR, Brice, A, Wood, NW, Heutink, P, Hardy, J, Singleton, AB, Dale, AM, Gasser, T, Andreassen, OA, Sharma, M, Conso, IPDG, Amer, BECN, Co, UKBE
Publikováno v:
Witoelar, A; Jansen, IE; Wang, Y; Desikan, RS; Gibbs, JR; Blauwendraat, C; et al.(2017). Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases. JAMA NEUROLOGY, 74(7), 780-792. doi: 10.1001/jamaneurol.2017.0469. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/3dn2j864
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::a85ef1126755d80c028e0ccfffa4e41e
http://www.escholarship.org/uc/item/3dn2j864
http://www.escholarship.org/uc/item/3dn2j864
Autor:
Carmona, DF, Vaglio, A, Mackie, SL, Hernández-Rodríguez, J, Monach, PA, Castaneda, S, Solans, R, Morado, IC, Narvaez, J, Ramentol-Sintas, M, Pease, CT, Dasgupta, B, Watts, R, Khalidi, N, Langford, CA, Ytterberg, S, Boiardi, L, Beretta, L, Govoni, M, Emmi, G, Bonatti, F, Cimmino, MA, Witte, T, Neumann, T, Holle, A, Schonau, V, Sailler, L, Papo, T, Haroche, J, Mahr, A, Mouthon, L, Molberg, O, Diamantopoulos, AP, Voskuyl, A, Brouwer, E, Daikeler, T, Berger, CT, Molloy, ES, O'Neill, L, Blockmans, D, Lie, BA, Mclaren, P, Vyse, TJ, Wijmenga, C, Allanore, Y, Koeleman, BPC, Spanish CGA Group, UKGCA Consortium, Vasculitis Clinical Research Consortium, Barrett, JH, Cid, MC, Salvarini, C, Merkel, PA, Morgan, AW, Gonzalez-Gay, MA, Martin, J
Giant cell arteritis (GCA) is the most common form of vasculitis in individuals older than 50 years in Western countries. To shed light onto the genetic background influencing susceptibility for GCA, we performed a genome-wide association screening i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d9c5ce8b625827ed76564ec7a3bc5c06
https://dspace.library.uu.nl/handle/1874/356608
https://dspace.library.uu.nl/handle/1874/356608
Autor:
Andreassen, Ole Andreas, Desikan, RS, Wang, Yunpeng, Thompson, WK, Schork, AJ, Zuber, Verena, Doncheva, NT, Ellinghaus, E, Mattingsdal, Morten, Franke, A, Lie, BA, Mills, Ian Geoffrey, Aukrust, Pål, McEvoy, LK, Djurovic, Srdjan, Karlsen, TH, Dale, AM
Publikováno v:
e0123057
PLoS ONE
PLoS ONE
Epidemiological studies suggest a relationship between blood lipids and immune-mediated diseases, but the nature of these associations is not well understood. We used genome-wide association studies (GWAS) to investigate shared single nucleotide poly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0df0f1498069535893e6f05813101ff5
https://hdl.handle.net/1956/9839
https://hdl.handle.net/1956/9839
Autor:
Andreassen, OA, Harbo, HF, Wang, Y, Thompson, WK, Schork, AJ, Mattingsdal, M, Zuber, V, Bettella, F, Ripke, S, Kelsoe, JR, Kendler, KS, O'Donovan, MC, Sklar, P, Psychiatric Genomics Consortium (PGC) Bipolar Disorder and Schizophrenia Work Groups, International Multiple Sclerosis Genetics Consortium (IMSGC), McEvoy, LK, Desikan, RS, Lie, BA, Djurovic, S, Dale, AM
Publikováno v:
Molecular psychiatry, vol 20, iss 2
Converging evidence implicates immune abnormalities in schizophrenia (SCZ), and recent genome-wide association studies (GWAS) have identified immune-related single-nucleotide polymorphisms (SNPs) associated with SCZ. Using the conditional false disco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::ba1e6a9a05afb55f678d8b5f0f7cd23b
https://escholarship.org/uc/item/39p9n9q8
https://escholarship.org/uc/item/39p9n9q8
Autor:
Dibbens, Lm, Mullen, S, Helbig, I, Mefford, Hc, Bayly, Ma, Bellows, S, Leu, C, Trucks, H, Obermeier, T, Wittig, M, Franke, A, Caglayan, H, Yapici, Z, Sander, T, Eichler, Ee, Scheffer, Ie, Mulley, Jc, Berkovic, Sf, De Jonghe, P, Suls, A, Hjalgrim, H, Madsen, Jm, Møller, Rs, Lehesjoki, Ae, Siren, A, Gaus, V, Janz, D, Schmitz, B, Elger, Ce, Hallmann, K, Kleefuß-Lie, Aa, Kunz, Ws, Raabe, A, Muhle, H, Ostertag, P, von Spiczak, S, Stephani, U, Lerche, H, Weber, Yg, Striano, P, Zara, F, Marini, C, Brilstra, Eh, Kastelijn-Nolst, Trenité, Koeleman, D, Bpc, de Kovel, Cgf, Lindhout, D, Swinkels, Mem, Yalcin, O, Baykan, B, Turkdogan, D, Dizdarer, G, Ozkara, C, Lee, Y, Müller-Quernheim, J, Fölster-Holst, R, Hofmann, S, Nebel, A., Schreiber, S, Schürmann, M, Rodriguez, E, Weidinger, S, Baurecht, H, Lie, Ba, Boberg, Km, Karlsen, Th.
Publikováno v:
Human molecular genetics
Dibbens, L M, Mullen, S, Helbig, I, Mefford, H C, Bayly, M A, Bellows, S, Leu, C, Trucks, H, Obermeier, T, Wittig, M, Franke, A, Caglayan, H, Yapici, Z, EPICURE Consortium, Sander, T, Eichler, E E, Scheffer, I E, Mulley, J C, Berkovic, S F & Møller, R S 2009, ' Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy : precedent for disorders with complex inheritance ', Human Molecular Genetics, vol. 18, no. 19, pp. 3626-31 . https://doi.org/10.1093/hmg/ddp311
Dibbens, L M, Mullen, S, Helbig, I, Mefford, H C, Bayly, M A, Bellows, S, Leu, C, Trucks, H, Obermeier, T, Wittig, M, Franke, A, Caglayan, H, Yapici, Z, EPICURE Consortium, Sander, T, Eichler, E E, Scheffer, I E, Mulley, J C, Berkovic, S F & Møller, R S 2009, ' Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy : precedent for disorders with complex inheritance ', Human Molecular Genetics, vol. 18, no. 19, pp. 3626-31 . https://doi.org/10.1093/hmg/ddp311
Microdeletion at chromosomal position 15q13.3 has been described in intellectual disability, autism spectrum disorders, schizophrenia and recently in idiopathic generalized epilepsy (IGE). Using independent IGE cohorts, we first aimed to confirm the
Autor:
Lie, Ba, Mora, B, Boland, A, Thorsby, E, Mazzilli, Mc, Absi, L, Arranz, E, Bonamico, M, Borelli, Iolanda, Corazza, Gr, De la Concha EG, Drubek, J, Fasano, Me, Fernandez, L, Garrote, Ja, Gay, C, Greco, L, Kerhin Brklijacic, V, Lolek, A, Li, H, Louka, As, Mantovani, V, Neuhausen, Sl, Percopo, S, Perz Bravo, F, Pozsonyi, Rosati, R, Rajczy, Salvaneschi, L, Schoch, G, Sollid, Lm, Testi, M, Thomson, G, Zone JJ Zunec, R.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______970::83858fb0812a907e90e9469f393d2b9c
http://hdl.handle.net/2318/50514
http://hdl.handle.net/2318/50514