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Candidate driver genes involved in genome maintenance and DNA repair in Sézary syndrome

Autor: Woollard, Wesley J., Pullabhatla, Venu, Lorenc, Anna, Patel, Varsha M., Butler, Rosie M., Bayega, Anthony, Begum, Nelema, Bakr, Farrah, Dedhia, Kiran, Fisher, Joshua, Aguilar-Duran, Silvia, Flanagan, Charlotte, Ghasemi, Aria A., Hoffmann, Ricarda M., Castillo-Mosquera, Nubia, Nuttall, Elisabeth A., Paul, Arisa, Roberts, Ceri A., Solomonidis, Emmanouil G., Tarrant, Rebecca, Yoxall, Antoinette, Beyers, Carl Z., Ferreira, Silvia, Tosi, Isabella, Simpson, Michael A., de Rinaldis, Emanuele, Mitchell, Tracey J., Whittaker, Sean J. ^*

Publikováno v: In Blood 30 June 2016 127(26):3387-3397

Intraindividual genome expression analysis reveals opposing immune reaction in psoriasis and eczema

Autor: Quaranta, Maria, Knapp, Bettina, Garzorz-Stark, Nathalie, Mattii, Martina, Pullabhatla, Venu, Pennino, Davide, Andreas, Christian, Traidl-Hoffmann, Claudia, Cavani, Andrea, Theis, Fabian J., Ring, Johannes, Schmidt-Weber, Carsten, Eyerich, Stephanie, Eyerich, K.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3341::3656063a569fff3af63cd6ba0d2f7c27
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/85367

De novo mutations implicate novel genes in systemic lupus erythematosus

Autor: Pullabhatla, Venu, Roberts, Amy L., Lewis, Myles J., Mauro, Daniele, Morris, David L., Odhams, Christopher A., Tombleson, Philip, Liljedahl, Ulrika, Vyse, Simon, Simpson, Michael A., Sauer, Sascha, de Rinaldis, Emanuele, Syvänen, Ann-Christine, Vyse, Timothy J.

The omnigenic model of complex disease stipulates that the majority of the heritability will be explained by the effects of common variation on genes in the periphery of core disease pathways. Rare variant associations, expected to explain far less o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0529c651a8376f9403244c369940a3d5
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-346884

Retinoic acid is essential for Th1 cell lineage stability and prevents transition to a Th17 cell program

Autor: Brown, Chrysothemis c., Esterhazy, Daria, Sarde, Aurelien, London, Mariya, Pullabhatla, Venu, Osma-garcia, Ines, Al-bader, Raya, Ortiz, Carla, Elgueta, Raul, Arno, Matthew, De rinaldis, Emanuele, Mucida, Daniel, Lord, Graham m., Noelle, Randolph j.

Publikováno v: Immunity
Brown, C C, Esterhazy, D, Sarde, A, London, M, Pullabhatla, V, Osma-Garcia, I, Al-Bader, R, Ortiz, C, Elgueta, R, Arno, M, de Rinaldis, E, Mucida, D, Lord, G M & Noelle, R J 2015, ' Retinoic Acid is essential for Th1 cell lineage stability and prevents transition to a th17 cell program ', Immunity, vol. 42, no. 3, pp. 499-511 . https://doi.org/10.1016/j.immuni.2015.02.003
Brown, C, Esterhazy, D, Sarde, A, London, M, Pullabhatla, V, Osma-garcia, I, Al-bader, R, Ortiz, C, Elgueta, R, Arno, M, De rinaldis, E, Mucida, D, Lord, G & Noelle, R 2015, ' Retinoic Acid Is Essential for Th1 Cell Lineage Stability and Prevents Transition to a Th17 Cell Program ', Immunity, vol. 42, no. 3, pp. 499-511 . https://doi.org/10.1016/j.immuni.2015.02.003

Summary CD4+ T cells differentiate into phenotypically distinct T helper cells upon antigenic stimulation. Regulation of plasticity between these CD4+ T-cell lineages is critical for immune homeostasis and prevention of autoimmune disease. However, t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::54800d7afe4acfe19d79c5092e9146f7
https://pubmed.ncbi.nlm.nih.gov/25769610