Disease relevant modifications of the methylome and transcriptome by particulate matter (PM(2.5)) from biomass combustion

por Heßelbach, Katharina, Kim, Gwang-Jin, Flemming, Stephan, Häupl, Thomas, Bonin, Marc, Dornhof, Regina, Günther, Stefan, Merfort, Irmgard, Humar, Matjaz
Publicado 2017

Particulate Matter (PM(2.5)) from Biomass Combustion Induces an Anti-Oxidative Response and Cancer Drug Resistance in Human Bronchial Epithelial BEAS-2B Cells

por Merk, Regina, Heßelbach, Katharina, Osipova, Anastasiya, Popadić, Désirée, Schmidt-Heck, Wolfgang, Kim, Gwang-Jin, Günther, Stefan, Piñeres, Alfonso García, Merfort, Irmgard, Humar, Matjaz
Publicado 2020

Sox9 and Sox8 protect the adult testis from male-to-female genetic reprogramming and complete degeneration

por Barrionuevo, Francisco J, Hurtado, Alicia, Kim, Gwang-Jin, Real, Francisca M, Bakkali, Mohammed, Kopp, Janel L, Sander, Maike, Scherer, Gerd, Burgos, Miguel, Jiménez, Rafael
Publicado 2016

Precision Mapping of COVID-19 Vulnerable Locales by Epidemiological and Socioeconomic Risk Factors, Developed Using South Korean Data

por Weinstein, Bayarmagnai, da Silva, Alan R., Kouzoukas, Dimitrios E., Bose, Tanima, Kim, Gwang Jin, Correa, Paola A., Pondugula, Santhi, Lee, YoonJung, Kim, Jihoo, Carpenter, David O.
Publicado 2021

Efficacy and Safety of Innovative Experimental Chimeric Antigen Receptor (CAR) T-cells versus Axicabtagene ciloleucel (Yescarta) for the Treatment of Relapsed/Refractory Large B-Ce...

por Weinstein, Bayarmagnai, Muresan, Bogdan, Solano, Sara, de Macedo, Antonio Vaz, Lee, YoonJung, Su, Yu-Chen, Ahn, Yeseul, Henriquez, Gabriela, Camargo, Cristina, Kim, Gwang-Jin, Carpenter, David O.
Publicado 2021

Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

por Radner, Franz P. W., Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith
Publicado 2013

Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans

por Radner, Franz P. W., Marrakchi, Slaheddine, Kirchmeier, Peter, Kim, Gwang-Jin, Ribierre, Florence, Kamoun, Bourane, Abid, Leila, Leipoldt, Michael, Turki, Hamida, Schempp, Werner, Heilig, Roland, Lathrop, Mark, Fischer, Judith
Publicado 2013

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

por Riedhammer, Korbinian M., Nguyen, Thanh-Minh T., Koşukcu, Can, Calzada-Wack, Julia, Li, Yong, Saygılı, Seha, Wimmers, Vera, Kim, Gwang-Jin, Chrysanthou, Marialena, Bakey, Zeineb, Kraiger, Markus, Sanz-Moreno, Adrián, Amarie, Oana V, Rathkolb, Birgit, Klein-Rodewald, Tanja, Garrett, Lillian, Hölter, Sabine M., Seisenberger, Claudia, Haug, Stefan, Marschall, Susan, Wurst, Wolfgang, Fuchs, Helmut, Gailus-Durner, Valerie, Wuttke, Matthias, de Angelis, Martin Hrabe, Ćomić, Jasmina, Doğan, Özlem Akgün, Özlük, Yasemin, Taşdemir, Mehmet, Ağbaş, Ayşe, Canpolat, Nur, Ćalışkan, Salim, Weber, Ruthild, Bergmann, Carsten, Jeanpierre, Cecile, Saunier, Sophie, Lim, Tze Y., Hildebrandt, Friedhelm, Alhaddad, Bader, Wu, Kaman, Antony, Dinu, Matschkal, Julia, Schaaf, Christian, Renders, Lutz, Schmaderer, Christoph, Meitinger, Thomas, Heemann, Uwe, Köttgen, Anna, Arnold, Sebastian, Ozaltin, Fatih, Schmidts, Miriam, Hoefele, Julia
Publicado 2023