Hepatitis Delta co-infection in humanized mice leads to pronounced induction of innate immune responses in comparison to HBV mono-infection
Giersch, Katja, Allweiss, Lena, Volz, Tassilo, Helbig, Martina, Bierwolf, Jeanette, Lohse, Ansgar W, Pollok, Joerg M, Petersen, Joerg, Dandri, Maura, Lütgehetmann, Marc
Published in Journal of hepatology (01.08.2015)
Published in Journal of hepatology (01.08.2015)
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Journal Article
Humanized chimeric uPA mouse model for the study of hepatitis B and D virus interactions and preclinical drug evaluation
Lütgehetmann, Marc, Mancke, Lida V., Volz, Tassilo, Helbig, Martina, Allweiss, Lena, Bornscheuer, Till, Pollok, Joerg M., Lohse, Ansgar W., Petersen, J., Urban, Stephan, Dandri, Maura
Published in Hepatology (Baltimore, Md.) (01.03.2012)
Published in Hepatology (Baltimore, Md.) (01.03.2012)
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Journal Article
Both interferon alpha and lambda can reduce all intrahepatic HDV infection markers in HBV/HDV infected humanized mice
Giersch, Katja, Homs, Maria, Volz, Tassilo, Helbig, Martina, Allweiss, Lena, Lohse, Ansgar W, Petersen, Jörg, Buti, Maria, Pollicino, Teresa, Sureau, Camille, Dandri, Maura, Lütgehetmann, Marc
Published in Scientific reports (16.06.2017)
Published in Scientific reports (16.06.2017)
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Journal Article
Does Nutrition Affect Endometriosis?
Helbig, Martina, Vesper, Anne-Sophie, Beyer, Ines, Fehm, Tanja
Published in Geburtshilfe und Frauenheilkunde (01.02.2021)
Published in Geburtshilfe und Frauenheilkunde (01.02.2021)
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Journal Article
Correlation between pain and depressive symptoms in patients with confirmed endometriosis during COVID-19 pandemic
Helbig, Martina, Schaal, Nora K., Drumm, Johannes, Fürst, Flurina, Reinhart, Lisa, Fehm, Tanja, Beyer, Ines
Published in Archives of gynecology and obstetrics (01.02.2024)
Published in Archives of gynecology and obstetrics (01.02.2024)
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Journal Article
The influence of being pregnant during the COVID-19 pandemic on birth expectations and antenatal bonding
Schaal, Nora K., Hagenbeck, Carsten, Helbig, Martina, Wulff, Verena, Märthesheimer, Sarah, Fehm, Tanja, Hepp, Philip
Published in Journal of reproductive and infant psychology (01.01.2023)
Published in Journal of reproductive and infant psychology (01.01.2023)
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Journal Article
Persistent hepatitis D virus mono-infection in humanized mice is efficiently converted by hepatitis B virus to a productive co-infection
Giersch, Katja, Helbig, Martina, Volz, Tassilo, Allweiss, Lena, Mancke, Lida V, Lohse, Ansgar W, Polywka, Susanne, Pollok, Jörg M, Petersen, Jörg, Taylor, John, Dandri, Maura, Lütgehetmann, Marc
Published in Journal of hepatology (01.03.2014)
Published in Journal of hepatology (01.03.2014)
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Journal Article
Retinal Layer Thicknesses in Early Age-Related Macular Degeneration: Results From the German AugUR Study
Brandl, Caroline, Brücklmayer, Christiane, Günther, Felix, Zimmermann, Martina E, Küchenhoff, Helmut, Helbig, Horst, Weber, Bernhard H F, Heid, Iris M, Stark, Klaus J
Published in Investigative ophthalmology & visual science (01.04.2019)
Published in Investigative ophthalmology & visual science (01.04.2019)
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Journal Article
Quantitative Analysis of OCT Characteristics in Patients with Achromatopsia and Blue-Cone Monochromatism
Barthelmes, Daniel, Sutter, Florian K, Kurz-Levin, Malaika M, Bosch, Martina M, Helbig, Horst, Niemeyer, Gunter, Fleischhauer, Johannes C
Published in Investigative ophthalmology & visual science (01.03.2006)
Published in Investigative ophthalmology & visual science (01.03.2006)
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Journal Article
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies
Carvill, Gemma L., Engel, Krysta L., Ramamurthy, Aishwarya, Cochran, J. Nicholas, Roovers, Jolien, Stamberger, Hannah, Lim, Nicholas, Schneider, Amy L., Hollingsworth, Georgie, Holder, Dylan H., Regan, Brigid M., Lawlor, James, Lagae, Lieven, Ceulemans, Berten, Bebin, E. Martina, Nguyen, John, Striano, Pasquale, Zara, Federico, Helbig, Ingo, Møller, Rikke S., von Spiczak, Sarah, Muhle, Hiltrud, Caglayan, Hande, Sterbova, Katalin, Craiu, Dana, Hoffman, Dorota, Lehesjoki, Anna-Elina, Selmer, Kaja, Depienne, Christel, Lemke, Johannes, Marini, Carla, Guerrini, Renzo, Neubauer, Bernd, Talvik, Tiina, Leguern, Eric, de Jonghe, Peter, Weckhuysen, Sarah, Barsh, Gregory S., Weckhuysen, Sarah, Meisler, Miriam, Berkovic, Samuel F., De Jonghe, Peter, Scheffer, Ingrid E., Myers, Richard M., Cooper, Gregory M., Mefford, Heather C.
Published in American journal of human genetics (06.12.2018)
Published in American journal of human genetics (06.12.2018)
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Journal Article
The life-saving benefit of dexamethasone in severe COVID-19 is linked to a reversal of monocyte dysregulation
Knoll, Rainer, Helbig, Elisa T., Dahm, Kilian, Bolaji, Olufemi, Hamm, Frederik, Dietrich, Oliver, van Uelft, Martina, Müller, Sophie, Bonaguro, Lorenzo, Schulte-Schrepping, Jonas, Petrov, Lev, Krämer, Benjamin, Kraut, Michael, Stubbemann, Paula, Thibeault, Charlotte, Brumhard, Sophia, Theis, Heidi, Hack, Gudrun, De Domenico, Elena, Nattermann, Jacob, Becker, Matthias, Beyer, Marc D., Hillus, David, Georg, Philipp, Loers, Constantin, Tiedemann, Janina, Tober-Lau, Pinkus, Lippert, Lena, Millet Pascual-Leone, Belén, Tacke, Frank, Rohde, Gernot, Suttorp, Norbert, Witzenrath, Martin, Saliba, Antoine-Emmanuel, Ulas, Thomas, Polansky, Julia K., Sawitzki, Birgit, Sander, Leif E., Schultze, Joachim L., Aschenbrenner, Anna C., Kurth, Florian
Published in Cell (08.08.2024)
Published in Cell (08.08.2024)
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Journal Article
FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants
Mitter, Diana, Pringsheim, Milka, Kaulisch, Marc, Plümacher, Kim Sarah, Schröder, Simone, Warthemann, Rita, Abou Jamra, Rami, Baethmann, Martina, Bast, Thomas, Büttel, Hans-Martin, Cohen, Julie S., Conover, Elizabeth, Courage, Carolina, Eger, Angelika, Fatemi, Ali, Grebe, Theresa A., Hauser, Natalie S., Heinritz, Wolfram, Helbig, Katherine L., Heruth, Marion, Huhle, Dagmar, Höft, Karen, Karch, Stephanie, Kluger, Gerhard, Korenke, G. Christoph, Lemke, Johannes R., Lutz, Richard E., Patzer, Steffi, Prehl, Isabelle, Hoertnagel, Konstanze, Ramsey, Keri, Rating, Tina, Rieß, Angelika, Rohena, Luis, Schimmel, Mareike, Westman, Rachel, Zech, Frank-Martin, Zoll, Barbara, Malzahn, Dörthe, Zirn, Birgit, Brockmann, Knut
Published in Genetics in medicine (01.01.2018)
Published in Genetics in medicine (01.01.2018)
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Journal Article
Genetic Risk Score Analysis Supports a Joint View of Two Classification Systems for Age-Related Macular Degeneration
Herold, Janina M., Zimmermann, Martina E., Gorski, Mathias, Günther, Felix, Weber, Bernhard H. F., Helbig, Horst, Stark, Klaus J., Heid, Iris M., Brandl, Caroline
Published in Investigative ophthalmology & visual science (01.09.2023)
Published in Investigative ophthalmology & visual science (01.09.2023)
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Journal Article
On the impact of different approaches to classify age-related macular degeneration: Results from the German AugUR study
Brandl, Caroline, Zimmermann, Martina E, Günther, Felix, Barth, Teresa, Olden, Matthias, Schelter, Sabine C, Kronenberg, Florian, Loss, Julika, Küchenhoff, Helmut, Helbig, Horst, Weber, Bernhard H F, Stark, Klaus J, Heid, Iris M
Published in Scientific reports (06.06.2018)
Published in Scientific reports (06.06.2018)
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Journal Article
Comparing Alternative Ranibizumab Dosages for Safety and Efficacy in Retinopathy of Prematurity: A Randomized Clinical Trial
Stahl, Andreas, Krohne, Tim U, Eter, Nicole, Oberacher-Velten, Isabel, Guthoff, Rainer, Meltendorf, Synke, Ehrt, Oliver, Aisenbrey, Sabine, Roider, Johann, Gerding, Heinrich, Jandeck, Claudia, Smith, Lois E H, Walz, Johanna M
Published in JAMA pediatrics (01.03.2018)
Published in JAMA pediatrics (01.03.2018)
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Journal Article
eP148 - Heterozygous ANKRD17 loss of function variants cause a syndrome with intellectual disability, speech delay and dysmorphism
Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta, Kaur, Anupriya, Kaur, Parmeet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia, Capuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra, Wilke, Martina, Thompson, Michelle, Bebin, Martina, Bijlsma, Emilia, Hoffer, Mariette, Peters-Scholte, Cacha, Slavotinek, Anne, Weiss, William, Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Yachelevich, Naomi, Wilaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Kloechner, Chiara, Kamphausen, Susanne, Jamra, Rami, Arelin, Maria, Innes, Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damien, de Burca, Anna, Kini, Usha, Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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Journal Article
Heterozygous ANKRD17 loss of function variants cause a syndrome with intellectual disability, speech delay and dysmorphism
Chopra, Maya, McEntagart, Meriel, Clayton-Smith, Jill, Platzer, Konrad, Shukla, Anju, Girisha, Katta, Kaur, Anupriya, Kaur, Parmeet, Pfundt, Rolph, Veenstra-Knol, Hermine, Mancini, Grazia, Capuccio, Gerarda, Brunetti-Pierri, Nicola, Kortüm, Fanny, Hempel, Maja, Denecke, Jonas, Lehman, Anna, Kleefstra, Tjitske, Stuurman, Kyra, Wilke, Martina, Thompson, Michelle, Bebin, Martina, Bijlsma, Emilia, Hoffer, Mariette, Peters-Scholte, Cacha, Slavotinek, Anne, Weiss, William, Yip, Tiffany, Hodoglugil, Ugur, Whittle, Amy, diMonda, Janette, Neira, Juanita, Yang, Sandra, Kirby, Amelia, Pinz, Hailey, Lechner, Rosan, Sleutels, Frank, Helbig, Ingo, McKeown, Sarah, Helbig, Katherine, Yachelevich, Naomi, Wilaert, Rebecca, Juusola, Jane, Semotok, Jennifer, Hadonou, Medard, Short, John, Lala, Sajel, Fernández-Jaen, Alberto, Pelayo, Janvier Porta, Kloechner, Chiara, Kamphausen, Susanne, Jamra, Rami, Arelin, Maria, Innes, Micheil, Niskakoski, Anni, Amin, Sam, Williams, Maggie, Evans, Julie, Smithson, Sarah, Smedley, Damien, de Burca, Anna, Kini, Usha, Lyonnet, Stanislas, Amiel, Jeanne, Gordon, Christopher
Published in Molecular genetics and metabolism (01.04.2021)
Published in Molecular genetics and metabolism (01.04.2021)
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