Antibodies against PEGylated enzymes: Treat them with respect!

Por Rutsch, Frank
Publicado no EBioMedicine (2018)

Generalized arterial calcification of infancy and pseudoxanthoma elasticum: two sides of the same coin

Por Nitschke, Yvonne, Rutsch, Frank
Publicado em 2012

Genetics in Arterial Calcification: Pieces of a Puzzle and Cogs in a Wheel

Por Rutsch, Frank, Nitschke, Yvonne, Terkeltaub, Robert
Publicado em 2011

Npp1 promotes atherosclerosis in ApoE knockout mice

Por Nitschke, Yvonne, Weissen-Plenz, Gabriele, Terkeltaub, Robert, Rutsch, Frank
Publicado em 2011

Cerebral vasculopathy is a common feature in Aicardi–Goutières syndrome associated with SAMHD1 mutations

Por du Moulin, Marcel, Nürnberg, Peter, Crow, Yanick J., Rutsch, Frank
Publicado em 2011

MDA5-Associated Neuroinflammation and the Singleton–Merten Syndrome: Two Faces of the Same Type I Interferonopathy Spectrum

Por Buers, Insa, Rice, Gillian I., Crow, Yanick J., Rutsch, Frank
Publicado no J Interferon Cytokine Res (2017)

Molecular diagnosis of generalized arterial calcification of infancy (GACI)

Por Kalal, Iravathy Goud, Seetha, Dayakar, Panda, Anuradha, Nitschke, Yvonne, Rutsch, Frank
Publicado em 2012

ENPP1-Fc prevents neointima formation in generalized arterial calcification of infancy through the generation of AMP

Por Nitschke, Yvonne, Yan, Yan, Buers, Insa, Kintziger, Kristina, Askew, Kim, Rutsch, Frank
Publicado no Exp Mol Med (2018)

Lmbrd1 expression is essential for the initiation of gastrulation

Por Buers, Insa, Pennekamp, Petra, Nitschke, Yvonne, Lowe, Chrishanthi, Skryabin, Boris V., Rutsch, Frank
Publicado no J Cell Mol Med (2016)

Generalized Arterial Calcification of Infancy: Fatal Clinical Course Associated with a Novel Mutation in ENPP1

Por Galletti, Silvia, Nitschke, Yvonne, Malavolti, Anna M., Aquilano, Giulia, Faldella, Giacomo, Corvaglia, Luigi, Rutsch, Frank
Publicado em 2011

Expression of NPP1 is regulated during atheromatous plaque calcification

Por Nitschke, Yvonne, Hartmann, Simone, Torsello, Giovanni, Horstmann, Rüdiger, Seifarth, Harald, Weissen-Plenz, Gabriele, Rutsch, Frank
Publicado em 2011

Kocuria rhizophila Adds to the Emerging Spectrum of Micrococcal Species Involved in Human Infections

Por Becker, Karsten, Rutsch, Frank, Uekötter, Andreas, Kipp, Frank, König, Jens, Marquardt, Thorsten, Peters, Georg, von Eiff, Christof
Publicado em 2008

Association of ENPP1 gene polymorphisms with hand osteoarthritis in a Chuvasha population

Por Suk, Eun-Kyung, Malkin, Ida, Dahm, Stefan, Kalichman, Leonid, Ruf, Nico, Kobyliansky, Eugene, Toliat, Mohammad, Rutsch, Frank, Nürnberg, Peter, Livshits, Gregory
Publicado em 2005

The Kuvan(®) Adult Maternal Paediatric European Registry (KAMPER) Multinational Observational Study: Baseline and 1-Year Data in Phenylketonuria Patients Responsive to Sapropterin

Por Trefz, Friedrich K., Muntau, Ania C., Lagler, Florian B., Moreau, Flavie, Alm, Jan, Burlina, Alberto, Rutsch, Frank, Bélanger-Quintana, Amaya, Feillet, François
Publicado no JIMD Rep (2015)

Cerebral Arterial Stenoses and Stroke: Novel Features of Aicardi-Goutières Syndrome Caused by the Arg164X Mutation in SAMHD1 Are Associated with Altered Cytokine Expression

Por Thiele, Holger, du Moulin, Marcel, Barczyk, Katarzyna, George, Christel, Schwindt, Wolfram, Nürnberg, Gudrun, Frosch, Michael, Kurlemann, Gerhard, Roth, Johannes, Nürnberg, Peter, Rutsch, Frank
Publicado em 2010

PC-1 Nucleoside Triphosphate Pyrophosphohydrolase Deficiency in Idiopathic Infantile Arterial Calcification

Por Rutsch, Frank, Vaingankar, Sucheta, Johnson, Kristen, Goldfine, Ira, Maddux, Betty, Schauerte, Petra, Kalhoff, Hermann, Sano, Kimihiko, Boisvert, William A., Superti-Furga, Andrea, Terkeltaub, Robert
Publicado em 2001

Influence of PAH Genotype on Sapropterin Response in PKU: Results of a Single-Center Cohort Study

Por Leuders, Sarah, Wolfgart, Eva, Ott, Torsten, du Moulin, Marcel, van Teeffelen-Heithoff, Agnes, Vogelpohl, Lydia, Och, Ulrike, Marquardt, Thorsten, Weglage, Josef, Feldmann, Reinhold, Rutsch, Frank
Publicado em 2013

Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders

Por Herholz, Jana, Meloni, Alessandra, Marongiu, Mara, Chiappe, Francesca, Deiana, Manila, Herrero, Carmen Roche, Zampino, Giuseppe, Hamamy, Hanan, Zalloum, Yusra, Waaler, Per Erik, Crisponi, Giangiorgio, Crisponi, Laura, Rutsch, Frank
Publicado em 2011

A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

Por Rutsch, Frank, MacDougall, Mary, Lu, Changming, Buers, Insa, Mamaeva, Olga, Nitschke, Yvonne, Rice, Gillian I., Erlandsen, Heidi, Kehl, Hans Gerd, Thiele, Holger, Nürnberg, Peter, Höhne, Wolfgang, Crow, Yanick J., Feigenbaum, Annette, Hennekam, Raoul C.
Publicado no Am J Hum Genet (2015)

SAMHD1-Deficient CD14+ Cells from Individuals with Aicardi-Goutières Syndrome Are Highly Susceptible to HIV-1 Infection

Por Berger, André, Sommer, Andreas F. R., Zwarg, Jenny, Hamdorf, Matthias, Welzel, Karin, Esly, Nicole, Panitz, Sylvia, Reuter, Andreas, Ramos, Irene, Jatiani, Asavari, Mulder, Lubbertus C. F., Fernandez-Sesma, Ana, Rutsch, Frank, Simon, Viviana, König, Renate, Flory, Egbert
Publicado em 2011