EQUATIONS OVER FINITE FIELDS : AN ELEMENTARY APPROACH.

Por SCHMIDT, WOLFGANG M
Publicado em C197

DIOPHANTINE APPROXIMATION.

Por SCHMIDT, WOLFGANG M
Publicado em C1980

SMALL FRACTIONAL PARTS OF POLYNOMIALS.

Por SCHMIDT, WOLFGANG M, CBMS.
Publicado em C197

In vivo profile of the human leukocyte microRNA response to endotoxemia

Por Schmidt, Wolfgang M, Spiel, Alexander O, Jilma, Bernd, Wolzt, Michael, Müller, Markus
Publicado em 2008

Microarray-Based Identification of Bacteria in Clinical Samples by Solid-Phase PCR Amplification of 23S Ribosomal DNA Sequences

Por Mitterer, Georg, Huber, Martin, Leidinger, Ernst, Kirisits, Claudia, Lubitz, Werner, Mueller, Manfred W., Schmidt, Wolfgang M.
Publicado em 2004

Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia

Por Schmidt, Wolfgang M., Rutledge, S. Lane, Schüle, Rebecca, Mayerhofer, Benjamin, Züchner, Stephan, Boltshauser, Eugen, Bittner, Reginald E.
Publicado no Am J Hum Genet (2015)

Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation

Por Skrabl-Baumgartner, Andrea, Plecko, Barbara, Schmidt, Wolfgang M., König, Nadja, Hershfield, Michael, Gruber-Sedlmayr, Ursula, Lee-Kirsch, Min Ae
Publicado no Pediatr Rheumatol Online J (2017)

Aggressiveness of human melanoma xenograft models is promoted by aneuploidy-driven gene expression deregulation

Por Mathieu, Véronique, Pirker, Christine, Schmidt, Wolfgang M., Spiegl-Kreinecker, Sabine, Lötsch, Daniela, Heffeter, Petra, Hegedus, Balazs, Grusch, Michael, Kiss, Robert, Berger, Walter
Publicado em 2012

Homozygous SYNE1 mutation causes congenital onset of muscular weakness with distal arthrogryposis: a genotype–phenotype correlation

Por Baumann, Matthias, Steichen-Gersdorf, Elisabeth, Krabichler, Birgit, Petersen, Britt-Sabina, Weber, Ulrike, Schmidt, Wolfgang M, Zschocke, Johannes, Müller, Thomas, Bittner, Reginald E, Janecke, Andreas R
Publicado no Eur J Hum Genet (2017)

DNA Damage, Somatic Aneuploidy, and Malignant Sarcoma Susceptibility in Muscular Dystrophies

Por Schmidt, Wolfgang M., Uddin, Mohammed H., Dysek, Sandra, Moser-Thier, Karin, Pirker, Christine, Höger, Harald, Ambros, Inge M., Ambros, Peter F., Berger, Walter, Bittner, Reginald E.
Publicado em 2011

SNP-array based whole genome homozygosity mapping: A quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients()

Por Papić, Lea, Fischer, Dirk, Trajanoski, Slave, Höftberger, Romana, Fischer, Carina, Ströbel, Thomas, Schmidt, Wolfgang M., Bittner, Reginald E., Schabhüttl, Maria, Gruber, Karin, Pieber, Thomas R., Janecke, Andreas R., Auer-Grumbach, Michaela
Publicado em 2011

Mutation in the Scyl1 gene encoding amino-terminal kinase-like protein causes a recessive form of spinocerebellar neurodegeneration

Por Schmidt, Wolfgang M, Kraus, Cornelia, Höger, Harald, Hochmeister, Sonja, Oberndorfer, Felicitas, Branka, Manuela, Bingemann, Sonja, Lassmann, Hans, Müller, Markus, Macedo-Souza, Lúcia Inês, Vainzof, Mariz, Zatz, Mayana, Reis, André, Bittner, Reginald E
Publicado em 2007

Colon cancer cell-derived 12(S)-HETE induces the retraction of cancer-associated fibroblast via MLC2, RHO/ROCK and Ca(2+) signalling

Por Stadler, Serena, Nguyen, Chi Huu, Schachner, Helga, Milovanovic, Daniela, Holzner, Silvio, Brenner, Stefan, Eichsteininger, Julia, Stadler, Mira, Senfter, Daniel, Krenn, Liselotte, Schmidt, Wolfgang M., Huttary, Nicole, Krieger, Sigurd, Koperek, Oskar, Bago-Horvath, Zsuzsanna, Brendel, Konstantin Alexander, Marian, Brigitte, de Wever, Oliver, Mader, Robert M., Giessrigl, Benedikt, Jäger, Walter, Dolznig, Helmut, Krupitza, Georg
Publicado no Cell Mol Life Sci (2016)