Apnea due to Inheritance of Atypical Pseudocholinesterase

Por Nixon, J. C., Thiel, C. J.
Publicado em 1964

Multiscale modeling reveals inhibitory and stimulatory effects of caffeine on acetaminophen‐induced toxicity in humans

Por Thiel, C, Cordes, H, Baier, V, Blank, LM, Kuepfer, L
Publicado no CPT Pharmacometrics Syst Pharmacol (2017)

PCR detection of Anaplasma phagocytophilum in goat flocks in an area endemic for tick-borne fever in Switzerland

Por Silaghi, C., Scheuerle, M.C., Friche Passos, L.M., Thiel, C., Pfister, K.
Publicado em 2011

Molecular karyotyping using an SNP array for genomewide genotyping

Por Rauch, A, Ruschendorf, F, Huang, J, Trautmann, U, Becker, C, Thiel, C, Jones, K, Reis, A, Nurnberg, P
Publicado em 2004

Pericentrin interacts with KASH domain-containing protein Syne-2

Por Falk, N, Kessler, K, Glöckner, J, Boldt, K, Ueffing, M, Roepman, R, Thiel, C, Brandstätter, JH, Gießl, A
Publicado no Cilia (2015)

Adhesion molecule expression and cell cycle control in cells of the immune system are sensitive to altered gravity

Por Ullrich, O, Thiel, C, Paulsen, K, Huber, K, Hemmersbach, R, von der Wiesche, M, Kroll, H, Zipp, F, Engelmann, F
Publicado no Cell Commun Signal (2009)

Systematic assessment of atypical deletions reveals genotype–phenotype correlation in 22q11.2

Por Rauch, A, Zink, S, Zweier, C, Thiel, C, Koch, A, Rauch, R, Lascorz, J, Huffmeier, U, Weyand, M, Singer, H, Hofbeck, M
Publicado em 2005

Identification of mutations in DYNC2LI1, a member of the mammalian cytoplasmic dynein 2 complex, expands the clinical spectrum of Jeune/ATD ciliopathies

Por Kessler, K, Falk, N, Wunderlich, I, Fröhlich, M, Hauer, N, Gießl, A, Brandstätter, JH, Sticht, H, Ekici, AB, Uebe, S, Seemanová, E, Reis, A, Roepman, R, Thiel, C
Publicado no Cilia (2015)

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

Por Hüffmeier, U, Lascorz, J, Becker, T, Schürmeier-Horst, F, Magener, A, Ekici, A B, Endele, S, Thiel, C T, Thoma-Uszynski, S, Mössner, R, Reich, K, Kurrat, W, Wienker, T F, Traupe, H, Reis, A
Publicado em 2009

Mutations in the Gene Encoding the Wnt-Signaling Component R-Spondin 4 (RSPO4) Cause Autosomal Recessive Anonychia

Por Bergmann, C. , Senderek, J. , Anhuf, D. , Thiel, C. T. , Ekici, A. B. , Poblete-Gutiérrez, P. , van Steensel, M. , Seelow, D. , Nürnberg, G. , Schild, H. H. , Nürnberg, P. , Reis, A. , Frank, J. , Zerres, K. 
Publicado em 2006

Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum

Por Ekici, A.B., Hilfinger, D., Jatzwauk, M., Thiel, C.T., Wenzel, D., Lorenz, I., Boltshauser, E., Goecke, T.W., Staatz, G., Morris-Rosendahl, D.J., Sticht, H., Hehr, U., Reis, A., Rauch, A.
Publicado em 2010