Down syndrome phenotype in a boy with a mosaic microduplication of chromosome 21q22

por Schnabel, Franziska, Smogavec, Mateja, Funke, Rudolf, Pauli, Silke, Burfeind, Peter, Bartels, Iris
Publicado 2018

Leupaxin stimulates adhesion and migration of prostate cancer cells through modulation of the phosphorylation status of the actin-binding protein caldesmon

por Dierks, Sascha, von Hardenberg, Sandra, Schmidt, Thomas, Bremmer, Felix, Burfeind, Peter, Kaulfuß, Silke
Publicado 2015

Leupaxin is expressed in mammary carcinoma and acts as a transcriptional activator of the estrogen receptor α

por KAULFUSS, SILKE, HERR, ANNA-MARIA, BÜCHNER, ANJA, HEMMERLEIN, BERNHARD, GÜNTHERT, ANDREAS R., BURFEIND, PETER
Publicado 2015

Prospects of estrogen receptor β activation in the treatment of castration-resistant prostate cancer

por Gehrig, Julia, Kaulfuß, Silke, Jarry, Hubertus, Bremmer, Felix, Stettner, Mark, Burfeind, Peter, Thelen, Paul
Publicado 2017

N-cadherin expression in malignant germ cell tumours of the testis

por Bremmer, Felix, Hemmerlein, Bernhard, Strauss, Arne, Burfeind, Peter, Thelen, Paul, Radzun, Heinz-Joachim, Behnes, Carl Ludwig
Publicado 2012

De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis

por Schwaibold, Eva Maria Christina, Bartels, Iris, Küster, Helmut, Lorenz, Michael, Burfeind, Peter, Adam, Ronja, Zoll, Barbara
Publicado 2014

Defective thrombus formation in mice lacking coagulation factor XII

por Renné, Thomas, Pozgajová, Miroslava, Grüner, Sabine, Schuh, Kai, Pauer, Hans-Ulrich, Burfeind, Peter, Gailani, David, Nieswandt, Bernhard
Publicado 2005

Testosterone metabolites inhibit proliferation of castration- and therapy-resistant prostate cancer

por Bremmer, Felix, Jarry, Hubertus, Unterkircher, Valerie, Kaulfuss, Silke, Burfeind, Peter, Radzun, Heinz-Joachim, Ströbel, Philipp, Thelen, Paul
Publicado 2018

Blockade of the PDGFR family together with SRC leads to diminished proliferation of colorectal cancer cells

por Kaulfuβ, Silke, Seemann, Henning, Kampe, Rovena, Meyer, Julia, Dressel, Ralf, König, Britta, Scharf, Jens-Gerd, Burfeind, Peter
Publicado 2013

Intragenic duplication of EHMT1 gene results in Kleefstra syndrome

por Schwaibold, Eva Maria Christina, Smogavec, Mateja, Hobbiebrunken, Elke, Winter, Lorenz, Zoll, Barbara, Burfeind, Peter, Brockmann, Knut, Pauli, Silke
Publicado 2014

Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation

por Auber, Bernd, Bruemmer, Verena, Zoll, Barbara, Burfeind, Peter, Boehm, Detlef, Liehr, Thomas, Brockmann, Knut, Wilichowski, Ekkehard, Argyriou, Loukas, Bartels, Iris
Publicado 2009

Targeting coagulation factor XII provides protection from pathological thrombosis in cerebral ischemia without interfering with hemostasis

por Kleinschnitz, Christoph, Stoll, Guido, Bendszus, Martin, Schuh, Kai, Pauer, Hans-Ulrich, Burfeind, Peter, Renné, Christoph, Gailani, David, Nieswandt, Bernhard, Renné, Thomas
Publicado 2006

Pelota interacts with HAX1, EIF3G and SRPX and the resulting protein complexes are associated with the actin cytoskeleton

por Burnicka-Turek, Ozanna, Kata, Aleksandra, Buyandelger, Byambajav, Ebermann, Linda, Kramann, Nadine, Burfeind, Peter, Hoyer-Fender, Sigrid, Engel, Wolfgang, Adham, Ibrahim M
Publicado 2010

Role of N-cadherin in proliferation, migration, and invasion of germ cell tumours

por Bremmer, Felix, Schallenberg, Simon, Jarry, Hubertus, Küffer, Stefan, Kaulfuss, Silke, Burfeind, Peter, Strauβ, Arne, Thelen, Paul, Radzun, Heinz Joachim, Ströbel, Philipp, Honecker, Friedemann, Behnes, Carl Ludwig
Publicado 2015

Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state

por Yigit, Gökhan, Sheffer, Ruth, Daana, Muhannad, Li, Yun, Kaygusuz, Emrah, Mor-Shakad, Hagar, Altmüller, Janine, Nürnberg, Peter, Douiev, Liza, Kaulfuss, Silke, Burfeind, Peter, Wollnik, Bernd, Brockmann, Knut
Publicado 2022

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

por Ganapathi, Mythily, Argyriou, Loukas, Martínez-Azorín, Francisco, Morlot, Susanne, Yigit, Gökhan, Lee, Teresa M., Auber, Bernd, von Gise, Alexander, Petrey, Donald S., Thiele, Holger, Cyganek, Lukas, Sabater-Molina, María, Ahimaz, Priyanka, Cabezas-Herrera, Juan, Sorlí-García, Moisés, Zibat, Arne, Siegelin, Markus D., Burfeind, Peter, Buchovecky, Christie M., Hasenfuss, Gerd, Honig, Barry, Li, Yun, Iglesias, Alejandro D., Wollnik, Bernd
Publicado 2020