Analysis of Drosophila Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer
Liu, Jiang, Ghanim, Murad, Xue, Lei, Brown, Christopher D, Iossifov, Ivan, Angeletti, Cesar, Hua, Sujun, Nègre, Nicolas, Ludwig, Michael, Stricker, Thomas, Al-Ahmadie, Hikmat A, Tretiakova, Maria, Camp, Robert L, Perera-Alberto, Montse, Rimm, David L, Xu, Tian, Rzhetsky, Andrey, White, Kevin P
Published in Science (American Association for the Advancement of Science) (27.02.2009)
Published in Science (American Association for the Advancement of Science) (27.02.2009)
Get full text
Journal Article
Ancestral resurrection of the Drosophila S2E enhancer reveals accessible evolutionary paths through compensatory change
Martinez, Carlos, Rest, Joshua S, Kim, Ah-Ram, Ludwig, Michael, Kreitman, Martin, White, Kevin, Reinitz, John
Published in Molecular biology and evolution (01.04.2014)
Published in Molecular biology and evolution (01.04.2014)
Get full text
Journal Article
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish
Baranowska Körberg, Izabella, Hofmeister, Wolfgang, Markljung, Ellen, Cao, Jia, Nilsson, Daniel, Ludwig, Michael, Draaken, Markus, Holmdahl, Gundela, Barker, Gillian, Reutter, Heiko, Vukojević, Vladana, Clementson Kockum, Christina, Lundin, Johanna, Lindstrand, Anna, Nordenskjöld, Agneta
Published in Human molecular genetics (15.09.2015)
Published in Human molecular genetics (15.09.2015)
Get full text
Journal Article
Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula
Brosens, Erwin, Marsch, Florian, de Jong, Elisabeth M, Zaveri, Hitisha P, Hilger, Alina C, Choinitzki, Vera Gisela, Hölscher, Alice, Hoffmann, Per, Herms, Stefan, Boemers, Thomas M, Ure, Benno M, Lacher, Martin, Ludwig, Michael, Eussen, Bert H, van der Helm, Robert M, Douben, Hannie, Van Opstal, Diane, Wijnen, Rene M H, Beverloo, H Berna, van Bever, Yolande, Brooks, Alice S, IJsselstijn, Hanneke, Scott, Daryl A, Schumacher, Johannes, Tibboel, Dick, Reutter, Heiko, de Klein, Annelies
Published in European journal of human genetics : EJHG (01.12.2016)
Published in European journal of human genetics : EJHG (01.12.2016)
Get full text
Journal Article
Lowe syndrome/Dent-2 disease: A comprehensive review of known and novel aspects
Recker, Florian, Reutter, Heiko, Ludwig, Michael
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2013)
Published in Journal of pediatric genetics (Birmingham, Ala.) (01.06.2013)
Get full text
Journal Article
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions
Krutzke, Sophia K, Engels, Hartmut, Hofmann, Andrea, Schumann, Madita M, Cremer, Kirsten, Zink, Alexander M, Hilger, Alina, Ludwig, Michael, Gembruch, Ulrich, Reutter, Heiko, Merz, Waltraut M
Published in Birth defects research. A Clinical and molecular teratology (01.01.2016)
Published in Birth defects research. A Clinical and molecular teratology (01.01.2016)
Get more information
Journal Article
Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?
Kause, Franziska, Reutter, Heiko, Marsch, Florian, Thiele, Holger, Altmüller, Janine, Ludwig, Michael, Zhang, Rong
Published in Molecular medicine reports (01.02.2018)
Published in Molecular medicine reports (01.02.2018)
Get full text
Journal Article