1. Characterization of a DmdEGFP reporter mouse as a tool to investigate dystrophin expression. Issue 1 (December 2016) Authors: Petkova, Mina; Morales-Gonzales, Susanne; Relizani, Karima; Gill, Esther; Seifert, Franziska; Radke, Josefine; Stenzel, Werner; Garcia, Luis; Amthor, Helge; Schuelke, Markus Journal: Skeletal muscle Issue: Volume 6:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Crucial Role of the Chaperonin GroES/EL for Heterologous Production of the Soluble Methane Monooxygenase from Methylomonas methanica MC09. (29th April 2022) Authors: Zill, Domenic; Lettau, Elisabeth; Lorent, Christian; Seifert, Franziska; Singh, Praveen K.; Lauterbach, Lars Journal: Chembiochem Issue: Volume 23:Number 12(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. MORC2 mutation causes severe spinal muscular atrophy-phenotype, cerebellar atrophy, and diaphragmatic paralysis. (29th October 2016) Authors: Schottmann, Gudrun; Wagner, Christiane; Seifert, Franziska; Stenzel, Werner; Schuelke, Markus Journal: Brain Issue: Volume 139:Part 12(2016:Dec.) Page Start: e70 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Recessive DEAF1 mutation associates with autism, intellectual disability, basal ganglia dysfunction and epilepsy. Issue 9 (5th June 2015) Authors: Rajab, Anna; Schuelke, Markus; Gill, Esther; Zwirner, Angelika; Seifert, Franziska; Morales Gonzalez, Susanne; Knierim, Ellen Journal: Journal of medical genetics Issue: Volume 52:Issue 9(2015) Page Start: 607 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Recessive REEP1 mutation is associated with congenital axonal neuropathy and diaphragmatic palsy. (December 2015) Authors: Schottmann, Gudrun; Seelow, Dominik; Seifert, Franziska; Morales-Gonzalez, Susanne; Gill, Esther; von Au, Katja; von Moers, Arpad; Stenzel, Werner; Schuelke, Markus Journal: Neurology Issue: Volume 1:Number 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Recessive truncating IGHMBP2 mutations presenting as axonal sensorimotor neuropathy. (3rd February 2015) Authors: Schottmann, Gudrun; Jungbluth, Heinz; Schara, Ulrike; Knierim, Ellen; Morales Gonzalez, Susanne; Gill, Esther; Seifert, Franziska; Norwood, Fiona; Deshpande, Charu; von Au, Katja; Schuelke, Markus; Senderek, Jan Journal: Neurology Issue: Volume 84:Number 5(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Synthesis and biological investigation of new carbonic anhydrase IX (CAIX) inhibitors. (25th March 2018) Authors: Vanchanagiri, Kranthi; Emmerich, Daniel; Bruschke, Monique; Bache, Matthias; Seifert, Franziska; Csuk, René; Vordermark, Dirk; Paschke, Reinhard Journal: Chemico-biological interactions Issue: Volume 284(2018) Page Start: 12 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗