Tauroursodeoxycholic acid reduces endoplasmic reticulum stress, trypsin activation, and acinar cell apoptosis while increasing secretion in rat pancreatic acini
Malo, A, Krüger, B, Seyhun, E, Schäfer, C, Hoffmann, R T, Göke, B, Kubisch, C H
Published in American journal of physiology: Gastrointestinal and liver physiology (01.10.2010)
Published in American journal of physiology: Gastrointestinal and liver physiology (01.10.2010)
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Journal Article
Clinical and genetic findings in a family with NMNAT1-associated Leber congenital amaurosis: case report and review of the literature
Hedergott, A., Volk, A. E., Herkenrath, P., Thiele, H., Fricke, J., Altmüller, J., Nürnberg, P., Kubisch, C., Neugebauer, A.
Published in Graefe's archive for clinical and experimental ophthalmology (01.12.2015)
Published in Graefe's archive for clinical and experimental ophthalmology (01.12.2015)
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Journal Article
Radiofrequency ablation after selective internal radiation therapy with Yttrium90 microspheres in metastatic liver disease—Is it feasible?
Hoffmann, R.T, Jakobs, T.F, Kubisch, C.H, Stemmler, H.J, Trumm, C, Tatsch, K, Helmberger, T.K, Reiser, M.F
Published in European journal of radiology (01.04.2010)
Published in European journal of radiology (01.04.2010)
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Journal Article
V42. De novo mutations in the FUS gene are a frequent cause of sporadic ALS in very young patients
Hübers, A, Volk, A, Just, W, Rosenbohm, A, Bierbaumer, N, Kathrin, M, Nicolai, M, Ingrid, G, Josef, H, Janine, A, Holger, T, Nürnberg, P, Weishaupt, J.H, Kubisch, C, Ludolph, A.C
Published in Clinical neurophysiology (01.08.2015)
Published in Clinical neurophysiology (01.08.2015)
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Journal Article
A Potassium Channel Mutation in Neonatal Human Epilepsy
Biervert, Christian, Schroeder, Björn C., Kubisch, Christian, Berkovic, Samuel F., Propping, Peter, Jentsch, Thomas J., Steinlein, Ortrud K.
Published in Science (American Association for the Advancement of Science) (16.01.1998)
Published in Science (American Association for the Advancement of Science) (16.01.1998)
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Journal Article
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression
Wilch, E, Azaiez, H, Fisher, RA, Elfenbein, J, Murgia, A, Birkenhäger, R, Bolz, H, Da Silva-Costa, SM, Del Castillo, I, Haaf, T, Hoefsloot, L, Kremer, H, Kubisch, C, Le Marechal, C, Pandya, A, Sartorato, EL, Schneider, E, Van Camp, G, Wuyts, W, Smith, RJH, Friderici, KH
Published in Clinical genetics (01.09.2010)
Published in Clinical genetics (01.09.2010)
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Journal Article
High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel
Borck, G, Rainshtein, L, Hellman-Aharony, S, Volk, AE, Friedrich, K, Taub, E, Magal, N, Kanaan, M, Kubisch, C, Shohat, M, Basel-Vanagaite, L
Published in Clinical genetics (01.09.2012)
Published in Clinical genetics (01.09.2012)
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Journal Article
Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDS
FISCHER, Dirk, WALTER, Maggie C, URBACH, Horst, SCHRÖDER, Rolf, KESPER, Kristina, PETERSEN, Jens A, AURINO, Stefania, NIGRO, Vincenzo, KUBISCH, Christian, MEINDL, Thomas, LOCHMÜLLER, Hanns, WILHELM, Kai
Published in Journal of neurology (01.05.2005)
Published in Journal of neurology (01.05.2005)
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Journal Article
Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias
Wollnik, Bernd, Schroeder, Björn C., Kubisch, Christian, Esperer, Hans D., Wieacker, Peter, Jentsch, Thomas J.
Published in Human molecular genetics (01.10.1997)
Published in Human molecular genetics (01.10.1997)
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Journal Article
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation
Vorgerd, M, Ricker, K, Ziemssen, F, Kress, W, Goebel, H H, Nix, W A, Kubisch, C, Schoser, B G, Mortier, W
Published in Neurology (26.12.2001)
Published in Neurology (26.12.2001)
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Journal Article
Genetic Association Study of Endothelin-1 and Its Receptors EDNRA and EDNRB in Migraine with Aura
Tikka-Kleemola, P, Kaunisto, MA, Hämäläinen, E, Todt, U, Göbel, H, Kaprio, J, Kubisch, C, Färkkilä, M, Palotie, A, Wessman, M, Kallela, M
Published in Cephalalgia (01.11.2009)
Published in Cephalalgia (01.11.2009)
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Journal Article
KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness
Kubisch, Christian, Schroeder, Björn C, Friedrich, Thomas, Lütjohann, Björn, El-Amraoui, Aziz, Marlin, Sandrine, Petit, Christine, Jentsch, Thomas J
Published in Cell (05.02.1999)
Published in Cell (05.02.1999)
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Journal Article
Improved visualization of carotid-jugular arteriovenous fistula by contrast-enhanced ultrasound
Clevert, D-A, Kubisch, C, Meimarakis, G, Zengel, P, Reiser, M
Published in Ultraschall in der Medizin (01.12.2010)
Published in Ultraschall in der Medizin (01.12.2010)
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Journal Article
Automatic Transfer Function Specification for Visual Emphasis of Coronary Artery Plaque
Glaßer, S., Oeltze, S., Hennemuth, A., Kubisch, C., Mahnken, A., Wilhelmsen, S., Preim, B.
Published in Computer graphics forum (01.03.2010)
Published in Computer graphics forum (01.03.2010)
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Journal Article
ClC-1 Chloride Channel Mutations in Myotonia Congenita: Variable Penetrance of Mutations Shifting the Voltage Dependence
Kubisch, Christian, Schmidt-Rose, Thomas, Fontaine, Bertrand, Bretag, Allan H., Jentsch, Thomas J.
Published in Human molecular genetics (01.10.1998)
Published in Human molecular genetics (01.10.1998)
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Journal Article
Variation of the serotonin transporter gene SLC6A4 in the susceptibility to migraine with aura
Todt, U, Freudenberg, J, Goebel, I, Heinze, A, Heinze-Kuhn, K, Rietschel, M, Göbel, H, Kubisch, C
Published in Neurology (14.11.2006)
Published in Neurology (14.11.2006)
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