I. Bartsch

发表

A transcription terminator located upstream of the mouse rDNA initiation site affects rRNA synthesis

H. Rosenbauer, I. Grummt, A. Kuhn, 1986, Cell.

Purification and characterization of TTFI, a factor that mediates termination of mouse ribosomal DNA transcription

I. Grummt, I. Bartsch, C. Schoneberg, 1988, Molecular and cellular biology.

Novel mutation in two brothers with Hermansky Pudlak syndrome type 3.

U. Koehler, B. Zieger, C. Simon-Gabriel, 2017, Blood cells, molecules & diseases.

Human endothelial cell septins: SEPT11 is an interaction partner of SEPT5

M. Huber, H. Rempp, B. Zieger, 2006, The Journal of pathology.

Characterization of human septin interactions

B. Zieger, I. Bartsch, K. Sandrock, 2011, Biological chemistry.

Septin Expression in Proliferative Retinal Membranes

J. Flammer, C. Prünte, B. Zieger, 2007, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Salmonella strains and mammalian cells genetically engineered for expression of sulfotransferases.

H. Glatt, C. Falany, A. Seidel, 1995, Toxicology letters.

Sulfotransferase-mediated activation of mutagens studied using heterologous expression systems.

H. Glatt, C. Falany, D. Phillips, 1998, Chemico-biological interactions.

Human endothelial and platelet septin SEPT11: Cloning of novel variants and characterisation of interaction partners

M. Huber, H. Rempp, B. Zieger, 2010, Thrombosis and Haemostasis.

Characterization of thyroid hormone sulfotransferases.

H. Glatt, T. Visser, M. Coughtrie, 1998, Chemico-biological interactions.

Specific interaction of the murine transcription termination factor TTF I with class-I RNA polymerases

I. Grummt, A. Kuhn, I. Bartsch, 1990, Nature.

Expression of human estrogen sulfotransferase in Salmonella typhimurium: differences between hHST and hEST in the enantioselective activation of 1-hydroxyethylpyrene to a mutagen.

H. Glatt, C. Falany, R. Landsiedel, 1998, Chemico-biological interactions.

Evolutionary changes of sequences and factors that direct transcription termination of human and mouse ribsomal genes

I. Grummt, I. Bartsch, C. Schoneberg, 1987, Molecular and cellular biology.

A large Swiss family with Bernard-Soulier syndrome

B. Zieger, W. Wuillemin, I. Bartsch, 2009, Hämostaseologie.

Novel mutation in Hermansky–Pudlak syndrome type 2 with mild immunological phenotype

S. Ehl, G. Schmitz, C. Aslanidis, 2013, Platelets.

Stable heterologous expression of hydroxysteroid sulphotransferase in Chinese hamster V79 cells and their use for toxicological investigations.

H. Glatt, A. Czich, S. Hornhardt, 1994, Chemico-biological interactions.

An undecamer DNA sequence directs termination of human ribosomal gene transcription.

I. Grummt, I. Bartsch, A. Smid, 1990, Nucleic acids research.

The mouse ribosomal gene terminator consists of three functionally separable sequence elements.

I. Grummt, A. Kuhn, I. Bartsch, 1988, The EMBO journal.

Deletion of human GP 1 BB and SEPT 5 is associated with Bernard-Soulier syndrome , platelet secretion defect , polymicrogyria , and develop-mental delay

P. Nurden, J. Oldenburg, I. Hainmann, 2018 .

Septins, a Novel Group of GTP-binding Proteins – Relevance in Hemostasis, Neuropathology and Oncogenesis

B. Zieger, I. Bartsch, K. Sandrock, 2009, Klinische Padiatrie.

Activation of propane 2-nitronate to a genotoxicant in V79-derived cell lines engineered for the expression of rat hepatic sulfotransferases.

H. Glatt, W. Meinl, M. Coughtrie, 1999, Mutation research.

Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay

P. Nurden, J. Oldenburg, I. Hainmann, 2011, Thrombosis and Haemostasis.

Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I.

W. Behnisch, A. Kulozik, A. Superti-Furga, 2010, Klinische Padiatrie.

Lethal phenotype of mice carrying a Sept11 null mutation

H. Omran, N. Loges, B. Zieger, 2011, Biological chemistry.

Compound Heterozygous Mutations in 2 Siblings with Hermansky-Pudlak Syndrome Type 1 (HPS1)

I. Hainmann, B. Zieger, I. Bartsch, 2010, Klinische Padiatrie.