B. Hartmann

发表

Decrypting the genome's alternative messages.

B. Hartmann, J. Valcárcel, 2009, Current opinion in cell biology.

Genome-wide Analysis of Alternative Pre-mRNA Splicing*

Britta Hartmann, Juan Valcárcel, B. Hartmann, 2008, Journal of Biological Chemistry.

Alternative splicing in Drosophila neuronal development

B. Hartmann, Carmen Mohr, 2014, Journal of neurogenetics.

Year : 2004 A simple molecular complex mediates widespread BMP-induced repression during Drosophila development

B. Hartmann, G. Pyrowolakis, M. Affolter, 2006 .

Sex-Specific Transcript Diversity in the Fly Head Is Established during Pupal Stages and Adulthood and Is Largely Independent of the Mating Process and the Germline

B. Hartmann, M. Blanchette, G. Pyrowolakis, 2017, Sexual Development.

How to Detect Isolated PEX10-Related Cerebellar Ataxia?

B. Hartmann, S. Thoms, E. Boltshauser, 2022, Neuropediatrics.

Loss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.

Mark T. Handley, B. Hartmann, A. Ebert, 2013, American journal of human genetics.

Tyrosinemia type II: Mutation update, 11 novel mutations and description of 5 independent subjects with a novel founder mutation

B. Hartmann, P. Huppke, C. Pérez-Cerdá, 2017, Clinical genetics.

Global analysis of alternative splicing regulation by insulin and wingless signaling in Drosophila cells

B. Hartmann, J. Valcárcel, R. Castelo, 2009, Genome Biology.

Combinatorial Gene Regulatory Functions Underlie Ultraconserved Elements in Drosophila

Britta Hartmann, B. Hartmann, Maria Warnefors, 2016, Molecular biology and evolution.

Results A Novel Approach for UCE Identification Finds More than 1 , 500 UCEs Shared across 12 Drosophila Genomes

B. Hartmann, Maria Warnefors, C. Alonso, 2016 .

HOX genes in the sepiolid squid Euprymna scolopes: Implications for the evolution of complex body plans

B. Hartmann, K. Fischbach, K. Ikeo, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantation.

B. Hartmann, C. Klein, J. Puck, 2013, The Journal of allergy and clinical immunology.

Distinct regulatory programs establish widespread sex-specific alternative splicing in Drosophila melanogaster.

B. Hartmann, J. Valcárcel, R. Castelo, 2011, RNA.

Pax6 in the sepiolid squid Euprymna scolopes: evidence for a role in eye, sensory organ and brain development

B. Hartmann, P. Callaerts, Patricia N. Lee, 2003, Mechanisms of Development.

160 kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndrome.

B. Hartmann, D. Wieczorek, T. Rosenbaum, 2013, European journal of medical genetics.

A simple molecular complex mediates widespread BMP-induced repression during Drosophila development.

Markus Affolter, Konrad Basler, Bruno Müller, 2004, Developmental cell.

Conversion of an Extracellular Dpp/BMP Morphogen Gradient into an Inverse Transcriptional Gradient

Markus Affolter, Konrad Basler, Bruno Müller, 2003, Cell.

Characterization of Schnurri : an integral component of the Dpp-signaling pathway in "Drosophila melanogaster"

B. Hartmann, 2004 .

Monoallelic Large Intragenic KRT5 Deletions Account for Genetically Unsolved Cases of Epidermolysis Bullosa Simplex.

B. Hartmann, C. Has, J. Kohlhase, 2017, The Journal of investigative dermatology.

DNA recognition by the brinker repressor--an extreme case of coupling between binding and folding.

B. Hartmann, S. Grzesiek, M. Affolter, 2006, Journal of molecular biology.

17 TGF-β Family Signaling in Drosophila

B. Hartmann, G. Pyrowolakis, M. Affolter, 2008 .

A novel mutation in the ABCA12 gene in a Turkish case of Harlequin ichthyosis

B. Hartmann, H. Gürkan, H. Tozkır, 2015, Clinical dysmorphology.

Cerebellar ataxia, mental retardation and dysequilibrium syndrome 1 (CAMRQ1) caused by an unusual constellation of VLDLR mutation

B. Hartmann, J. Gärtner, D. Morris-Rosendahl, 2013, Journal of Neurology.

Large deletions in the NSDHL gene in two patients with CHILD syndrome.

B. Hartmann, R. Happle, J. Fischer, 2015, Acta Dermato-Venereologica.

HOX genes in the sepiolid sq Implications for the evolutiol

B. Hartmann, P. Callaerts, Patricia N. Lee, 2016 .

Large homozygous RAB3GAP1 gene microdeletion causes Warburg Micro Syndrome 1

B. Hartmann, D. Horn, E. Klopocki, 2014, Orphanet Journal of Rare Diseases.

Distinct regulatory programs establish widespread sex-specific alternative splicing in Drosophila melanogaster.

B. Hartmann, J. Valcárcel, R. Castelo, 2011, RNA.