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Institution

Heidelberg University

EducationHeidelberg, Germany
About: Heidelberg University is a education organization based out in Heidelberg, Germany. It is known for research contribution in the topics: Population & Transplantation. The organization has 62066 authors who have published 119109 publications receiving 4678423 citations. The organization is also known as: Ruprecht-Karls-Universität Heidelberg & University of Heidelberg.
Topics: Population, Transplantation, Galaxy, Cancer, Stars


Papers
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Journal ArticleDOI
Dominik Sturm1, Hendrik Witt2, Hendrik Witt1, Volker Hovestadt1, Dong Anh Khuong-Quang3, David T.W. Jones1, Carolin Konermann1, Elke Pfaff1, Martje Tönjes1, Martin Sill1, Sebastian Bender1, Marcel Kool1, Marc Zapatka1, Natalia Becker1, Manuela Zucknick1, Thomas Hielscher1, Xiaoyang Liu3, Adam M. Fontebasso4, Marina Ryzhova, Steffen Albrecht4, Karine Jacob3, Marietta Wolter5, Martin Ebinger6, Martin U. Schuhmann6, Timothy E. Van Meter7, Michael C. Frühwald8, Holger Hauch, Arnulf Pekrun, Bernhard Radlwimmer1, Tim Niehues9, Gregor Von Komorowski, Matthias Dürken, Andreas E. Kulozik2, Jenny Madden10, Andrew M. Donson10, Nicholas K. Foreman10, Rachid Drissi11, Maryam Fouladi11, Wolfram Scheurlen9, Andreas von Deimling2, Andreas von Deimling1, Camelia M. Monoranu12, Wolfgang Roggendorf12, Christel Herold-Mende2, Andreas Unterberg2, Christof M. Kramm13, Jörg Felsberg5, Christian Hartmann14, Benedikt Wiestler2, Wolfgang Wick2, Till Milde1, Till Milde2, Olaf Witt2, Olaf Witt1, Anders Lindroth1, Jeremy Schwartzentruber3, Damien Faury3, Adam Fleming3, Magdalena Zakrzewska15, Pawel P. Liberski15, Krzysztof Zakrzewski16, Peter Hauser17, Miklós Garami17, Almos Klekner18, László Bognár18, Sorana Morrissy19, Florence M.G. Cavalli19, Michael D. Taylor19, Peter van Sluis20, Jan Koster20, Rogier Versteeg20, Richard Volckmann20, Tom Mikkelsen21, Kenneth Aldape22, Guido Reifenberger5, V. Peter Collins23, Jacek Majewski3, Andrey Korshunov1, Peter Lichter1, Christoph Plass1, Nada Jabado3, Stefan M. Pfister2, Stefan M. Pfister1 
TL;DR: It is demonstrated that each H3F3A mutation defines an epigenetic subgroup of GBM with a distinct global methylation pattern, and that they are mutually exclusive with IDH1 mutations, which characterize a third mutation-defined subgroup.

1,557 citations

Journal ArticleDOI
TL;DR: In this article, a new exact evolution equation for the scale dependence of an effective action was derived, which allows one to deal with the infrared problems of theories with massless modes in less than four dimensions which are relevant for the high temperature phase transition in particle physics or the computation of critical exponents in statistical mechanics.

1,557 citations

Journal ArticleDOI
22 Feb 2013-Science
TL;DR: A melanoma-prone family through linkage analysis and high-throughput sequencing was investigated and a disease-segregating germline mutation in the promoter of the telomerase reverse transcriptase (TERT) gene, which encodes the catalytic subunit of telomersase, caused up to twofold increase in transcription.
Abstract: Cutaneous melanoma occurs in both familial and sporadic forms. We investigated a melanoma-prone family through linkage analysis and high-throughput sequencing and identified a disease-segregating germline mutation in the promoter of the telomerase reverse transcriptase (TERT) gene, which encodes the catalytic subunit of telomerase. The mutation creates a new binding motif for Ets transcription factors and ternary complex factors (TCFs) near the transcription start and, in reporter gene assays, caused up to twofold increase in transcription. We then screened the TERT promoter in sporadic melanoma and observed recurrent ultraviolet signature somatic mutations in 125 of 168 (74%) of human cell lines derived from metastatic melanomas, 45 of 53 corresponding metastatic tumor tissues (85%), and 25 of 77 (33%) primary melanomas. The majority of those mutations occurred at two positions in the TERT promoter and also generated binding motifs for Ets/TCF transcription factors.

1,557 citations

Journal ArticleDOI
TL;DR: The expression patterns of 13 GABAA receptor subunit encoding genes (alpha 1-alpha 6, beta 1-beta 3, gamma 1-gamma 3, delta) were determined in adult rat brain by in situ hybridization as discussed by the authors.
Abstract: The expression patterns of 13 GABAA receptor subunit encoding genes (alpha 1-alpha 6, beta 1-beta 3, gamma 1-gamma 3, delta) were determined in adult rat brain by in situ hybridization. Each mRNA displayed a unique distribution, ranging from ubiquitous (alpha 1 mRNA) to narrowly confined (alpha 6 mRNA was present only in cerebellar granule cells). Some neuronal populations coexpressed large numbers of subunit mRNAs, whereas in others only a few GABAA receptor-specific mRNAs were found. Neocortex, hippocampus, and caudate-putamen displayed complex expression patterns, and these areas probably contain a large diversity of GABAA receptors. In many areas, a consistent coexpression was observed for alpha 1 and beta 2 mRNAs, which often colocalized with gamma 2 mRNA. The alpha 1 beta 2 combination was abundant in olfactory bulb, globus pallidus, inferior colliculus, substantia nigra pars reticulata, globus pallidus, zona incerta, subthalamic nucleus, medial septum, and cerebellum. Colocalization was also apparent for the alpha 2 and beta 3 mRNAs, and these predominated in areas such as amygdala and hypothalamus. The alpha 3 mRNA occurred in layers V and VI of neocortex and in the reticular thalamic nucleus. In much of the forebrain, with the exception of hippocampal pyramidal cells, the alpha 4 and delta transcripts appeared to codistribute. In thalamic nuclei, the only abundant GABAA receptor mRNAs were those of alpha 1, alpha 4, beta 2, and delta. In the medial geniculate thalamic nucleus, alpha 1, alpha 4, beta 2, delta, and gamma 3 mRNAs were the principal GABAA receptor transcripts. The alpha 5 and beta 1 mRNAs generally colocalized and may encode predominantly hippocampal forms of the GABAA receptor. These anatomical observations support the hypothesis that alpha 1 beta 2 gamma 2 receptors are responsible for benzodiazepine I (BZ I) binding, whereas receptors containing alpha 2, alpha 3, and alpha 5 contribute to subtypes of the BZ II site. Based on significant mismatches between alpha 4/delta and gamma mRNAs, we suggest that in vivo, the alpha 4 subunit contributes to GABAA receptors that lack BZ modulation.

1,557 citations

Journal ArticleDOI
P. L. Nolan1, A. A. Abdo2, A. A. Abdo3, Markus Ackermann  +290 moreInstitutions (53)
TL;DR: The second Fermi-LAT catalog (2FGL) as mentioned in this paper includes source location regions, defined in terms of elliptical fits to the 95% confidence regions and spectral fits in terms either power-law, exponentially cutoff power law, or log-normal forms.
Abstract: We present the second catalog of high-energy γ-ray sources detected by the Large Area Telescope (LAT), the primary science instrument on the Fermi Gamma-ray Space Telescope (Fermi), derived from data taken during the first 24 months of the science phase of the mission, which began on 2008 August 4. Source detection is based on the average flux over the 24 month period. The second Fermi-LAT catalog (2FGL) includes source location regions, defined in terms of elliptical fits to the 95% confidence regions and spectral fits in terms of power-law, exponentially cutoff power-law, or log-normal forms. Also included are flux measurements in five energy bands and light curves on monthly intervals for each source. Twelve sources in the catalog are modeled as spatially extended. We provide a detailed comparison of the results from this catalog with those from the first Fermi-LAT catalog (1FGL). Although the diffuse Galactic and isotropic models used in the 2FGL analysis are improved compared to the 1FGL catalog, we attach caution flags to 162 of the sources to indicate possible confusion with residual imperfections in the diffuse model. The 2FGL catalog contains 1873 sources detected and characterized in the 100 MeV to 100 GeV range of which we consider 127 as being firmly identified and 1171 as being reliably associated with counterparts of known or likely γ-ray-producing source classes.

1,541 citations


Authors

Showing all 62427 results

NameH-indexPapersCitations
Nicholas G. Martin1921770161952
Jing Wang1844046202769
Chris Sander178713233287
Kenneth C. Anderson1781138126072
Zena Werb168473122629
Marc Weber1672716153502
Volker Springel165746123399
Ira Pastan1601286110069
Wolfgang Wagner1562342123391
Jovan Milosevic1521433106802
Hermann Brenner1511765145655
Robert J. Sternberg149106689193
Margaret A. Pericak-Vance149826118672
Andreas Pfeiffer1491756131080
Rajesh Kumar1494439140830
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023191
2022729
20216,243
20206,124
20195,659
20185,388