Manfred Gessler

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Genel erişim

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59 makale

13 makale

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Finansman sağlayan kuruluşun getirdiği zorunluluğa dayalı olarak

Katkıda bulunan yazarlar

Norbert GrafProfessor of Paediatric Oncologyuks.eu üzerinde doğrulanmış e-posta adresine sahip
Andreas FischerProfessor for Clinical Chemistry, Göttingen Universitymed.uni-goettingen.de üzerinde doğrulanmış e-posta adresine sahip
Gordan VujanicSidra Medicine, Doha, Qatarsidra.org üzerinde doğrulanmış e-posta adresine sahip
Prof. Dr. Hans-Peter LenhofCenter for Bioinformatics, Saarland Informatics Campus, Saarland Universitybioinf.uni-sb.de üzerinde doğrulanmış e-posta adresine sahip
Eckart MeeseProfessor für Humangenetik, Saarland Universityuks.eu üzerinde doğrulanmış e-posta adresine sahip
Harm van TinterenHoofd Trial en Datacentrum, Prinses Maxima Centrumprinsesmaximacentrum.nl üzerinde doğrulanmış e-posta adresine sahip
Webster CaveneeLudwig Institute, University of California San Diegoucsd.edu üzerinde doğrulanmış e-posta adresine sahip
Andreas KellerProfessor for Clinical Bioinformatics, Center for Bioinformatics, Saarland Informatics Campusccb.uni-saarland.de üzerinde doğrulanmış e-posta adresine sahip
Nicole LudwigSaarland Universitymx.uni-saarland.de üzerinde doğrulanmış e-posta adresine sahip
Stuart Orkindfci.harvard.edu üzerinde doğrulanmış e-posta adresine sahip
Maureen O'SullivanTrinity College, OR the national Children's Research Centre OR Our lady's Children's Hospital ORtcd.ie üzerinde doğrulanmış e-posta adresine sahip
Michael SendtnerProfessor of Clinical Neurobiology, Wuerzburg University, Germanymail.uni-wuerzburg.de üzerinde doğrulanmış e-posta adresine sahip
Tim KehlAlgorithm Engineer, AI Lab Saarbrücken, ZF Groupbioinf.uni-sb.de üzerinde doğrulanmış e-posta adresine sahip
Georges NemerProfessor of Genomics and Precision Medicine, Hamad Bin Khalifa Universityhbku.edu.qa üzerinde doğrulanmış e-posta adresine sahip
Benoit G. BruneauSenior Investigator, Gladstone Institute of Cardiovascular Disease; Professor of Pediatrics, UCSFgladstone.ucsf.edu üzerinde doğrulanmış e-posta adresine sahip
Mona Nemeruniversity of ottawauottawa.ca üzerinde doğrulanmış e-posta adresine sahip
Birgit SamansTechnische Hochschule Mittelhessen/Faculty of Health Sciencesges.thm.de üzerinde doğrulanmış e-posta adresine sahip
Torsten PietschProfessor and Chairman, Institute of Neuropathology, University of Bonnuni-bonn.de üzerinde doğrulanmış e-posta adresine sahip
Helen McNeillWashington University School of Medicine in St. Louis, University of Toronto , Lunenfeld Tanenbaumlunenfeld.ca üzerinde doğrulanmış e-posta adresine sahip
David GisselssonProfessor of Molecular Pathology, Lund Universitymed.lu.se üzerinde doğrulanmış e-posta adresine sahip

Takip et

Manfred Gessler

Biocenter, Dev. Biochemistry, Wuerzburg University

biozentrum.uni-wuerzburg.de üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa

Pediatric kidney tumors Molecular genetics


Başlık Alıntılara göre sırala Yıla göre sırala Başlığa göre sırala	Alıntı yapanlar Alıntı yapanlar	Yıl
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping M Gessler, A Poustka, W Cavenee, RL Neve, SH Orkin, GAP Bruns Nature 343 (6260), 774-778, 1990	1656	1990
The landscape of genomic alterations across childhood cancers SN Gröbner, BC Worst, J Weischenfeldt, I Buchhalter, K Kleinheinz, ... Nature 555 (7696), 321-327, 2018	1495	2018
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease BG Bruneau, G Nemer, JP Schmitt, F Charron, L Robitaille, S Caron, ... Cell 106 (6), 709-721, 2001	1253	2001
The Notch target genes Hey1 and Hey2 are required for embryonic vascular development A Fischer, N Schumacher, M Maier, M Sendtner, M Gessler Genes & development 18 (8), 901-911, 2004	832	2004
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families A Vortkamp, M Gessler, KH Grzeschik Nature 352, 539-540, 1991	675	1991
Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease S Saburi, I Hester, E Fischer, M Pontoglio, V Eremina, M Gessler, ... Nature genetics 40 (8), 1010-1015, 2008	585	2008
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ... Nature genetics 45 (9), 1044-1049, 2013	572	2013
Delta–Notch—and then? Protein interactions and proposed modes of repression by Hes and Hey bHLH factors A Fischer, M Gessler Nucleic acids research 35 (14), 4583-4596, 2007	515	2007
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1+/− KTS splice isoforms B Klamt, A Koziell, F Poulat, P Wieacker, P Scambler, P Berta, M Gessler Human molecular genetics 7 (4), 709-714, 1998	459	1998
Epithelial Notch signaling regulates interstitial fibrosis development in the kidneys of mice and humans B Bielesz, Y Sirin, H Si, T Niranjan, A Gruenwald, S Ahn, H Kato, ... The Journal of clinical investigation 120 (11), 4040-4054, 2010	410	2010
Sarcoma classification by DNA methylation profiling C Koelsche, D Schrimpf, D Stichel, M Sill, F Sahm, DE Reuss, M Blattner, ... Nature communications 12 (1), 498, 2021	398	2021
Spectrum of hSNF5IINI1 somatic mutations in human cancer and genotype-phenotype correlations N Sévenet, A Lellouch-Tubiana, D Schofield, K Hoang-Xuan, M Gessler, ... Human molecular genetics 8 (13), 2359-2368, 1999	346	1999
Rationale for the treatment of Wilms tumour in the UMBRELLA SIOP–RTSG 2016 protocol MM Van Den Heuvel-eibrink, JA Hol, K Pritchard-Jones, H Van Tinteren, ... Nature Reviews Urology 14 (12), 743-752, 2017	343	2017
Mutations in the SIX1/2 pathway and the DROSHA/DGCR8 miRNA microprocessor complex underlie high-risk blastemal type Wilms tumors J Wegert, N Ishaque, R Vardapour, C Geörg, Z Gu, M Bieg, B Ziegler, ... Cancer cell 27 (2), 298-311, 2015	339	2015
Hey genes: a novel subfamily of hairy-and Enhancer of split related genes specifically expressed during mouse embryogenesis C Leimeister, A Externbrink, B Klamt, M Gessler Mechanisms of development 85 (1-2), 173-177, 1999	325	1999
Hypoxia-mediated activation of Dll4-Notch-Hey2 signaling in endothelial progenitor cells and adoption of arterial cell fate H Diez, A Fischer, A Winkler, CJ Hu, AK Hatzopoulos, G Breier, M Gessler Experimental cell research 313 (1), 1-9, 2007	304	2007
Comparative analysis of the human and mouse Hey1 promoter: Hey genes are new Notch target genes MM Maier, M Gessler Biochemical and biophysical research communications 275 (2), 652-660, 2000	300	2000
Integrated regulation of Toll-like receptor responses by Notch and interferon-γ pathways X Hu, AY Chung, I Wu, J Foldi, J Chen, JD Ji, T Tateya, YJ Kang, J Han, ... Immunity 29 (5), 691-703, 2008	287	2008
Hey2 regulation by FGF provides a Notch-independent mechanism for maintaining pillar cell fate in the organ of Corti A Doetzlhofer, ML Basch, T Ohyama, M Gessler, AK Groves, N Segil Developmental cell 16 (1), 58-69, 2009	276	2009
The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol GM Vujanić, M Gessler, AHAG Ooms, P Collini, A Coulomb-l’Hermine, ... Nature Reviews Urology 15 (11), 693-701, 2018	251	2018

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