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Neue Krankheit entdeckt - Innovations-Report
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Detlev Schindler vom Institut für Humangenetik der Universität ...
"Er neigte ein wenig zur Fülle" | Lokalsport
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WER ERKENNT WEN Detlev Schindler war nicht nur Torhüter, sondern auch Trainer und Schiedsrichter. Die Fußballplätze in der Region ...
Physicians & MDs
Autor: Detlev Schindler - PubMed | Infodoctor
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Últimas Publicaciones. A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.
Network Profiles
LinkedIn: Detlev Schindler | LinkedIn
Detlev Schindlers berufliches Profil anzeigen LinkedIn ist das weltweit größte berufliche Netzwerk, das Fach- und Führungskräften wie Detlev Schindler dabei ...
Interests
EDC4: New gene involved in familial breast cancer | EurekAlert ...
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Milan (Italy); Detlev Schindler from the University of Wurzburg, ...
New gene mutation associated with defective DNA repair and Fanconi...
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Fanconi anemia is a rare genetic disease characterized by hematologic symptoms and high cancer risk. Mutations in nearly 20 different genes have been...
Table of contents | Journal of Medical Genetics
jmg.bmj.com
Nienke J H van Os, Luciana Chessa, Corry M R Weemaes, Marcel van Deuren, Alice Fiévet, Judith van Gaalen, Nizar Mahlaoui, Nel Roeleveld, Christoph Schrader, Detlev Schindler, Alexander M R Taylor, Bart P C Van de Warrenburg, Thilo Dörk, Michèl A A P Willemsen
Business Profiles
Xing: Detlev Schindler - Principal Scientist - Medizinisches Xing
oder kontaktieren Sie Detlev Schindler direkt bei XING.
Researchgate: Detlev Schindler
Würzburg, Bavaria, Germany
Celebrities & Politicians
Schindler, Detlev in "Dizionario di Medicina"
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Schindler, Detlev
Pediatra e genetista tedesco. Prof., dal 1997, nel dipartimento di genetica umana dell’univ. di Würzburg. Il suo campo di ricerca comprende...
Books & Literature
Detlev Schindler | Longdom Publishing SL
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https://www.longdom.org/author-profile/detlev-schindler
Cached
Detlev Schindler , Journal of Genetic Syndromes & Gene Therapy.
Diagnostic Cytogenetics - Google Books Result
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Anemia and Related Hematological Disorders DETLEV SCHINDLER AND ...
Carbohydrate and Glycoprotein Metabolism; Maternal Phenylketonuria -...
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394 finding by Dr C. Jakobs, Amsterdam, was elevated plasma galactitol and/or sorbitol levels in some cataract patients with quite normal activities of the...
Diagnostic Cytogenetics - Google Books
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Flow Cytometric Testing for Syndromes with Chromosomal Instability, Aplastic Anemia and Related Hematological Disorders DETLEV SCHINDLER AND ...
Related Documents
References Subscriptions Permissions Email Alerts A Severe ...
citeseerx.ist.psu.edu
References Subscriptions Permissions Email Alerts A Severe Form of Human Combined Immunodeficiency Due to Mutations in DNA (2013) ... and Ulrich Duffner and Ulrich Pannicke and Elisabeth Nikolopoulos and Anke Peters and Marzenna Orlowska-volk and Detlev Schindler and Friedrich Barbara Selle and Anselm Enders and Paul Fisch and Klaus ...
Detlev Schindler - Academia.edu
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Detlev Schindler studies Cardiothoracic Surgery, Medical Education & Training, and Global Public Health.
CiteSeerX — Roles of brca2 (fancd1) in Oocyte Nuclear Architecture,...
citeseerx.ist.psu.edu
... Ruth A. Bremiller , Lin Yan , Indrajit N , Adam Johnston , John P. Kanki , Erin M. Gray , Xinjun He , Jan Spitsbergen , Detlev Schindler , John H. Postlethwait ...
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause ...
papers.ssrn.com
Campbell, Stefan Aretz, Detlev Schindler, Tom van Wezel, Nicoline ...
Scientific Publications
Premature Chromosome Condensation in Humans Associated with...
www.sciencedirect.com
Heidemarie Neitzel,; Luitgard M. Neumann,; Detlev Schindler,; Andreas Wirges,; Holger Tönnies,; Marc Trimborn,; Alice Krebsova,; Reyk Richter,; Karl ...
Exploring the link between MORF4L1 and risk of breast cancer | Breast...
breast-cancer-research.biomedcentral.com
... Anthony Renwick, Nazneen Rahman, Julia Kühl, Kornelia Neveling, Detlev Schindler, María J Ramírez, María Castellà, Gonzalo Hernández, ...
Prof. Schindler - Institut fuer Humangenetik
www.biozentrum.uni-wuerzburg.de
Detlev Schindler received his M.D. degree from the University of Würzburg School of Medicine. He is board certified in Pediatrics, Medical and Human Genetics. Since he is a Professor in the Department of Human Genetics. He heads the Division of Somatic Cell and biochemical Genetics within the Department of Human Genetics
Publications
Publications Authored by Detlev Schindler | PubFacts
www.pubfacts.com
Publications Authored by Detlev Schindler
Identification of the Fanconi Anemia Complementation Group I Gene,...
www.hindawi.com
... Haitjema,1 Sietske T. Bakker,1 Jûrgen Steltenpool,1 Dezsö Schuler,2 Sheila Mohan,3Detlev Schindler,4 Fré Arwert,1 Gerard Pals,1 Christopher G. Mathew,5 ...
Fanconi Anemia | SpringerLink
link.springer.com
Detlev Schindler, Kornelia Neveling, ... Fanconi–Turler syndrome, Landsteiner–Fanconi–Andersen syndrome, or Zinsser–Fanconi syndrome,
Mutation of the RAD51C gene in a Fanconi anemia-like disorder. |...
www.pubfacts.com
... , Marcel Freund, Linda Hartmann, David Grimwade, Roland G Roberts, Heiner Schaal, Shehla Mohammed, Nazneen Rahman, Detlev Schindler, Christopher G Mathew
Reports & Statements
Wikipedia: Schindler disease - Wikipedia
Schindler disease was named after Detlev Schindler ( ) M.D., the first author of a paper detailing the disease. It also named after the Japanese Biochemist and Physician, Hiro Kanzaki ( ), who further studied it and released papers detailing the disease in
Wikipedia: Talk:Schindler disease - Wikipedia
Who . Who is it named after? Rmhermen 02:59, 12 November (UTC) It was first called Schindler disease in 1988, after Detlev Schindler, M.D., the first author in
Microcephaly, short stature, and limb abnormality disorder ...
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· Author notes. These author contributed equally: Solveig Schulz, Martin A. Mensah, Detlev Schindler, and Karim Kentouche. Affiliations. Center of Human Genetics, Jena ...
nature.com search
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& Detlev Schindler. Nature Genetics 44, Research | 08 October Localisation of a Fanconi anaemia gene to chromosome 9p. Kathrin Saar, Detlev Schindler
Miscellaneous
Detlev Schindler | LinkedIn
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View Detlev Schindler's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Detlev Schindler discover
(PDF) New mutations in the ATM gene and clinical data of ...
www.academia.edu
Neurogenetics (2011) 12:273–282 DOI s ORIGINAL ARTICLE New mutations in the ATM gene and clinical data of 25 AT patients Ilja Demuth & Véronique Dutrannoy & Wilson Marques Jr & Heidemarie Neitzel & Detlev Schindler & Petja S. Dimova & Krystyna H. Chrzanowska & Veneta Bojinova & Hanna Gregorek & Luitgard M. Graul-Neumann & Arpad von Moers & Ilka Schulze …
A recurrent 11q aberration pattern characterizes a subset of ...
www.slaop.org
Grzegorz Rymkiewicz,18 Detlev Schindler,19 Matthias Schlesner,20 Rene´ Scholtysik,14 Carsten Schwaenen,21
New Disease Discovered - innovations-report.com
www.innovations-report.com
The woman's organism does not form enough RAD50 proteins. Moreover, the residual proteins do not execute their function sufficiently. "There are a residual quantity and a residual function, and possibly this is the only reason why the patient is still alive", says Detlev Schindler.
A Severe Form of Human Combined Immunodeficiency Due to ...
www.jimmunol.org
Elisabeth Nikolopoulos, Anke Peters, Marzenna Orlowska-Volk, Detlev Schindler,
...
Human RAD52 – a novel player in DNA repair in cancer and ...
haematologica.org
René Martin Linka, Roland Meisel, Christian Mielke, Tim Niehues, Detlev Schindler, ...
Identification of the Fanconi anemia complementation group I gene,...
research.vumc.nl
T. Bakker, Jurgen Steltenpool, Dezso Schuler, Sheila Mohan, Detlev Schindler, ...
Neues Krebsgen - Organische-Chemie.ch
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des Humangenetikers Detlev Schindler gemeinsam mit ...
Neuroaxonal Dystrophy Due to Lysosomal α-N Scite.ai
scite.ai
Deficiency. Detlev Schindler, David F. Bishop, David E. Wolfe, Anne M. Wang,
Heinz ...
British Library EThOS: Characterisation of human SLX4/FANCP, a...
ethos.bl.uk
DNA damage ; Fanconi anemia ; Interstrand crosslink repair ; SLX4
Fanconi Anemia Core Complex Gene Promoters Harbor Conserved...
journals.plos.org
Affiliation Department of Human Genetics, University of Wurzburg, Wurzburg, Germany. ⨯. Detlev Schindler. Affiliation Department of Human ...
JCI - Fanconi anemia signaling network regulates the spindle assembly...
www.jci.org
Specimens from patients with FA were obtained from Detlev Schindler (University of Wuerzburg, Wuerzburg, Germany), Hans Joenje (VU University, Amsterdam, ...
Labor Sanobis - Gesundheitscampus
gesundheitscampus.com
Dr. Detlev Schindler (Facharzt für Humangenetik). Die Sanobis GmbH ist eine Nebenbetriebsstätte des MVZ Taunus aus Bad Homburg. Letzteres unterhält eine ...
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