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Gendefekt legt die Blutbildung lahm und erhöht das Krebsrisiko
www.innovations-report.de
Von Würzburger Seite waren an diesem Forschungserfolg Professor Detlev Schindler und seine Doktoranden Kornelia Neveling und Reinhard Kalb vom Institut für Humangenetik beteiligt. Die Wissenschaftler fanden heraus, dass bei Patienten mit der sehr seltenen Blutkrankheit Fanconi-Anämie ein Gen namens BRIP1 defekt sein kann.
| NDAQ:BNGO | Press Release | Bionano Genomics Inc.
stockhouse.com
Dr. Kornelia Neveling from Radboud UMC will present on repeat expansion disorder testing using OGM. Scientific presentations and poster sessions from ... ›
Programm der 20. Jahrestagung der Deutschen Gesellschaft ...
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Workshop (W 3) Cancer genetics Moderatoren: Karl Heinimann (Basel), Kornelia Neveling (Würzburg) BERLIN W3 01 Role of common variants for familial ...
Bionano Genomics Announces ESHG Lineup Featuring
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Dr. Kornelia Neveling, Radboud University Medical Centre, Netherlands, Long-read technologies identify a hidden inverted duplication in a family with ... › news › Bi...
Netzwerk-Profile
Interessen
Detection and interpretation of de novo mutations and structural ...
cordis.europa.eu
... Ellen Kater-Baats; Djie Tjwan Thung; Irma Derks-Prinsen; Lean Beulen; Hanneke Mieloo; Kornelia Neveling ... Twitter · Facebook · LinkedIn · E-mail ... › results
Table of contents | Journal of Medical Genetics
jmg.bmj.com
Muhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, Yar Muhammad Khan, Maleeha Azam, Nadia Khalida Waheed, Christian P Hamel, Tamar ...
Firmen-Mitarbeiter
Marcel Martin — Lehrstuhl 11 Algorithm Engineering
ls11-www.cs.tu-dortmund.de
Marcel Martin, Sven Rahmann. Aligning Flowgrams to DNA Sequences German Conference on Bioinformatics, DOI: OASIcs.GCB Claudia Voigt, André Mégarbané, Kornelia Neveling, Johanna Christina Czeschik ...
Ausbildung
Germline mutations in breast and ovarian cancer pedigrees establish...
kclpure.kcl.ac.uk
... Christoph Engel and Bertram Mueller-Myhsok and Kornelia Neveling and Marion Kiechle and Mathew, {Christopher G.} and Detlev Schindler and Schmutzler, ...
Bücher
OPUS Würzburg | Suchen
opus.bibliothek.uni-wuerzburg.de
Author. Neveling, Kornelia (2); Blanco, Ignacio (1); Bogliolo, Massimo (1); Bonifaci, Núria (1); Brunet, Joan (1); Gómez-Baldó, Laia (1); Lázaro, Conxi (1); Martrat, ...
Programm der 20. Jahrestagung der Deutschen Gesellschaft für ...ur.booksc.me › book
ur.booksc.me
... Kornelia Neveling (Würzburg) BERLIN W3 01 Role of common variants for familial prostate cancer susceptibility Maier C (Ulm) W3 02 Predisposition for ...
Encyclopedia of Cancer - Google Books
books.google.co.uk
This comprehensive encyclopedic reference provides rapid access to focused information on topics of cancer research for clinicians, research scientists and...
Fanconi Anemia: A Paradigmatic Disease for the Understanding of...
books.google.co.uk
Kornelia Neveling Department of Human Genetics, University of Würzburg, Biocenter B107, Am Hubland, Würzburg (Germany) , Fax ...
Dokumente zum Namen
Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a...
papers.ssrn.com
Biallelic germline mutations affecting NTHL1 predispose to adenomatous polyposis and colorectal cancer, but the complete phenotype is unknown, which hampers pat
British Journal of Haematology: Vol 133, No 2 - Wiley Online Library
onlinelibrary.wiley.com
Kirsten Huck, Helmut Hanenberg, Sonja Gudowius, Roland Fenk, Reinhard Kalb, Kornelia Neveling, Beate Betz, Dieter Niederacher, Rainer Haas, Ulrich Göbel, ... › toc
[PDF] 2006_TZA.pdf - Tumorgenetische Arbeitstagungtumorgenetische-arbeitstagung.de › archiv_TGA › TGA_Abstracts › 2...
tumorgenetische-arbeitstagung.de
Kornelia Neveling, Würzburg ab 19:00. ABENDESSEN ab ca. 21:00 OHRENSCHMAUS MIT DEM ORTHOPÄDISCHEN QUARTETT. MAGDEBURG. Ort: Restaurant. Freitag, 12.
expanding the phenotypes associated with EFTUD2 mutations
www.scienceopen.com
— Kornelia Neveling. Johanna Christina Czeschik. Beate Albrecht. Bert Callewaert. Florian von Deimling. Andreas Hehr. Marie Falkenberg Smeland. › do...
Wissenschaftliche Veröffentlichungen
Exploring the link between MORF4L1 and risk of breast cancer | Breast...
breast-cancer-research.biomedcentral.com
· Julia Kühl, Kornelia Neveling & Detlev Schindler. Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, ...
Real-Time DNA Sequencing from Single Polymerase Molecules
www.science.org
von J Eid · · Zitiert von: — ... Jaap Oostrik,; Simone van den Heuvel,; Kornelia Neveling,; Ronald Pennings,; Hannie Kremer,; Erwin van Wijk, ... FacebookTwitterLinkedinemail. › doi › abs
The American Journal of Human Genetics | Vol 87, Issue 4, Pages...
www.sciencedirect.com
Linda Hartmann, Kornelia Neveling, Stephanie Borkens, Hildegard Schneider, ... Heiner Schaal. Pages : Download PDF. Article preview. select article ...
Next generation cytogenetics is on its way - ScienceDaily
www.sciencedaily.com
— The American Journal of Human Genetics, 2021; DOI: j.ajhg ; Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, Michiel ... ›
Veröffentlichungen allgemein
Neoplasia, Ageing, and Genetic Instability due to Defective Caretaker...
www.hindawi.com
Neoplasia, Ageing, and Genetic Instability due to Defective Caretaker Genes: undefined
Artikel & Meinungen
Wikipedia: Célula germinal (humana) - Wikipedia, la enciclopedia libre
Al contrario de las células somáticas que se dividen por mitosis originando la mayor parte de Christian Kubisch, Hans E Wichmann, Karin Kast, Helmut Deißler, Christoph Engel, Bertram Müller-Myhsok, Kornelia Neveling, Marion Kiechle, ...
Mutation of the RAD51C gene in a Fanconi anemia–like disorder |...
www.nature.com
Christopher Mathew and colleagues report a homozygous germline mutation of RAD51C in a Fanconi anemia-like disorder. Mutation of RAD51C, encoding a protein...
Identification of ADHD risk genes in extended pedigrees by combining...
www.nature.com
· Jordi Corominas, Marieke Klein, Marc Pauper, Kornelia Neveling, Geert Poelmans, Alejandro Arias Vasquez & Barbara Franke.
Mutations in the chromatin modifier gene KANSL1 cause the 17q
www.nature.com
Bert DeVries and colleagues identify mutations in the chromatin regulator KANSL1 in 17q microdeletion syndrome. This syndrome is characterized by...
Sonstiges
Z-Library single sign on
1lib.domains
Z-Library single sign on | Z-Library. Download books for free. Find books
Bas E. Dutilh - Utrecht University Metagenomics Group MGX
tbb.bio.uu.nl
»LinkedIn »Frontiers ... Maartje A.H.J. van Kessel, Bas E. Dutilh, Kornelia Neveling, Michael P. Kwint, Joris A. Veltman, Gert Flik, Mike S.M. Jetten, ... › dutilh
NIPT: praktische aspecten, eerste resultaten en een blik vooruit....
docplayer.nl
Kornelia Neveling (PhD) en Lean Beulen (MD) 4 th November en een blik vooruit (II) Lean Beulen en Kornelia Neveling regionale bijeenkomst SPN d.d..
Functional genomics identifies type I interferon pathway as ...
europepmc.org
von SP Smeekens · · Zitiert von: 139 — Furthermore, the authors thank Kornelia Neveling and Petra de Vries for technical assistance with the RNA sequencing experiments. › pmc › pm...
Kornelia Neveling: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن لائن ...ur.booksc.eu › ...
ur.booksc.eu
Z-Library پروجیکٹ کا حصہ دنیا کا سب سے بڑا سائنسی مضامین اسٹور ہے۔ 70,000,000+ مضامین مفت سے۔ Are you familiar with a high-risk merchant or do you process ...
RNA Sequencing Elucidates Drug-Specific Mechanisms of ...
journals.asm.org
von JA Schildkraut · Zitiert von: 5 — ... F. L. Wertheim, Kornelia Neveling, Wouter Hoefsloot, Jakko van Ingen https://orcid.org Authors Info & Affiliations. › doi › AA...
Neues Krebsgen: Defekt erhöht Risiko schon bei Kindern
medizinarium.de
Forscher haben ein Gen identifiziert, das bei Beschädigung zu Krebserkrankungen führen kann. Sind seine beiden Kopien defekt, besteht bereits ab dem frühen...
Resume - Crisly.nl
crisly.nl
LinkedIN: http://www.linkedin.com/in/crislanting ... Ronny Derk, Alexander Hoischen, Sjoert A H Pegge, Kornelia Neveling, Ronald J E Pennings, Hannie Kremer › resume
Veille technologique – AChro-puce
acpa-achropuce.com
Mariangela Sabatella, Tuomo Mantere, Esmé Waanders, Kornelia Neveling, Arjen R Mensenkamp, Freerk van Dijk, Jayne Y Hehir-Kwa, Ronnie Derks, Michael Kwint, ... › veille...
Verburg Curven. Rosalinde Snijders - PDF Free Download
docplayer.nl
https://nl.linkedin.com/in/rogierhavelaar ... NIPT Dr. Kornelia Neveling Wetenschappelijk onderzoeker, afdeling Genetica, ... › V...
All transcript variants in gene C8orf37 - Global Variome shared LOVD
databases.lovd.nl
Curator: Kornelia Neveling · C8orf37 homepage · View transcripts · View variants · View individuals · View diseases · View screenings · Submit new data · LOVD ...
[PDF] Molecular Characterization of Novel Mutations in Fanconi ...
oa.mg
Sarah Reid, Detlev Schindler, Helmut Hanenberg, Karen Barker, Sandra Hanks, Reinhard Kalb, Kornelia Neveling, Patrick Kelly, Sheila Seal, Marcel Freund, ... › work
Altmetric – Biallelic mutations in PALB2 cause Fanconi anemia subtype...
www.altmetric.com
Sarah Reid, Detlev Schindler, Helmut Hanenberg, Karen Barker, Sandra Hanks, Reinhard Kalb, Kornelia Neveling, Patrick Kelly, Sheila Seal, Marcel Freund, ...
Bionano Genomics Symposium - Labroots
www.labroots.com
— Kornelia Neveling, PhD. Scientific Researcher Translational Genomics, Radboud - University Medical Center, Nijmegen, The Netherlands. › agenda
Mutations in the chromatin modifier gene KANSL1 cause the ...
www.sigmaaldrich.com
— David A Koolen, Jamie M Kramer, Kornelia Neveling, Willy M Nillesen, Heather L Moore-Barton, Frances V Elmslie, Annick Toutain, Jeanne Amiel ... › pa...
Aus dem Institut für Humangenetik der Universität Würzburg Vorstand:...
docplayer.org
Die mittlere Überlebenszeit der FA-Patienten beträgt 24 Jahre (Kutler et al., ) Kornelia Neveling, Reinhard Kalb, Michaela Gross Institut für Humangenetik, Klinik für Dermatologie und Allergologie HELIOS Klinikum Berlin-Buch.
Identification of pathogenic gene variants in small families with...
moh-it.pure.elsevier.com
... Kornelia Neveling, Marisol Del Rosario, Gausiya Hira, Santina Reitano, Aurelio Vitello, Pinella Failla, Donatella Greco, Marco Fichera, Ornella Galesi, ...
BRCA testing by single-molecule molecular inversion probes —...
research.tue.nl
Kornelia Neveling, Arjen R. Mensenkamp, Ronny Derks, Michael Kwint, Hicham Ouchene, Marloes Steehouwer, Bart Van Lier, Ermanno Bosgoed, Alwin Rikken ...
Molecular Vision: Exome sequencing identifies a novel and a recurrent...
www.molvis.org
Muhammad Ajmal,1 ,2 ,3 Muhammad Imran Khan,1 ,2Kornelia Neveling,2 ,4 Ali Tayyab,3 Sulman Jaffar,3 ,5 Ahmed Sadeque,1 Humaira Ayub ...
Verwandte Suchanfragen zu Kornelia Neveling
| Sandra Hanks Marcel Freund Reinhard Kalb | Detlev Schindler Christoph Engel Holger Hoehn | Julia Kuehl Hildegard Schneider Sarah Reid |
Person "Neveling" (1) Vorname "Kornelia" (4713) Name "Neveling" (170) |
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