133 Infos zu Raymonda Varon-mateeva

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2 Aktuelle Nachrichten

Raymonda Varon-Mateeva - Knowledia News

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Neue Krankheit entdeckt – Orpha Selbsthilfe

... Amanda Kijas, Markus Stumm, Alexandra Sobeck, Britta Wieland, Raymonda Varon, Yaniv Lerenthal, Martin F. Lavin, Detlev Schindler, and Thilo Dörk, ...

5 Profile in Sozialen Netzwerken

Facebook: Raymonda Varon-Mateeva | Facebook

LinkedIn: Raymonda Varon | LinkedIn

Raymonda Varons berufliches Profil anzeigen LinkedIn ist das weltweit größte professionelle Netzwerk, das Fach- und Führungskräften wie Raymonda Varon ...

Verfasser Suchresultate

Treffer von 42 für Suche: 'Raymonda Varon', Suchdauer: 0.3s. Sortieren. Relevanz, Nach Datum, absteigend, Nach Datum, aufsteigend, Signatur ...

3 Hobbys & Interessen

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in...

Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome. Raymonda Varon. x. Raymonda Varon. Search for ...

Prevalence of BRCA1/2 germline mutations in families with...

Caroline Scholz,16 Bernd Auber,16 Raymonda Varon-Manteeva,17 Dorothee Speiser,18. Judit Horvath,19 Nadine Lichey,19 Pauline ...

1 Business-Profile

patentbuddy: Raymonda Varon-Mateeva

BENAROYA RESEARCH INSTITUTE AT VIRGINIA MASON, Berlin, DE

2 Infos zur Ausbildung

Mutational spectrum in a worldwide study of 29,700 families with...

Stanford Libraries' official online search tool for books, media, journals, databases, government documents and more.

Evaluation of polygenic risk scores King's Research Portal

von KB Kuchenbaecker · · Zitiert von: 258 — ... Eric Hahnen, Jan Hauke, Karin Kast, Alfons Meindl, Dieter Niederacher, Raymonda Varon-Mateeva, Shan Wang-Gohrke, Barbara Wappenschmidt, Laure Barjhoux, ... › portal

8 Bücher zum Namen

An original phylogenetic approach identified UGent Biblio

von S Blein · · Zitiert von: 28 — ... Nina Ditsch, Norbert Arnold, Raymonda Varon-Mateeva, Rita K Schmutzler, Sabine Preisler-Adams, Nadja Bogdanova Markov, Shan Wang-Gohrke, ... › publication

OPUS Würzburg | Suchen

... Simone ; Niederacher, Dieter ; Preisler-Adams, Sabine ; Gadzicki, Dorothea ; Varon-Mateeva, Raymonda ; Deissler, Helmut ; Gehrig, Andrea ; Sutter, Christian ...

Journal of the National Cancer Institute: JNCI.

... Christian Sutter , Norbert Arnold , Helmut Deissler , Raymonda Varon - Mateeva , Karin Kast , Dieter Niederacher , Dorothea Gadzicki , Trinidad Caldes ...

Molekularmedizinische Grundlagen von nicht-hereditären ...

Raymonda Varon et al. und James P. Carney et al. identifizieren Nibrin, ein Reparaturprotein für DNA-Doppelstrangbrüche, das beim Nijmegen-breakage-Syndrom ...

10 Dokumente

CiteSeerX — Nibrin, a novel DNA double-strand break repair ...

von R Varon · · Zitiert von: — by Raymonda Varon , Christine Vissinga , Matthias Platzer , Karen M. Cerosaletti , Krystyna H. Chrzanowska , Kathrin Saar , Georg Beckmann , Eva Seemanová ... › summ...

The NBN founder mutation—Evidence for a country specific ...

von KH Chrzanowska — Raymonda Varon,. Raymonda Varon. Institute of Medical and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany. › abs

provisional PDF - OnCommunity

Raymonda Varon-Mateeva (). Helmut Deissler (). Andrea Gehrig ...

Cancer Risk of Heterozygotes With the NBN Founder Mutation

von E Seemanová · · Zitiert von: 121 — Raymonda Varon,. Raymonda Varon. Affiliations of authors: Department of Clinical Genetics, Institute of Biology and Medical Genetics (ES) ... von R Varon · · Zitiert von: 26 — Raymonda Varon, Klaus Magdorf, Doris Staab, Hans-Ulrich Wahn, Michael Krawczak, Karl Sperling, André Reis; Recurrent nasal polyps as a monosymptomatic form ... › jnci › a... › article

11 Wissenschaftliche Publikationen

DFG GEPRIS - Dr. Raymonda Varon

Dr. Raymonda Varon, Institut für Humangenetik (CVK)Berlin

657del5 Mutation of the Nijmegen Breakage Syndrome Gene ...

von M TEKIN · · Zitiert von: 7 — kindly provided by Raymonda Varon (Institute of Human Genetics, Charité Hum- boldt University, Germany). Results. Mutation screening in all four families ... › stable

Investigating the effects of additional truncating variants in ...

von I Sepahi · · Zitiert von: 8 — Raymonda Varon. Institute for Clinical Genetics, Dresden, Germany. Evelin Schröck. Department of Obstetrics and Gynaecology, ... › ...

BibTeX-Output - IMISE Leipzig

... van Hest and Liliana Varesco and Raymonda Varon-Mateeva and Alessandra Viel and Jeroen Vierstrate and Roberta Villa and Anna von Wachenfeldt and Philipp ... › ...

10 Allgemeine Veröffentlichungen

Identification of four novel susceptibility loci for CORE

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Authors. Fergus J. Couch · Raymonda Varon-Mateeva. › redirect › display

Evidence for the deficiency of β-glucosidase-activating factor in...

Reduced activity of β-glucosidase was shown in the cultured skin fibroblasts of four patients with I-cell disease when the enzyme was tested without the use of...

A novel mutation in GJA8 associated with jellyfish-like BioMedSearch

Vanita Vanita,1 Jai Rup Singh,1 Daljit Singh,2 Raymonda Varon,3 Karl Sperling3. 1Centre for Genetic Disorders, Guru Nanak Dev University ...

The Best of AACR Journals Papers: Page 5

... Helmut Deissler, Doroteha Gadzicki, Sabine Preisler-Adams, Raymonda Varon-Mateeva, Ines Schönbuchner, Heidrun Gevensleben, Dominique Stoppa-Lyonnet, ... › publ...

2 Meinungen & Artikel

Chromosome instability and nibrin protein variants in NBS...

Article

Clinical ascertainment of Nijmegen breakage syndrome (NBS ...

von R Varon · · Zitiert von: 206 — Raymonda Varon, Karl Sperling & André Reis. Department of Medical Genetics, Charles University, Prague, Czech Republic. Eva Seemanova. › articles

77 Webfunde aus dem Netz

Raymonda Varon | LinkedIn

View Raymonda Varon's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Raymonda Varon discover ...

Raymonda Varon - Suchen 学术

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Varon-Mateeva, Raymonda: 免费的Z-Library数字图书馆

Varon-Mateeva, Raymonda: 免费的Z-Library数字图书馆| BookSC. Download books for free. Find books. Raymonda Varon-Mateeva: 免费的Z-Library数字图书馆| BookSC. Download books for free. Find books. › Varon-Mat... › Raymonda ...

Varon-Mateeva, Raymonda Person - VIVO

Varon-Mateeva, Raymonda Person. Contact. scroll to property group menus. Contact. full name. Raymonda Varon-Mateeva. ©2022 VIVO Project | Terms of Use ... › display

Orphanet: Dr Raymonda VARON MATEEVA

Das Portal für seltene Krankheiten und Orphan Drugs

Raymonda Varon

Raymonda Varon. Details · Publications ... Maren Runte, Peter M. Kroisel, Gabriele Gillessen-Kaesbach, Raymonda Varon, more.

Additional file 6: of Male breast cancer in BRCA1 and BRCA2 ...

... Raymonda Varon-Mateeva (Bidrager); Javier Benitez (Ophavsperson); Ana Osorio (Ophavsperson); Gabriella Ivady (Ophavsperson); Debra Frost (Ophavsperson) ... › datasets › addi...

Association of Genomic Domains in BRCA1 and BRCA2 with ...

von VL Patel · · Zitiert von: 38 — ... Liselotte P. van Hest, Liliana Varesco, Raymonda Varon-Mateeva, Alessandra Viel, Jeroen Vierstrate, Roberta Villa, Anna von Wachenfeldt, ... › associati...

Association of the Variants CASP8 D302H and CASP10 V410I ...

von C Engel · · Zitiert von: 51 — ... Laurence Gladieff, Nancy Uhrhammer, Yves-Jean Bignon, Alfons Meindl, Norbert Arnold, Raymonda Varon-Mateeva, Dieter Niederacher, Sabine Preisler-Adams, ... › p...

Availability: Fine-Scale Mappin Katalog K.UTB

... Silvia Tognazzo, Elizabeth J van Rensburg, Liliana Varesco, Raymonda Varon-Mateeva, Athanassios Vratimos, Jeffrey N Weitzel, Lesley McGuffog, Judy Kirk, ... › Ed...

Benjamin Varon

The publication was a collaboration between Zakhari Stoyanov Publishing House and Raymonda Varon-Mateeva, daughter of the remarkable thinker.

Identification of ten variants associated with Read by QxMD

... Ans M W van den Ouweland, Elizabeth J van Rensburg, Liliana Varesco, Raymonda Varon-Mateeva, Ana Vega, Alessandra Viel, Joseph Vijai, Daniel Vincent, ... › read › ide...

Biologie des systèmes du cancer | Institut Curie

... Mattias Van Heetvelde, Els Van Nieuwenhuysen, Elizabeth J van Rensburg, Adriaan Vanderstichele, Raymonda Varon-Mateeva, Ana Vega, Digna Velez Edwards, ... › equipe › barillot

Candidate Genetic Modifiers for Breast and Ovarian Cancer ...

... D Gareth R Evans, Debra Frost, Diana Eccles, Angela Brady, Jackie Cook, Marc Tischkowitz, Raymonda Varon-Mateeva, Mark E Robson, Barbara Wappenschmidt, ... › publications › ca...

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants...

... {Elizabeth J} and Liliana Varesco and Raymonda Varon-Mateeva and Athanassios Vratimos and Weitzel, {Jeffrey N} and Lesley McGuffog and Judy Kirk and ...

New Disease Discovered

New Disease Discovered Amanda Kijas, Markus Stumm, Alexandra Sobeck, Britta Wieland, Raymonda Varon, Yaniv Lerenthal, ... More articles from Life Sciences:

Candidate Genetic Modifiers for Breast and Ovarian Cancer ...

von P Peterlongo · · Zitiert von: 28 — ... Nina Ditsch Norbert Arnold Raymonda Varon-Mateeva Barbara Wappenschmidt Shan Wang Brigitte Bressac-de Paillerets Bruno Buecher Capucine Delnatte Claude ... › hal

MSS/CCFDN-Gen

Dr. von Arpad Moers

Common alleles at 6q25.1 and 1p11.2 are Hal-Inria

von AC Antoniou · · Zitiert von: 104 — ... K Schmutzler Barbara Wappenschmidt 86 Christoph Engel 87 Alfons Meindl 88 Ina Ruehl 89Raymonda Varon-Mateeva 90 Karin Kast 91 Helmut Deissler 92 Dieter ... › hal

Common alleles at 6q25.1 and 1p11.2 are Sigma-Aldrich

— ... Alfons Meindl, Ina Ruehl, Raymonda Varon-Mateeva, Karin Kast, Helmut Deissler, Dieter Niederacher, Norbert Arnold, Dorothea Gadzicki, ... › pa...

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