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News
Kinder als Dozenten - Fürth - nordbayern.de
www.nordbayern.de
FÜRTH - Ein ungewöhnliches Schulprojekt in den Ferien: In Zusammenarbeit mit der Fürther VHS hat der Verein „Besonders begabte Kinder“ einen sogenannten...
Netzwerk-Profile
ICQ Benutzer: Steffen Uebe (Steefn)
, Männlich, Alter: 27
ICQ Benutzer: Steffen Uebe (Uartseieu)
, Alter: 34
Interessen
Rheuma Tolerance for Cure | RTCure Project | Results | H2020
cordis.europa.eu
— Author(s): Thomas Wohlfahrt, Simon Rauber, Steffen Uebe, Markus Luber, Alina Soare, Arif Ekici, Stefanie Weber, Alexandru-Emil Matei, ... › project
Business-Profile
Steffen UEBE | Dr. rer. nat. | Institute of Human Genetics
www.researchgate.net
› profile › Steffen-Uebe
Private Homepages
Dr. rer. nat. Steffen Uebe - Scientist - Humangenetik Erlangen
www.humangenetik.uk-erlangen.de
› kontakt › s...
Dr. rer. nat. Steffen Uebe - wissenschaftlicher Mitarbeiter
www.uk-erlangen.de
› kontakt › visitenkarte › st...
Kontakt | B+M Poly Pool
www.polypool.de
Steffen Uebe. Werkstattleiter/Prokurist. B+M Pool Dach GmbH. + · . Thorsten Jenetzky. Techniker / Verkaufsberater ... › kontakt
ASBMR e-News Weekly: April 28, Edition
www.asbmr.org
— Yasunori Omata, Hiroyuki Okada, Steffen Uebe, Naohiro Izawa, Arif B. Ekici, Kerstin Sarter, Taku Saito, Georg Schett, Sakae Tanaka, ... › about › as...
Projekte
snver-help Mailing List for SNVer
sourceforge.net
[Snver-help] Cannot read split target file by tab, Uebe, Steffen <Steffen.Uebe@uk...> :14:45. [Snver-help] Java not recognized on launch, Sean ...
EU H2020 Project "RTCURE (Rheuma Tolerance for Cure)"
www.fabiodisconzi.com
2019, Thomas Wohlfahrt, Simon Rauber, Steffen Uebe, Markus Luber, Alina Soare, ... not embedded into any word file), twitter account, linkedin page, etc. › p...
Bücher
PLOS Genetics: Rare Copy Number Variants Are a Common Cause of Short...
journals.plos.org
· Steffen Uebe. Affiliation Institute of Human Genetics, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany. Arif B. Ekici.
EIF3F-related neurodevelopmental disorder: delineating and ...
www.authorea.com
von U Hueffmeier · — Ulrike Hueffmeier,; Cornelia Kraus,; Miriam Reuter,; Steffen Uebe,; Mary-Alice Abbott,; Syed Ahmed,; Kristyn Rawson,; Eileen Barr,; Hong Li, ... › users › articles
Meet the First Author IFMRS HubLE
www.huble.org
... Daniel Eriksson, Anne Schnelzer, Jutta Jordan, Martin Eberhardt, Ulrike Schleicher, Jürgen Rech, Andreas Ramming, Steffen Uebe, Arif Ekici, Juan D. Cañete, ...
AACR Proceedings: Part B April
books.google.co.uk
Michael Stürzl, Maximilian Fuchs, Meik Kunz, Nicholas Dickel, Bernt Popp, Steffen Uebe, Arif B. Ekici, Carol I. Geppert, Susanne Merkel, Vera S. Schellerer, ...
Dokumente zum Namen
MedicalResearch.com: Medical Research Exclusive Interviews February …
de.slideshare.net
MedicalResearch.com features exclusive interviews with medical researchers from major and specialty medical and health care journals and meetings.
Kategorie Vorname Name schnellste Zeit Platzierung …
daten.verwaltungsportal.de
Zeit Seite 3 Kategorie Vorname Name Alter Startnummer schnellste Zeit m50 Steffen Uebe :21,31 m30 Tobias Burkhardt :21,53 m40 Thomas ...
Manifestation of epilepsy in a patient with EED‐related ...
onlinelibrary.wiley.com
von KLML Hetzelt · — Steffen Uebe,. Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg FAU, Erlangen, ... › abs
Kirchenbote/Der Ruf zur Kirche - Bergkirche Seiffen
bergkirche-seiffen.de
Mai Hanna Marie und Jonas Finn Uebe, Kinder von Steffen Uebe und Nicole geb. Hochheimer aus Kefenrod/Hessen Gott hat uns nicht gegeben den Geist der Furcht, ...
Wissenschaftliche Veröffentlichungen
Expanding the clinical spectrum of COL1A1 mutations in different...
ojrd.biomedcentral.com
Lucia Mauri,; Steffen Uebe,; Heinrich Sticht,; Urs Vossmerbaeumer,; Nicole Weisschuh,; Emanuela Manfredini,; Edoardo Maselli,; Mariacristina Patrosso,; Robert N. Weinreb,; Silvana Penco,; André Reis and; Francesca PasuttoEmail authorView ORCID ID profile. Orphanet Journal of Rare Diseases : ...
Orphanet Journal of Rare Diseases | Articles
ojrd.biomedcentral.com
Encompassing all aspects of rare diseases and orphan drugs, Orphanet Journal of Rare Diseases features high quality reviews and original articles in ...
Veröffentlichungen allgemein
A Homozygous Mutation in GPT2 Associated with Nonsyndromic...
link.springer.com
Intellectual disability is a highly heterogeneous disease that affects the central nervous system and impairs patients’ ability to function independently....
Programm 2018www.adf-online.de › uploads › Programm-AG-Genetik-der-ADF-2018
www.adf-online.de
Wollnik, Köln. 10:55-11: Ulrike Hüffmeier, Sabine Löhr, Arif B. Ekici, Steffen Uebe, Michaela Köhm, Frank. Behrens, Beate Böhm, Michael ...
GPFrontend and GPGraphics: graphical analysis tools for genetic...
link.springer.com
Most software packages for whole genome association studies are non-graphical, purely text based programs originally designed to run with UNIX-like operating...
Wikidata:WikiProject Source MetaData/Wikidata lists/Items about...
www.wikidata.org
, Rahul Kanwar, Stefan K Schulze Meike Gölzenleuchter Hauke Werner, Angela Garding Ramona B Jung Gabrielle Mengus Steffen Uebe
Video & Audio
Movie 2
movie.biologists.com
▶Fabian Pridöhl, Matthias Weißkopf, Nikolaus Koniszewski, Andreas Sulzmaier, Steffen Uebe, Arif B. Ekici ...
Artikel & Meinungen
A common variant mapping to CACNA1A is associated with susceptibility...
www.nature.com
Tin Aung, Chiea-Chuen Khor and colleagues report the results of a genome-wide association study of exfoliation syndrome. They replicate a known association at...
Common variants at TRAF3IP2 are associated with susceptibility to...
www.nature.com
André Reis and colleagues report a genome-wide association study identifying a susceptibility locus at TRAF3IP2 for psoriatic arthritis and psoriasis.
Prevalence of hereditary tubulointerstitial kidney Nature
www.nature.com
von B Popp · · Zitiert von: 2 — Bernt Popp, Arif B. Ekici, Steffen Uebe, André Reis & Cornelia Kraus. Institute of Human Genetics, University of Leipzig Hospitals and ... › articles
Sonstiges
Pin by Steffen Uebe on Kitchen | Barn doors sliding, White barn door,...
www.pinterest.it
Steffen Uebe hat diesen Pin entdeckt. Entdecke (und sammle) deine eigenen Pins bei Pinterest.
Choline transporter‐like1 (CHER1) is crucial for plasmodesmata...
www.bionity.com
Max E. Kraner, Katrin Link, Michael Melzer, Arif B. Ekici, Steffen Uebe, Pablo Tarazona, Ivo Feussner, Jörg Hofmann, Uwe Sonnewald : Journal: The Plant Journal ...
GMS | 20. Wissenschaftliche Jahrestagung der DGPP Deutsche...
www.egms.de
Uebe S; Volz-Peters A; Berger R; Kunz J; Autoren ... Steffen Uebe - Institut für Humangenetik, Universitätsklinikum MarburgMarburg
CoMon variants at TRAF3IP2 are aSociated with susceptibility to ...www.research.manchester.ac.uk › portal › export
www.research.manchester.ac.uk
author = "Ulrike H{\"u}ffmeier and Steffen Uebe and Ekici, {Arif B.} and John Bowes and Emiliano Giardina and Eleanor Korendowych and Kristina Juneblad and ...
In a Nutshell IFMRS HubLEwww.huble.org › In a Nutshell
www.huble.org
... Martin Eberhardt, Ulrike Schleicher, Jürgen Rech, Andreas Ramming, Steffen Uebe, Arif Ekici, Juan D. Cañete, Xiaoxiang Chen, Tobias Bäuerle, Julio Vera, ...
A common variant mapping to CACNA1A is DSpace Home
dsp.sbmu.ac.ir
von T Aung · Zitiert von: 89 — Steffen Uebe. Jeffrey M. Harder. Anita S.Y. Chan. Anita S.Y. Chan. Mei Chin Lee. Kathryn P. Burdon. Kathryn P. Burdon. Yury S. Astakhov. Khaled K. Abu-Amero. › handle
Publications | Hochschule Bonn-Rhein-Sieg (H-BRS)www.h-brs.de › publicationsh-brs-institute-members-0
www.h-brs.de
... Regina Trollmann, Steffen Uebe, Arif B. Ekici, André Reis: HIBCH deficiency in a patient with phenotypic characteristics of mitochondrial disorders.
Auria Biobank - Publications
www.auria.fi
... Owen M. Siggs, Terri Young, Veronique Vitart, Alberta A.H.J. Thiadens, Juha Karjalainen, Steffen Uebe, Ronald B. Melles, K. Saidas Nair, Robert Luben, ... › julkaisut
A new missense mutation in PLA2G6 gene among a family with infantile...
www.infona.pl
... PLA2G6 gene among a family with infantile neuroaxonal dystrophy INAD. Ola Gebril, Steffen Uebe, Miriam Reuter, Johannes Schumacher, Rami Abou Jamra, ...
Altmetric – PTPN22 is associated with susceptibility to psoriatic...
www.altmetric.com
John Bowes, Sabine Loehr, Ashley Budu-Aggrey, Steffen Uebe, Ian N Bruce, Marie Feletar, Helena Marzo-Ortega, Philip Helliwell, Anthony W Ryan, David Kane, Eleanor Korendowych, Gerd-Marie Alenius, Emiliano Giardina, Jonathan Packham, Ross McManus, Oliver FitzGerald, Matthew A Brown, Frank Behrens, Harald ...
8ème Conférence d'exament de la CIABT : événement parallèle organisé...
cd-geneve.delegfrance.org
... l'Ambassadeur Alice Guitton, l'Ambassadeur Susanne Baumann, le Lieutenant -Colonel Kai Hoberg, le Dr Steffen Uebe et le Dr. Lorna Miller.
B&M Pooldach GmbH, Wilkau-Haßlau - North Data
www.northdata.de
Neueintragung Anschrift: Gewerbering 5 GF André Bogmann GF Gerald Mück Prokura Steffen Uebe Wortmarke: B ... › Amtsgericht+Chemnitz+HR...
Mutations in the mitochondrial gene C12ORF65 lead to syndromic...
www.infona.pl
Steffen Uebe. Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Schwabachanlage 10, Erlangen, ...
Personen und Einrichtungen
univis.fau.de
... PD Dr. Thiel, Christian, App ; Dr. rer. nat. Uebe, Steffen, App ; Zahnleiter, Diana; PD Dr. med. Zweier, Christiane, App
TALPID3 controls centrosome and cell polarity and the human ortholog...
elifesciences.org
Steffen Uebe. Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, ... DOI: http://dx.doi.org eLife eLife digest.
Fra-2 regulates B cell development by enhancing IRF4 and Foxo1 ...rupress.org › jem › article-abstract
rupress.org
· Steffen Uebe,. Steffen Uebe. 2. Institute of Human Genetics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
Best Episodes of Epigenetics Podcast | Podchaser
www.podchaser.com
... Active Motif on LinkedIn Active Motif on Facebook Steffen Uebe, Arif B. Ekici, Vadym Gnatkovsky, and Katja Kobow. › episo...
Rare Copy Number Variants Are a Common Cause of Short Stature - PDF...
docplayer.net
Rare Copy Number Variants Are a Common Cause of Short Stature Diana Zahnleiter 1, Steffen Uebe 1, Arif B. Ekici 1, Juliane Hoyer 1, Antje Wiesener
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