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News
Defekt gen förklarar Kostmanns sjukdom | Karolinska Institutet, KI
www.mynewsdesk.com
En svensk-tysk forskargrupp vid Karolinska Institutet, Uppsala universitet och Hannover Medical School har hittat en gen som förklarar gåtan med severe...
Report from the Paediatric Diseases Working Party EBMT
www.ebmt.org
— This exciting session was closed by the joint presentation from Matthias Ballmaier and Manuela Germeshausen from Germany on the state-of-art ... › ebmt › news
Netzwerk-Profile
WikiGenes - Manuela Germeshausen
www.wikigenes.org
Affiliations. Department of Pediatric Hematology and Oncology/Molecular Hematopoiesis, Medizinische Hochschule HannoverD
Business-Profile
Xing: Manuela Germeshausen - Biologin - Medizinische Hochschule Hannover |...
Manuela Germeshausen, Hannover: Berufserfahrung, Kontaktdaten, Portfolio und weitere Infos: Erfahr mehr – oder kontaktier Manuela Germeshausen direkt bei ...
Stephanie King Hannover Medical School | MHH
www.researchgate.net
Stephanie King; Manuela Germeshausen · Gabriele Strauss; [...] Matthias Ballmaier. Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare bone marrow ... Manuela Germeshausen · Phil Ancliff · Jaime Estrada; [...] Matthias Ballmaier. Key Points Germ line mutations in MECOM cause a heterogeneous bone marrow ... › Step... › profile › Markus-Metzler
Ausbildung
Coelomic fluid proteins as basic components of innate ...
journals.scholarsportal.info
Authors. Natalia Gavrikova · Cornelia Zeidler · Martin Stanulla · Manuela Germeshausen · Beate Schwinzer · Karl Welte ... › ...
Projekte
M34
www.hector-stiftung.de
Julia Skokowa, Gunnar Cario, Murat Uenalan, Axel Schambach, Manuela Germeshausen, Kartin Battmer, Cornelia Zeidler, Ulrich Lehmann, Matthias Eder, Christopher Baum, Rudolf Grosschedl, Martin Stanulla, Michaela Scherr & Karl Welte LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia Nature Medicine (2006) Letizia …
Bücher
Advances in the understanding of congenital amegakaryocytic...
ur.booksc.org
Advances in the understanding of congenital amegakaryocytic thrombocytopenia | Matthias Ballmaier; Manuela Germeshausen | download | BookSC. Download books for...
Dokumente zum Namen
A Naturally Occurring Extracellular α−β Clasp Contributes to ...
pubs.acs.org
von AN Vomund · · Zitiert von: 14 — ... Peter Collins, Deborah French, Remi Favier, Kathleen Freson, Bruce Furie, Manuela Germeshausen, Cedric Ghevaert, Keith Gomez, ... › doi › abs
Manuela Germeshausen - Academia.eduindependent.academia.edu › ManuelaGermeshausen
independent.academia.edu
Manuela Germeshausen studies Next generation sequencing, Molecular Cell Biology, and Cancer Research.
a heterogeneous inherited bone marrow failure syndrome with ...
ashpublications.org
von M Germeshausen · · Zitiert von: 64 — Manuela Germeshausen, Phil Ancliff, Jaime Estrada, Markus Metzler, Eva Ponstingl, Horst Rütschle, Dirk Schwabe, Richard H. Scott, Sule Unal, Angela Wawer, ... › MECO...
Wissenschaftliche Veröffentlichungen
… siblings with homozygous G6PC3 mutations expand our...
bmcmedgenet.biomedcentral.com
17 Aug 2012, Reviewed, Reviewer Report - Manuela Germeshausen. 24 Oct 2012, Author responded, Author comments - Michael Woods. Resubmission - Version 2.
Gusal Pracht – ScienceOpen
www.scienceopen.com
Authors: Cornelia Zeidler, Gusal Pracht, Manuela Germeshausen … All publications. Record: found; Orcid: not found; Profile: not found ...
Orphanet Journal of Rare Diseases | 5th european conference on rare...
preview-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
genetic and phenotypic characteristics of a CORE
core.ac.uk
Cornelia Zeidler · Gusal Pracht · Manuela Germeshausen · Karl Welte. Publication date: Publisher: Springer Nature. Doi: DOI: s1-p › display
Artikel & Meinungen
LEF-1 is crucial for neutrophil granulocytopoiesis and its
www.nature.com
von J Skokowa · — Julia Skokowa, Gunnar Cario, Murat Uenalan, Axel Schambach, Manuela Germeshausen, Karin Battmer, Cornelia Zeidler, Ulrich Lehmann,. › articles
HAX1 deficiency causes autosomal recessive severe congenital...
www.nature.com
· Christoph Klein, Giridharan Appaswamy, Manuela Germeshausen, Inga Sandrock, Chozhavendan Rathinam, Kaan Boztug, Beate Schwinzer, Georg Bohn, ...
Sonstiges
Granulocyte colony-stimulating factor receptor mutations in a ...
slideplayer.com
Manuela Germeshausen et al leukemia secondary to severe congenital neutropenia by Manuela Germeshausen, Matthias Ballmaier, Harald Schulze, Karl Welte, ... › slide
Manuela%20Germeshausen: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن...
ur.booksc.eu
Manuela%20Germeshausen: مفت ڈاؤنلوڈ. ای بک لائبریری۔ Z-Library پر آن لائن کتابوں کی دکانیں | BookSC. Download books for free. Find books
Manuela%20Germeshausen: मुफ़्त में डाउनलोड. ई-बुक पुस्तकालय....
hi.booksc.me
Manuela%20Germeshausen: मुफ़्त में डाउनलोड. ई-बुक पुस्तकालय. Z-Library में ऑन लाइन पुस्तकों की दुकान | BookSC. Download books for free. Find books
EUPLANE
www.gesundheitsforschung-bmbf.de
Dr. Manuela Germeshausen Adresse: Medizinische Hochschule Hannover, Zentrum Kinderheilkunde und Jugendmedizin, Klinik für Pädiatrische Hämatologie und Onkologie, AG Germeshausen/Ballmaier Hannover: Europäisches Netzwerk für die Erforschung der Pathophysiologie von zwei Formen hereditärer Thrombozytopenien, THC2 und …
A high-throughput sequencing test for diagnosing inherited bleeding,...
hal.archives-ouvertes.fr
... Peter Collins C. Daugherty Rémi Favier Deborah French Bruce Furie Michael Gattens Manuela Germeshausen Cedric Ghevaert Anne C Goodeve A. Guerrero Daniel ...
A high-throughput sequencing test for Repository@Hull
hull-repository.worktribe.com
Manuela Germeshausen. Cedric Ghevaert. Anne C. Goodeve. Jose A. Guerrero. Profile Image. Dr Dan Hampshire .uk. Lecturer in Genetics. › ...
A novel mutation in the MECOM gene causing radioulnar synostosis ...read.qxmd.com › read › a-novel-mutation-in-the-m...
read.qxmd.com
Manuela Germeshausen, Phil Ancliff, Jaime Estrada, Markus Metzler, Eva Ponstingl, Horst Rütschle, Dirk Schwabe, Richard H Scott, Sule Unal, Angela Wawer, ...
A high-throughput sequencing test for diagnosing inherited ...
research-information.bris.ac.uk
von I Simeoni · · Zitiert von: 170 — ... Deborah L French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cedric Ghevaert, Anne Goodeve, Jose Guerrero, Daniel J Hampshire, ... › ...
Advances in the understanding of congenital amegakaryocytic ...
www.academia.edu
Profile image of Manuela Germeshausen ... thrombocytopenia Matthias Ballmaier and Manuela Germeshausen Department of Paediatric Haematology and Oncology, ... › Advan...
A high-throughput sequencing test for diagnosing inherited bleeding,...
research-information.bris.ac.uk
Loredana Bury, Marco Cattaneo, Peter Collins, Louise C Daugherty, Rémi Favier, Deborah L French, Bruce Furie, Michael Gattens, Manuela Germeshausen, ...
Clinical implications of ELA2-, HAX1-, and G-CSF-receptor ...
read.qxmd.com
Cornelia Zeidler, Manuela Germeshausen, Christoph Klein, Karl Welte. British Journal of Haematology 2009, 144 (4): › read
Congenital amegakaryocytic thrombocytopenia - Not a single ...
pubmed.ncbi.nlm.nih.gov
von M Germeshausen · · Zitiert von: 7 — Authors. Manuela Germeshausen , Matthias Ballmaier. Affiliations. 1 Central Research Facility Cell Sorting Hannover Medical School, Hannover, Germany. von M Germeshausen · · Zitiert von: 64 — Manuela Germeshausen , Phil Ancliff , Jaime Estrada , Markus Metzler , Eva Ponstingl , Horst Rütschle , Dirk Schwabe , Richard H Scott , Sule Unal , Angela ... › ...
Csf3r - Sigma-Aldrich
www.sigmaaldrich.com
Results of 52 — RAS and CSF3R mutations in severe congenital neutropenia. Manuela Germeshausen et al. Blood, 114(16), ( ). › se...
Download Figures (PPT) - Experimental Hematology
www.exphem.org
Harald Schulze, Matthias Ballmaier, Karl Welte, Manuela Germeshausen. Experimental Hematology. Volume 28 Issue 3 Pages (March 2000). › article › ppt
Clinic, pathogenic mechanisms and drug testing of two inherited...
moh-it.pure.elsevier.com
Alessandra Balduini, Hana Raslova, Christian A. Di Buduo, Alessandro Donada, Matthias Ballmaier, Manuela Germeshausen, Carlo L. Balduini. Research ...
Familial thrombocytosis caused by the novel germ-line mutation...
www.research.ed.ac.uk
El-Harith Abdelghaffar El-Harith, Cornelia Roesl, Matthias Ballmaier, Manuela Germeshausen, Hildegard Frye-Boukhriss, Nils von Neuhoff, Christian Becker, ...
G5758 | Sigma-Aldrich
www.sigmaaldrich.com
Results of 64 — Manuela Germeshausen et al. Haematologica, 95(7), ( ). Severe congenital neutropenia a clinically and genetically ... › se...
Digenic mutations in severe congenital neutropenia — Italian...
moh-it.pure.elsevier.com
Digenic mutations in severe congenital neutropenia. Manuela Germeshausen, Cornelia Zeidler, Manfred Stuhrmann, Marina Lanciotti, Matthias Ballmaier, Karl ...
Verwandte Suchanfragen zu Manuela Germeshausen
| Harald Schulze Christoph Klein Murat Uenalan | Ulrich Lehmann Peter Collins Karin Battmer | Magda Grudzien Martin Stanulla Beate Schwinzer |
Personen Vorname "Manuela" (35206) Name "Germeshausen" (46) |
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