Ulrike Nuber
Ulrike Nuber
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Transcriptional dynamics of the embryonic stem cell switch
V Chickarmane, C Troein, UA Nuber, HM Sauro, C Peterson
PLoS computational biology 2 (9), e123, 2006
CD133 is not present on neurogenic astrocytes in the adult subventricular zone, but on embryonic neural stem cells, ependymal cells, and glioblastoma cells
CV Pfenninger, T Roschupkina, F Hertwig, D Kottwitz, E Englund, ...
Cancer research 67 (12), 5727-5736, 2007
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
UA Nuber, S Kriaucionis, TC Roloff, J Guy, J Selfridge, C Steinhoff, ...
Human molecular genetics 14 (15), 2247-2256, 2005
Desmosomes and cytoskeletal architecture in epithelial differentiation: cell type-specific plaque components and intermediate filament anchorage.
A Schmidt, HW Heid, S Schäfer, UA Nuber, R Zimbelmann, WW Franke
European journal of cell biology 65 (2), 229-245, 1994
Neural precursor cells induce cell death of high-grade astrocytomas through stimulation of TRPV1
K Stock, J Kumar, M Synowitz, S Petrosino, R Imperatore, ESJ Smith, ...
Nature medicine 18 (8), 1232-1238, 2012
Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation
VM Kalscheuer, K Freude, L Musante, LR Jensen, HG Yntema, J Gécz, ...
Nature genetics 35 (4), 313-315, 2003
The widespread human desmocollin Dsc2 and tissue-specific patterns of synthesis of various desmocollin subtypes.
UA Nuber, S Schäfer, A Schmidt, PJ Koch, WW Franke
European journal of cell biology 66 (1), 69-74, 1995
Gene expression changes in the course of neural progenitor cell differentiation
U Gurok, C Steinhoff, B Lipkowitz, HH Ropers, C Scharff, UA Nuber
Journal of Neuroscience 24 (26), 5982-6002, 2004
Comparative study of methyl-CpG-binding domain proteins
TC Roloff, HH Ropers, UA Nuber
BMC genomics 4, 1-9, 2003
Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
UA Nuber, S Schäfer, S Stehr, HR Rackwitz, WW Franke
European journal of cell biology 71 (1), 1-13, 1996
Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarrays
F Erdogan, R Kirchner, W Mann, HH Ropers, UA Nuber
Nucleic Acids Research 29 (7), e36-e36, 2001
Long‐term maintenance of hematopoietic stem cells does not require contact with embryo‐derived stromal cells in cocultures
RAJ Oostendorp, C Robin, C Steinhoff, S Marz, R Bräuer, UA Nuber, ...
Stem Cells 23 (6), 842-851, 2005
Autocrine fibroblast growth factor 18 mediates dexamethasone‐induced osteogenic differentiation of murine mesenchymal stem cells
Z Hamidouche, O Fromigué, U Nuber, P Vaudin, JC Pages, R Ebert, ...
Journal of cellular physiology 224 (2), 509-515, 2010
Gene expression profile of mouse bone marrow stromal cells determined by cDNA microarray analysis
G Wieczorek, C Steinhoff, R Schulz, M Scheller, M Vingron, HH Ropers, ...
Cell and Tissue Research 311 (2), 227-237, 2003
Chromatin, epigenetics and stem cells
TC Roloff, UA Nuber
European journal of cell biology 84 (2-3), 123-135, 2005
GRISEA, a putative copper-activated transcription factor fromPodospora anserina involved in differentiation and senescence
HD Osiewacz, U Nuber
Molecular and General Genetics MGG 252, 115-124, 1996
X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications
R Sudbrak, G Wieczorek, UA Nuber, W Mann, R Kirchner, F Erdogan, ...
Human molecular genetics 10 (1), 77-83, 2001
Prospectively isolated CD133/CD24‐positive ependymal cells from the adult spinal cord and lateral ventricle wall differ in their long‐term in vitro self‐renewal and in vivo …
CV Pfenninger, C Steinhoff, F Hertwig, UA Nuber
Glia 59 (1), 68-81, 2011
Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and Esx1 mutation
U Singh, LE Fohn, T Wakayama, J Ohgane, C Steinhoff, B Lipkowitz, ...
Developmental Dynamics: An Official Publication of the American Association …, 2004
Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation
UA Nuber, S Tinschert, S Mundlos, I Hauber
American Journal of Medical Genetics Part A 125 (3), 261-266, 2004
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