T. Enklaar

发表

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

Thomas Eggermann, Jerry Pelletier, R. Cencic, 2016, Clinical Epigenetics.

Beckwith–Wiedemann syndrome: multiple molecular mechanisms

D. Prawitt, B. Zabel, T. Enklaar, 2006, Expert Reviews in Molecular Medicine.

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor.

Peter Schmidtke, Jerry Pelletier, Bernhard Zabel, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family.

A. Winterpacht, D. Prawitt, B. Zabel, 2000, Genomics.

The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites

M. Cubellis, B. Horsthemke, J. Beygo, 2012, Human molecular genetics.

Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis

R. Crazzolara, C. Bergmann, D. Prawitt, 2017, Pediatric blood & cancer.

Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.

S. Bens, R. Siebert, J. Richter, 2016, Epigenomics.

In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself

A. Hasenburg, D. Prawitt, W. Brenner, 2018, Cell Communication and Signaling.

TRPM5 regulates glucose-stimulated insulin secretion

R. Penner, A. Fleig, D. Prawitt, 2010, Pflügers Archiv - European Journal of Physiology.

TRPM 5 regulates glucose-stimulated insulin secretion

R. Penner, A. Fleig, D. Prawitt, 2010 .

Genomic structure and in vivo expression of the human organic anion transporter 1 (hOAT1) gene.

David J. Buttler, G. Reid, G. Burckhardt, 2000, Biochemical and biophysical research communications.

Identification and characterization of MTR1, a novel gene with homology to melastatin (MLSN1) and the trp gene family located in the BWS-WT2 critical region on chromosome 11p15.5 and showing allele-specific expression.

J. Pelletier, A. Winterpacht, D. Prawitt, 2000, Human molecular genetics.

Premature senescence is a primary fail-safe mechanism of ERBB2-driven tumorigenesis in breast carcinoma cells.

Jan G Hengstler, Peter Schmidtke, Steffen Schmitt, 2005, Cancer research.

Microdeletion and IGF2 loss of imprinting in a cascade causing Beckwith-Wiedemann syndrome with Wilms' tumor

D. Housman, J. Pelletier, D. Reutzel, 2005, Nature Genetics.

Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation

R. Cencic, J. Pelletier, T. Eggermann, 2016, Clinical Epigenetics.

Beckwith-Wiedemann-Syndrom

D. Prawitt, B. Zabel, T. Enklaar, 2010 .

Mapping and structure of DMXL1, a human homologue of the DmX gene from Drosophila melanogaster coding for a WD repeat protein.

B. Zabel, E. Schmidt, E R Schmidt, 2000, Genomics.

Adding efficiency: The role of the CAN ion channels TRPM4 and TRPM5 in pancreatic islets

D. Prawitt, B. Zabel, L. Brixel, 2010, Islets.

Human CLAPS2 encoding AP17, a small chain of the clathrin-associated protein complex: cDNA cloning and chromosomal assignment to 19q13.2-->q13.3.

A. Winterpacht, M. Fuhry, S. Endele, 1996, Cytogenetics and Cell Genetics.