Claudia Baumann

VEGF-A and -C but not -B mediate increased vascular permeability in preserved lung grafts.

Circulatory arrest during PBPC apheresis in an unrelated donor.

Targeted deletion of the epididymal receptor HE6 results in fluid dysregulation and male infertility.

Factors affecting the efficacy of peripheral blood progenitor cells collections by large-volume leukaphereses with standardized processing volumes.

Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts.

Systematic linkage disequilibrium analysis of SLC12A8 at PSORS5 confirms a role in susceptibility to psoriasis vulgaris.

Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis.

Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells.

Association of ATRX with pericentric heterochromatin and the Y chromosome of neonatal mouse spermatogonia.

ATRX marks the inactive X chromosome (Xi) in somatic cells and during imprinted X chromosome inactivation in trophoblast stem cells.

Persistence of histone H2AX phosphorylation after meiotic chromosome synapsis and abnormal centromere cohesion in poly (ADP-ribose) polymerase (Parp-1) null oocytes.

NEDD1 is crucial for meiotic spindle stability and accurate chromosome segregation in mammalian oocytes.

Sticky platelet syndrome as a possible cause for free flap failure--a case report.

The E3 ubiquitin ligase Itch regulates sorting nexin 9 through an unconventional substrate recognition domain.

Loss of maternal ATRX results in centromere instability and aneuploidy in the mammalian oocyte and pre-implantation embryo.

Chromatin configuration and epigenetic landscape at the sex chromosome bivalent during equine spermatogenesis.

Lymphoid-specific helicase (HELLS) is essential for meiotic progression in mouse spermatocytes.

Role of ATRX in chromatin structure and function: implications for chromosome instability and human disease.

Quantitative comparison of the expression of antimicrobial peptides in the oral mucosa and extraoral skin.

Tyrosine kinase expression profile in clear cell renal cell carcinoma.

Role of polycomb group protein cbx2/m33 in meiosis onset and maintenance of chromosome stability in the Mammalian germline.

Alterations of global histone H4K20 methylation during prostate carcinogenesis.

Amniotic membrane as part of a skin substitute for full-thickness wounds: an experimental evaluation in a porcine model.

Chromatin structure and ATRX function in mouse oocytes.

Identification of prostaglandin receptors in human ureters.

Histone hyperacetylation during meiosis interferes with large-scale chromatin remodeling, axial chromatid condensation and sister chromatid separation in the mammalian oocyte.

Early dynamic fate changes in haemogenic endothelium characterized at the single-cell level.

Alterations of global histone H3K9 and H3K27 methylation levels in bladder cancer.

Evaluation of human amniotic membrane as a wound dressing for split-thickness skin-graft donor sites.

Single-cell analyses of regulatory network perturbations using enhancer-targeting TALEs suggest novel roles for PU.1 during haematopoietic specification.

Mouse BRWD1 is critical for spermatid postmeiotic transcription and female meiotic chromosome stability.

T-bet- and STAT4-dependent IL-33 receptor expression directly promotes antiviral Th1 cell responses.

ATRX contributes to epigenetic asymmetry and silencing of major satellite transcripts in the maternal genome of the mouse embryo.

Lack of protein kinase C-delta (PKCδ) disrupts fertilization and embryonic development.

Arginine methyltransferases mediate an epigenetic ovarian response to endometriosis.