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Scientific Publications

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in J Mol Med

Dysfunction of dysferlin-deficient hearts

  • K. Wenzel
  • C. Geier
  • F. Qadri
  • N. Huebner
  • H. Schulz
  • B. Erdmann
  • V. Gross
  • D. Bauer
  • R. Dechend
  • R. Dietz
  • K.J. Osterziel
  • S. Spuler
  • C. Oezcelik
in J Allergy Clin Immunol

A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema

  • F. Schulz
  • I. Marenholz
  • R. Foelster-Holst
  • C. Chen
  • A. Sternjak
  • R. Baumgrass
  • J. Esparza-Gordillo
  • C. Grueber
  • R. Nickel
  • S. Schreiber
  • M. Stoll
  • M. Kurek
  • F. Rueschendorf
  • N. Huebner
  • U. Wahn
  • Y.A. Lee
in Mol Psychiatr

Association and linkage of allelic variants of the dopamine transporter gene in ADHD

  • S. Friedel
  • K. Saar
  • S. Sauer
  • A. Dempfle
  • S. Walitza
  • T. Renner
  • M. Romanos
  • C. Freitag
  • C. Seitz
  • H. Palmason
  • A. Scherag
  • C. Windemuth-Kieselbach
  • B.G. Schimmelmann
  • C. Wewetzer
  • J. Meyer
  • A. Warnke
  • K.P. Lesch
  • R. Reinhardt
  • B. Herpertz-Dahlmann
  • M. Linder
  • A. Hinney
  • H. Remschmidt
  • H. Schaefer
  • K. Konrad
  • N. Huebner
  • J. Hebebrand
in Genome Biol

Transcriptomic and phenotypic analysis of murine embryonic stem cell derived BMP2+ lineage cells: an insight into mesodermal patterning

  • M.X. Doss
  • S. Chen
  • J. Winkler
  • R. Hippler-Altenburg
  • M. Odenthal
  • C. Wickenhauser
  • S. Balaraman
  • H. Schulz
  • O. Hummel
  • N. Huebner
  • N. Ghosh-Choudhury
  • I. Sotiriadou
  • J. Hescheler
  • A. Sachinidis
in Nat Genet

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus

  • M.A. Lee-Kirsch
  • M. Gong
  • D. Chowdhury
  • L. Senenko
  • K. Engel
  • Y.A. Lee
  • U. de Silva
  • S.L. Bailey
  • T. Witte
  • T.J. Vyse
  • J. Kere
  • C. Pfeiffer
  • S. Harvey
  • A. Wong
  • S. Koskenmies
  • O. Hummel
  • K. Rohde
  • R.E. Schmidt
  • A.F. Dominiczak
  • M. Gahr
  • T. Hollis
  • F.W. Perrino
  • J. Lieberman
  • N. Huebner
in PLoS Biol

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis

  • C. Soederhaell
  • I. Marenholz
  • T. Kerscher
  • F. Rueschendorf
  • J. Esparza-Gordillo
  • M. Worm
  • C. Gruber
  • G. Mayr
  • M. Albrecht
  • K. Rohde
  • H. Schulz
  • U. Wahn
  • N. Huebner
  • Y.A. Lee
in Biochem Biophys Res Commun

The c-Myb functions as a downstream target of PDGF-mediated survival signal in vascular smooth muscle cells

  • Y. Chen
  • H. Xu
  • J. Liu
  • C. Zhang
  • A. Leutz
  • X. Mo
in Physiol Genomics

Quantitative genetic basis of arterial phenotypes in the Brown Norway rat

  • L. Kota
  • M. Osborne-Pellegrin
  • H. Schulz
  • J. Behmoaras
  • M. Coutard
  • M. Gong
  • N. Huebner
in J Mol Med

A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus

  • M.A. Lee-Kirsch
  • D. Chowdhury
  • S. Harvey
  • M. Gong
  • L. Senenko
  • K. Engel
  • C. Pfeiffer
  • T. Hollis
  • M. Gahr
  • F.W. Perrino
  • J. Lieberman
  • N. Huebner
in Biol Chem

Expression of the protein phosphatase 1 inhibitor KEPI is downregulated in breast cancer cell lines and tissues and involved in the regulation of the tumor suppressor EGR1 via the MEK-ERK pathway

  • K. Wenzel
  • K. Daskalow
  • F. Herse
  • S. Seitz
  • U. Zacharias
  • J.A. Schenk
  • H. Schulz
  • N. Huebner
  • B. Micheel
  • P.M. Schlag
  • K.J. Osterziel
  • C. Ozcelik
  • S. Scherneck
  • B. Jandrig