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in Eur J Hum Genet

Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy

  • Z.T. Kabaeva
  • A. Perrot
  • B. Wolter
  • R. Dietz
  • N. Cardim
  • J.M. Correia
  • H.D. Schulte
  • A.A. Aldashev
  • M.M. Mirrakhimov
  • K.J. Osterziel
in Herz

Fabry disease: focus on cardiac manifestations and molecular mechanisms

  • A. Perrot
  • K.J. Osterziel
  • M. Beck
  • R. Dietz
  • C. Kampmann
in Z Kardiol

The heart in Anderson Fabry disease

  • C. Kampmann
  • C.M. Wiethoff
  • A. Perrot
  • M. Beck
  • R. Dietz
  • K.J. Osterziel
in FEBS Lett

The LIM domain protein Lmo2 binds to AF6, a translocation partner of the MLL oncogene

  • V. Begay-Mueller
  • S. Ansieau
  • A. Leutz
in Circulation

Calcineurin in human heart hypertrophy

  • O. Ritter
  • S. Hack
  • K. Schuh
  • N. Roethlein
  • A. Perrot
  • K.J. Osterziel
  • H.D. Schulte
  • L. Neyses
in Science

Mediation of hippocampal mossy fiber long-term potentiation by presynaptic Ih channels

  • J. Mellor
  • R.A. Nicoll
  • D. Schmitz
in J Neurosci

Glutamine uptake by neurons: interaction of protons with system a transporters

  • F.A. Chaudhry
  • D. Schmitz
  • R.J. Reimer
  • P. Larsson
  • A.T. Gray
  • R. Nicoll
  • M. Kavanaugh
  • R.H. Edwards
in Rev Neurosci

Axonal gap junctions between principal neurons: a novel source of network oscillations, and perhaps epileptogenesis

  • R.D. Traub
  • A. Draguhn
  • M.A. Whittington
  • T. Baldeweg
  • A. Bibbig
  • E.H. Buhl
  • D. Schmitz