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Wissenschaftliche Publikationen

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/ J Genet Genomics

Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation

  • X. Su
  • Y. Feng
  • S.A. Rahman
  • S. Wu
  • G. Li
  • F. Rüschendorf
  • L. Zhao
  • H. Cui
  • J. Liang
  • L. Fang
  • H. Hu
  • S. Froehler
  • Y. Yu
  • G. Patone
  • O. Hummel
  • Q. Chen
  • K. Raile
  • F.C. Luft
  • S. Bähring
  • K. Hussain
  • W. Chen
  • J. Zhang
  • M. Gong
/ J Genet Genomics

Phosphatidylinositol 4-kinase β mutations cause nonsyndromic sensorineural deafness and inner ear malformation

  • X. Su
  • Y. Feng
  • S.A. Rahman
  • S. Wu
  • G. Li
  • F. Rüschendorf
  • L. Zhao
  • H. Cui
  • J. Liang
  • L. Fang
  • H. Hu
  • S. Froehler
  • Y. Yu
  • G. Patone
  • O. Hummel
  • Q. Chen
  • K. Raile
  • F.C. Luft
  • S. Bähring
  • K. Hussain
  • W. Chen
  • J. Zhang
  • M. Gong
/ Cell Mol Life Sci

MACC1 regulates clathrin-mediated endocytosis and receptor recycling of transferrin receptor and EGFR in colorectal cancer

  • F. Imbastari
  • M. Dahlmann
  • A. Sporbert
  • C. Ciolli Mattioli
  • T. Mari
  • F. Scholz
  • L. Timm
  • S. Twamley
  • R. Migotti
  • W. Walther
  • G. Dittmar
  • A. Rehm
  • U. Stein
/ Front Physiol

Activation of tripartite motif containing 63 expression by transcription factor EB and transcription factor binding to immunoglobulin heavy chain enhancer 3 is regulated by protein kinase D and class IIa histone deacetylases

  • C. Pablo Tortola
  • B. Fielitz
  • Y. Li
  • J. Rüdebusch
  • F.C. Luft
  • J. Fielitz
/ Acta Physiol

Adaptive physiological water conservation explains hypertension and muscle catabolism in experimental chronic renal failure

  • J. Kovarik
  • N. Morisawa
  • J. Wild
  • A. Marton
  • K. Takase-Minegishi
  • S. Minegishi
  • S. Daub
  • J.M. Sands
  • J.D. Klein
  • J.L. Bailey
  • J.P. Kovalik
  • M. Rauh
  • S. Karbach
  • K.F. Hilgers
  • F. Luft
  • A. Nishiyama
  • D. Nakano
  • K. Kitada
  • J. Titze
/ Acta Physiol

Aestivation motifs explain hypertension and muscle mass loss in mice with psoriatic skin barrier defect

  • J. Wild
  • R. Jung
  • T. Knopp
  • P. Efentakis
  • D. Benaki
  • A. Grill
  • J. Wegner
  • M. Molitor
  • V. Garlapati
  • N. Rakova
  • L. Markó
  • A. Marton
  • E. Mikros
  • T. Muenzel
  • S. Kossmann
  • M. Rauh
  • D. Nakano
  • K. Kitada
  • F. Luft
  • A. Waisman
  • P. Wenzel
  • J. Titze
  • S. Karbach
/ Internist

Molekulargenetik der humanen Hypertonie [Molecular genetics of human hypertension]

  • F.C. Luft
/ Circulation

Phosphodiesterase 3A and arterial hypertension

  • M. Ercu
  • L. Markó
  • C. Schächterle
  • D. Tsvetkov
  • Y. Cui
  • S. Maghsodi
  • T.U.P. Bartolomaeus
  • P.G. Maass
  • K. Zühlke
  • N. Gregersen
  • N. Hübner
  • R. Hodge
  • A. Mühl
  • B. Pohl
  • R. Molé-Illas
  • A. Geelhaar
  • S. Walter
  • H. Napieczynska
  • S. Schelenz
  • M. Taube
  • A. Heuser
  • Y.M. Anistan
  • F. Qadri
  • M. Todiras
  • R. Plehm
  • E. Popova
  • R. Langanki
  • J. Eichhorst
  • M. Lehmann
  • B. Wiesner
  • M. Russwurm
  • S.K. Forslund
  • I. Kamer
  • D.N. Müller
  • M. Gollasch
  • A. Aydin
  • S. Bähring
  • M. Bader
  • F.C. Luft
  • E. Klussmann
/ Physiol Rep

Effects of hemodialysis on plasma oxylipins

  • B. Gollasch
  • G. Wu
  • I. Dogan
  • M. Rothe
  • M. Gollasch
  • F.C. Luft
/ FASEB J

Hypochlorhydria reduces mortality in heart failure caused by Kcne2 gene deletion

  • U. Lisewski
  • C. Köhncke
  • L. Schleussner
  • B. Purfürst
  • S.M. Lee
  • A. De Silva
  • R.W. Manville
  • G.W. Abbott
  • T.K. Roepke