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Scientific Publications

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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
/ Z Kardiol

Ca2+ channels, Ca2+ sparks, and regulation of arterial smooth muscle function

  • M. Gollasch
  • M. Loehn
  • M. Fuerstenau
  • M.T. Nelson
  • F.C. Luft
  • H. Haller
/ FASEB J

Protein kinase Calpha targeting is regulated by temporal and spatial changes in intracellular free calcium concentration [Ca2+]i

  • C. Maasch
  • S. Wagner
  • C. Lindschau
  • G. Alexander
  • K. Buchner
  • M. Gollasch
  • F.C. Luft
  • H. Haller
/ J Hypertens

Ca2+ channels, 'quantized' Ca2+ release, and differentiation of myocytes in the cardiovascular system

  • M. Gollasch
  • M. Loehn
  • M. Fuerstenau
  • M.T. Nelson
  • F.C. Luft
  • H. Haller
/ J Biomed Biotechnol

Role of ryanodine receptor subtypes in initiation and formation of calcium sparks in arterial smooth muscle: comparison with striated muscle

  • K. Essin
  • M. Gollasch
/ J Neurol

Clinical and genetic features in a family with CADASIL and high lipoprotein (a) values

  • M. Gong
  • F. Rueschendorf
  • P. Marx
  • H. Schulz
  • H.G. Kraft
  • N. Huebner
  • H.C. Koennecke
/ EMBO J

Gq-coupled receptors as mechanosensors mediating myogenic vasoconstriction

  • M. Mederos y Schnitzler
  • U. Storch
  • S. Meibers
  • P. Nurwakagari
  • A. Breit
  • K. Essin
  • M. Gollasch
  • T. Gudermann
/ J Orofac Orthop

Die primaere Durchbruchsstoerung (PFE) - klinische und molekulargenetische Analyse [Primary failure of eruption (PFE) - clinical and molecular genetics analysis]

  • A. Stellzig-Eisenhauer
  • E. Decker
  • P. Meyer-Marcotty
  • C. Rau
  • B.S. Fiebig
  • W. Kress
  • K. Saar
  • F. Rueschendorf
  • N. Huebner
  • T. Grimm
  • E. Witt
  • B.H. Weber
/ Am J Hum Genet

Mutations in SPINT2 cause a syndromic form of congenital sodium diarrhea

  • P. Heinz-Erian
  • T. Mueller
  • B. Krabichler
  • M. Schranz
  • C. Becker
  • F. Rueschendorf
  • P. Nuernberg
  • B. Rossier
  • M. Vujic
  • I.W. Booth
  • C. Holmberg
  • C. Wijmenga
  • G. Grigelioniene
  • C.M. Kneepkens
  • S. Rosipal
  • M. Mistrik
  • M. Kappler
  • L. Michaud
  • L.C. Doczy
  • V.M. Siu
  • M. Krantz
  • H. Zoller
  • G. Utermann
  • A.R. Janecke
/ Hypertension

Role of the multidomain protein spinophilin in blood pressure and cardiac function regulation

  • A.C. da Costa-Goncalves
  • J. Tank
  • R. Plehm
  • A. Diedrich
  • M. Todiras
  • M. Gollasch
  • A. Heuser
  • M. Wellner
  • M. Bader
  • J. Jordan
  • F.C. Luft
  • V. Gross