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Scientific Publications

1038 Results:
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/ Oncotarget

RAGE mediates S100A4-induced cell motility via MAPK/ERK and hypoxia signaling and is a prognostic biomarker for human colorectal cancer metastasis

  • M. Dahlmann
  • A. Okhrimenko
  • P. Marcinkowski
  • M. Osterland
  • P. Herrmann
  • J. Smith
  • C.W. Heizmann
  • P.M. Schlag
  • U. Stein
/ 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
/ Front Immunol

Pro-inflammatory TNF-α and IFN-γ promote tumor growth and metastasis via induction of MACC1

  • D. Kobelt
  • C. Zhang
  • I.A. Clayton-Lucey
  • R. Glauben
  • C. Voss
  • B. Siegmund
  • U. Stein
/ Am J Physiol Renal Physiol

Renal effects of Tamm-Horsfall protein (uromodulin) deficiency in mice

  • S. Bachmann
  • K. Mutig
  • J. Bates
  • P. Welker
  • B. Geist
  • V. Gross
  • F.C. Luft
  • N. Alenina
  • M. Bader
  • B.J. Thiele
  • K. Prasadan
  • H.S. Raffi
  • S. Kumar
/ J Gene Med

Use of the nuclease inhibitor aurintricarboxylic acid (ATA) for improved non-viral intratumoral in vivo gene transfer by jet-injection

  • W. Walther
  • U. Stein
  • R. Siegel
  • I. Fichtner
  • P.M. Schlag
/ J Med Genet

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

  • A.M. Kaindl
  • F. Rueschendorf
  • S. Krause
  • H.H. Goebel
  • K. Koehler
  • C. Becker
  • D. Pongratz
  • J. Mueller-Hoecker
  • P. Nuernberg
  • G. Stoltenburg-Didinger
  • H. Lochmueller
  • A. Huebner
/ Regul Pept

Altered renal response to acute volume expansion in transgenic rats harboring the human tissue kallikrein gene

  • K.T. Passaglio
  • O. Baltatu
  • R.P. Machado
  • A.M. Dos Reis
  • J.B. Pesquero
  • M. Bader
  • R.A. Santos
/ J Med Genet

Molecular karyotyping using an SNP array for genomewide genotyping

  • A. Rauch
  • F. Rueschendorf
  • J. Huang
  • U. Trautmann
  • C. Becker
  • C. Thiel
  • K.W. Jones
  • A. Reis
  • P. Nuernberg
/ Hypertension

Weight loss and the renin-angiotensin-aldosterone system

  • S. Engeli
  • J. Boehnke
  • K. Gorzelniak
  • J. Janke
  • P. Schling
  • M. Bader
  • F.C. Luft
  • A.M. Sharma
/ Nat Genet

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

  • L.A. Metherell
  • J.P. Chapple
  • S. Cooray
  • A. David
  • C. Becker
  • F. Rueschendorf
  • D. Naville
  • M. Begeot
  • B. Khoo
  • P. Nuernberg
  • A. Huebner
  • M.E. Cheetham
  • A.J.L. Clark