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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
/ Nat Biomed Eng

Enhanced precision and efficiency

  • S. Bashir
  • R. Kühn
/ Brain Commun

Subcellular localisation and formation of huntingtin aggregates correlates with symptom onset and progression in a Huntington's disease model

/ 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
/ Nutrition

Intestinal expression of TLR gene changes early after gastric bypass and association with type 2 diabetes remission

  • P. Sala
  • R.S.M.M. Torrinhas
  • D.C. Fonseca
  • N.M. Machado
  • J. Singer
  • P. Singer
  • G.R. Ravacci
  • G. Belarmino
  • B.A.M. Ferreira
  • M. Marques
  • R. K. Ishida
  • I.F.M.S. Guarda
  • E.G.H. de Moura
  • P. Sakai
  • M.A. Santo
  • D.Y. Sunaga
  • S.B. Heymsfield
  • D.P.S. Bezerra
  • M.L. Corrêa-Giannella
  • D.L. Waitzberg
/ Parkinsonism Relat Disord

Cognitive impairment in multiple system atrophy is related to white matter damage detected by the T1w/T2w ratio

  • M.A. Andrade-Navarro
  • G. Cooper
  • S. Hirano
  • H. Yokota
  • M. Mori
  • K. Shimizu
  • M. Yakiyama
  • C. Finke
  • A.U. Brandt
  • F. Paul
  • S. Kuwabara
/ Med Clin North Am

What have we learned from the genetics of hypertension?

  • F.C. Luft
/ J Clin Invest

S-sulfocysteine/NMDA receptor-dependent signaling underlies neurodegeneration in molybdenum cofactor deficiency

  • A. Kumar
  • B. Dejanovic
  • F. Hetsch
  • M. Semtner
  • D. Fusca
  • S. Arjune
  • J.A. Santamaria-Araujo
  • A. Winkelmann
  • S. Ayton
  • A.I. Bush
  • P. Kloppenburg
  • J.C. Meier
  • G. Schwarz
  • A.A. Belaidi
/ Mol Ther

CRISPR/Cas9-mediated ELANE mutation correction in hematopoietic stem and progenitor cells to treat severe congenital neutropenia

  • N.T. Tran
  • R. Graf
  • A. Wulf-Goldenberg
  • M. Stecklum
  • G. Strauß
  • R. Kühn
  • C. Kocks
  • K. Rajewsky
  • V.T. Chu
/ J Physiol

Master and commander? FoxO's role in muscle atrophy

  • H.T. Langer