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in J Neurosci Res

Glial cell line‐derived neurotrophic factor increases matrix metallopeptidase 9 and 14 expression in microglia and promotes microglia‐mediated glioma progression

  • Y. Huang
  • B. Zhang
  • H. Haneke
  • V. Haage
  • M. Lubas
  • Y. Yuan
  • P. Xia
  • E. Motta
  • C. Nanvuma
  • O. Dzaye
  • F. Hu
  • H. Kettenmann
in Eur J Med Chem

Design and synthesis of novel fluorescently labeled analogs of vemurafenib targeting MKK4

  • T. Kircher
  • T. Pantsar
  • A. Oder
  • J.P. von Kries
  • M. Juchum
  • B. Pfaffenrot
  • P. Kloevekorn
  • W. Albrecht
  • R. Selig
  • S. Laufer
in Brain Behav Immun

Deletion of muscarinic acetylcholine receptor 3 in microglia impacts brain ischemic injury

  • A. Costa
  • V. Haage
  • S. Yang
  • S. Wegner
  • B. Ersoy
  • B. Ugursu
  • A. Rex
  • G. Kronenberg
  • K. Gertz
  • M. Endres
  • S.A. Wolf
  • H. Kettenmann
in J Med Chem

From pyrazolones to azaindoles: evolution of active-site SHP2 inhibitors based on scaffold hopping and bioisosteric replacement

  • Y. Mostinski
  • G.J.J.E. Heynen
  • M.P. López-Alberca
  • J. Paul
  • S. Miksche
  • S. Radetzki
  • D. Schaller
  • E. Shanina
  • C. Seyffarth
  • Y. Kolomeets
  • N. Ziebart
  • J. de Schryver
  • S. Oestreich
  • M. Neuenschwander
  • Y. Roske
  • U. Heinemann
  • C. Rademacher
  • A. Volkamer
  • J.P. von Kries
  • W. Birchmeier
  • M. Nazaré
in Exp Cell Res

Down-regulation of Aquaporin-1 mediates a microglial phenotype switch affecting glioma growth

  • F. Hu
  • Y. Huang
  • M. Semtner
  • K. Zhao
  • Z. Tan
  • O. Dzaye
  • H. Kettenmann
  • K. Shu
  • T. Lei
in Genes

Genetic spectrum of syndromic and non-syndromic hearing loss in Pakistani families

  • J. Doll
  • B. Vona
  • L. Schnapp
  • F. Rüschendorf
  • I. Khan
  • S. Khan
  • N. Muhammad
  • S. Alam Khan
  • H. Nawaz
  • A. Khan
  • N. Ahmad
  • S.M. Kolb
  • L. Kühlewein
  • J.D.J. Labonne
  • L.C. Layman
  • M.A.H. Hofrichter
  • T. Röder
  • M. Dittrich
  • T. Müller
  • T.D. Graves
  • I.K. Kong
  • I. Nanda
  • H.G. Kim
  • T. Haaf
in 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
in 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
in Neurobiol Dis

Neurofibromatosis 1 - mutant microglia exhibit sexually-dimorphic cyclic AMP-dependent purinergic defects

  • N. Elmadany
  • F. Logiacco
  • A. Buonfiglioli
  • V. Haage
  • E.C. Wright-Jin
  • A. Schattenberg
  • R. Papawassiliou
  • H. Kettenmann
  • M. Semtner
  • D.H. Gutmann
in Acta Neuropathol Commun

Activation of Toll-like receptor 5 in microglia modulates their function and triggers neuronal injury

  • M. Ifuku
  • L. Hinkelmann
  • L.D. Kuhrt
  • I.E. Efe
  • V. Kumbol
  • A. Buonfiglioli
  • C. Krüger
  • P. Jordan
  • M. Fulde
  • M. Noda
  • H. Kettenmann
  • S. Lehnardt