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/ Hum Mol Genet

The progressive ankyloses protein ANK facilitates clathrin- and adaptor-mediated membrane traffic at the trans-Golgi network-to-endosome interface

  • W. Seifert
  • Y. Posor
  • P. Schu
  • G. Stenbeck
  • S. Mundlos
  • S. Klaassen
  • P. Nürnberg
  • V. Haucke
  • U. Kornak
  • J. Kühnisch
/ Nat Genet

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

  • A. Sifrim
  • M.P. Hitz
  • A. Wilsdon
  • J. Breckpot
  • S.H.A. Turki
  • B. Thienpont
  • J. McRae
  • T.W. Fitzgerald
  • T. Singh
  • G.J. Swaminathan
  • E. Prigmore
  • D. Rajan
  • H. Abdul-Khaliq
  • S. Banka
  • U.M.M. Bauer
  • J. Bentham
  • F. Berger
  • S. Bhattacharya
  • F. Bu'Lock
  • N. Canham
  • I.G. Colgiu
  • C. Cosgrove
  • H. Cox
  • I. Daehnert
  • A. Daly
  • J. Danesh
  • A. Fryer
  • M. Gewillig
  • E. Hobson
  • K. Hoff
  • T. Homfray
  • A.K. Kahlert
  • A. Ketley
  • H.H. Kramer
  • K. Lachlan
  • A.K. Lampe
  • J.J. Louw
  • A.K. Manickara
  • D. Manase
  • K.P. McCarthy
  • K. Metcalfe
  • C. Moore
  • R. Newbury-Ecob
  • S.O. Omer
  • W.H. Ouwehand
  • S.M. Park
  • M.J. Parker
  • T. Pickardt
  • M.O. Pollard
  • L. Robert
  • D.J. Roberts
  • J. Sambrook
  • K. Setchfield
  • B. Stiller
  • C. Thornborough
  • O. Toka
  • H. Watkins
  • D. Williams
  • M. Wright
  • S. Mital
  • P.E.F. Daubeney
  • B. Keavney
  • J. Goodship
  • R.M. Abu-Sulaiman
  • S. Klaassen
  • C.F. Wright
  • H.V. Firth
  • J.C. Barrett
  • K. Devriendt
  • D.R. FitzPatrick
  • J.D. Brook
  • M.E. Hurles
/ Eur Radiol

Value of cardiovascular MR in diagnosing left ventricular non-compaction cardiomyopathy and in discriminating between other cardiomyopathies

  • M. Grothoff
  • M. Pachowsky
  • J. Hoffmann
  • M. Posch
  • S. Klaassen
  • L. Lehmkuhl
  • M. Gutberlet
/ J Hypertens

MWF rats with spontaneous albuminuria inherit a reduced efficiency of nephron induction during early nephrogenesis in comparison to SHRs

  • L. Schulte
  • A. Schulz
  • J. Unland
  • H. Schulz
  • N. Hubner
  • K.M. Schmidt-Ott
  • R. Kreutz
/ PLoS Genet

Rare copy number variants contribute to congenital left-sided heart disease

  • M.P. Hitz
  • L.P. Lemieux-Perreault
  • C. Marshall
  • Y. Feroz-Zada
  • R. Davies
  • S.W. Yang
  • A.C. Lionel
  • G. D'Amours
  • E. Lemyre
  • R. Cullum
  • J.L. Bigras
  • M. Thibeault
  • P. Chetaille
  • A. Montpetit
  • P. Khairy
  • B. Overduin
  • S. Klaassen
  • P. Hoodless
  • P. Awadalla
  • J. Hussin
  • Y. Idaghdour
  • M. Nemer
  • A.F. Stewart
  • C. Boerkoel
  • S.W. Scherer
  • A. Richter
  • M.P. Dube
  • G. Andelfinger
/ Nat Med

RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

  • W. Guo
  • S. Schafer
  • M.L. Greaser
  • M.H. Radke
  • M. Liss
  • T. Govindarajan
  • H. Maatz
  • H. Schulz
  • S.E. Lincoln
  • A.M. Parrish
  • V. Dauksaite
  • P. Vakeel
  • S. Klaassen
  • B. Gerull
  • L. Thierfelder
  • V. Regitz-Zagrosek
  • T.A. Hacker
  • K.W. Saupe
  • G.W. Dec
  • P.T. Ellinor
  • C.A. MacRae
  • B. Spallek
  • R. Fischer
  • A. Perrot
  • C. Ozcelik
  • K. Saar
  • N. Hubner
  • M. Gotthardt
/ Am J Cardiol

Predictors of adverse outcome in adolescents and adults with isolated left ventricular noncompaction

  • M. Greutmann
  • M.L. Mah
  • C.K. Silversides
  • S. Klaassen
  • C.H. Attenhofer Jost
  • R. Jenni
  • E.N. Oechslin