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Scientific Publications

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/ Eur J Cancer

In vivo models for endocrine-dependent breast carcinomas: special considerations of clinical relevance

  • I. Fichtner
  • M. Becker
  • R. Zeisig
  • A. Sommer
/ Transplantation

Extracorporeal photopheresis in graft-versus-host disease: ultraviolet radiation mediates T cell senescence in vivo

  • S. Lee
  • B. Doerken
  • C.A. Schmitt
/ Am J Med Genet

Recurrent NF1 gene mutation in a patient with oligosymptomatic neurofibromatosis type 1 (NF1)

  • A. Buske
  • A. Gewies
  • R. Lehmann
  • K. Ruether
  • B. Algermissen
  • P. Nuernberg
  • S. Tinschert
/ Am J Hum Genet

A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort

  • J. Hampe
  • S. Schreiber
  • S.H. Shaw
  • K.F. Lau
  • S. Bridger
  • A.J. Macpherson
  • L.R. Cardon
  • H. Sakul
  • T.J. Harris
  • A. Buckler
  • J. Hall
  • P. Stokkers
  • S.J. van Deventer
  • P. Nuernberg
  • M.M. Mirza
  • J.C. Lee
  • J.E. Lennard-Jones
  • C.G. Mathew
  • M.E. Curran
/ Am J Med Genet

Novel twelve-generation kindred of fatal familial insomnia from germany representing the entire spectrum of disease expression

  • A. Harder
  • K. Jendroska
  • F. Kreuz
  • T. Wirth
  • C. Schafranka
  • N. Karnatz
  • A. Theallier-Janko
  • J. Dreier
  • K. Lohan
  • D. Emmerich
  • J. Cervos-Navarro
  • O. Windl
  • H.A. Kretzschmar
  • P. Nuernberg
  • R. Witkowski
/ Am J Med Genet

Two independent mutations in a family with neurofibromatosis type 1 (NF1)

  • A. Klose
  • H. Peters
  • S. Hoffmeyer
  • A. Buske
  • A. Lueder
  • D. Hess
  • R. Lehmann
  • P. Nuernberg
  • S. Tinschert
/ Nat Genet

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

  • K.J. Nowak
  • D. Wattanasirichaigoon
  • H.H. Goebel
  • M. Wilce
  • K. Pelin
  • K. Donner
  • R.L. Jacob
  • C. Huebner
  • K. Oexle
  • J.R. Anderson
  • C.M. Verity
  • K.N. North
  • S.T. Iannaccone
  • C.R. Mueller
  • P. Nuernberg
  • F. Muntoni
  • C. Sewry
  • I. Hughes
  • R. Sutphen
  • A.G. Lacson
  • K.J. Swoboda
  • J. Vigneron
  • C. Wallgren-Pettersson
  • A.H. Beggs
  • N.G. Laing
/ Am J Med Genet

McCune-Albright syndrome: clinical and molecular evidence of mosaicism in an unusual giant patient

  • S. Tinschert
  • H. Gerl
  • A. Gewies
  • H.P. Jung
  • P. Nuernberg
/ Electrophoresis

Changes in methylation patterns identified by two-dimensional DNA fingerprinting

  • K. Uhlmann
  • K. Marczinek
  • J. Hampe
  • G. Thiel
  • P. Nuernberg
/ Hum Mutat

A novel missense mutation 14259 G>A in the mitochondrial NADH dehydrogenase 6 gene (MTND6)

  • I. Aguilera
  • J.R. Garcia-Lozano
  • J. Bautista
  • A. Nunez-Roldan