Roche (Sweden)

Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss

Christopher J. Klein, Maria Victoria Botuyan, Yanhong Wu et al. · Nature Genetics · 2011 · 391 citations · Full text

Neurodegenerative Diseases, Mendelian Disorder, Genetic Disorder +8

IκBα Deficiency Results in a Sustained NF-κB Response and Severe Widespread Dermatitis in Mice

John F. Klement, Nancy R. Rice, Bruce D. Car et al. · Molecular and Cellular Biology · 1996 · 341 citations · Full text

Signal Transduction Pathways, Immunology, Immune Regulation +23

Genome Sequencing and Mapping Reveal Loss of Heterozygosity as a Mechanism for Rapid Adaptation in the Vegetable Pathogen <i>Phytophthora capsici</i>

Kurt Lamour, Joann Mudge, Daniel Gobena et al. · Molecular Plant-Microbe Interactions · 2012 · 273 citations · Full text

Genetics, Plant Pathology, Genomics +16

Response to Rituximab Induction Is a Predictive Marker in B-Cell Post-Transplant Lymphoproliferative Disorder and Allows Successful Stratification Into Rituximab or R-CHOP Consolidation in an International, Prospective, Multicenter Phase II Trial

Ralf Ulrich Trappe, Daan Dierickx, Heiner Zimmermann et al. · Journal of Clinical Oncology · 2017 · 219 citations · Full text

Molecular cloning and sequence determination of rat preproenkephalin cDNA: sensitive probe for studying transcriptional changes in rat tissues.

Richard Howells, D L Kilpatrick, Ramesh R. Bhatt et al. · Proceedings of the National Academy of Sciences · 1984 · 191 citations · Full text

Sequence Determination, Molecular Regulation, Molecular Biology +22