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Matrix Biology : Journal of the International Society for Matrix Biology|May 14, 2013
Identification of a Ninein (NIN) mutation in a family with spondyloepimetaphyseal dysplasia with joint laxity (leptodactylic type)-like phenotypeMelanie Grosch, Barbara Grüner, Stephanie Spranger, et al.
American Journal of Medical Genetics. Part A|January 12, 2005
Dominant negative mutations in the C-propeptide of COL2A1 cause platyspondylic lethal skeletal dysplasia, torrance type, and define a novel subfamily within the type 2 collagenopathiesAndreas Zankl, Luitgard Neumann, Jaako Ignatius, et al.
Plos One|March 26, 2013
Chemerin is an antimicrobial agent in human epidermisMagdalena Banas, Katarzyna Zabieglo, Gopinath Kasetty, et al.
Biochemical and Biophysical Research Communications|August 31, 2000
Genomic structure and in vivo expression of the human organic anion transporter 1 (hOAT1) geneA Bahn, D Prawitt, D Buttler, et al.
Nature Protocols|January 30, 2021
Determination of G-protein-coupled receptor oligomerization by molecular brightness analyses in single cellsAli Işbilir, Robert Serfling, Jan Möller, et al.
MMWR. Morbidity and Mortality Weekly Report|August 7, 2015
Lack of Measles Transmission to Susceptible Contacts from a Health Care Worker with Probable Secondary Vaccine Failure - Maricopa County, Arizona, 2015Jefferson Jones, Ron Klein, Saskia Popescu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 20, 2007
Stromal complement receptor CD21/35 facilitates lymphoid prion colonization and pathogenesisMark D Zabel, Mathias Heikenwalder, Marco Prinz, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|April 25, 2008
Automatic home monitoring of implantable cardioverter defibrillatorsJens Cosedis Nielsen, Hans Kottkamp, Markus Zabel, et al.
Plos One|April 25, 2014
Amyloid-β and proinflammatory cytokines utilize a prion protein-dependent pathway to activate NADPH oxidase and induce cofilin-actin rods in hippocampal neuronsKeifer P Walsh, Laurie S Minamide, Sarah J Kane, et al.
Endocrine|April 9, 2017
Mutations in proteasome-related genes are associated with thyroid hemiagenesisBartlomiej Budny, Ewelina Szczepanek-Parulska, Tomasz Zemojtel, et al.
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