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Digestive Diseases and Sciences|April 4, 2007
CARD15 genotype-phenotype relationships in a small inflammatory bowel disease population with severe disease affection statusNigel P S Crawford, Daniel W Colliver, M Robert Eichenberger, et al.
Science (New York, N.Y.)|May 30, 2009
A role for the CHC22 clathrin heavy-chain isoform in human glucose metabolismStéphane Vassilopoulos, Christopher Esk, Sachiko Hoshino, et al.
Clinical Genetics|September 17, 2013
A systematic approach to assessing the clinical significance of genetic variantsH Duzkale, J Shen, H McLaughlin, et al.
Cardiogenetics|September 25, 2013
Familial dilated cardiomyopathy associated with congenital defects in the setting of a novel VCL mutation (Lys815Arg) in conjunction with a known MYPBC3 variantQuinn S Wells, Natalie L Ausborn, Birgit H Funke, et al.
Dalton Transactions (Cambridge, England : 2003)|April 5, 2019
Red-emitting K3HF2WO2F4:Mn4+ for application in warm-white phosphor-converted LEDs - optical properties and magnetic resonance characterizationThomas Jansen, Lena Marie Funke, Jürgen Gorobez, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|November 6, 2016
Toll-like receptor 4 activation attenuates profibrotic response in control lung fibroblasts but not in fibroblasts from patients with IPFSimone Ebener, Sandra Barnowski, Carlos Wotzkow, et al.
Pediatric Research|October 17, 1998
Plasma levels and gene expression of granulocyte colony-stimulating factor, tumor necrosis factor-alpha, interleukin (IL)-1beta, IL-6, IL-8, and soluble intercellular adhesion molecule-1 in neonatal early onset sepsisR Berner, C M Niemeyer, J U Leititis, et al.
Respiratory Research|January 30, 2020
Correction to: Azithromycin has enhanced effects on lung fibroblasts from idiopathic pulmonary fibrosis (IPF) patients compared to controlsKristina Krempaska, Sandra Barnowski, Jacopo Gavini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2016
Navigating highly homologous genes in a molecular diagnostic setting: a resource for clinical next-generation sequencingDiana Mandelker, Ryan J Schmidt, Arunkanth Ankala, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohortG Kuhlenbäumer, K Berger, A Huge, et al.
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