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Gene|June 15, 1988
Alkali myosin light chains in man are encoded by a multigene family that includes the adult skeletal muscle, the embryonic or atrial, and nonsarcomeric isoformsU Seidel, E Bober, B Winter, et al.
Rheumatology International|November 1, 2011
Incidence and clinical features of hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) and spectrum of mevalonate kinase (MVK) mutations in German childrenE Lainka, U Neudorf, P Lohse, et al.
The Journal of Biological Chemistry|December 15, 1989
An initiation codon mutation in the apoC-II gene (apoC-II Paris) of a patient with a deficiency of apolipoprotein C-IIS S Fojo, J L de Gennes, J Chapman, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 17, 2012
Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosisT Kümpfel, L-A Gerdes, T Wacker, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 3, 2010
Association of the interleukin-23 receptor gene variant rs11209026 with Crohn's disease in German childrenM Lacher, S Schroepf, J Helmbrecht, et al.
Neoplasma|August 11, 2007
Germline VHL gene mutations in three Serbian families with von Hippel-Lindau diseaseB R Stanojevic, P Lohse, G G Neskovic, et al.
Ecological Applications : a Publication of the Ecological Society of America|March 16, 2026
Marine heatwave and keystone predator loss drive broad-scale decline and hinder recovery of a rocky intertidal kelpFrancis D Gerraty, Karah N Cox-Ammann, Melissa A Douglas, et al.
Digestion|May 1, 2004
Extended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical featuresU Schiemann, Y Müller-Koch, M Gross, et al.
Journal of Lipid Research|January 1, 1993
Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn)H G Klein, P Lohse, N Duverger, et al.
Human Gene Therapy|February 15, 2001
Phenotypic correction of lipid storage and growth arrest in wolman disease fibroblasts by gene transfer of lysosomal acid lipaseU J Tietge, G Sun, S Czarnecki, et al.
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