P Lohse - Concepedia

Author

P Lohse

Ludwig-Maximilians-Universität München

Also Known As

P Lohse, P. Lohse, Peter Lohse, Pia Lohse, Sylke Maas

Publications

584

Citations

H-Index

Concepts

All Affiliations

Ludwig-Maximilians-Universität München National Institutes of Health Heidelberg University National Heart Lung and Blood Institute

About

P Lohse is an author at Ludwig-Maximilians-Universität München specializing in medicine, natural sciences, and biochemistry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	172
2	Natural Sciences	3	4	132
3	Biochemistry	3	4	132
4	Biology	1	1	60
5	Cell Biology	1	1	28

P Lohse

Publications

426

Citations

H-Index

Page 1

	Year	Citations
MRP8 and MRP14, phagocyte-specific danger signals, are sensitive biomarkers of disease activity in cryopyrin-associated periodic syndromes Helmut Wittkowski, J. B. Kuemmerle‐Deschner, Judith Austermann, Annals of the Rheumatic Diseases	2011	68
Microsatellite instability, loss of heterozygosity, and loss of hMLH1 and hMSH2 protein expression in endometrial carcinoma Gloria Peiró, Joachim Diebold, Peter Lohse, Human Pathology Tumor BiologySomatic VariantMedicineMicrosatellite InstabilityPathology	2002	61
Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met). Hanns‐Georg Klein, P Lohse, P. Haydn Pritchard, Journal of Clinical Investigation Lecithin-cholesterol Acyltransferase GeneGeneticsHyperlipidemiaMolecular GeneticsLecithin-cholesterol Acyltransferase	1992	60
Molecular analysis of the <i>MVK</i> and <i>TNFRSF1A</i> genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: A low‐penetrance <i>TNFRSF1A</i> variant in a heterozygous <i>MVK</i> carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa S Stojanov, Peter Lohse, P Lohse, Arthritis & Rheumatism	2004	42
Long-term follow-up and treatment of congenital alveolar proteinosis Matthias Griese, Jan Ripper, Anke Sibbersen, BMC Pediatrics	2011	35
R116C Mutation of Cationic Trypsinogen in a Turkish Family with Recurrent Pancreatitis Illustrates Genetic Microheterogeneity of Hereditary Pancreatitis Gerda Tautermann, H. Ruebsamen, Michael Till Beck, Digestion	2001	28
Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu). W. Alexander Mann, P Lohse, Richard E. Gregg, Journal of Clinical Investigation Dominant ExpressionLipid PeroxidationHyperlipidemiaKinetic CharacteristicsMutant Apoe Gene	1995	28
Familial Mediterranean fever in Germany: clinical presentation and amyloidosis risk Darius Ebrahimi‐Fakhari, Ute Hegenbart, P Lohse, Scandinavian Journal of Rheumatology	2012	28
Tumor necrosis factor receptor 1-associated periodic syndrome without fever: cytokine profile before and during etanercept treatment Henner Morbach, Petra Richl, S Stojanov, Rheumatology International InflammationCytokineAutoimmune DiseaseEtanercept TreatmentPathogenesis	2009	23
Human lysosomal acid lipase/cholesteryl ester hydrolase and human gastric lipase: site-directed mutagenesis of Cys227 and Cys236 results in substrate-dependent reduction of enzymatic activity P Lohse, P Lohse, S Chahrokh-Zadeh, Journal of Lipid Research Bioorganic ChemistryLipid SynthesisBiochemistryHuman Gastric LipaseNatural Sciences	1997	22

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