C. P. J. Maury - Concepedia

Author

C. P. J. Maury

University of Helsinki ORCID

Also Known As

C P Maury, C. P. J. Maury, C. Peter J. Maury, C.P Maury, C.P.J. Maury, Carl Peter J. Maury

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Helsinki

About

C. P. J. Maury is an author at University of Helsinki specializing in medicine, pathology, and alzheimer's disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	429
2	Natural Sciences	3	3	101
3	Immunology	3	3	91
4	Biochemistry	2	2	52
5	Cell Biology	2	2	52

C. P. J. Maury

Publications

Citations

H-Index

Page 1

	Year	Citations
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene C. P. J. Maury, Juha Kere, Riina Tolvanen, FEBS Letters	1990	137
Finnish hereditary amyloidosis C. P. J. Maury, K. Alii, Marc Baumann FEBS Letters	1990	118
Amyloid and the origin of life: self-replicating catalytic amyloids as prebiotic informational and protometabolic entities C. P. J. Maury Cellular and Molecular Life Sciences	2018	106
Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease C. P. J. Maury, Juha Kere, Riina Tolvanen, Genomics UrologyMedicineGeneticsRenal PathologyAsn187 Gelsolin Mutation	1992	64
Isolation and characterization of cardiac amyloid in familial amyloid polyneuropathy type IV (Finnish): relation of the amyloid protein to variant gelsolin C. P. J. Maury Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease CardiomyopathyAlzheimer's DiseaseAmyloid ProteinCardiac AmyloidProtein Misfolding	1990	63
Familial amyloidosis, Finnish type: G654 → A mutation of the gelsolin gene in Finnish families and an unrelated American family Albert de la Chapelle, Juha Kere, George H. Sack, Genomics Genetic DisorderGeneticsFinnish FamiliesGenetic EpidemiologyPathology	1992	63
Amyloid fibril formation in gelsolin-derived amyloidosis. Definition of the amyloidogenic region and evidence of accelerated amyloid formation of mutant Asn-187 and Tyr-187 gelsolin peptides. C. P. J. Maury, Eeva‐Liisa Nurmiaho‐Lassila, Hernan Rossi PubMed	1994	59
Origin of life. Primordial genetics: Information transfer in a pre-RNA world based on self-replicating beta-sheet amyloid conformers C. P. J. Maury Journal of Theoretical Biology Protein AssemblyGeneticsGenomic MechanismMolecular BiologyMolecular Genetics	2015	49
Comparative study of serum amyloid-related protein SAA, C-reactive protein, and beta 2-microglobulin as markers of renal allograft rejection. C. P. J. Maury, A.-M. Teppo PubMed Renal PathologyImmunologyPathologyRejection DiagnosisGlomerulonephritis	1984	43
Variant plasma gelsolin responsible for familial amyloidosis (Finnish type) has defective actin severing activity Alan G. Weeds, John Gooch, Paul McLaughlin, FEBS Letters Amyloid ProteinPathologyMolecular BiologyCytoskeletonProtein Phase Separation	1993	40

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