proline and Amyloidosis

proline has been researched along with Amyloidosis in 22 studies

Research

Studies (22)

Timeframe	Studies, this research(%)	All Research%
pre-1990	3 (13.64)	18.7374
1990's	5 (22.73)	18.2507
2000's	8 (36.36)	29.6817
2010's	4 (18.18)	24.3611
2020's	2 (9.09)	2.80

Authors

Authors	Studies
Berk, JL; Burks, EJ; Chen, H; Chiu, A; Choate, LA; Connors, LH; Cuddy, SAM; Cui, H; Dasari, S; Gibson, VM; Hu, Y; Joshi, T; Klimtchuk, ES; McPhail, ED; Nedelkov, D; Prokaeva, T; Sanchorawala, V; Siddiqi, O; Spencer, B	1
Cappelli, C; Delbarba, A; Di Lodovico, E; Facchetti, F; Facondo, P; Ferlin, A; Fisogni, S; Izzi, C; Maffezzoni, F; Pezzaioli, LC; Scolari, F	1
Kelly, JW; Morgan, GJ; Usher, GA	1
Hilvert, D; Torbeev, VY	1
Bellotti, V; Chen, W; Clatworthy, IR; Gillmore, JD; Giorgetti, S; Hawkins, PN; Mangione, PP; Marchese, L; Marcoux, J; Monti, M; Pepys, MB; Porcari, M; Porcari, R; Pucci, P; Raimondi, S; Relini, A; Robinson, CV; Serpell, LC; Stoppini, M; Taylor, GW; Tennent, GA; Wood, SP	1
Frosch, MP; Greenberg, SM; Nakagawa, K; Sheikh, SI; Snuderl, M	1
Barbiroli, A; Bellotti, V; Bolognesi, M; Bonomi, F; Colombo, M; Giorgetti, S; Grandori, R; Raimondi, S; Ricagno, S; Santambrogio, C	1
Fernandes, R; Palha, JA; Saraiva, MJ; Sousa, MM; Taboada, A; Vieira, P	1
PERKOFF, GT	1
Coriu, D; Dispenzieri, A; Murphy, CL; Solomon, A; Stevens, FJ; Wang, S; Weiss, DT	1
Arbustini, E; Bellotti, V; Bergonzi, C; Calabresi, L; Donadei, S; Giorgetti, S; Gregorini, G; Marciano, S; Merlini, G; Obici, L; Palladini, G; Perfetti, V; Scolari, F; Verga, L	1
Affeldt, JA; Aldave, AJ; Gutmark, JG; Klintworth, GK; Meallet, MA; Rao, NA; Small, KW; Udar, N; Yellore, VS	1
Colón, W; Kelly, JW; Lai, Z; McCutchen, SL; Miroy, GJ	1
Higuchi, K; Naiki, H; Nakakuki, K; Shimada, A; Takeda, T	1
Ferlini, A; Forabosco, A; Gobbi, P; Mencucci, R; Michelucci, R; Plasmati, R; Salvi, F; Salvi, G; Santangelo, M; Volpe, R	1
Damas, AM; Merlini, G; Saraiva, MJ; Sebastião, MP	1
Fast, J; Håkansson, M; Linse, S; Svensson, A	1
Fersht, AR; Galani, D; Perrett, S	1
Buxbaum, JN; Jacobson, DR; Kane, I; McFarlin, DE	1
Almeida, MR; Altland, K; Costa, PP; Gawinowicz, M; Moreira, P; Rauh, S; Saraiva, MJ	1
Braun, HJ	1
Kissane, JM	1

Reviews

3 review(s) available for proline and Amyloidosis

Article	Year
FAMILIAL ASPECTS OF DIFFUSE RENAL DISEASES. Annual review of medicine, 1964, Volume: 15 Topics: Amyloidosis; Angiokeratoma; Blood; Congenital Abnormalities; Deafness; Genetics, Medical; Hematuria; Humans; Hydroxyproline; Kidney; Kidney Diseases; Nephritis; Paralyses, Familial Periodic; Polycystic Kidney Diseases; Proline; Skin Neoplasms; Urticaria	1964
[Properties of the amyloid and views on the pathogenesis of amyloidosis]. Medizinische Klinik, 1972, Oct-06, Volume: 67, Issue:40 Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Animals; Antigens; Birefringence; Caseins; Glycosaminoglycans; Humans; Hydroxyproline; Lipids; Molecular Conformation; Proline; Solubility; Staining and Labeling; Tryptophan	1972
Hereditary disorders of the kidney. II. Hereditary nephropathies. Perspectives in pediatric pathology, 1973, Volume: 1 Topics: Adolescent; Adult; Aldosterone; Amyloidosis; Bone Resorption; Child; Child, Preschool; Female; Glomerulonephritis; Humans; Infant; Juxtaglomerular Apparatus; Kidney; Kidney Calculi; Kidney Diseases; Kidney Neoplasms; Laurence-Moon Syndrome; Lipodystrophy; Male; Metabolic Diseases; Middle Aged; Muscular Atrophy; Nail-Patella Syndrome; Nephritis; Nephrotic Syndrome; Potassium; Proline; Renal Tubular Transport, Inborn Errors	1973

Other Studies

19 other study(ies) available for proline and Amyloidosis

Article	Year
A novel substitution of proline (P32L) destabilises β2-microglobulin inducing hereditary systemic amyloidosis. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2022, Volume: 29, Issue:4 Topics: Amyloid; Amyloidosis; Amyloidosis, Familial; beta 2-Microglobulin; Humans; Proline	2022
Testicular Involvement is a Hallmark of Apo A-I Leu75Pro Mutation Amyloidosis. The Journal of clinical endocrinology and metabolism, 2020, 12-01, Volume: 105, Issue:12 Topics: Adolescent; Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Amyloidosis; Apolipoprotein A-I; Cohort Studies; Databases, Factual; Genetic Predisposition to Disease; Humans; Italy; Leucine; Male; Middle Aged; Mutation, Missense; Proline; Retrospective Studies; Testicular Diseases; Testis; Young Adult	2020
Incomplete Refolding of Antibody Light Chains to Non-Native, Protease-Sensitive Conformations Leads to Aggregation: A Mechanism of Amyloidogenesis in Patients? Biochemistry, 2017, Dec-19, Volume: 56, Issue:50 Topics: Alanine; Amyloid; Amyloidosis; Circular Dichroism; Endopeptidases; Humans; Immunoglobulin Light Chains; Kinetics; Models, Molecular; Proline; Protein Aggregates; Protein Conformation; Protein Folding; Thermodynamics	2017
Both the cis-trans equilibrium and isomerization dynamics of a single proline amide modulate β2-microglobulin amyloid assembly. Proceedings of the National Academy of Sciences of the United States of America, 2013, Dec-10, Volume: 110, Issue:50 Topics: Amides; Amyloidosis; beta 2-Microglobulin; Chromatography, Gel; Chromatography, High Pressure Liquid; Circular Dichroism; Dialysis; Humans; Isomerism; Magnetic Resonance Spectroscopy; Models, Molecular; Molecular Structure; Proline; Protein Conformation; Solubility	2013
Proteolytic cleavage of Ser52Pro variant transthyretin triggers its amyloid fibrillogenesis. Proceedings of the National Academy of Sciences of the United States of America, 2014, Jan-28, Volume: 111, Issue:4 Topics: Amino Acid Sequence; Amyloid; Amyloidosis; Crystallography, X-Ray; Humans; Hydrogen Bonding; Molecular Conformation; Molecular Sequence Data; Phenotype; Prealbumin; Proline; Proteolysis; Serine	2014
A new Thr49Pro transthyretin gene mutation associated with leptomeningeal amyloidosis. Journal of the neurological sciences, 2008, Sep-15, Volume: 272, Issue:1-2 Topics: Amyloidosis; DNA Mutational Analysis; Humans; Magnetic Resonance Imaging; Male; Meninges; Middle Aged; Mutation; Prealbumin; Proline; Threonine	2008
The effects of an ideal beta-turn on beta-2 microglobulin fold stability. Journal of biochemistry, 2011, Volume: 150, Issue:1 Topics: Alzheimer Disease; Amino Acid Substitution; Amyloid; Amyloidosis; beta 2-Microglobulin; Crystallography, X-Ray; Humans; Mutation; Proline; Protein Folding; Protein Stability; Protein Structure, Secondary	2011
Evidence for early cytotoxic aggregates in transgenic mice for human transthyretin Leu55Pro. The American journal of pathology, 2002, Volume: 161, Issue:5 Topics: Amyloid; Amyloid Neuropathies, Familial; Amyloidosis; Animals; Coloring Agents; Congo Red; Genetic Vectors; Humans; Immunohistochemistry; Intestine, Small; Leucine; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Microscopy, Immunoelectron; Mutation; Oxidative Stress; Prealbumin; Proline; RNA, Messenger; Skin	2002
Hepatic amyloidosis resulting from deposition of the apolipoprotein A-I variant Leu75Pro. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis, 2003, Volume: 10, Issue:4 Topics: Amino Acid Sequence; Amino Acid Substitution; Amyloidosis; Apolipoprotein A-I; DNA; Female; Genetic Variation; Humans; Leucine; Liver; Liver Diseases; Mass Spectrometry; Middle Aged; Molecular Sequence Data; Mutation; Plasma; Polymorphism, Restriction Fragment Length; Proline; Sequence Homology, Amino Acid	2003
Liver biopsy discloses a new apolipoprotein A-I hereditary amyloidosis in several unrelated Italian families. Gastroenterology, 2004, Volume: 126, Issue:5 Topics: Aged; Amyloidosis; Apolipoprotein A-I; Biopsy; DNA; Female; Heterozygote; Humans; Italy; Leucine; Liver; Male; Microscopy, Immunoelectron; Middle Aged; Mutation; Pedigree; Proline	2004
Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene. American journal of ophthalmology, 2004, Volume: 138, Issue:5 Topics: Adult; Alanine; Amyloid; Amyloidosis; Aspartic Acid; Cornea; Corneal Dystrophies, Hereditary; DNA Mutational Analysis; Exons; Extracellular Matrix Proteins; Female; Glutamine; Haplotypes; Humans; Mutation, Missense; Pedigree; Proline; Transforming Growth Factor beta	2004
Comparison of lethal and nonlethal transthyretin variants and their relationship to amyloid disease. Biochemistry, 1995, Oct-17, Volume: 34, Issue:41 Topics: Amino Acid Sequence; Amyloidosis; Base Sequence; DNA Primers; Electrophoresis, Polyacrylamide Gel; Genes, Lethal; Genetic Variation; Humans; Hydrogen-Ion Concentration; Kinetics; Leucine; Lysosomes; Macromolecular Substances; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Point Mutation; Prealbumin; Proline; Protein Denaturation; Protein Structure, Secondary; Recombinant Proteins; Structure-Activity Relationship	1995
Genetic analysis of murine senile amyloidosis. Laboratory investigation; a journal of technical methods and pathology, 1993, Volume: 68, Issue:3 Topics: Aging; Amyloidosis; Animals; Dementia; DNA; Genotype; Glutamine; Mice; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Protein Precursors; Serum Amyloid A Protein; Spectrometry, Fluorescence	1993
Transthyretin-related TTR hereditary amyloidosis of the vitreous body. Clinical and molecular characterization in two Italian families. Ophthalmic paediatrics and genetics, 1993, Volume: 14, Issue:1 Topics: Adult; Aged; Alanine; Amyloidosis; Eye Diseases; Female; Humans; Lens Diseases; Male; Middle Aged; Mutation; Pedigree; Prealbumin; Proline; Ultrasonography; Vitreous Body	1993
The molecular interaction of 4'-iodo-4'-deoxydoxorubicin with Leu-55Pro transthyretin 'amyloid-like' oligomer leading to disaggregation. The Biochemical journal, 2000, Oct-01, Volume: 351, Issue:Pt 1 Topics: Amino Acid Substitution; Amyloidosis; Benzothiazoles; Crystallization; Doxorubicin; Humans; Iodine; Leucine; Models, Molecular; Prealbumin; Proline; Protein Binding; Protein Structure, Secondary; Thiazoles; X-Ray Diffraction	2000
An extended hydrophobic core induces EF-hand swapping. Protein science : a publication of the Protein Society, 2001, Volume: 10, Issue:5 Topics: Amino Acid Substitution; Amyloidosis; Apoproteins; Binding Sites; Calbindins; Calcium; Chromatography, Gel; Crystallography, X-Ray; Dimerization; EF Hand Motifs; Kinetics; Methionine; Models, Molecular; Mutation; Proline; Protein Structure, Quaternary; Protein Structure, Tertiary; S100 Calcium Binding Protein G; Structure-Activity Relationship; Thermodynamics	2001
Folding of the yeast prion protein Ure2: kinetic evidence for folding and unfolding intermediates. Journal of molecular biology, 2002, Jan-11, Volume: 315, Issue:2 Topics: Amyloidosis; Dimerization; Fluorescence; Glutathione Peroxidase; Guanidine; Isomerism; Kinetics; Models, Biological; Mutation; Prions; Proline; Protein Denaturation; Protein Folding; Protein Renaturation; Protein Structure, Tertiary; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Solutions; Thermodynamics; Water	2002
Transthyretin Pro55, a variant associated with early-onset, aggressive, diffuse amyloidosis with cardiac and neurologic involvement. Human genetics, 1992, Volume: 89, Issue:3 Topics: Amyloidosis; Base Sequence; Cardiomyopathies; Cell Line, Transformed; Female; Humans; Male; Molecular Sequence Data; Mutation; Nucleic Acid Conformation; Pedigree; Peripheral Nervous System Diseases; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Prealbumin; Proline	1992
Characterization of a basic transthyretin variant--TTR Arg 102--in the German population. Biochimica et biophysica acta, 1991, Oct-21, Volume: 1097, Issue:3 Topics: Amyloidosis; Arginine; Base Sequence; Exons; Female; Genetic Testing; Genetic Variation; Germany; Humans; Molecular Sequence Data; Mutation; Peptide Mapping; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Prealbumin; Pregnancy; Proline	1991