Caracciolo, Domenico, marchese,
Attributed to Domenico Caracciolo by Goldsmiths' Library. Includes 6-page quotation in French from Jacques Necker. Book.
0000 - Gale Group | The Making of Modern World
P. Grippo, Elio Parisi, Clementina Carestia, Eduardo Scarano,
... and its nonrandom distributionPasquale Grippo, Elio Parisi, Clementina Carestia, and Eduardo ScaranoCite this: Biochemistry 1970, 9, 13, ...
Tópico(s): Metal complexes synthesis and properties
1970 - American Chemical Society | Biochemistry
Errata: p. [6]. Book.
0000 - Gale Group | The Making of Modern World
Qiuying Huang, Xudong Wang, Ning Tang, Tizhen Yan, Ping Chen, Qingge Li,
... N.F. Esposito M. Nigro V. Gaudiano C. Carestia C. Sequence variations of the alpha-globin genes: ... N.F. Esposito M. Nigro V. Gaudiano C. Carestia C. Sequence variations of the alpha-globin genes: ...
Tópico(s): Forensic and Genetic Research
2017 - Elsevier BV | Journal of Molecular Diagnostics
Book.
0000 - Gale Group | World Scholar Latin America
... que las epidemias «puras», sin relación con una carestía de los cereales, no parecían haber ejercido una ... crisis es la epidemia, sin la cual la carestía apenas podría mostrar sus efectos sobre la mortalidad».
Tópico(s): Climate Change and Health Impacts
1988 - Centro de Estudios Constitucionales | Revista de Historia Económica / Journal of Iberian and Latin American Economic History
Capriata di Sardigliano, Vasallo Domenico,
Attributed to V.D. Capriata di Sardigliano--Cf. NUC pre-1956. Book.
0000 - Gale Group | The Making of Modern World
... a part of the work of the Abbé Carestia, one of the most assiduous researchers of the Valsesian flora. The Abbé Antonio Carestia, born in 1825 and died in 1908 at ... with exception of a species list, prepared by Carestia for publication by the Italian Alpine Club (Varallo Sesia Section). The collection of the Abbé Carestia left at his death, are conserved in large ... in the Calderini Museum. The catalogue of the Carestia collections included in this papers, limited to the ... owing to excange of specimens, the collections of Carestia are found in many Herbaria, Italian and foreign; ...
Tópico(s): Lichen and fungal ecology
1954 - Taylor & Francis | Giornale botanico italiano
"Tassa general de los precios a que se han de vender las mercaderias ...": leaves [1]-17 (3rd group). Book.
0000 - Gale Group | The Making of Modern World
Tópico(s): Insect and Arachnid Ecology and Behavior
1967 - | Mosquito news
Errata: p. [6]. Book.
0000 - Gale Group | The Making of Modern World
Piero Pucci, Clementina Carestia, G Fioretti, A.M. Mastrobuoni, Livio Pagano,
A procedure using fast atom bombardment mass spectrometry was developed for mapping the proteolytic digest of proteins. The procedure was successfully applied to the tryptic peptides of the human β-globin chain. Almost all the expected peptides were identified by direct analysis of the peptide mixture on the mass spectrometer. Peptide recognition along the β-globin chain sequence was easily made on the basis of their molecular weight. The general applicability of this mapping procedure in the analysis ...
Tópico(s): Protein Structure and Dynamics
1985 - Elsevier BV | Biochemical and Biophysical Research Communications
... Office Policy, Noticias Diversas, Western Province Floods, A Carestia Da Vida Em Inglaterra, Vienna Sidetracked, Beira Tide ...
1913 - Gale Group | NCCO EuropeAfrica
Clementina Carestia, Livio Pagano, G Fioretti, A Mastrobuoni,
In order to evaluate the feasibility of first trimester prenatal diagnosis of beta-thalassaemia by restriction fragment length polymorphism (RFLP) in Campania, one of the most affected regions in Southern Italy, DNA polymorphism analysis was performed on 40 unrelated patients, affected with homozygous beta-thalassaemia, and on their parents. Frequency of the presence of the Hinc II epsilon, Hind III G gamma and A gamma, Hinc II psi beta and 3' psi beta, Ava II psi beta, Ava II beta and Bam HI 3' ...
Tópico(s): Hemoglobinopathies and Related Disorders
1987 - Wiley | British Journal of Haematology
Clementina Carestia, Livio Pagano, G. F Ioretti, A Mastrobuoni,
Summary In order to evaluate the feasibility of first trimester prenatal diagnosis of β‐thalassaemia by restriction fragment length polymorphism (RFLP) in Campania, one of the most affected regions in Southern Italy, DNA polymorphism analysis was performed on 40 unrelated patients, affected with homozygous β‐thalassaemia, and on their parents. Frequency of the presence of the Hinc II ε, Hind III G γ and A γ, Hinc II SPSβ and SPSβ, Ava II SPSβ, Ava II β and Bam HI 3′β sites have been determined in ...
Tópico(s): Hemoglobinopathies and Related Disorders
1987 - Wiley | British Journal of Haematology
Maria De Angioletti, Giuseppina Lacerra, Carlo Gaudiano, Gabriella Mastrolonardo, Leonilde Pagano, Lucia Mastrullo, Santa Masciandaro, Clementina Carestia,
We characterized mutations and haplotypes of the δ-globin gene (HBD, MIM# 142000) in two regions of southern Italy. Mutations were discovered by screening for individuals with Hb A2 A), Hb A2-Campania (g.302C>A), Hb A2-Lucania (g.393C>G), and Hb A2-Capri (g.443G>T)]. Hb A2-Lucania was not inherited but had arisen in the propositus. Two were novel mutations in the noncoding regions: the substitutions IVS2+6T>A, presumably affecting the splicing, and g.-126A>T in the GATA motif presumably affecting transcription. ...
Tópico(s): Iron Metabolism and Disorders
2002 - Wiley | Human Mutation
Giuseppina Lacerra, Rosario Testa, Maria De Angioletti, Gino Schilirò, Clementina Carestia,
We report a new unstable variant identified in three carriers of a family from East Sicily; it was named Hb Bronte after the place from which the family originated. DNA sequencing from nucleotides −181 to +894 (α1) and to +884 (α2) revealed a GTG→GGG substitution at codon 93 of the α2‐globin gene. The MCV and MCH values were at the lower end of the normal range in the carriers. On cation exchange high performance liquid chromatography (HPLC), the Hb A2 level was apparently increased to around 6%, and ...
Tópico(s): Iron Metabolism and Disorders
2003 - Taylor & Francis | Hemoglobin
Maria De Angioletti, Giuseppina Lacerra, V. Sabato, Clementina Carestia,
Summary A family from the Southeast of Italy was found to have a novel β ‐globin mutant, β +45 G→C, with the features of a silent β ‐thalassaemia mutation. It was asymptomatic in two heterozygotes, but its interaction with the severe thalassaemia mutation β ‐IVS‐II‐654 C→T worsened the haematological and biosynthetic phenotype in two compound heterozygotes; moreover, another compound heterozygote, who was also heterozygote for the α α α anti3·7 , suffered from thalassaemia intermedia. The mutation was ...
Tópico(s): DNA and Nucleic Acid Chemistry
2003 - Wiley | British Journal of Haematology
Eric J. Sorenson, A. J. Windbank, J. N. Mandrekar, William R. Bamlet, Stanley H. Appel, C. Armon, P. E. Barkhaus, P. Bosch, Khrista Boylan, William S. David, Eva L. Feldman, Jonathan D. Glass, Laurie Gutmann, J. Katz, Wendy King, Carestia Luciano, Leo McCluskey, S. Nash, D. S. Newman, R. M. Pascuzzi, E. Pioro, L. J. Sams, S. Scelsa, Ericka P. Simpson, S. H. Subramony, Ezgi Tiryaki, C. A. Thornton,
Background: Previous human clinical trials of insulin-like growth factor type I (IGF-1) in amyotrophic lateral sclerosis (ALS) have been inconsistent. This phase III, randomized, double-blind, placebo-controlled study was undertaken to address whether IGF-1 benefited patients with ALS. Methods: A total of 330 patients from 20 medical centers were randomized to receive 0.05 mg/kg body weight of human recombinant IGF-1 given subcutaneously twice daily or placebo for 2 years. The primary outcome measure was change ...
Tópico(s): Cancer-related gene regulation
2008 - Lippincott Williams & Wilkins | Neurology
Giuseppina Lacerra, Clelia Scarano, Laura F. Lagona, Rosario Testa, Daniela Caruso, Emilia Medulla, Maria G. Friscia, Lucia Mastrullo, Mercedes Caldora, Romeo Prezioso, Carlo Gaudiano, Carmelo Magnano, M. A. Romeo, Gennaro Musollino, Francesca Di Noce, Clementina Carestia,
The increase of Hb A2 (α2δ2) beyond the upper limit [2.0–2.2/3.3–3.4% of the total hemoglobin (Hb)] is an invaluable tool in the hematological screening of β-thalassemia (β-thal) carriers. Factors decreasing Hb A2 percentages can hinder correct diagnosis. In order to analyze the genotype-phenotype relationship, we characterized δ-, β- and α-globin genotypes in 190 families where the probands had Hb A2 values of ≤2.0% or were β-thal heterozygotes with normal Hb A2 levels. Hb A2 was measured with cation ...
Tópico(s): Neonatal Health and Biochemistry
2010 - Taylor & Francis | Hemoglobin
Ana María Rincón, C. Aguado, Lourdes R. Desviat, Rocío Sánchez-Alcudia, Magdalena Ugarte, Belén Pérez,
... pseudoexons) in the mRNA.7Lacerra G Sierakowska H Carestia C Fucharoen S Summerton J Weller D Kole ...
Tópico(s): RNA modifications and cancer
2007 - Elsevier BV | The American Journal of Human Genetics
Giuseppina Lacerra, Gennaro Musollino, Francesca Di Noce, Romeo Prezioso, Clementina Carestia,
We report the conditions of a multiplex-amplifiction refractory mutation system (ARMS) for genotyping for nine known mutations of the α2-globin gene and of the ARMS assay for the detection of α1 Hb J-Oxford and −α3.7 -AC. The method is reproducible, reliable, simple, rapid, inexpensive and provides genotype diagnosis in >70% of point-mutation carriers in Mediterranean countries. Moreover, it allows investigation of the structure of mutated alleles by sequencing ARMS-amplicons.
Tópico(s): Iron Metabolism and Disorders
2007 - Ferrata Storti Foundation | Haematologica
M R Cesarone, Gianni Belcaro, Giovanni B. Agus, Michele Georgiev, B.M. Errichi, Roberto Marinucci, Silvia Errichi, A Filippini, L Pellegrini, A Ledda, G. Vinciguerra, A. Ricci, G Cipollone, M Lania, G. Gizzi, E. Ippolito, P. Bavera, F. Fano, Mark Dugall, R Adovasio, L. Gallione, G. Del Boccio, Umberto Cornelli, Robert D. Steigerwalt, G. Acerbi, M. Cacchio, A. Di Renzo, Masako Hosoi, Stefano Stuard, Massimiliano Marco Corsi Romanelli, L. Di Ciano, Emilio Simeone, G. Collevecchio, Maria Giovanna Grossi, F. Di Giambattista, F. Carestia, A Zukowski,
Superficial vein thrombosis is characterized by clotting of superficial veins (ie, following direct trauma) with minimal inflammatory components. Superficial thrombophlebitis is a minimally thrombotic process of superficial veins associated with inflammatory changes and/or infection. Treatments generally include analgesics, elastic compression, anti-inflammatory agents, exercise and ambulation, and, in some cases, local or systemic anticoagulants. It is better to avoid bed rest and reduced mobility. ...
Tópico(s): Diagnosis and Treatment of Venous Diseases
2007 - SAGE Publishing | Angiology
Giuseppina Lacerra, Christian Scarano, Gennaro Musollino, Angela Flagiello, Piero Pucci, Clementina Carestia,
We report a novel alpha2-globin gene allele with the mutation cod 117 TTC>TCC or alpha 117(GH5)Phe>Ser detected in three carriers with alpha-thalassemia phenotype. The mutated mRNA was present in the reticulocytes in the same amount as the normal one, but no chain or hemoglobin variant were detected. Most likely the amino acid substitution impairs the interaction of the alpha-chain variant with the AHSP and prevents its stabilizing effect, thus leading to the alpha-chain pool reduction.
Tópico(s): Erythrocyte Function and Pathophysiology
2007 - Ferrata Storti Foundation | Haematologica
P. D. Crittenden, Xavier Llimona, Leopoldo G. Sancho,
... was measured in Thyrea girardii (Durieu & Mont.) Bagl. & Carestia and Thyrea confusa Henssen, lichens containing a unicellular ...
Tópico(s): Biocrusts and Microbial Ecology
2007 - Canadian Science Publishing | Canadian Journal of Botany
Julia Etulain, Soledad Negrotto, Agostina Carestia, Roberto Gabriel Pozner, María Albertina Romaniuk, Lina Paola D’Atri, Giannoula Klement, Mirta Schattner,
Acidosis is one of the hallmarks of tissue injury such as trauma, infection, inflammation, and tumour growth. Although platelets participate in the pathophysiology of all these processes, the impact of acidosis on platelet biology has not been studied outside of the quality control of laboratory aggregation assays or platelet transfusion optimization. Herein, we evaluate the effect of physiologically relevant changes in extracellular acidosis on the biological function of platelets, placing particular ...
Tópico(s): Blood Coagulation and Thrombosis Mechanisms
2011 - Thieme Medical Publishers (Germany) | Thrombosis and Haemostasis
Roghieh Hajiboland, Fereshteh Farhanghi, Mahboobeh Aliasgharpour,
... los primordios foliares y los haces vasculares con carestía de B.
Tópico(s): Plant Micronutrient Interactions and Effects
2012 - University of Murcia | Anales de Biología
Yuuri Hirooka, Amy Y. Rossman, Gary J. Samuels, Christian Lechat, Priscila Chaverrí,
... lonicerae (Seeler) Hirooka, Rossman & P. Chaverri, Pleonectria rosellinii (Carestia) Hirooka, Rossman & P. Chaverri, Pleonectria rubicarpa (Cooke) Hirooka, ...
Tópico(s): Yeasts and Rust Fungi Studies
2012 - Elsevier BV | Studies in Mycology
G Fioretti, Maria De Angioletti, L. Paganol, Giuseppina Lacerra, A. Viola, Costanzo De Bonis, A Scarallo, Clementina Carestia,
AbstractWe detected Hb D-Los Angeles [β121(GH4)Glu→Gln], the most common hemoglobin variant after Hb S and Hb Lepore-Boston, in six unrelated families in Southern Italy. Ten patients were studied; eight patients were heterozygotes and two were compound heterozygotes for the hemoglobin variant and the β-thalassemia codon 39 (C→T) nonsense mutation. The β-globin gene sequence was characterized by polymerase chain reaction direct sequencing; restriction fragment length polymorphisms were defined by Southern ...
Tópico(s): Iron Metabolism and Disorders
1993 - Taylor & Francis | Hemoglobin
Produção Nacional
João José Reis, Márcia Gabriela D. de Aguiar,
This article is a study of a food riot in Bahia in 1858. The authors describe the events, discuss the profile of the protestors, analyze the movement as a defense of the"moral economy" and emphasize its political magnitude.
Tópico(s): Food, Nutrition, and Cultural Practices
1996 - UNIVERSIDADE DE SÃO PAULO | Revista de História