Carla Bini

Dr. Carla Bini

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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LBLivia Beccacece
Livia Beccacece
PAPaolo Abondio
Paolo Abondio
CBCarla Bini
Carla Bini
SPSusi Pelotti
Susi Pelotti
DLDonata Luiselli
Donata Luiselli
Cardiovascular diseases are the leading cause of global deaths, and many risk factors contribute to their pathogenesis. In this context, prostanoids, which derive from arachidonic acid, have attracted attention for their involvement in cardiovascular homeostasis and inflammatory processes. Prostanoids are the target of several drugs, but it has been shown that some of them increase the risk of thrombosis. Overall, many studies have shown that prostanoids are tightly associated with cardiovascular diseases and that several polymorphisms in genes involved in their synthesis and function increase the risk of developing these pathologies. In this review, we focus on molecular mechanisms linking prostanoids to cardiovascular diseases and we provide an overview of genetic polymorphisms that increase the risk for cardiovascular disease.

1 November 2020 in Forensic Science International: Genetics
Verified
Journal Article
Closed access
CTChiara Turchi
Chiara Turchi
CPCarlo Previderè
Carlo Previderè
CBCarla Bini
Carla Bini
ECEugenia Carnevali
Eugenia Carnevali
PGPierangela Grignani
Pierangela Grignani
PFPAOLO FATTORINI
PAOLO FATTORINI

1 March 2015 in Forensic Science International: Genetics
Verified
Journal Article
Closed access
CBCarla Bini
Carla Bini
LRLaura Natalia Riccardi
Laura Natalia Riccardi
SCStefania Ceccardi
Stefania Ceccardi
FCFrancesco Carano
Francesco Carano
SSStefania Sarno
Stefania Sarno
SPSusi Pelotti
Susi Pelotti

27 September 2023 in Forensic Science International
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Journal Article
Open access
EGElena Giovannini
Elena Giovannini
Mariana RoccaroMariana Roccaro
Mariana Roccaro
APAngelo Peli
Angelo Peli
SBSimone Bianchini
Simone Bianchini
CBCarla Bini
Carla Bini
PFPaolo Fais
Paolo Fais
Dog bites pose a significant global public health issue and are the most common type of injury caused by animals. While most dog bites result in minor harm, they can also lead to severe or even fatal consequences. In cases involving serious injury or death, forensic pathologists investigate various aspects, including the crime scene, the injuries sustained by the victim, and the characteristics of the dog suspected to have caused the bite. The aim of this study is to provide a systematic review of the literature on the medical-legal implications of dog bites in forensic practice, in order to recognize the dog bite victim features, the injuries and their consequences related to, and to identify the offending dogs. The literature search was performed using PubMed, Scopus and Web of Science from January 1980 to March 2023. Eligible studies have investigated issues of interest to forensic medicine about dog bites to humans. A total of 116 studies met the inclusion criteria and were included in the review and they were organized and discussed by issue of interest (biting dog features, dog bite victim features, anatomical distribution of dog bites, injuries related to dog bites, cause of death, bite features, dog identification and post-mortem dog depredation). The findings of this systematic review highlight the importance of bite mark analysis in reconstructing the events leading to the attack and identifying the dog responsible. In medical forensic evaluations of dog bite cases, a multidisciplinary approach is crucial. This approach involves thorough analysis of the crime scene, identification of risk factors, examination of dog characteristics, and assessment of the victim's injuries. By combining expertise from both human and veterinary forensic fields, a comprehensive understanding can be achieved in dog bite cases.

1 April 2021 in Free Radical Biology and Medicine
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Journal Article
Open access
SNSimona Neri
Simona Neri
SGSerena Guidotti
Serena Guidotti
CBCarla Bini
Carla Bini
SPSusi Pelotti
Susi Pelotti
SDStefania D’ADamo
Stefania D’ADamo
RBRosa Maria Borzì
Rosa Maria Borzì
During osteoarthritis development, chondrocytes are subjected to a functional derangement. This increases their susceptibility to stressful conditions such as oxidative stress, a characteristic of the aging tissue, which can further provoke extrinsic senescence by DNA damage responses. It was previously observed that IκB kinase α knockdown increases the replicative potential of primary human OA chondrocytes cultured in monolayer and the survival of the same cells undergoing hypertrophic-like differentiation in 3-D. In this paper we investigated whether IKKα knockdown could modulate oxidative stress-induced senescence of OA chondrocytes undergoing a DDR and particularly the involvement in this process of the DNA mismatch repair system, the principal mechanism for repair of replicative and recombinational errors, devoted to genomic stability maintenance in actively replicating cells. This repair system is also implicated in oxidative stress-mediated DNA damage repair. We analyzed microsatellite instability and expression of the mismatch repair components in human osteoarthritis chondrocytes after IKKα knockdown and H2O2 exposure. Only low MSI levels and incidence were detected and exclusively in IKKα proficient cells. Moreover, we found that IKKα proficient and deficient chondrocytes differently regulated MMR proteins after oxidative stress, both at mRNA and protein level, suggesting a reduced susceptibility of IKKα deficient cells. Our data suggest an involvement of the MMR system in the response to oxidative stress that tends to be more efficient in IKKαKD cells. This argues for a partial contribution of the MMR system to the better ability to recover DNA damage already observed in these cells.

23 February 2024 in Children
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EGElena Giovannini
Elena Giovannini
MBMaria Paola Bonasoni
Maria Paola Bonasoni
JPJennifer P Pascali
Jennifer P Pascali
CBCarla Bini
Carla Bini
GPGuido Pelletti
Guido Pelletti
PFPaolo Fais
Paolo Fais
The two primary classes of opioid substances are morphine and its synthetic derivative, heroin. Opioids can cross the placental barrier, reaching fetal circulation. Therefore, at any gestational age, the fetus is highly exposed to pharmacologically active opioid metabolites and their associated adverse effects. This review aimed to investigate all the studies reported in a timeframe of forty years about prenatal and postnatal outcomes of opioid exposition during pregnancy. Clinical and toxicological aspects, as well as pharmacogenetic and epigenetic research focusing on fetal and infant effects of opioid use during pregnancy together with their medico-legal implications are exposed and discussed.