Mara Rigamonti
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Explore the profile of Mara Rigamonti including associated specialties, affiliations and a list of published articles.
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11
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70
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Recent Articles
1.
Tomanelli M, Guffanti F, Vargiu G, Micotti E, Rigamonti M, Tumiatti F, et al.
Front Oncol
. 2025 Jan;
14:1504938.
PMID: 39763604
Introduction: Lung cancer is the first cause of cancer death in the world, due to a delayed diagnosis and the absence of efficacy therapies. KRAS mutation occurs in 25% of...
2.
Santin Y, Chiesa M, Alfonso A, Doghri Y, Kang R, Haidar F, et al.
Sci Adv
. 2024 Dec;
10(50):eadt1670.
PMID: 39671481
Biological age, which reflects the physiological state of an individual, offers a better predictive value than chronological age for age-related diseases and mortality. Nonetheless, determining accurate functional features of biological...
3.
Fuochi S, Rigamonti M, OConnor E, de Girolamo P, DAngelo L
Front Big Data
. 2024 Jun;
7:1390467.
PMID: 38831953
Undisturbed home cage recording of mouse activity and behavior has received increasing attention in recent years. In parallel, several technologies have been developed in a bid to automate data collection...
4.
Faydaver M, El Khatib M, Russo V, Rigamonti M, Raspa M, Di Giacinto O, et al.
Front Vet Sci
. 2024 Jan;
10:1281040.
PMID: 38179329
Introduction: Tendon disorders present significant challenges in the realm of musculoskeletal diseases, affecting locomotor activity and causing pain. Current treatments often fall short of achieving complete functional recovery of the...
5.
Fuochi S, Rigamonti M, Raspa M, Scavizzi F, de Girolamo P, DAngelo L
Sci Rep
. 2023 Jul;
13(1):10851.
PMID: 37407633
In this longitudinal study we compare between and within-strain variation in the home-cage spatial preference of three widely used and commercially available mice strains-C57BL/6NCrl, BALB/cAnNCrl and CRL:CD1(ICR)-starting from the first...
6.
Golini E, Rigamonti M, Raspa M, Scavizzi F, Falcone G, Gourdon G, et al.
Front Behav Neurosci
. 2023 Mar;
17:1130055.
PMID: 36935893
Myotonic dystrophy type 1 (DM1) is a dominantly inherited neuromuscular disease caused by the abnormal expansion of CTG-repeats in the 3'-untranslated region of the Dystrophia Myotonica Protein Kinase (DMPK) gene,...
7.
Peres C, Sellitto C, Nardin C, Putti S, Orsini T, Di Pietro C, et al.
EBioMedicine
. 2023 Feb;
89:104453.
PMID: 36736132
Background: Keratitis ichthyosis deafness (KID) syndrome is a rare disorder caused by hemichannel (HC) activating gain-of-function mutations in the GJB2 gene encoding connexin (Cx) 26, for which there is no...
8.
Corsi G, Picard K, Di Castro M, Garofalo S, Tucci F, Chece G, et al.
Glia
. 2021 Sep;
70(1):89-105.
PMID: 34487590
Microglia, the brain's resident macrophages, actively contribute to the homeostasis of cerebral parenchyma by sensing neuronal activity and supporting synaptic remodeling and plasticity. While several studies demonstrated different roles for...
9.
Lavigna G, Masone A, Bouybayoune I, Bertani I, Lucchetti J, Gobbi M, et al.
Neurobiol Dis
. 2021 Aug;
158:105455.
PMID: 34358614
Fatal familial insomnia (FFI) is a dominantly inherited prion disease linked to the D178N mutation in the gene encoding the prion protein (PrP). Symptoms, including insomnia, memory loss and motor...
10.
Fuochi S, Rigamonti M, Iannello F, Raspa M, Scavizzi F, de Girolamo P, et al.
Lab Anim (NY)
. 2021 Jun;
50(8):215-223.
PMID: 34155410
Mouse strains differ markedly in all behaviors, independently of their genetic background. We undertook this study to disentangle the diurnal activity and feature key aspects of three non-genetically altered mouse...