Alba Marin-Moreno
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Explore the profile of Alba Marin-Moreno including associated specialties, affiliations and a list of published articles.
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29
Citations
234
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Recent Articles
11.
Cali I, Espinosa J, Nemani S, Marin-Moreno A, Camacho M, Aslam R, et al.
Acta Neuropathol Commun
. 2021 Mar;
9(1):55.
PMID: 33766126
Current classifications of sporadic Creutzfeldt-Jakob disease (sCJD) identify five subtypes associated with different disease phenotypes. Most of these histopathological phenotypes (histotypes) co-distribute with distinct pairings of methionine (M)/valine (V) genotypes...
12.
Espinosa J, Andreoletti O, Marin-Moreno A, Lugan S, Aguilar-Calvo P, Cassard H, et al.
mBio
. 2021 Mar;
12(2).
PMID: 33727358
Early studies in transgenic mouse lines have shown that the coexpression of endogenous murine prion protein (PrP) and transgenic PrP from another species either inhibits or allows the propagation of...
13.
Espinosa J, Marin-Moreno A, Aguilar-Calvo P, Torres J
Neuropathol Appl Neurobiol
. 2020 Nov;
47(4):506-518.
PMID: 33253417
Aims: The amino acid sequence of prion protein (PrP) is a key determinant in the transmissibility of prion diseases. While PrP sequence is highly conserved among mammalian species, minor changes...
14.
Marin-Moreno A, Espinosa J, Torres J
Prog Mol Biol Transl Sci
. 2020 Sep;
175:147-177.
PMID: 32958231
Prions are unique agents that challenge the molecular biology dogma by transmitting information on the protein level. They cause neurodegenerative diseases that lack of any cure or treatment called transmissible...
15.
Toivonen J, Sanz-Rubio D, Lopez-Perez O, Marin-Moreno A, Bolea R, Osta R, et al.
Biomolecules
. 2020 Jun;
10(6).
PMID: 32549330
MicroRNAs (miRNAs) may contribute to the development and pathology of many neurodegenerative diseases, including prion diseases. They are also promising biomarker candidates due to their stability in body fluids. We...
16.
Cassard H, Huor A, Espinosa J, Douet J, Lugan S, Aron N, et al.
mBio
. 2020 Jun;
11(3).
PMID: 32546613
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently classified according to the methionine/valine polymorphism at codon 129 of the gene and the proteinase K-digested abnormal prion protein (PrP) isoform identified by...
17.
Marin-Moreno A, Huor A, Espinosa J, Douet J, Aguilar-Calvo P, Aron N, et al.
Emerg Infect Dis
. 2020 May;
26(6):1130-1139.
PMID: 32441630
Classical bovine spongiform encephalopathy (BSE) is the only zoonotic prion disease described to date. Although the zoonotic potential of atypical BSE prions have been partially studied, an extensive analysis is...
18.
Torres J, Marin-Moreno A, Andreoletti O, Espinosa J, Beringue V, Aguilar P, et al.
Food Saf (Tokyo)
. 2020 Apr;
4(4):105-109.
PMID: 32231913
Dietary exposure to Bovine Spongiform Encephalopathy (BSE) contaminated bovine tissues is considered as the origin of variant Creutzfeldt-Jakob disease (vCJD) in humans. To date, BSE agent is the only recognized...
19.
Espinosa J, Marin-Moreno A, Aguilar-Calvo P, Benestad S, Andreoletti O, Torres J
J Infect Dis
. 2020 Mar;
221(12):2085.
PMID: 32119741
No abstract available.
20.
Espinosa J, Marin-Moreno A, Aguilar-Calvo P, Benestad S, Andreoletti O, Torres J
J Infect Dis
. 2020 Jan;
223(6):1103-1112.
PMID: 31919511
Although experimental transmission of bovine spongiform encephalopathy (BSE) to pigs and transgenic mice expressing pig cellular prion protein (PrPC) (porcine PrP [PoPrP]-Tg001) has been described, no natural cases of prion...