UNAI
GALICIA GARCIA
PROFESORADO ADJUNTO
SHIFA
JEBARI BENSLAIMAN
INVESTIGADOR/A PREDOCTORAL
Publications by the researcher in collaboration with SHIFA JEBARI BENSLAIMAN (16)
2024
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Aterosklerosiaren fisiopatologia: disfuntzio endotelialetik plakaren hausturara
Osagaiz: osasun-zientzien aldizkaria, Vol. 8, Núm. 1, pp. 119-132
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OptiMo-LDLr: An Integrated In Silico Model with Enhanced Predictive Power for LDL Receptor Variants, Unraveling Hot Spot Pathogenic Residues
Advanced Science, Vol. 11, Núm. 13
2023
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Predictive Modeling and Structure Analysis of Genetic Variants in Familial Hypercholesterolemia: Implications for Diagnosis and Protein Interaction Studies
Current Atherosclerosis Reports, Vol. 25, Núm. 11, pp. 839-859
2021
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MLb-LDLr.xlsx
figshare
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MLb-LDLr.xlsx
figshare
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MLb-LDLr: LDLaren hartzailearen aldaeren eragina aurresatekoikasketa automatikoko eredua
Osasun zientzak: IV. Ikergazte Nazioarteko Ikerteta Euskaraz. 2021eko ekainaren 9, 10 eta . Gasteiz, Euskal Herria.
2020
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Cholesterol efflux efficiency of reconstituted HDL is affected by nanoparticle lipid composition
Biomedicines, Vol. 8, Núm. 10
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Hiperkolesterolemia Familiarra: patofisiologia, diagnostikoa eta tratamendua
Osagaiz: osasun-zientzien aldizkaria, Vol. 4, Núm. 1, pp. 69-80
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Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR
Scientific reports, Vol. 10, Núm. 1, pp. 1727
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Pathophysiology of type 2 diabetes mellitus
International Journal of Molecular Sciences, Vol. 21, Núm. 17, pp. 1-34
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Statin treatment-induced development of type 2 diabetes: From clinical evidence to mechanistic insights
International Journal of Molecular Sciences, Vol. 21, Núm. 13, pp. 1-25
2019
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The Arg499His gain-of-function mutation in the C-terminal domain of PCSK9
Atherosclerosis, Vol. 289, pp. 162-172
2018
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Familial hypercholesterolemia: The most frequent cholesterol metabolism disorder caused disease
International Journal of Molecular Sciences, Vol. 19, Núm. 11
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Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition
PLoS ONE, Vol. 13, Núm. 10
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Validation of LDLr activity as a tool to improve genetic diagnosis of familial hypercholesterolemia: A retrospective on functional characterization of LDLr variants
International Journal of Molecular Sciences, Vol. 19, Núm. 6
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p.(Asp47Asn) and p.(Thr62Met): non deleterious LDL receptor missense variants functionally characterized in vitro
Scientific Reports, Vol. 8, Núm. 1