166 results on '"Palacios, Lourdes"'
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2. On the density of CV0(X)⊗A in CV0(X,A)
3. On m-convexity in CV(0)(X,A)
4. Diagnostic yield of sequencing familial hypercholesterolemia genes in individuals with primary hypercholesterolemia
5. Rendimiento diagnóstico de la secuenciación de genes de hipercolesterolemia familiar en sujetos con hipercolesterolemia primaria
6. PattRec: An easy-to-use CNV detection tool optimized for targeted NGS assays with diagnostic purposes
7. On bornologicalness in locally convex algebras
8. On Some Properties of A Inherited by C b (X, A)
9. On the density of CV0(X)⊗A in CV0(X,A)
10. Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR
11. Multipliers in some perfect locally m-pseudo-convex algebras
12. On Some Properties of A Inherited by C b(X, A)
13. On TQ-Algebras
14. Association between socioeconomic level and cardiovascular risk in the Peruvian population
15. On some properties of CV_{(0)}(X, A)
16. On m-convexity in $$CV_{(0)}(X,A)$$
17. Asociación entre nivel socioeconómico y riesgo cardiovascular en la población peruana
18. Leu22_Leu23 Duplication at the Signal Peptide of PCSK9 Promotes Intracellular Degradation of LDLr and Autosomal Dominant Hypercholesterolemia
19. A DNA Microarray for the Detection of Point Mutations and Copy Number Variation Causing Familial Hypercholesterolemia in Europe
20. MULTIPLIERS IN LOCALLY CONVEX *-ALGEBRAS
21. Supplemental Material Leu22_Leu23 duplication at the signal peptide of PCSK9 promotes intracellular degradation of LDLr and autosomal dominant hypercholesterolemia
22. Leu22_Leu23 Duplication at the Signal Peptide of PCSK9 Promotes Intracellular Degradation of LDLr and Autosomal Dominant Hypercholesterolemia
23. Phase Behavior and Structure of Systems Based on Mixtures of n-Hentriacontane and Melissic Acid
24. Molecular characterization of familial hypercholesterolemia in Spain
25. Análisis funcional de mutaciones en el promotor del LDLR y su relación con la hipercolesterolemia familiar
26. Clinical evaluation of the Procleix SARS-CoV-2 assay, a sensitive, high-throughput test that runs on an automated system
27. The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes
28. Educational inclusion as the axis of public policies in the province of Santa Fe from 2014 to 2019
29. Functional Characterization and Classification of Frequent Low-Density Lipoprotein Receptor Variants
30. On some properties of CV(0) (X, A).
31. Infection of primary hepatocytes with adenoviral vectors alters biliary lipid metabolism
32. Diagnostic yield of sequencing familial hypercholesterolemia genes in individuals with primary hypercholesterolemia
33. New contributions to the study of common double mutants in the human LDL receptor gene
34. Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR
35. Mutation type classification and pathogenicity assignment of sixteen missense variants located in the EGF-precursor homology domain of the LDLR
36. Overexpression of SND p102, a rat homologue of p100 coactivator, promotes the secretion of lipoprotein phospholipids in primary hepatocytes
37. Functional characterization of splicing and ligand-binding domain variants in the LDL receptor
38. Functional analysis of LDLR promoter and 5′ UTR mutations in subjects with clinical diagnosis of familial www.hgvs.orghypercholesterolemia
39. Rendimiento diagnóstico de la secuenciación de genes de hipercolesterolemia familiar en sujetos con hipercolesterolemia primaria
40. Antigen-stimulated PBMC transcriptional protective signatures for malaria immunization
41. Association between socioeconomic level and cardiovascular risk in the Peruvian population.
42. Debates actuales en torno al voto migrante en la Ciudad de Buenos Aires (artículos)
43. Replacement of Cysteine at Position 46 in the First Cysteine-Rich Repeat of the LDL Receptor
44. Replacement of Cysteine at Position 46 in the First Cysteine-Rich Repeat of the LDL Receptor
45. El e-book científico-técnico: panorama de los diferentes modelos comerciales
46. The leucine stretch length of PCSK9 signal peptide and its role in development of autosomal dominant hypercholesterolaemia: unravelling the activities of P.LEU23DEL AND P.LEU22_LEU23DUP variants
47. A Characterization of C*-normed Algebras via Positive Functionals
48. The leucine stretch length of PCSK9 signal peptide and its role in development of autosomal dominant hypercholesterolaemia: Unravelling the activities of P.LEU23DEL and P.LEU22_LEU23DUP variants
49. Functional characterization of LDL receptor missense variants located in the first cysteine-rich repeat in ligand binding domain of low density lipoprotein receptor
50. Homozygous truncating mutation in prenatally expressed skeletal isoform of TTN gene results in arthrogryposis multiplex congenita and myopathy without cardiac involvement
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