65 results on '"Peltonen L"'
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2. Polymer incorporation method affects the physical stability of amorphous indomethacin in aqueous suspension
3. Neuronal ceroid lipofuscinosis genes, CLN2, CLN3 and CLN5 are spatially and temporally co-expressed in a developing mouse brain
4. Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) project
5. Mesoporous materials as controlled drug delivery formulations
6. Stability and CMC determinations of amphiphilic (DSPEPEG(3400)-CTT2) peptide constructs by microtensiometry
7. P2.32 The frequency of myotonic dystrophy type 2 (DM2) and type 1 (DM1) mutations in the population
8. New Biotechnology
9. S5.2 – BBMRI
10. Abstract: P1138 OSBPL10, A NOVEL CANDIDATE GENE FOR LOW HDL AND HIGH TG TRAITS, REGULATES CELLULAR LIPID METABOLISM
11. Abstract: 529 KNOCK-OUT MODELS IN MICE AND MEN SUGGEST A PROATHEROGENIC ROLE FOR USF1
12. Better understanding of dissolution behaviour of amorphous drugs by in situ solid-state analysis using Raman spectroscopy
13. Biocompatibility of mesoporous silicon microparticles
14. Solvent-mediated solid phase transformations of carbamazepine—Effects of simulated intestinal fluid and fasted state simulated intestinal fluid
15. Drug dissolution studies on mesoporous silicon particles—A theoretical approach
16. Drug polymorphism causes problems on reliable pharmaceutical solubility testing
17. Nanocrystallization of indomethacin by wet ball-milling technique
18. Improved insight into the dissolution behavior of amorphous drugs by in situ solid-state analysis
19. ESTROGEN RECEPTOR GENE POLYMORPHISM AND CARDIOVASCULAR DISEASE RISK IN THE FINNISH POPULATION
20. OSBP-RELATED PROTEIN 10 (OSBPL10/ORP10), A NOVEL REGULATOR OF LIPID HOMEOSTASIS
21. OC3.09.4 PREVALENCE OF LACTASE PERSISTENCE AND THE PERFORMANCE OF A NEW NON INVASIVE GENETIC TEST IN ADULT PATIENTS
22. Surface pressure measurements in particle interaction and stability studies of poly(lactic acid) nanoparticles
23. 99 – Predicting schizophrenia spectrum disorders with psychological scales – The Northern Finland 1966 Birth Cohort
24. Microtensiometry—A novel tool for fast drug solubility screening in 96-well plates
25. WO15-OR-3 LINKAGE DISEQUILIBRIUM ANALYSIS OF USF1 REGION AND REPLICATION OF ASSOCIATION IN DYSLIPIDEMIC FAMILIES
26. LB-OR-6 TRANSCRIPT PROFILES FROM MUSCLE AND FAT EXPOSE MOLECULAR MECHANISM BEHIND USF1 ASSOCIATED DYSLIPIDEMIA WITH ALLELE- SPECIFIC EFFECTS ON THE VESSEL WALL
27. Trait Components Provide Tools to Dissect the Genetic Susceptibility of Migraine
28. Effect of nanoprecipitation on the physicochemical properties of low molecular weight poly(l-lactic acid) nanoparticles loaded with salbutamol sulphate and beclomethasone dipropionate
29. DNA extraction yield is associated with several phenotypic characteristics: results from two large population surveys
30. A novel channel flow method in determination of solubility properties and dissolution profiles of theophylline tablets
31. Minimum Description Length Block Finder, a Method to Identify Haplotype Blocks and to Compare the Strength of Block Boundaries
32. 1P-0228 A quantitative trait locus on chromosome 10p11 influences variation in plasma HDL-C levels in Finnish dyslipidemic families
33. Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study
34. Seasonal Affective Disorder and Serotonin-Related Polymorphisms
35. Fine mapping of the human familial combined hyperlipidemia locus on chromosome 1q21-q23 using conserved synteny to the mouse locus on chromosome 3
36. Small low density lipoprotein particles in familial combined hyperlipidemia
37. A Genome-wide scan for low HDL-Cholesterol in genetically isolated finnish families with premature coronary heart disease
38. Genetics of the neuronal ceroid lipofuscinoses
39. Association of FXIII Val34Leu with decreased risk of myocardial infarction in Finnish males
40. Fine-Scale Mapping of a Novel Dementia Gene, PLOSL, by Linkage Disequilibrium
41. Attitudes towards genetic testing: analysis of contradictions
42. 1.P.131 The occurrence of small dense low density lipoprotein particles in familial combined hyperlipidemia
43. 1.P.260 Candidate gene analysis in familial combined hyperlipidemia
44. The Visual Assignment of Genes by Fiber-Fish: BTF3 Protein Homologue Gene (BTF3) and a Novel Pseudogene of Human RNA Helicase A (DDX9P) on 13q22
45. 1-31-24 Immune system genes in multiple sclerosis: Genetic association and linkage analyses on TCRβ, IGH, IL-1ra/IL-1β and IFN-γ loci
46. Acceptance of genetic testing in a general population: age, education and gender differences
47. Chromosome X DNA markers and bipolar disorder
48. Loci on chromosomes 3p, 6p, and 8p do not contribute to schizophrenia in a Finnish family sample
49. Efficient Construction of a Physical Map by Fiber-Fish of the CLN5 Region: Refined Assignment and Long-Range Contig Covering the Critical Region on 13q22
50. Distal myopathies and overlapping forms and intrafamiliar variability between distal myopathies and limb-girdle muscular dystrophies
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