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HUMAN MOLECULAR GENETICS
Rivista
Codice:
E078692
ISSN:
0964-6906
Dati Generali
Dati Generali
Pubblicazioni (22)
Pulisci
Ordina Pubblicazioni:
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decrescente
A correlation between the relative predisposition of MHC class II alleles to type 1 diabetes and the structure of their proteins
Articolo
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration
Articolo
An archipelago of CpG islands in Xq28: identification and fine mapping of 20 new genes of the human X chromosome
Articolo
Apoptotic mechanisms in mutant LRRK2-mediated cell death
Articolo
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Articolo
Conditional linkage disequilibrium analysis of a complex disease superlocus, IDDM1 in the HLA region, reveals the presence of independent modifying gene effects influencing the type 1 diabetes risk encoded by the major HLA-DQB1,-DRB1 disease loci
Articolo
Confirmation of the DRB1-DQB1 loci as the major component of IDDM1 in the isolated founder population of Sardinia
Articolo
DRB1-DQA1-DQB1 loci and multiple sclerosis predisposition in the Sardinian population
Articolo
Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
Articolo
Evaluation of fine mapping strategies for a multifactorial disease locus: systematic linkage and association analysis of IDDM1 in the HLA region on chromosome 6p21
Articolo
Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21
Articolo
Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11
Articolo
GWAS of genetic factors affecting white blood cell morphological parameters in Sardinians uncovers influence of chromosome 11 innate immunity gene cluster on eosinophil morphology
Articolo
Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of european ancestry
Articolo
Major factors influencing linkage disequilibrium by analysis of different chromosome regions in distinct populations: demography chromosome recombination frequency and selection
Articolo
Mitochondrial genetic variation is enriched in G-quadruplex regions that stall DNA synthesis in vitro
Articolo
Saturation multipoint linkage mapping of chromosome 6q in type 1 diabetes
Articolo
The co-inheritance of type 1 diabetes and multiple sclerosis in Sardinia cannot be explained by genotype variation in the HLA region alone
Articolo
The inter-regional distribution of HLA class II haplotypes indicates the suitability of the Sardinian population for case-control association studies in complex diseases
Articolo
Transmission of haplotypes of microsatellite markers rather than single marker alleles in the mapping of a putative type 1 diabetes susceptibility gene (IDDM6)
Articolo
Vitamin D receptor binding, chromatin states and association with multiple sclerosis
Articolo
Vitamin D receptor binding, chromatin states and association with multiple sclerosis.
Articolo
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