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The fit of the genetic relative risk models of the human leucocyte antigen (HLA) in the risk of insulin-dependent diabetes mellitus in the Finnish population
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Diploid genome reconstruction from shotgun sequencing
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Studies On The Induction Of Alloreactive And Antigen-Specific Cytotoxic T Cells By Synthetic Peptides
Differential gene expression in normal and transformed NIH3T3 cells
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Censored survival models for genetic epidemiology: A Gibbs sampling approach
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Human linkage analysis of pseudoautosomal sequences using single sperm typing
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Cytolytic T-lymphocyte recognition of class I molecules
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Creation of cytotoxic T cell epitopes using synthetic peptides
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The role of the thymus in the development of T-cell proliferation in the MRL/Mp Ipr Ipr murine model
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Immunologic and biochemical detection of cell surface alterations following morphological transformation or mutation of C3H/10T1/2 Cl 8 cells by chemical carcinogens
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Inference for stochastic models of molecular data
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Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations
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Pre-transplant conditioning and the role of the microenvironment during hematopoietic reconstitution
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Role of GH/IGF-1 signaling in oxidative stress, DNA damage and cancer
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Discovery of complex pathways from observational data
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Lessons learned conducting a clinical study
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Multivariate methods for extracting genetic associations from correlated data
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Genetic variations in gene from the cytochrome P450 family may account for differential response to pioglitazone therapy in the Hispanic women
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Polygenic analyses of complex traits in complex populations
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Association testing of polymorphisms in the vitamin D metabolism and signaling pathway with multiple sclerosis across multiple populatuions
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The informationalization of race: communication technologies and genomics in the information age
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A population genomics approach to the study of speciation in flowering columbines
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Screening and association testing of coding variation in steroid hormone coactivator and corepressor genes in relationship with breast cancer risk in multiple populations
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Clinical and molecular genetic studies on families with inherited dental anomalies
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