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Posts
- Category: Genetics News (continued)
- A navigator for human genome epidemiology
- A new approach to estimate parameters of speciation models with application to apes
- A new drug target for Huntington's disease
- A new identity for the elusive intestinal stem cell
- A new locus for split hand/foot malformation with long bone...
- A new multipoint method for genome-wide association studies by imputation of genotypes
- A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies
- A New Study Finds That Genetic Variation Affects Smoking Cessation Treatment, UK
- A new test promises to reveal babyA s sex at six weeks
- A New Theory Of MHC Evolution: Beyond Selection On The Immune Genes
- A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus
- A Note on Algorithms for Genotype and Allele Elimination in Complex...
- A Novel Gene Found For Childhood-Onset Asthma
- A Novel Marker Of Colorectal Carcinoma
- A Pacemaker is a Network [A Blog Around The Clock]
- A Personal Touch
- A phenylalanine in DGAT is a key determinant of oil content and composition in maize
- A plea for a rare disease: Illness turns muscles into bone
- A polymorphism of the -opioid receptor is linked to alcohol misuse among adolescents
- A Powerful New Tool For Researchers: Cancer Genomics Browser
- A promoter polymorphism in the CASP8 gene is not associated with cancer risk
- A QTL for rice grain width and weight encodes a previously unknown RING-type E3 ubiquitin ligase
- A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
- A quantitative trait locus regulating rice grain width
- A Rare Breed: Fainting Goats
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures
- A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome
- A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes
- A restricted spectrum of NRAS mutations causes Noonan syndrome
- A Rice Protein Linked To Infectious Disease Resistance
- A robust statistical method for case-control association testing with copy number variation
- A root of hair loss found?
- A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
- A Shoulder to Rely Upon Hope with hospice
- A single gene network accurately predicts phenotypic effects of gene perturbation in Caenorhabditis elegans
- A single positively selected West Nile viral mutation confers increased virogenesis in American crows
- A six-nucleotide insertion-deletion polymorphism in the CASP8 promoter is associated with susceptibility to multiple cancers
- A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes
- A Step Closer To Creating Safe Embryonic-Like Stem Cells
- A step forward for restless legs syndrome
- A structural-maintenance-of-chromosomes hinge domain–containing protein is required for RNA-directed DNA methylation
- A supersized list of obesity genes
- A survey of genetic human cortical gene expression
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
- A Tale of Two Scientific Consensuses
- A tall story: New research adds to growing body of knowledge of genetics of height
- A TARBP2 mutation in human cancer impairs microRNA processing and DICER1 function
- A textbook for all seasons
- A timely guide to the genome
- A transcriptome atlas of rice cell types uncovers cellular, functional and developmental hierarchies
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Suggested Reading:
Introduction to Genetic Analysis (Introduction to Genetic Analysis (Griffiths))The author team welcomes a new coauthor, Sean B. Carroll, a recognized leader in the field of evolutionary development, to this new edition of Introdu... Read More >
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