Latest papers

Polymorphisms of chicken toll-like receptor 1 type 1 and type 2 in different breeds.

Quantitative trait loci associated with the humoral innate immune response in chickens were confirmed in a cross between Green-Legged Partridgelike and White Leghorn.

The proteome of Mycoplasma pneumoniae, a supposedly "simple" cell.

A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Replication and explorations of high-order epistasis using a large advanced intercross line pedigree.

Suppression of reactive oxygen species in cells with multiple mitochondrial DNA deletions by exogenous protein-coding RNAs.

RNA-mediated restoration of mitochondrial function in cells harboring a Kearns Sayre Syndrome mutation.

Inactivation of IL11 Signaling Causes Craniosynostosis, Delayed Tooth Eruption, and Supernumerary Teeth

Fine mapping of five Loci associated with low-density lipoprotein cholesterol detects variants that double the explained heritability.

Genetic architecture of body weight, condition factor and age of sexual maturation in Icelandic Arctic charr (Salvelinus alpinus).

Genome-wide genetic marker discovery and genotyping using next-generation sequencing.

DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation.

Gain-of-function mutations of ARHGAP31, a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies.

A transcribed pseudogene of MYLK promotes cell proliferation.

SNP-array based whole genome homozygosity mapping: A quick and powerful tool to achieve an accurate diagnosis in LGMD2 patients

[Gene RAD31 is identical to gene MEC1 of yeast Saccharomyces cerevisiae].

Mouse ES and iPS cells can form similar definitive endoderm despite differences in imprinted genes. LID - 10.1172/JCI43853 [doi] LID - 43853 [pii]

Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS.

The mouse QTL map helps interpret human genome-wide association studies for HDL cholesterol.