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in J Allergy Clin Immunol

A common haplotype of the IL-31 gene influencing gene expression is associated with nonatopic eczema

F. Schulz et al.
in Hum Mol Genet

SNP genome scanning localises oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner ear disease and FADD in ocular coloboma

C.Y. Gregory-Evans et al.
in J Med Genet

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays

J. Hoyer et al.
in Aging Cell

Mitochondrial DNA deletions induce the adenosine monophosphate-activated protein kinase energy stress pathway and result in decreased secretion of some proteins

A. Prigione et al.
in PLoS Biol

Variants in a novel epidermal collagen gene (COL29A1) are associated with atopic dermatitis

C. Soederhaell et al.
in Autophagy

Mitochondrial DNA deletions and chloramphenicol treatment stimulate the autophagic transcript ATG12

A. Prigione et al.
in PLoS Genet

Genome-wide linkage analysis of malaria infection intensity and mild disease

C. Timmann et al.
in Hum Genet

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

H. Najmabadi et al.
in J Integr Bioinform

Flexible web-based integration of distributed large-scale human protein interaction maps

G. Chaurasia et al.
in Free Radic Biol Med

Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcript

M. Alemi et al.