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Nature Genetics

Sun, 2009-08-16 18:25 — sciencestaff

Publishes the very highest quality research in genetics.

Differentiation stage determines potential of hematopoietic cells for reprogramming into induced pluripotent stem cells
Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia
Germline genomic variants associated with childhood acute lymphoblastic leukemia
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse
Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer
Mutations in PYCR1 cause cutis laxa with progeroid features
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer
Genomic privacy and limits of individual detection in a pool
Posterior malformations in Dact1 mutant mice arise through misregulated Vangl2 at the primitive streak
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
Personalized copy number and segmental duplication maps using next-generation sequencing
Tcf3 and Tcf4 are essential for long-term homeostasis of skin epithelia
p53 deletion impairs clearance of chromosomal-instable stem cells in aging telomere-dysfunctional mice
Analysis of the tyrosine kinome in melanoma reveals recurrent mutations in ERBB4
Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

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