Journal Article (223)
121.
Journal Article
82 (4), pp. 714 - 724 (2010)
Presence of late embryogenesis abundant (LEA) proteins in a nondesiccated, diapausing invertebrate embryo (Rotifers). Biology of Reproduction 122.
Journal Article
15 (4), pp. 2478 - 2490 (2010)
Automation in the high-throughput selection of random combinatorial libraries-different approaches for select applications. Molecules 123.
Journal Article
67 (7), pp. e45 - e48 (2010)
Correspondence to Sand et al. “Critical Reappraisal of a Catechol-O-Methyltransferase Transversion Variant in Schizophrenia”. Biological Psychiatry 124.
Journal Article
31 (4), pp. 477 - 483 (2010)
Quantifying the effect of sequence variation on regulatory interactions. Hum Mutation 125.
Journal Article
12 (2), pp. 195 - 213 (2010)
An Expressed Sequence Tag Analysis of the Intertidal Brown Seaweeds Fucus serratus (L.) and F. vesiculosus (L.) (Heterokontophyta, Phaeophyceae) in Response to Abiotic Stressors. Marine Biotechnology (New York, N.Y.) 126.
Journal Article
131, pp. 508 - 514 (2010)
Novel mutations in Indian patients with autosomal recessive infantile malignant osteopetrosis. Indian J Med Res 127.
Journal Article
464 (7289), pp. 757 - 762 (2010)
The genome of a songbird. Nature 128.
Journal Article
38 (11), p. e122 - e122 (2010)
An inducible RNA interference system for the functional dissection of mouse embryogenesis. Nucleic Acids Research 129.
Journal Article
152A (4), pp. 870 - 874 (2010)
Three novel mutations in the ANK membrane protein cause craniometaphyseal dysplasia with variable conductive hearing loss. American Journal of Medical Genetics Part A 130.
Journal Article
152A (4), pp. 1008 - 1012 (2010)
Characterization of an interstitial 4q32 deletion in a patient with mental retardation and a complex chromosome rearrangement. American Journal of Medical Genetics. Part A. 131.
Journal Article
A transcriptional roadmap to the induction of pluripotency in somatic cells. (2010)
132.
Journal Article
Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree1. Molecular Psychiatry, pp. 1 - 13 (2010)
133.
Journal Article
2010, p. epub - epub (2010)
Cloning, tissue expression analysis, and functional characterization of two Δ6-desaturase variants of sea bass (Dicentrarchus labrax L.). Marine Biotechnology 134.
Journal Article
77 (6), pp. 541 - 551 (2010)
Novel missense mutations in the ubiquitination-related gene UBE2A cause a recognizable X-linked mental retardation syndrome. Clinical Genetics: an International Journal of Genetics in Medicine 135.
Journal Article
26 (6), pp. 722 - 729 (2010)
Microindel detection in short-read sequence data. Bioinformatics 136.
Journal Article
86 (3), pp. 434 - 439 (2010)
Deletion and point mutations of PTHLH cause brachydactyly type E. The American Journal of Human Genetics 137.
Journal Article
285 (19), pp. 14438 - 14449 (2010)
Tumor necrosis factor receptor superfamily member 19 (TNFRSF19) regulates differentiation fate of human mesenchymal (stromal) stem cells through canonical Wnt signalling and C/EBP. The Journal of Biological Chemistry 138.
Journal Article
464 (7286), pp. 250 - 255 (2010)
The primary transcriptome of the major human pathogen Helicobacter pylori. Nature 139.
Journal Article
38 (13), pp. 4246 - 4253 (2010)
Chromatin methylation activity of Dnmt3a and Dnmt3a/3L is guided by interaction of the ADD domain with the histone H3 tail. Nucleic Acids Research 140.
Journal Article
50 (4), pp. S19 - S22 (2010)
Evaluation of the LightCycler(R) 1536 Instrument for high-throughput quantitative real-time PCR. Methods