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- 2008
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Mark
Subjects heterozygous for genetic loss of function of the thiazide-sensitive cotransporter have reduced blood pressure
- Contribution to journal › Article
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Mark
Novel expression and transcriptional regulation of FoxJ1 during oro-facial morphogenesis
- Contribution to journal › Article
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Mark
A risk haplotype of STAT4 for systemic lupus erythematosus is over-expressed, correlates with anti-dsDNA and shows additive effects with two risk alleles of IRF5
- Contribution to journal › Article
- 2007
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Mark
Reduced cell proliferation and increased apoptosis are significant pathological mechanisms in a murine model of mild pseudoachondroplasia resulting from a mutation in the C-terminal domain of COMP
- Contribution to journal › Article
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Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
- Contribution to journal › Article
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Mark
COG8 deficiency causes new congenital disorder of glycosylation type IIh
- Contribution to journal › Article
- 2006
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Mark
Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease
- Contribution to journal › Article
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Mark
Laminin {alpha}1 chain improves laminin {alpha}2 chain deficient peripheral neuropathy.
- Contribution to journal › Article
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Mark
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
- Contribution to journal › Article
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Mark
Cholinergic neuronal defect without cell loss in Huntington's disease.
- Contribution to journal › Article
