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- 2005
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Mark
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy
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- Contribution to journal › Article
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Mark
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome
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- Contribution to journal › Article
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Mark
The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient {beta}-cell mass and exocytosis.
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- Contribution to journal › Article
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Mark
Orexin loss in Huntington's disease.
(
- Contribution to journal › Article
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Mark
Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
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- Contribution to journal › Article
- 2004
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Mark
Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice.
(
- Contribution to journal › Article
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Mark
Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3.
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- Contribution to journal › Article
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Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
- 2003
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Mark
A genome wide scan for early onset primary hypertension in Scandinavians.
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- Contribution to journal › Article
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Mark
Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma
(
- Contribution to journal › Article