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- 2011
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Mark
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
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- Contribution to journal › Article
- 2010
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Mark
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias
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- Contribution to journal › Article
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Mark
Altered expression and distribution of cathepsins in neuronopathic forms of Gaucher disease and in other sphingolipidoses
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- Contribution to journal › Article
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Mark
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons
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- Contribution to journal › Article
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Mark
Integrative genomics identifies DSCR1 (RCAN1) as a novel NFAT-dependent mediator of phenotypic modulation in vascular smooth muscle cells
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- Contribution to journal › Article
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Mark
A comprehensive analysis of common IGF1, IGFBP1 and IGFBP3 genetic variation with prospective IGF-I and IGFBP-3 blood levels and prostate cancer risk among
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- Contribution to journal › Article
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Mark
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes
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- Contribution to journal › Article
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Mark
The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.
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- Contribution to journal › Article
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Mark
Fatal outcome due to deficiency of subunit 6 of the conserved oligomeric Golgi complex leading to a new type of congenital disorders of glycosylation
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- Contribution to journal › Article
- 2009
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Mark
Tissue-specific alternative splicing of TCF7L2
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- Contribution to journal › Article