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- 2024
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Mark
Statistical Combination of ATLAS Run 2 Searches for Charginos and Neutralinos at the LHC
(
- Contribution to journal › Article
- 2023
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Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
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- Contribution to journal › Article
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Mark
First-Line Venetoclax Combinations in Chronic Lymphocytic Leukemia.
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- Contribution to journal › Article
- 2022
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Mark
Genetic Landscape of the ACE2 Coronavirus Receptor
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- Contribution to journal › Article
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Mark
Pharmacological targeting of MTHFD2 suppresses acute myeloid leukemia by inducing thymidine depletion and replication stress
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- Contribution to journal › Article
- 2021
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Mark
Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element
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- Contribution to journal › Article
- 2017
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Mark
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutations
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- Contribution to journal › Article
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Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
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- Contribution to journal › Article
- 2016
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Mark
Global binding pattern of the Wilms' tumor gene 1 (WT1) +17AA -KTS isoform in leukemic cells
2016) American Association for Cancer Research (AACR) 107th Annual Meeting 2016 In Cancer Research 76(14 Suppl.).(
- Contribution to journal › Published meeting abstract
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Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
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- Contribution to journal › Article
- 2015
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Mark
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation
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- Contribution to journal › Article
- 2014
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Mark
IL-17 protects T cells from apoptosis and contributes to development of ALPS-like phenotypes
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- Contribution to journal › Article
- 2001
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Mark
Somatic mosaicism in hemophilia A: A fairly common event
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- Contribution to journal › Article
- 1995
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Mark
Evaluation of the relationship between protein S and C4b-binding protein isoforms in hereditary protein S deficiency demonstrating type I and type III deficiencies to be phenotypic variants of the same genetic disease
(
- Contribution to journal › Article