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Year Number of Results
2017 3
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2020 15
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2024 13

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SMAD6-deficiency in human genetic disorders.
Luyckx I, Verstraeten A, Goumans MJ, Loeys B. Luyckx I, et al. NPJ Genom Med. 2022 Nov 21;7(1):68. doi: 10.1038/s41525-022-00338-5. NPJ Genom Med. 2022. PMID: 36414630 Free PMC article. Review.
The role of ErbB4 in cancer.
Segers VFM, Dugaucquier L, Feyen E, Shakeri H, De Keulenaer GW. Segers VFM, et al. Cell Oncol (Dordr). 2020 Jun;43(3):335-352. doi: 10.1007/s13402-020-00499-4. Epub 2020 Mar 26. Cell Oncol (Dordr). 2020. PMID: 32219702 Review.
Pathophysiology and clinical relevance of atrial myopathy.
Tubeeckx MRL, De Keulenaer GW, Heidbuchel H, Segers VFM. Tubeeckx MRL, et al. Basic Res Cardiol. 2024 Apr;119(2):215-242. doi: 10.1007/s00395-024-01038-0. Epub 2024 Mar 12. Basic Res Cardiol. 2024. PMID: 38472506 Review.
Advances and challenges in modeling inherited peripheral neuropathies using iPSCs.
Van Lent J, Prior R, Pérez Siles G, Cutrupi AN, Kennerson ML, Vangansewinkel T, Wolfs E, Mukherjee-Clavin B, Nevin Z, Judge L, Conklin B, Tyynismaa H, Clark AJ, Bennett DL, Van Den Bosch L, Saporta M, Timmerman V. Van Lent J, et al. Exp Mol Med. 2024 Jun 3. doi: 10.1038/s12276-024-01250-x. Online ahead of print. Exp Mol Med. 2024. PMID: 38825644 Free article. Review.
91 results