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Annemieke M. Timmermans

Researcher at Erasmus University Rotterdam

Publications -  14
Citations -  624

Annemieke M. Timmermans is an academic researcher from Erasmus University Rotterdam. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 9, co-authored 10 publications receiving 511 citations. Previous affiliations of Annemieke M. Timmermans include Erasmus University Medical Center.

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Identification of a Putative Protein Profile Associated with Tamoxifen Therapy Resistance in Breast Cancer

TL;DR: Extracellular matrix metalloproteinase inducer levels were higher in therapy-resistant tumors and significantly associated with an earlier tumor progression following first line tamoxifen treatment (hazard ratio, 1.87) and ENPP1, EIF3E, and GNB4 were significant associated with progression-free survival upon tamoxIFen treatment for recurrent disease.
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Detection of circulating tumor cells in breast cancer may improve through enrichment with anti-CD146

TL;DR: The use of CD146 is introduced to detect EpCAM-negative CTCs, thereby improving CTC detection and combined use of anti-CD146 and anti-EpCAM is likely to improve C TC detection in breast cancer patients.
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Tumor cell migration screen identifies SRPK1 as breast cancer metastasis determinant

TL;DR: Examination of genes that modulate migration indicated that SRPK1, encoding the splicing factor kinase SRSF protein kinase 1, is relevant to breast cancer outcomes, as it was highly expressed in basal breast cancer.
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Breast cancer genomics and immuno-oncological markers to guide immune therapies.

TL;DR: The characteristics of infiltrating leukocytes in healthy and malignant breast tissue, the prognostic and predictive values of immune cell subsets across different BC subtypes and the various existing immune evasive mechanisms are reviewed.
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CD49f-based selection of circulating tumor cells (CTCs) improves detection across breast cancer subtypes

TL;DR: The tested cytokeratins provided no substantial benefit, but adding CD49f to CK8/18/19 as a selection marker resulted in improved recovery of normal-like cell lines, likely to further improve CTC detection in breast cancer.