Lynette Foo on Muck Rack

Lynette Foo

As seen in: Cell Press, Stem Cell Reports

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Looking to raise your team's performance in Singapore? We have a cooking team building programme available for you. We offer both challenging programmes that build up the pressure, such as Hell's Kitchen, as more friendly, social and fun formats for casual get-togethers. Palate Sensations Team Building – Singapore, Chromos #01-03, 10 Biopolis Rd, Singapore 138670, +65 6478 9746

Articles

ApoE4 disrupts intracellular trafficking and iron homeostasis in a reproducible iPSC-based model of human brain endothelial cells

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By Luisa Bell, Shane Clerkin, Nadine Stokar-Regenscheit, Xandor M. Spijkers, Claire Simonneau, Angélique Augustin, Barbara Höllbacher, Lia D’Abate, Joanna Ficek-Pascual, Kim Schneider, Thomas L. Maurissen, Chiara Zanini, Christine Becker, Alex Odermatt, Lynette Foo, Martina Pigoni, Roberto Villaseñor, Sila Rizalar, Antoine Rizkallah, Nienke R. Wevers, Christelle Zundel, Sabrina Golling
| Stem Cell Reports Verified
ArticleVolume 20, Issue 9102607Open access 1Roche Pharma Research and Early Development (pRED), Roche Innovation Center Basel, Basel, Switzerland 2Department of Pharmaceutical Sciences, University of Basel, Basel, Switzerland 3MIMETAS BV, Oegstgeest, the Netherlands Publication History: Received October 26, 2024; Revised July 28, 2025; Accepted July 28, 2025; Published online August 21, 2025 DOI: 10.1016/j.stemcr.2025.102607 External LinkAlso available on ScienceDirect External Link...
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snRNA-seq stratifies multiple sclerosis patients into distinct white matter glial responses

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By Will Macnair, Daniela Calini, Eneritz Agirre, Julien Bryois, Sarah Jäkel, Rebecca Smith, Petra Kukanja, Nadine Stokar-Regenscheit, Virginie Ott, Lynette Foo, Ludovic Collin, Sven Schippling, Eduard Urich, Erik Nutma, Manuel C. Marzin, Federico An
| Cell Press Verified
See Figure S13 for an overview of the analysis workflow. Sample swap checks via genotyping We genotyped all samples included in this study using the GSAv3 illumina CHIP. Genotypes were imputed using the Haplotype Reference Consortium (HRC) reference panel (version r1.1)73 and lifted over to GRCh38. Genotype processing and quality control was performed using Plink v1.9.74 SNPs with imputation score <0.4 or with missingness greater than 5% were excluded. We used MBV75 to identify sample swaps.
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Single-nucleus and spatial transcriptomic profiling of human temporal cortex and white matter reveals novel associations with AD pathology

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By Julien Bryois, Daniela Calini, Lynette Foo
| biorxiv.org
Abstract Alzheimer's disease (AD) is a neurodegenerative disorder with complex pathological manifestations and is the leading cause of cognitive decline and dementia in elderly individuals. A major goal in AD research is to identify new therapeutic pathways by studying the molecular and cellular changes in the disease, either downstream or upstream of the pathological hallmarks.
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