A. T. Ten Asbroek

发表

Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Robert H. Brown, M. Weale, F. Baas, 2017, Science Translational Medicine.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Annelot M. Dekker, Robert H. Brown, F. Baas, 2016, Nature Genetics.

Comparison of schwann cell and sciatic nerve transcriptomes indicates that mouse is a valid model for the human peripheral nervous system

J. Ruijter, F. Baas, A. T. Ten Asbroek, 2006, Journal of neuroscience research.

A review of treatment modalities in gyrate atrophy of the choroid and retina (GACR).

H. Waterham, R. Houtkooper, C. V. van Karnebeek, 2021, Molecular genetics and metabolism.

UvA-DARE ( Digital Academic Repository ) In vivo tumor growth inhibition and biodistribution studies of locked nucleic acid ( LNA ) antisense oligonucleotides

Frank Baas, F. Baas, H. Olsson, 2017 .

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Annelot M. Dekker, Ashley R. Jones, F. Baas, 2016, Nature Genetics.

The Role of Small Molecules and Their Effect on the Molecular Mechanisms of Early Retinal Organoid Development

A. T. Ten Asbroek, A. Bergen, C. Boon, 2021, International journal of molecular sciences.

ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function

Robert H. Brown, F. Baas, A. Al-Chalabi, 2018, Neurobiology of Aging.

The involvement of human ribonucleases H1 and H2 in the variation of response of cells to antisense phosphorothioate oligonucleotides.

Frank Baas, F. Baas, A. T. Ten Asbroek, 2002, European journal of biochemistry.

Ribonuclease H1 maps to chromosome 2 and has at least three pseudogene loci in the human genome.

F. Baas, A. T. Ten Asbroek, B. Janssen, 2002, Genomics.

Myelin and Axon Pathology in a Long-Term Study of PMP22-Overexpressing Mice

F. Baas, J. Muddle, A. T. Ten Asbroek, 2011, Journal of neuropathology and experimental neurology.

Expression profiling of sciatic nerve in a Charcot‐Marie‐Tooth disease type 1a mouse model

F. Baas, A. T. Ten Asbroek, C. Verhamme, 2005, Journal of neuroscience research.

Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis

Hannah A. Pliner, John D. Eicher, Janel O. Johnson, 2021, JAMA Neurology.

The circadian clock regulates RPE-mediated lactate transport via SLC16A1 (MCT1).

A. T. Ten Asbroek, A. Bergen, M. Felder-Schmittbuhl, 2020, Experimental eye research.

The Analysis of Embryoid Body Formation and Its Role in Retinal Organoid Development

A. T. Ten Asbroek, J. T. ten Brink, Andrea Heredero Berzal, 2024, International journal of molecular sciences.

An alternative approach to produce versatile retinal organoids with accelerated ganglion cell development

A. T. Ten Asbroek, A. Bergen, N. Jansonius, 2021, Scientific Reports.

The Road towards Gene Therapy for X-Linked Juvenile Retinoschisis: A Systematic Review of Preclinical Gene Therapy in Cell-Based and Rodent Models of XLRS

A. T. Ten Asbroek, Andrea Heredero Berzal, Isa van der Veen, 2024, International journal of molecular sciences.

Stable transformation of Trypanosoma brucei.

P. Borst, A. T. Ten Asbroek, C. Mol, 1993, Molecular and biochemical parasitology.

Tumor genotype-specific growth inhibition in vivo by antisense oligonucleotides against a polymorphic site of the large subunit of human RNA polymerase II.

F. Baas, M. Aalders, A. T. Ten Asbroek, 2002, Cancer research.