prof. dr. ir. Björn Menten
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Long-read sequencing enables full characterization of previously unresolved structural variation
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- Conference Paper
- C3
- open access
Long-read sequencing resolves (complex) cryptic structural variation in patients with syndromic intellectual disability
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Structural variants disrupt a critical regulatory region downstream of FOXG1
(2023) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 31(Supplement 1). p.28-28 -
Effect of biphasic CAPA-IVM on ovarian tissue oocytes of transgender men
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- Journal Article
- A1
- open access
Retained chromosomal integrity following CRISPR-Cas9-based mutational correction in human embryos
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- Journal Article
- A1
- open access
Characterization of ovarian tissue oocytes from transgender men reveals poor calcium release and embryo development, which might be overcome by spindle transfer
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- Journal Article
- A1
- open access
Single-cell profiling identifies a novel human polyclonal unconventional T cell lineage
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- Journal Article
- A1
- open access
Generation of human induced pluripotent stem cell line UGENTi001-A from a patient with Marfan syndrome carrying a heterozygous c.7754 T > C variant in FBN1 and the isogenic control UGENT001-A-1 using CRISPR/Cas9 editing
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Spindle transfer rescues poor embryo development of in vitro matured ovarian tissue oocytes from transgender men
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Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models