prof. dr. Frank Peelman
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- Journal Article
- A2
- open access
Deep mutational scanning of proteins in mammalian cells
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- Journal Article
- A1
- open access
The biologist’s guide to the glucocorticoid receptor’s structure
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- Journal Article
- A1
- open access
Selective IL-1 activity on CD8+ T cells empowers antitumor immunity and synergizes with neovasculature-targeted TNF for full tumor eradication
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- Journal Article
- A1
- open access
An affinity-enhanced, broadly neutralizing heavy chain-only antibody protects against SARS-CoV-2 infection in animal models
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- Journal Article
- A1
- open access
Specific targeting of IL-1β activity to CD8+ T cells allows for safe use as a vaccine adjuvant
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Selected IL-1 activity on CD8+ T cells allows for safe enhancement of cellular immune responses
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- Journal Article
- A1
- open access
Safe eradication of large established tumors using neovasculature-targeted tumor necrosis factor-based therapies
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- Journal Article
- A1
- open access
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone‐rod dystrophy, hearing loss and reduced male fertility
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Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
(2019) -
Expansion of the role and functional characterization of a missense variant in CEP78 associated with cone-rod dystrophy and hearing loss
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Towards the use of interleukin-1β as vaccine adjuvant
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- Journal Article
- A1
- open access
The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond
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- Journal Article
- A1
- open access
Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
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IL-1β AcTaleukins : towards potent yet safe adjuvants for tumor vaccination
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Biallelic loss-of-function variants in RAX2, encoding a homeobox-containing Rax transcription factor, cause autosomal recessive inherited retinal disease
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Functional characterization of N-terminal TIMP3 mutation underlying Sorsby fundus dystrophy in Belgian and French pedigrees
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- Journal Article
- A1
- open access
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development
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Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritis
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IL-1β AcTaleukins : towards potent yet safe adjuvants for tumor vaccination
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- Journal Article
- A1
- open access
TYK2-induced phosphorylation of Y640 suppresses STAT3 transcriptional activity