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Profil bibliographique

Matty Meijers

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

46Publications signalées
1562Citations signalées
0Affiliations récentes

Les domaines associés

DNA Repair MechanismsGenetic factors in colorectal cancerPARP inhibition in cancer therapyCarcinogens and Genotoxicity AssessmentBRCA gene mutations in cancer

Les publications récentes

Accès ouvert 2023 other OpenAlex

Data Supplement from Functional Ex Vivo Assay to Select Homologous Recombination–Deficient Breast Tumors for PARP Inhibitor Treatment

Kishan A.T. Naipal, Nicole S. Verkaik, Najim Ameziane, Carolien H. M. van Deurzen et autres

Figure S1: Schematic workflow of RAD51IRIF assay and accessory experimental timeline. Figure S2: Validation of RAD51 IRIF immunostaining: 2 hours post IR is optimal for RAD51 focus formation which are only formed in GEMININ positive cells Figure S3: ᵞ-H2AX and 53BP1 nuclear …

0 citations
Accès ouvert 2023 other OpenAlex

Data Supplement from Functional Ex Vivo Assay to Select Homologous Recombination–Deficient Breast Tumors for PARP Inhibitor Treatment

Kishan A.T. Naipal, Nicole S. Verkaik, Najim Ameziane, Carolien H. M. van Deurzen et autres

Figure S1: Schematic workflow of RAD51IRIF assay and accessory experimental timeline. Figure S2: Validation of RAD51 IRIF immunostaining: 2 hours post IR is optimal for RAD51 focus formation which are only formed in GEMININ positive cells Figure S3: ᵞ-H2AX and 53BP1 nuclear …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Functional Ex Vivo Assay to Select Homologous Recombination–Deficient Breast Tumors for PARP Inhibitor Treatment

Kishan A.T. Naipal, Nicole S. Verkaik, Najim Ameziane, Carolien H. M. van Deurzen et autres

Abstract Purpose: Poly(ADP-ribose) polymerase (PARP) inhibitors are promising targeted treatment options for hereditary breast tumors with a homologous recombination (HR) deficiency caused by BRCA1 or BRCA2 mutations. However, the functional consequence of BRCA gene mutations is not always known and tumors can …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Frequent Homologous Recombination Deficiency in High-grade Endometrial Carcinomas

Marthe M. de Jonge, Aurélie Auguste, Lise M. van Wijk, Philip C. Schouten et autres

AbstractPurpose: The elevated levels of somatic copy-number alterations (SCNAs) in a subset of high-risk endometrial cancers are suggestive of defects in pathways governing genome integrity. We sought to assess the prevalence of homologous recombination deficiency (HRD) in endometrial cancers and its association …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Functional Ex Vivo Assay to Select Homologous Recombination–Deficient Breast Tumors for PARP Inhibitor Treatment

Kishan A.T. Naipal, Nicole S. Verkaik, Najim Ameziane, Carolien H. M. van Deurzen et autres

Abstract Purpose: Poly(ADP-ribose) polymerase (PARP) inhibitors are promising targeted treatment options for hereditary breast tumors with a homologous recombination (HR) deficiency caused by BRCA1 or BRCA2 mutations. However, the functional consequence of BRCA gene mutations is not always known and tumors can …

0 citations
Accès ouvert 2023 other OpenAlex

Data from Frequent Homologous Recombination Deficiency in High-grade Endometrial Carcinomas

Marthe M. de Jonge, Aurélie Auguste, Lise M. van Wijk, Philip C. Schouten et autres

AbstractPurpose: The elevated levels of somatic copy-number alterations (SCNAs) in a subset of high-risk endometrial cancers are suggestive of defects in pathways governing genome integrity. We sought to assess the prevalence of homologous recombination deficiency (HRD) in endometrial cancers and its association …

0 citations

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