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Publications by Ad Geurts van Kessel

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-Tumor Phenotype

Cancer Cell
Cancer ResearchOncologyCell Biology
2019English

BTG1 Regulates Glucocorticoid Receptor Autoinduction in Acute Lymphoblastic Leukemia

Blood
BiochemistryImmunologyCell BiologyHematology
2010English

NTHL1 and MUTYH Polyposis Syndromes: Two Sides of the Same Coin?

Journal of Pathology
Forensic MedicinePathology
2017English

Cancer Risk in Patients With Noonan Syndrome Carrying a PTPN11 Mutation

European Journal of Human Genetics
Genetics
2011English

Microarray Analyses Reveal Strong Influence of DNA Copy Number Alterations on the Transcriptional Patterns in Pancreatic Cancer: Implications for the Interpretation of Genomic Amplifications

Oncogene
Cancer ResearchGeneticsMolecular Biology
2005English

Detection of Chromosome Aneuploidies in Chorionic Villus Samples by Multiplex Ligation-Dependent Probe Amplification

Journal of Molecular Diagnostics
Forensic MedicinePathologyMolecular Medicine
2009English

Control of O -Glycan Branch Formation

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2000English

Analysis of Von Hippel—Lindau Mutations With Comparative Genomic Hybridization in Sporadic and Hereditary Hemangioblastomas: Possible Genetic Heterogeneity

Journal of Neurosurgery
SurgeryNeurology
2002English

Holoprosencephaly and Preaxial Polydactyly Associated With a 1.24 Mb Duplication Encompassing FBXW11 at 5q35.1

Journal of Human Genetics
Genetics
2006English

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