Petra G.M. van Overveld

ORCID: 0000-0003-0216-5004
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About
Contact & Profiles
Research Areas
  • Bone health and treatments
  • Radiopharmaceutical Chemistry and Applications
  • TGF-β signaling in diseases
  • Muscle Physiology and Disorders
  • Medical Imaging and Pathology Studies
  • Cancer Cells and Metastasis
  • RNA Research and Splicing
  • Bone and Dental Protein Studies
  • Genetic Neurodegenerative Diseases
  • Medical Imaging Techniques and Applications
  • Genetics and Neurodevelopmental Disorders
  • Management of metastatic bone disease
  • Prostate Cancer Treatment and Research
  • Neurogenetic and Muscular Disorders Research
  • Cardiomyopathy and Myosin Studies
  • Tissue Engineering and Regenerative Medicine
  • 3D Shape Modeling and Analysis
  • Software Engineering and Design Patterns
  • Logic, programming, and type systems
  • Chromosomal and Genetic Variations
  • Genomic variations and chromosomal abnormalities
  • bioluminescence and chemiluminescence research
  • Research Data Management Practices
  • Nanoplatforms for cancer theranostics
  • Periodontal Regeneration and Treatments

Leiden University Medical Center
2000-2011

Neurology, Inc
2007

Leiden University
2007

Centre for Human Drug Research
2005

Center for Human Genetics
2004

Radboud University Nijmegen
2003

Radboud University Medical Center
2003

Philips (Netherlands)
1999

Abstract Bone morphogenetic protein 7 (BMP7) counteracts the physiological epithelial-to-mesenchymal transition (EMT), a process that is indicative of epithelial plasticity. Because EMT involved in cancer, we investigated whether BMP7 plays role breast cancer growth and metastasis. In this study, show decreased expression primary significantly associated with formation clinically overt bone metastases patients ≥10 years follow-up. line these clinical observations, inversely related to...

10.1158/0008-5472.can-06-2490 article EN Cancer Research 2007-09-15

Abstract Facioscapulohumeral muscular dystrophy (FSHD) progressively affects the facial, shoulder, and upper arm muscles is associated with contractions of polymorphic D4Z4 repeat array in 4q35. Recently, we demonstrated that FSHD alleles are hypomethylated at D4Z4. To study potential relationships between hypomethylation both residual size clinical severity, compared severity score methylation unrelated patients. Correcting for age examination improves parameter to define provides further...

10.1002/ana.20625 article EN Annals of Neurology 2005-09-21

Chromosomal rearrangements occur more frequently in subtelomeric domains than other regions of the genome and are often associated with human pathology. To further elucidate plasticity domains, we examined 3.3 kb D4Z4 repeat array on chromosome 4 its homologue 10 208 Dutch blood donors by pulsed field gel electrophoresis. These repeats known to rearrange partial deletions this polymorphic facioscapulohumeral muscular dystrophy (FSHD), an autosomal dominant myopathy. Our results show that...

10.1093/hmg/9.19.2879 article EN Human Molecular Genetics 2000-11-01

<b><i>Objective:</i></b> Autosomal dominant facioscapulohumeral muscular dystrophy (FSHD) is associated with a contraction of the D4Z4 repeat array on chromosome 4. So far, homozygosity or compound heterozygosity for FSHD alleles has not been described, and it debated whether absence such subjects because rarity lethality disorder. <b><i>Methods:</i></b> Two unrelated families in which probands are heterozygous two FSHD-sized were studied. Clinical examination, pulsed-field gel...

10.1212/wnl.61.7.909 article EN Neurology 2003-10-14

We consider the problem of real-time animation a cartoon character which is represented by skeleton implicit surface. If character's motions permit constant topology for skin, it possible to reduce computing an approximation surface solve only one scalar equation per point fixed number points; these points define shape triangle mesh with topology. present algorithm, and demonstrate its working in model walking legs.

10.1109/cgi.1999.777957 article EN 1999-01-01

&lt;div&gt;Abstract&lt;p&gt;Bone morphogenetic protein 7 (BMP7) counteracts the physiological epithelial-to-mesenchymal transition (EMT), a process that is indicative of epithelial plasticity. Because EMT involved in cancer, we investigated whether BMP7 plays role breast cancer growth and metastasis. In this study, show decreased expression primary significantly associated with formation clinically overt bone metastases patients ≥10 years follow-up. line these clinical observations,...

10.1158/0008-5472.c.6495063.v1 preprint EN 2023-03-30

&lt;div&gt;Abstract&lt;p&gt;Bone morphogenetic protein 7 (BMP7) counteracts the physiological epithelial-to-mesenchymal transition (EMT), a process that is indicative of epithelial plasticity. Because EMT involved in cancer, we investigated whether BMP7 plays role breast cancer growth and metastasis. In this study, show decreased expression primary significantly associated with formation clinically overt bone metastases patients ≥10 years follow-up. line these clinical observations,...

10.1158/0008-5472.c.6495063 preprint EN 2023-03-30
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