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A. De Vos

Researcher at Vrije Universiteit Brussel

Publications -  64
Citations -  4199

A. De Vos is an academic researcher from Vrije Universiteit Brussel. The author has contributed to research in topics: Embryo transfer & Preimplantation genetic diagnosis. The author has an hindex of 34, co-authored 57 publications receiving 4027 citations. Previous affiliations of A. De Vos include University of California & University of California, Berkeley.

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Three-dimensional structure of an oncogene protein: catalytic domain of human c-H-ras p21.

TL;DR: A resolution of the normal human c-H-ras oncogene protein lacking a flexible carboxyl-terminal 18 residue reveals that the protein consists of a six-stranded beta sheet, four alpha helices, and nine connecting loops that indicate additional regions in the molecule that may possibly participate in other cellular functions.
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Metabolic fate of glucose in purified islet cells. Glucose-regulated anaplerosis in beta cells.

TL;DR: In this paper, the authors examined the anaplerosis of glucose carbon in purified rat islets using specific 14C-labeled glucose tracers and concluded that 25% of the glucose carbon entering the Krebs cycle via anaphylaxis is channeled into protein synthesis.
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Crystal structures at 2.2 A resolution of the catalytic domains of normal ras protein and an oncogenic mutant complexed with GDP.

TL;DR: Comparison with GTP-analog complexes of ras proteins suggests that the valine side-chain may inhibit GTP hydrolysis in two possible ways: (1) interacting directly with the gamma-phosphate and altering its orientation or the conformation of protein residues around the phosphates; and/or (2) preventing either the departure of gamma- phosphate on GTP Hydrolysis or the entrance of a nucleophilic group to attack the gamma.
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Heterogeneity in Glucose Sensitivity Among Pancreatic Beta-cells Is Correlated To Differences in Glucose Phosphorylation Rather Than Glucose-transport

TL;DR: Comparison of glucose metabolism in two beta‐cell subpopulations separated on the basis of the presence or absence of a metabolic redox shift at 7.5 mM glucose shows heterogeneity in glucose metabolism cannot be attributed to differences in GLUT2 mRNA levels or in glucose transport.
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Impact of cleavage-stage embryo biopsy in view of PGD on human blastocyst implantation: a prospective cohort of single embryo transfers

TL;DR: The clinical outcome of 1- cell biopsy was significantly better than that of 2-cell biopsy, even when adjusted for availability of genetically transferable embryos.