Prof. dr. S.J.L. (Sander) van den Heuvel Head of Department Science Biology Professor Science Biology Biodynamics and Biocomplexity Developmental Biology +31 30 253 3573
[email protected] Hugo R. Kruytgebouw Padualaan 8 Kamer O 507 3584 CH Utrecht Welcome to the Van den Heuvel lab Our research focuses on the coordinated regulation of cell division and differentiation in the context of animal development. Our goal is to obtain a deeper understanding, at the molecular and systems level, of the mechanisms that control two important developmental decisions:
Sander van den Heuvel Orthona
Sander van den Heuvel +31 30 253 3573
[email protected] Padualaan 8 3584 CH Utrecht The Netherlands BIOLOGY OFFICE Phone: +31 30 253 3084 Email:
[email protected] Contact Research Prof. dr. Sander van den Heuvel Our research focuses on the coordinated regulation of cell division and differentiation in the context of animal development. Sander van den Heuvel Group leader. Prof. Sander van den Heuvel +31 (0)30 253 3573 Room O.507 Vincent Portegijs Lab Manager. Dr. Vincent Portegijs +31 (0)30 253 3028 Room O.510 Alexander Blackwell Postdoctoral Fellow. Dr. Alexander Blackwell +31 (0)30 253 3475 Room O.511. Sander van den Heuvel's lab | Utrecht University (UU) Overview Advance your research 20+ million members 135+ million publication pages 2.3+ billion citations Featured research Dose-dependent. Prof. dr. S.J.L. (Sander) van den Heuvel - Universiteit Utrecht Medewerkers Organogram Prof. dr. S.J.L. (Sander) van den Heuvel Hoofd departement Bètawetenschappen Biologie Hoogleraar Bètawetenschappen Biologie Biodynamics and Biocomplexity Developmental Biology 030 253 3573
[email protected] Hugo R. Kruytgebouw Padualaan 8 Kamer O 507
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Sander van den Heuvel Utrecht University | UU · Division of Developmental Biology Connect with experts in your field Join ResearchGate to contact this researcher and connect with your scientific. Sander van den Heuvel Biography We study the regulation of cell division in the context of animal development. Our efforts aim to address (1) how cells can divide asymmetrically to form daughter cells with different fates, and (2) how cell proliferation and differentiation are coordinated during animal development. Edward T Kipreos Sander van den Heuvel 30846544 PMC6404260 10.1534/genetics.118.301643 cell division patterns has come from studies in various genetic model systems. The nematode Caenorhabditis elegans has only about 1000 somatic cells and approximately twice as many germ cells in the adult hermaphrodite. Caenorhabditis elegans cell-cycle genes have been identified over the past decade, including at least two distinct Cyclin-Dependent Kinases (CDKs), their cyclin partners, positive and negative regulators, and downstream targets.
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Sander van den Heuvel The single C. elegans member of the retinoblastoma gene family, lin-35 Rb, was originally identified as a synthetic Multivulva (synMuv) gene [1]. Suzan Ruijtenberg 1 , Sander van den Heuvel 2 Affiliations 1 Developmental Biology, Department of Biology, Faculty of Sciences, Utrecht University, Padualaan 8, 3584 CH Utrecht, the Netherlands.
Suzan Ruijtenberg and Sander van den Heuvel Developmental Biology, Department of Biology, Faculty of Sciences, Utrecht University, Utrecht, The Netherlands ARTICLE HISTORY Received 10 August 2015 Revised 4 October 2015 Accepted 12 November 2015 ABSTRACT Cell proliferation and differentiation show a remarkable inverse relationship. Precursor. Neem rechtstreeks contact op met Sander. Bekijk het profiel van Sander van den Heuvel op LinkedIn, de grootste professionele community ter wereld. Sander heeft 1 functie op zijn of haar profiel. Bekijk het volledige profiel op LinkedIn om de connecties van Sander en vacatures bij vergelijkbare bedrijven te zien.
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Prof. dr. S.J.L. (Sander) van den Heuvel. Head of Department. Biology. Professor. Developmental Biology +31 30 253 3573.
[email protected]. Profile Publications Activities Teaching Ancillary activities Contact. Profile Publications Activities Teaching Ancillary activities Contact. Research areas - 2054 DOI: 10.1126/science.8266103 Abstract The key cell-cycle regulator Cdc2 belongs to a family of cyclin-dependent kinases in higher eukaryotes. Dominant-negative mutations were used to address the requirement for kinases of this family in progression through the human cell cycle.
