Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35

Por Wijmenga, Cisca, Deaven, Larry, Frants, Rune R.
Publicado em 1992

The D4Z4 Repeat–Mediated Pathogenesis of Facioscapulohumeral Muscular Dystrophy

Por van der Maarel, Silvère M., Frants, Rune R.
Publicado em 2005

Epigenetic Mechanisms of Facioscapulohumeral Muscular Dystrophy

Por de Greef, Jessica C., Frants, Rune R., van der Maarel, Silvère M.
Publicado em 2008

A Locus Linked to p16 Modifies Melanoma Risk in Dutch Familial Atypical Multiple Mole Melanoma (FAMMM) Syndrome Families

Por van der Velden, Pieter A., Sandkuijl, Lodewijk A., Bergman, Wilma, Hille, Elysée T.M., Frants, Rune R., Gruis, Nelleke A.
Publicado em 1999

Contractions of D4Z4 on 4qB Subtelomeres Do Not Cause Facioscapulohumeral Muscular Dystrophy

Por Lemmers, Richard J. F. L., Wohlgemuth, Mariëlle, Frants, Rune R., Padberg, George W., Morava, Eva, van der Maarel, Silvère M.
Publicado em 2004

Melanocortin-1 Receptor Variant R151C Modifies Melanoma Risk in Dutch Families with Melanoma

Por van der Velden, Pieter A., Sandkuijl, Lodewijk A., Bergman, Wilma, Pavel, Stan, van Mourik, Leny, Frants, Rune R., Gruis, Nelleke A.
Publicado em 2001

Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle

Por Huang, Yanchao, de Morrée, Antoine, van Remoortere, Alexandra, Bushby, Kate, Frants, Rune R., Dunnen, Johan Tden, van der Maarel, Silvère M.
Publicado em 2008

A Cascade of Complex Subtelomeric Duplications during the Evolution of the Hominoid and Old World Monkey Genomes

Por van Geel, Michel, Eichler, Evan E., Beck, Amy F., Shan, Zhihong, Haaf, Thomas, van der Maarel, Silvère M., Frants, Rune R., de Jong, Pieter J.
Publicado em 2002

High levels of dietary stearate promote adiposity and deteriorate hepatic insulin sensitivity

Por Havekes Louis M, Frants Rune R, Voshol Peter J, Ouwens Margriet, Bijland Silvia, Guigas Bruno, van den Berg Sjoerd AA, Romijn Johannes A, van Dijk Ko
Publicado em 2010-03-01

Mechanism and Timing of Mitotic Rearrangements in the Subtelomeric D4Z4 Repeat Involved in Facioscapulohumeral Muscular Dystrophy

Por Lemmers, Richard J. L. F., van Overveld, Petra G. M., Sandkuijl, Lodewijk A., Vrieling, Harry, Padberg, George W., Frants, Rune R., van der Maarel, Silvère M.
Publicado em 2004

Genetic Architecture of Plasma Adiponectin Overlaps With the Genetics of Metabolic Syndrome–Related Traits

Por Henneman, Peter, Aulchenko, Yurii S., Frants, Rune R., Zorkoltseva, Irina V., Zillikens, M. Carola, Frolich, Marijke, Oostra, Ben A., van Dijk, Ko Willems, van Duijn, Cornelia M.
Publicado em 2010

High levels of dietary stearate promote adiposity and deteriorate hepatic insulin sensitivity

Por van den Berg, Sjoerd AA, Guigas, Bruno, Bijland, Silvia, Ouwens, Margriet, Voshol, Peter J, Frants, Rune R, Havekes, Louis M, Romijn, Johannes A, van Dijk, Ko Willems
Publicado em 2010

Worldwide Population Analysis of the 4q and 10q Subtelomeres Identifies Only Four Discrete Interchromosomal Sequence Transfers in Human Evolution

Por Lemmers, Richard J.L.F., van der Vliet, Patrick J., van der Gaag, Kristiaan J., Zuniga, Sofia, Frants, Rune R., de Knijff, Peter, van der Maarel, Silvère M.
Publicado em 2010

Proteomic Analysis of the Dysferlin Protein Complex Unveils Its Importance for Sarcolemmal Maintenance and Integrity

Por de Morrée, Antoine, Hensbergen, Paul J., van Haagen, Herman H. H. B. M., Dragan, Irina, Deelder, André M., ’t Hoen, Peter A. C., Frants, Rune R., van der Maarel, Silvère M.
Publicado em 2010

Dysferlin Regulates Cell Adhesion in Human Monocytes

Por de Morrée, Antoine, Flix, Bàrbara, Bagaric, Ivana, Wang, Jun, van den Boogaard, Marlinde, Grand Moursel, Laure, Frants, Rune R., Illa, Isabel, Gallardo, Eduard, Toes, Rene, van der Maarel, Silvère M.
Publicado em 2013

Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: Combined analysis of an international consortium

Por Sarfarazi, Mansoor, Wijmenga, Cisca, Upadhyaya, Meena, Weiffenbach, Barbara, Hyser, Craig, Mathews, Kathy, Murray, Jeffrey, Gilbert, John, Pericak-Vance, Margaret, Lunt, Peter, Frants, Rune R., Jacobsen, Stephen, Harper, Peter S., Padberg, George W.
Publicado em 1992

Purkinje Cell-Specific Ablation of Ca(V)2.1 Channels is Sufficient to Cause Cerebellar Ataxia in Mice

Por Todorov, Boyan, Kros, Lieke, Shyti, Reinald, Plak, Petra, Haasdijk, Elize D., Raike, Robert S., Frants, Rune R., Hess, Ellen J., Hoebeek, Freek E., De Zeeuw, Chris I., van den Maagdenberg, Arn M. J. M.
Publicado em 2011

Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2

Por Guida, Serena, Trettel, Flavia, Pagnutti, Stefano, Mantuano, Elide, Tottene, Angelita, Veneziano, Liana, Fellin, Tommaso, Spadaro, Maria, Stauderman, Kenneth A., Williams, Mark E., Volsen, Stephen, Ophoff, Roel A., Frants, Rune R., Jodice, Carla, Frontali, Marina, Pietrobon, Daniela
Publicado em 2001

Specific Sequence Variations within the 4q35 Region Are Associated with Facioscapulohumeral Muscular Dystrophy

Por Lemmers, Richard J. L. F. , Wohlgemuth, Mariëlle , van der Gaag, Kristiaan J. , van der Vliet, Patrick J. , van Teijlingen, Corrie M. M. , de Knijff, Peter , Padberg, George W. , Frants, Rune R. , van der Maarel, Silvère M. 
Publicado em 2007

The expression of type III hyperlipoproteinemia: involvement of lipolysis genes

Por Henneman, Peter, van der Sman-de Beer, Femke, Moghaddam, Payman Hanifi, Huijts, Petra, Stalenhoef, Anton FH, Kastelein, John JP, van Duijn, Cornelia M, Havekes, Louis M, Frants, Rune R, van Dijk, Ko Willems, Smelt, Augustinus HM
Publicado em 2009