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A fast method for quantitative proteomics based on a combination between two-dimensional electrophoresis and 15N-metabolic labelling.
Published in:
Electrophoresis, 2005, v. 26, n. 16, p. 3191
By:
- Ambrosius 4;P. 4;L. Snijders;
- Marjon 4;G. 4;J. de Vos;
- Bart de Koning;
- Phillip 4;C. Wright
Publication type:
Article
Archaeal MBF1 binds to 30S and 70S ribosomes via its helix-turn-helix domain.
Published in:
Biochemical Journal, 2014, v. 462, n. 2, p. 373, doi. 10.1042/BJ20131474
By:
- BLOMBACH, Fabian;
- LAUNAY, Helene;
- SNIJDERS, Ambrosius P. L.;
- ZORRAQUINO, Violeta;
- Hao WU;
- DE KONING, Bart;
- BROUNS, Stan J. J.;
- ETTEMA, Thijs J. G.;
- CAMILLONI, Carlo;
- CAVALLI, Andrea;
- VENDRUSCOLO, Michele;
- DICKMAN, Mark J.;
- CABRITA, Lisa D.;
- LA TEANA, Anna;
- BENELLI, Dario;
- LONDEI, Paola;
- CHRISTODOULOU, John;
- VAN DER OOST, John
Publication type:
Article
Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1270, doi. 10.1038/ejhg.2015.44
By:
- Vrijenhoek, Terry;
- Kraaijeveld, Ken;
- Elferink, Martin;
- de Ligt, Joep;
- Kranendonk, Elcke;
- Santen, Gijs;
- Nijman, Isaac J;
- Butler, Derek;
- Claes, Godelieve;
- Costessi, Adalberto;
- Dorlijn, Wim;
- van Eyndhoven, Winfried;
- Halley, Dicky JJ;
- van den Hout, Mirjam CGN;
- van Hove, Steven;
- Johansson, Lennart F;
- Jongbloed, Jan DH;
- Kamps, Rick;
- Kockx, Christel EM;
- de Koning, Bart
Publication type:
Article
Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 9, p. 1142, doi. 10.1038/ejhg.2014.279
By:
- Vrijenhoek, Terry;
- Kraaijeveld, Ken;
- Elferink, Martin;
- de Ligt, Joep;
- Kranendonk, Elcke;
- Santen, Gijs;
- Nijman, Isaac J;
- Butler, Derek;
- Claes, Godelieve;
- Costessi, Adalberto;
- Dorlijn, Wim;
- van Eyndhoven, Winfried;
- Halley, Dicky J J;
- van den Hout, Mirjam C G N;
- van Hove, Steven;
- Johansson, Lennart F;
- Jongbloed, Jan D H;
- Kamps, Rick;
- Kockx, Christel E M;
- de Koning, Bart
Publication type:
Article
Correction: Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.
Published in:
2021
By:
- Almomani, Rowida;
- Marchi, Margherita;
- Sopacua, Maurice;
- Lindsey, Patrick;
- Salvi, Erika;
- de Koning, Bart;
- Santoro, Silvia;
- Magri, Stefania;
- Smeets, Hubert J. M.;
- Boneschi, Filippo Martinelli;
- Malik, Rayaz A.;
- Ziegler, Dan;
- Hoeijmakers, Janneke G. J.;
- Bönhof, Gidon;
- Dib-Hajj, Sulayman;
- Waxman, Stephen G.;
- Merkies, Ingemar S. J.;
- Lauria, Giuseppe;
- Faber, Catharina G.;
- Gerrits, Monique M.
Publication type:
Correction Notice
Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing.
Published in:
PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0238467
By:
- Almomani, Rowida;
- Marchi, Margherita;
- Sopacua, Maurice;
- Lindsey, Patrick;
- Salvi, Erika;
- Koning, Bart de;
- Santoro, Silvia;
- Magri, Stefania;
- Smeets, Hubert J. M.;
- Martinelli Boneschi, Filippo;
- Malik, Rayaz R.;
- Ziegler, Dan;
- Hoeijmakers, Janneke G. J.;
- Bönhof, Gidon;
- Dib-Hajj, Sulayman;
- Waxman, Stephen G.;
- Merkies, Ingemar S. J.;
- Lauria, Giuseppe;
- Faber, Catharina G.;
- Gerrits, Monique M.
Publication type:
Article
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.
Published in:
2013
By:
- Gerards, Mike;
- Kamps, Rick;
- van Oevelen, Jo;
- Boesten, Iris;
- Jongen, Eveline;
- de Koning, Bart;
- Scholte, Hans R;
- de Angst, Isabel;
- Schoonderwoerd, Kees;
- Sefiani, Abdelaziz;
- Ratbi, Ilham;
- Coppieters, Wouter;
- Karim, Latifa;
- de Coo, René;
- van den Bosch, Bianca;
- Smeets, Hubert
Publication type:
Journal Article
Exome sequencing reveals a novel Moroccan founder mutation in SLC19A3 as a new cause of early-childhood fatal Leigh syndrome.
Published in:
Brain: A Journal of Neurology, 2013, v. 136, n. 3, p. 882, doi. 10.1093/brain/awt013
By:
- Gerards, Mike;
- Kamps, Rick;
- van Oevelen, Jo;
- Boesten, Iris;
- Jongen, Eveline;
- de Koning, Bart;
- Scholte, Hans R.;
- de Angst, Isabel;
- Schoonderwoerd, Kees;
- Sefiani, Abdelaziz;
- Ratbi, Ilham;
- Coppieters, Wouter;
- Karim, Latifa;
- de Coo, René;
- van den Bosch, Bianca;
- Smeets, Hubert
Publication type:
Article
Politieke Integriteitsaffaires in Nederland: de jaarlijkse Index.
Published in:
Beleid en Maatschappij (1875712X), 2024, v. 51, n. 2, p. 118, doi. 10.5553/BenM/138900692024004
By:
- Huberts, Leo;
- Kaptein, Muel;
- De Koning, Bart;
- Eising, Lotte
Publication type:
Article
Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause.
Published in:
Frontiers in Genetics, 2018, p. N.PAG, doi. 10.3389/fgene.2018.00400
By:
- Theunissen, Tom E. J.;
- Nguyen, Minh;
- Kamps, Rick;
- Hendrickx, Alexandra T.;
- Sallevelt, Suzanne C. E. H.;
- Gottschalk, Ralph W. H.;
- Calis, Chantal M.;
- Stassen, Alphons P. M.;
- de Koning, Bart;
- Mulder-Den Hartog, Elvira N. M.;
- Schoonderwoerd, Kees;
- Fuchs, Sabine A.;
- Hilhorst-Hofstee, Yvonne;
- de Visser, Marianne;
- Vanoevelen, Jo;
- Szklarczyk, Radek;
- Gerards, Mike;
- de Coo, Irenaeus F. M.;
- Hellebrekers, Debby M. E. I.;
- Smeets, Hubert J. M.
Publication type:
Article
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51508-1
By:
- Janssen, Anouk E. J.;
- Koeck, Rebekka M.;
- Essers, Rick;
- Cao, Ping;
- van Dijk, Wanwisa;
- Drüsedau, Marion;
- Meekels, Jeroen;
- Yaldiz, Burcu;
- van de Vorst, Maartje;
- de Koning, Bart;
- Hellebrekers, Debby M. E. I.;
- Stevens, Servi J. C.;
- Sun, Su Ming;
- Heijligers, Malou;
- de Munnik, Sonja A.;
- van Uum, Chris M. J.;
- Achten, Jelle;
- Hamers, Lars;
- Naghdi, Marjan;
- Vissers, Lisenka E. L. M.
Publication type:
Article
Specific MRIi Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects.
Published in:
Frontiers in Neurology, 2016, v. 7, p. 1, doi. 10.3389/fneur.2016.00203
By:
- Theunissen, Tom E. J.;
- Szklarczyk, Radek;
- Gerards, Mike;
- Hellebrekers, Debby M. E. I.;
- Mulder-Den Hartog, Elvira N. M.;
- Vanoevelen, Jo;
- Kamps, Rick;
- de Koning, Bart;
- Rutledge, S. Lane;
- Schmitt-Mechelke, Thomas;
- van Berkel, Carola G. M.;
- van der Knaap, Marjo S.;
- de Coo, Irenaeus F. M.;
- Smeets, Hubert J. M.
Publication type:
Article

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