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Bioimage

Bio-Image Summer School Paris 2005

Author name initial(s) from year to year Publication type Display format limit
14 Publications
1 Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11)
MWJ. Luijendijk, E. Van Wijk, AMLC. Bischoff, E. Krieger, PLM. Huygen, RJE. Pennings, HG. Brunner, CWRJ. Cremers, FPM. Cremers, H. Kremer,
Hum. Genet. (2004) 115-2 p.149
2 A conformation-specific interhelical salt bridge in the K+ binding site of gastric H,K-ATPase
JB. Koenderink, HGP. Swarts, PHGM. Willems, E. Krieger, JJHHM. De Pont,
J. Biol. Chem. (2004) 279-16 p.16417
3 A structural and dynamic model for the interaction of interleukin-8 and glycosaminoglycans: Support from isothermal fluorescence titrations
E. Krieger, E. Geretti, B. Brandner, B. Goger, TNC. Wells, AJ. Kungl,
Proteins (2004) 54-4 p.768
4 A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26)
E. Van Wijk, E. Krieger, MH. Kemperman, EMR. De Leenheer, PLM. Huygen, CWRJ. Cremers, FPM. Cremers, H. Kremer,
J. Med. Genet. (2003) 40-12 p.879
5 Fluorescence analysis of the Hansenula polymorpha peroxisomal targeting signal-1 receptor, Pex5p
R. Boteva, A. Koek, NV. Visser, AJWG. Visser, E. Krieger, T. Zlateva, M. Veenhuis, I. Van Der Klei,
Eur. J. Biochem. (2003) 270-21 p.4332
6 Quantitative evaluation of experimental NMR restraints
SB. Nabuurs, CAEM. Spronk, E. Krieger, H. Maassen, G. Vriend, GW. Vuister,
J. Am. Chem. Soc. (2003) 125-39 p.12026
7 DJ-1 (PARK7), a novel gene for autosomal recessive, early onset parkinsonism
V. Bonifati, P. Rizzu, F. Squitieri, E. Krieger, N. Vanacore, JC. Van Swieten, A. Brice, CM. Van Duijn, B. Oostra, G. Meco, P. Heutink,
Neurol. Sci. (2003) 24-3 p.159
8 The precision of NMR structure ensembles revisited
CAEM. Spronk, SB. Nabuurs, AMJJ. Bonvin, E. Krieger, GW. Vuister, G. Vriend,
J. Biomol. NMR (2003) 25-3 p.225
9 Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism
V. Bonifati, P. Rizzu, MJ. Van Baren, O. Schaap, GJ. Breedveld, E. Krieger, MCJ. Dekker, F. Squitieri, P. Ibanez, M. Joosse, JW. Van Dongen, N. Vanacore, JC. Van Swieten, A. Brice, G. Meco, CM. Van Duijn, BA. Oostra, P. Heutink,
Science (2003) 299-5604 p.256
10 A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebral ataxia
JC. Van Swieten, E. Brusse, BM. De Graaf, E. Krieger, R. Van De Graaf, I. De Koning, A. Maat-kievit, P. Leegwater, D. Dooijes, BA. Oostra, P. Heutink,
Am. J. Hum. Genet. (2003) 72-1 p.191
11 Increasing the precision of comparative models with YASARA NOVA - a self-parameterizing force field
E. Krieger, G. Koraimann, G. Vriend,
Proteins (2002) 47-3 p.393
12 Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63
PHG. Duijf, KRJ. Vanmolkot, P. Propping, W. Friedl, E. Krieger, F. Mckeon, V. Dotsch, HG. Brunner, H. Van Bokhoven,
Hum. Mol. Genet. (2002) 11-7 p.799
13 Identification of different binding sites in the dendritic cell-specific receptor DC-SIGN for intercellular adhesion molecule 3 and HIV-1
TBH. Geijtenbeek, GCF. Van Duijnhoven, SJ. Van Vliet, E. Krieger, G. Vriend, CG. Figdor, Y. Van Kooyk,
J. Biol. Chem. (2002) 277-13 p.11314
14 Model@Home: distributed computing in bioinformatics using a screensaver based approach
E. Krieger, G. Vriend,
Bioinformatics (2002) 18-2 p.315

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