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Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes

Neurology, 2006-10, Vol.67 (7), p.1242

2006

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Magnetic properties of square Py nanowires: Irradiation dose and geometry dependence

Journal of applied physics, 2015-05, Vol.117 (17)

2015

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Bridging the gap: heparan sulfate and Scube2 assemble Sonic hedgehog release complexes at the surface of producing cells

Scientific reports, 2016-05, Vol.6 (1), p.26435-26435, Article 26435

2016

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Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

American journal of human genetics, 2000-04, Vol.66 (4), p.1432-1436

2000

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Blockade of chemokine signaling in patients with multiple sclerosis

Neurology, 2006-11, Vol.67 (10), p.1880

2006

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Development of magnetic nanoactuator systems

Microelectronic engineering, 2011-08, Vol.88 (8), p.2263-2266

2011

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Magnetic bead nanoactuator

Microelectronic engineering, 2012-10, Vol.98, p.582-586

2012

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Mammalian SNM1 is required for genome stability

Molecular genetics and metabolism, 2008-05, Vol.94 (1), p.38-45

2008

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Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Nature genetics, 1995-11, Vol.11 (3), p.341-343

1995

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Silicon-plasmonic internal-photoemission detector for 40 Gbit/s data reception

Optica, 2016-07, Vol.3 (7), p.741

2016

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Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

American journal of human genetics, 2006-12, Vol.79 (6), p.1030-1039

2006

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Fifty-Four New Gene-Based Canine Microsatellite Markers

The Journal of heredity, 2005-11, Vol.96 (7), p.843-846

2005

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Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Journal of cardiac failure, 2001-09, Vol.7 (3), p.249-256

2001

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Pseudo exchange bias due to rotational anisotropy

Journal of magnetism and magnetic materials, 2016-08, Vol.412, p.7-10

2016

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Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes

American journal of ophthalmology, 2007, Vol.143 (1), p.194-195

2007

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Oral interferon beta-1a in relapsing-remitting multiple sclerosis: a double-blind randomized study

Multiple sclerosis, 2003-08, Vol.9 (4), p.342-348

2003

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Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

American journal of human genetics, 2000-05, Vol.66 (5), p.1540-1551

2000

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Sensitivity optimization of injection-molded photonic crystal slabs for biosensing applications

Optical materials express, 2013-05, Vol.3 (5), p.556-565

2013

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P129 Severe iron overload in patients with myelodysplastic syndromes (MDS) enrolled in a large study of deferasirox (Exjade®, ICL670)

Leukemia research, 2007, Vol.31, p.S109-S110

2007

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A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Nature genetics, 1993-06, Vol.4 (2), p.202-205

1993

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Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer

Molecular medicine (Cambridge, Mass.), 1998-07, Vol.4 (7), p.468-479

1998

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Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases

Genomics (San Diego, Calif.), 1995-09, Vol.29 (1), p.285-287

1995

Volltextzugriff (PDF)

24 Tumor-infiltrerende lymfocyten en relatie met uitkomst en HPV-status bij peniscarcinoom

Tijdschrift voor urologie, 2014-10, Vol.4 (7), p.169-169

2014

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Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Cytogenetic and genome research, 2009-09, Vol.125 (3), p.165-175

2009

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Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

Mammalian genome, 1999-04, Vol.10 (4), p.381-384

1999

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Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes

Magnetic properties of square Py nanowires: Irradiation dose and geometry dependence

Bridging the gap: heparan sulfate and Scube2 assemble Sonic hedgehog release complexes at the surface of producing cells

Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2

Blockade of chemokine signaling in patients with multiple sclerosis

Development of magnetic nanoactuator systems

Magnetic bead nanoactuator

Mammalian SNM1 is required for genome stability

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p

Silicon-plasmonic internal-photoemission detector for 40 Gbit/s data reception

Mutations of Presenilin Genes in Dilated Cardiomyopathy and Heart Failure

Fifty-Four New Gene-Based Canine Microsatellite Markers

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease

Pseudo exchange bias due to rotational anisotropy

Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes

Oral interferon beta-1a in relapsing-remitting multiple sclerosis: a double-blind randomized study

Localization of the Fanconi Anemia Complementation Group D Gene to a 200-kb Region on Chromosome 3p25.3

Sensitivity optimization of injection-molded photonic crystal slabs for biosensing applications

P129 Severe iron overload in patients with myelodysplastic syndromes (MDS) enrolled in a large study of deferasirox (Exjade®, ICL670)

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews

Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer

Cloning and Characterization of a Human cDNA (INPPL1) Sharing Homology with Inositol Polyphosphate Phosphatases

24 Tumor-infiltrerende lymfocyten en relatie met uitkomst en HPV-status bij peniscarcinoom

Topo IIIα and BLM Act within the Fanconi Anemia Pathway in Response to DNA-Crosslinking Agents

Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome

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