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Items: 10

1.

A strategy for the prior processing of high-resolution mass spectral data obtained from high-dimensional combined fractional diagonal chromatography.

Valkenborg D, Thomas G, Krols L, Kas K, Burzykowski T.

J Mass Spectrom. 2009 Apr;44(4):516-29. doi: 10.1002/jms.1527.

PMID:
19065607
2.

Using a Poisson approximation to predict the isotopic distribution of sulphur-containing peptides in a peptide-centric proteomic approach.

Valkenborg D, Assam P, Thomas G, Krols L, Kas K, Burzykowski T.

Rapid Commun Mass Spectrom. 2007;21(20):3387-91.

PMID:
17891751
3.

Functional analysis of cyclin-dependent kinase inhibitors of Arabidopsis.

De Veylder L, Beeckman T, Beemster GT, Krols L, Terras F, Landrieu I, van der Schueren E, Maes S, Naudts M, Inzé D.

Plant Cell. 2001 Jul;13(7):1653-68.

4.

Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.

Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, van Regenmorter N, Martin JJ, Van Broeckhoven C.

Hum Mol Genet. 1998 Feb;7(2):177-86.

PMID:
9425224
5.

Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1.

Krols L, Martin JJ, David G, Van Regemorter N, Benomar A, Löfgren A, Stevanin G, Dürr A, Brice A, Van Broeckhoven C.

Hum Genet. 1997 Feb;99(2):225-32.

PMID:
9048926
6.

Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees.

De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C.

Eur J Hum Genet. 1996;4(5):260-6.

PMID:
8946171
7.

Report and abstracts of the Fourth International Workshop on Human Chromosome 2 Mapping 1996.

Spur NK, Bashir R, Bushby K, Cox A, Cox S, Hilde Brandt F, Hill N, Kao FT, Krols L, Marzella R, Miller N, Nothwang HG, Rocchi M, Sarfarazi M, Stratakis CA, Wallgren-Petterson C, Naylor S.

Cytogenet Cell Genet. 1996;73(4):255-73. No abstract available.

PMID:
8751373
8.

Report of the sixth international workshop on human chromosome 3 mapping 1995.

Naylor SL, Carritt B, Boileau C, Beroud C, Alexander C, Allderdice P, Alimov A, Ashworth T, Bonifas J, Bugert P, Buys CH, Chipperfield MA, Deng G, Drabkin H, Gemmill RM, Grompe M, Joensuu T, Jonasdottir A, Gizatullin R, Krols L, Leach RJ, Lott ST, Killary A, Martinsson T, Messiaen L, et al.

Cytogenet Cell Genet. 1996;72(4):255-70. No abstract available.

PMID:
8641130
9.

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12-p21.1.

Benomar A, Krols L, Stevanin G, Cancel G, LeGuern E, David G, Ouhabi H, Martin JJ, Dürr A, Zaim A, et al.

Nat Genet. 1995 May;10(1):84-8.

PMID:
7647798
10.

On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family.

Martin JJ, Van Regemorter N, Krols L, Brucher JM, de Barsy T, Szliwowski H, Evrard P, Ceuterick C, Tassignon MJ, Smet-Dieleman H, et al.

Acta Neuropathol. 1994;88(4):277-86.

PMID:
7839819

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