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Results: 1-25/97
Authors:
Massat, I
Souery, D
Del-Favero, J
Oruc, L
Jakovljevic, M
Folnegovic, V
Adolfsson, R
Kaneva, R
Papadimitriou, G
Dikeos, D
Jazin, E
Milanova, V
Van Broeckhoven, C
Mendlewicz, J
Citation: I. Massat et al., Lack of association between GABRA3 and unipolar affective disorder: a multicentre study, IN J NEUROP, 4(3), 2001, pp. 273-278
Authors:
Lerer, B
Macciardi, F
Segman, RH
Adolfsson, R
Blackwood, D
Blairy, S
Del Favero, J
Dikeos, DG
Kaneva, R
Lilli, R
Massat, I
Milanova, V
Muir, W
Noethen, M
Oruc, L
Petrova, T
Papadimitriou, GN
Rietschel, M
Serretti, A
Souery, D
Van Gestel, S
Van Broeckhoven, C
Mendlewicz, J
Citation: B. Lerer et al., Variability of 5-HT2C receptor cys23ser polymorphism among European populations and vulnerability to affective disorder, MOL PSYCHI, 6(5), 2001, pp. 579-585
Authors:
Van Goethem, G
Dermaut, B
Lofgren, A
Martin, JJ
Van Broeckhoven, C
Citation: G. Van Goethem et al., Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions, NAT GENET, 28(3), 2001, pp. 211-212
Authors:
Ismailov, SM
Fedotov, VP
Dadali, EL
Polyakov, AV
Van Broeckhoven, C
Ivanov, VI
De Jonghe, P
Timmerman, V
Evgrafov, OV
Citation: Sm. Ismailov et al., A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21, EUR J HUM G, 9(8), 2001, pp. 646-650
Authors:
De Jonghe, C
Esselens, C
Kumar-Singh, S
Craessaerts, K
Serneels, S
Checler, F
Annaert, W
Van Broeckhoven, C
De Strooper, B
Citation: C. De Jonghe et al., Pathogenic APP mutations near the gamma-secretase cleavage site differentially affect A beta secretion and APP C-terminal fragment stability, HUM MOL GEN, 10(16), 2001, pp. 1665-1671
Authors:
Meuleman, J
Pou-Serradell, A
Lofgren, A
Ceuterick, C
Martin, JJ
Timmerman, V
Van Broeckhoven, C
De Jonghe, P
Citation: J. Meuleman et al., A novel 3 '-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies, NEUROMUSC D, 11(4), 2001, pp. 400-403
Authors:
Van Tendeloo, VFI
Van Broeckhoven, C
Berneman, ZN
Citation: Vfi. Van Tendeloo et al., Gene therapy: principles and applications to hematopoietic cells, LEUKEMIA, 15(4), 2001, pp. 523-544
Authors:
Van Tendeloo, VFI
Van Broeckhoven, C
Berneman, ZN
Citation: Vfi. Van Tendeloo et al., Gene-based cancer vaccines: an ex vivo approach, LEUKEMIA, 15(4), 2001, pp. 545-558
Authors:
Michalik, A
Kazantsev, A
Van Broeckhoven, C
Citation: A. Michalik et al., Method to introduce stable, expanded, polyglutamine-encoding CAG/CAA trinucleotide repeats into CAG repeat-containing genes, BIOTECHNIQU, 31(2), 2001, pp. 250
Authors:
De Jonghe, P
Mersivanova, I
Nelis, E
Del Favero, J
Martin, JJ
Van Broeckhoven, C
Evgrafov, OC
Timmerman, V
Citation: P. De Jonghe et al., Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E, ANN NEUROL, 49(2), 2001, pp. 245-249
Authors:
Goossens, D
Del-Favero, J
Van Broeckhoven, C
Citation: D. Goossens et al., Trinucleotide repeat expansions: Do they contribute to bipolar disorder?, BRAIN RES B, 56(3-4), 2001, pp. 243-257
Authors:
Ceuterick-de Groote, C
De Jonghe, P
Timmerman, V
Van Goethem, G
Lofgren, A
Ceulemans, B
Van Broeckhoven, C
Martin, JJ
Citation: C. Ceuterick-de Groote et al., Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsy, PATH RES PR, 197(3), 2001, pp. 193-198
Authors:
Theuns, J
Feuk, L
Dermaut, B
Del-Favero, J
Roks, G
Van den Bossche, D
Corsmit, E
Van den Broeck, M
van Duijn, CM
Cruts, M
Brookes, AJ
Van Broeckhoven, C
Citation: J. Theuns et al., The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease, HUM GENET, 108(6), 2001, pp. 552-553
Authors:
Meuleman, J
Kuhlenbaumer, G
Audenaert, D
Hunermund, G
Hor, H
Young, P
Stogbauer, F
Ringelstein, EB
Van Broeckhoven, C
De Jonghe, P
Timmerman, V
Citation: J. Meuleman et al., Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy(HNA), HUM GENET, 108(5), 2001, pp. 390-393
Authors:
Dermaut, B
Roks, G
Theuns, J
Rademakers, R
Houwing-Duistermaat, JJ
Serneels, S
Hofman, A
Breteler, MMB
Cruts, M
Van Broeckhoven, C
van Duijn, CM
Citation: B. Dermaut et al., Variable expression of presenilin 1 is not a major determinant of risk forlate-onset Alzheimer's Disease, J NEUROL, 248(11), 2001, pp. 935-939
Authors:
Kuhlenbaumer, G
Meuleman, J
De Jonghe, P
Falck, B
Young, P
Hunermund, G
Van Broeckhoven, C
Timmerman, V
Stogbauer, F
Citation: G. Kuhlenbaumer et al., Hereditary neuralgic amyotrophy (HNA) is genetically heterogeneous, J NEUROL, 248(10), 2001, pp. 861-865
Authors:
Van Everbroeck, B
Croes, EA
Pals, P
Dermaut, B
Jansen, G
van Duijn, CM
Cruts, M
Van Broeckhoven, C
Martin, JJ
Cras, P
Citation: B. Van Everbroeck et al., Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob Disease phenotype, NEUROSCI L, 313(1-2), 2001, pp. 69-72
Authors:
Arango, D
Cruts, M
Torres, O
Backhovens, H
Serrano, ML
Villareal, E
Montanes, P
Matallana, D
Cano, C
Van Broeckhoven, C
Jacquier, M
Citation: D. Arango et al., Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid beta precursor protein and presenilin genes in Colombia, AM J MED G, 103(2), 2001, pp. 138-143
Authors:
Slooter, AJC
Bots, ML
Havekes, LM
del Sol, AI
Cruts, M
Grobbee, DE
Hofman, A
Van Broeckhoven, C
Witteman, JCM
van Duijn, CM
Citation: Ajc. Slooter et al., Apolipoprotein E and carotid artery atherosclerosis - The Rotterdam study, STROKE, 32(9), 2001, pp. 1947-1952
Authors:
Roks, G
Cruts, M
Slooter, AJC
Dermaut, B
Hofman, A
Van Broeckhoven, C
Van Duijn, CM
Citation: G. Roks et al., The cystatin C polymorphism is not associated with early onset Alzheimer'sdisease, NEUROLOGY, 57(2), 2001, pp. 366-367
Authors:
Roymans, D
Vissenberg, K
De Jonghe, C
Grobben, B
Claes, P
Verbelen, JP
Van Broeckhoven, C
Slegers, H
Citation: D. Roymans et al., Phosphatidylinositol 3-kinase activity is required for the expression of glial fibrillary acidic protein upon cAMP-dependent induction of differentiation in rat C6 glioma, J NEUROCHEM, 76(2), 2001, pp. 610-618
Identification of the tumor metastasis suppressor Nm23-H1/Nm23-R1 as a constituent of the centrosome
Authors:
Roymans, D
Vissenberg, K
De Jonghe, C
Willems, R
Engler, G
Kimura, N
Grobben, B
Claes, P
Verbelen, JP
Van Broeckhoven, C
Slegers, H
Citation: D. Roymans et al., Identification of the tumor metastasis suppressor Nm23-H1/Nm23-R1 as a constituent of the centrosome, EXP CELL RE, 262(2), 2001, pp. 145-153
CAG repeat expansion in the TATA box-binding protein gene causes autosomaldominant cerebellar ataxia
Authors:
Fujigasaki, H
Martin, JJ
De Deyn, PP
Camuzat, A
Deffond, D
Stevanin, G
Dermaut, B
Van Broeckhoven, C
Durr, A
Brice, A
Citation: H. Fujigasaki et al., CAG repeat expansion in the TATA box-binding protein gene causes autosomaldominant cerebellar ataxia, BRAIN, 124, 2001, pp. 1939-1947
Authors:
Van Tendeloo, VFI
Ponsaerts, P
Lardon, F
Nijs, G
Lenjou, M
Van Broeckhoven, C
Van Bockstaele, DR
Berneman, ZN
Citation: Vfi. Van Tendeloo et al., Highly efficient gene delivery by mRNA electroporation in human hematopoietic cells: superiority to lipofection and passive pulsing of mRNA and to electroporation of plasmid cDNA for tumor antigen loading of dendritic cells, BLOOD, 98(1), 2001, pp. 49-56
Authors:
Souery, D
Van Gestel, S
Massat, I
Blairy, S
Adolfsson, R
Blackwood, D
Del-Favero, J
Dikeos, D
Jakovljevic, M
Kaneva, R
Lattuada, E
Lerer, B
Lilli, L
Milanova, V
Muir, W
Nothen, M
Oruc, L
Papadimitriou, G
Propping, P
Schulze, T
Serretti, A
Shapira, B
Smeraldi, E
Stefanis, C
Thomson, M
Van Broeckhoven, C
Mendlewicz, J
Citation: D. Souery et al., Tryptophan hydroxylase polymorphism and suicidality in unipolar and bipolar affective disorders: A multicenter association study, BIOL PSYCHI, 49(5), 2001, pp. 405-409