Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("CASSIMAN, J.-J")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 239

  • Page / 10
Export

Selection :

  • and

QUALITY GENETIC SERVICES FOR THE POPULATION, NOW AND IN THE FUTURECASSIMAN, J.-J.Bulletin et mémoires de l'Académie Royale de Médecine de Belgique. 2010, Vol 165, Num 10-12, pp 475-482, issn 0377-8231, 8 p.Article

The involvement of the cell matrix receptors, or VLA integrins, in the morphogenetic behavior of normal and malignant cells is gradually being uncoveredCASSIMAN, J.-J.Cancer genetics and cytogenetics. 1989, Vol 41, Num 1, pp 19-32, issn 0165-4608Article

Conseil génétique sur base moléculaire dans la chorée de Huntington = Huntington disease: genetic counselling and molecular biologyCASSIMAN, J. J.Journal de génétique humaine. 1989, Vol 37, Num 1, pp 13-24, issn 0021-7743, 12 p.Article

Mutagenic potential of anti-herpes agentsDE CLERCQ, E; CASSIMAN, J.-J.Life sciences (1973). 1986, Vol 38, Num 3, pp 281-289, issn 0024-3205Article

Forensic medicine and the polymerase chain reaction techniqueDECORTE, R; CASSIMAN, J.-J.Journal of medical genetics. 1993, Vol 30, Num 8, pp 625-633, issn 0022-2593Article

Reevaluation of the importance of polymorphic HLA class II alleles and amino acids in the susceptibility of individuals of different populations to type I diabetesZAMANI, M; CASSIMAN, J.-J.American journal of medical genetics. 1998, Vol 76, Num 2, pp 183-194, issn 0148-7299Article

Cellular ageing of Alzheimer's disease and Down syndrome cells in cultureCARMELIET, G; DAVID, G; CASSIMAN, J.-J et al.Mutation research. DNAging : genetic instability and aging. 1991, Vol 256, Num 2-6, pp 221-231, issn 0921-8734Article

Inhibition of the degradation of the precursor and of the mature β1 integrin subunit by different protein synthesis inhibitors and by ATP depletionVEKEMAN, S; JASPERS, M; CASSIMAN, J.-J et al.FEBS letters. 1993, Vol 327, Num 2, pp 207-212, issn 0014-5793Article

Peptide transporter genes (TAP) polymorphisms and genetic susceptibility to rheumatoid arthritisVANDEVYVER, C; GEUSENS, P; CASSIMAN, J.-J et al.British journal of rheumatology. 1995, Vol 34, Num 3, pp 207-214, issn 0263-7103Article

Evaluation of a decontamination protocol for hair shafts before mtDNA sequencingJEHAES, E; GILISSEN, A; CASSIMAN, J.-J et al.Forensic science international. 1998, Vol 94, Num 1-2, pp 65-71, issn 0379-0738Article

Myelin basic protein gene polymorphism is not associated with chronic progressive multiple sclerosisVANDEVYVER, C; STINISSEN, P; CASSIMAN, J.-J et al.Journal of neuroimmunology. 1994, Vol 52, Num 1, pp 97-99, issn 0165-5728Article

Heterogeneity of phenylketonuria in BelgiumVERELST, P; FRANCOIS, B; CASSIMAN, J. J et al.Developmental brain dysfunction. 1993, Vol 6, Num 1-3, pp 97-108, issn 1019-5815Article

Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reactionSPAEPEN, M; ANGULO, A. F; MARYNEN, P et al.FEMS microbiology letters. 1992, Vol 99, Num 1, pp 89-94, issn 0378-1097Article

Attitudes towards predictive testing in Huntington's disease: a recent survey in BelgiumEVERS-KIEBOOMS, G; CASSIMAN, J. J; VAN DEN BERGHE, H et al.Journal of medical genetics. 1987, Vol 24, Num 5, pp 275-279, issn 0022-2593Article

Quadruplex fluorescent STR typing system (HUMVWA, HUMTH01, D21S11 and HPRT) with sequence-defined allelic ladders identification of a new allele at D21S11XIAO, F.-X; GILISSEN, A; CASSIMAN, J.-J et al.Forensic science international. 1998, Vol 94, Num 1-2, pp 39-46, issn 0379-0738Article

Identification of internal variation in the pseudoautosomal VNTR DXYS17, with nonrandom distribution of the alleles on the X and the Y chromosomesDECORTE, R; WU, R; MARYNEN, P et al.American journal of human genetics. 1994, Vol 54, Num 3, pp 506-515, issn 0002-9297Article

T cell receptor delta locus polymorphism in rheumatoid arthritisVANDEVYVER, C; GEUSENS, P; CASSIMAN, J.-J et al.European journal of immunogenetics. 1994, Vol 21, Num 6, pp 479-483, issn 0960-7420Article

Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR geneCUPPENS, H; MARYNEN, P; DE BOECK, C et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 3, pp 693-697, issn 0888-7543Article

Identification of a new frameshift mutation and a duplication polymorphism in the CFTR gene in the Algerian populationCUPPENS, H; LOUMI, O; MARYNEN, P et al.Human molecular genetics (Print). 1992, Vol 1, Num 4, pp 283-284, issn 0964-6906Article

The probabilistic interpretation of correlation coefficients in population geneticsMEULEPAS, E; CASSIMAN, J. J; VAN DEN BERGHE, H et al.Theoretical population biology (Print). 1991, Vol 39, Num 3, pp 301-314, issn 0040-5809Article

Human pregnancy zone protein and α2-macroglobulin: high-affinity binding of complexes to the same receptor on fibroblasts and characterization by monoclonal antibodiesVAN LEUVEN, F; CASSIMAN, J.-J; VAN DEN BERGHE, H et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 35, pp 16622-16625, issn 0021-9258Article

Identification of seven rather infrequent and one novel CFTR mutation in the Belgian populationHUI TENG; CUPPENS, H; DE BOECK, C et al.Human molecular genetics (Print). 1994, Vol 3, Num 12, pp 2249-2250, issn 0964-6906Article

Changes in the adhesive behavior of human osteosarcoma clonal cell lines upon prolonged in vitro culture recovered by cloningDE MARTELAERE, D; CASSIMAN, J.-J; VAN DEN BERGHE, H et al.Cell biology international reports. 1985, Vol 9, Num 12, pp 1109-1113, issn 0309-1651Article

Presymptomatic and predictive genetic testing in minors : a systematic review of guidelines and position papersBORRY, P; STULTIENS, L; NYS, H et al.Clinical genetics. 2006, Vol 70, Num 5, pp 374-381, issn 0009-9163, 8 p.Article

Characterization of 19 disease-associated missense mutations in the regulatory domain of the cystic fibrosis transmembrane conductance regulatorVANKEERBERGHEN, A; LIN WEI; JASPERS, M et al.Human molecular genetics (Print). 1998, Vol 7, Num 11, pp 1761-1769, issn 0964-6906Article

  • Page / 10