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EVIDENCE IN VITRO FOR A PARTICIPATION OF THE ARGININE REPRESSOR IN CUMULATIVE REPRESSION OF ESCHERICHIA COLI CARBAMOYLPHOSPHATE SYNTHASELISSENS W; CUNIN R; GLANSDORFF N et al.1979; ARCH. INTERNATION. PHYSIOL. BIOCHIM.; BEL; DA. 1979; VOL. 87; NO 3; PP. 630-632; BIBL. 6 REF.Article

Preimplantation genetic diagnosis : current status and new developmentsLISSENS, W; SERMON, K.Human reproduction (Oxford. Print). 1997, Vol 12, Num 8, pp 1756-1761, issn 0268-1161Article

SYNTHESIS IN VITRO OF THE CATALYTIC SUBUNIT OF ESCHERICHIA COLI ASPARTATE CARBAMOYLTRANSFERASEFELLER A; LISSENS W; GLANSDORFF N et al.1978; ARCH. INTERNATION. PHYSIOL. BIOCHIM.; BEL; DA. 1978; VOL. 86; NO 4; PP. 941-942; BIBL. 7 REF.Article

ROLE OF TRANSCRIPTIONAL REGULATION AND ENZYME INACTIVATION IN THE SYNTHESIS OF ESCHERICHIA COLI CARBAMOYLPHOSPHATE SYNTHASEPIERARD A; LISSENS W; HALLEUX P et al.1980; J. BACTERIOL.; USA; DA. 1980; VOL. 141; NO 1; PP. 382-385; BIBL. 19 REF.Article

IN VITRO SYNTHESIS OF ESCHERICHIA COLI CARBAMOYLPHOSPHATE SYNTHASE: EVIDENCE FOR PARTICIPATION OF THE ARGININE REPRESSOR IN CUMULATIVE REPRESSIONLISSENS W; CUNIN R; KELKER N et al.1980; J. BACTERIOL.; USA; DA. 1980; VOL. 141; NO 1; PP. 58-66; BIBL. 38 REF.Article

Is β-glucuronidase a clinical useful biomarker for an acute organophosphorus poisoning?SABBE, M. B; DESRUELLES, D; LISSENS, W et al.Human & experimental toxicology. 2008, Vol 27, Num 5, pp 431-433, issn 0960-3271, 3 p.Article

PATTERNS OF POLARITY IN THE ESCHERICHIA COLI CARAB GENE CLUSTERGIGOT D; CRABEEL M; FELLER A et al.1980; J. BACTERIOL.; ISSN 0021-9193; USA; DA. 1980; VOL. 143; NO 2; PP. 914-920; BIBL. 36 REF.Article

TRANSCRIPTION POLARITY OF THE CAR AB GENE CLUSTER OF ESCHERICHIA COLIGIGOT D; CRABEEL M; FELLER A et al.1978; ARCH. INTERNATION. PHYSIOL. BIOCHIM.; BEL; DA. 1978; VOL. 86; NO 4; PP. 915-916; BIBL. 5 REF.Article

PROMOTER MAPPING AND SELECTION OF OPERATOR MUTANTS BY USING INSERTION OF BACTERIOPHAGE MU IN THE ARG ECBH DIVERGENT OPERON OF ESCHERICHIA COLI K-12BENY G; BOYEN A; CHARLIER D et al.1982; J. BACTERIOL.; ISSN 0021-9193; USA; DA. 1982; VOL. 151; NO 1; PP. 62-67; BIBL. 19 REF.Article

Pyruvate dehydrogenase (PDH) deficiency caused by a 21-base pair insertion mutation in the E1α subunitDE MEIRLEIR, L; LISSENS, W; VAMOS, E et al.Human genetics. 1992, Vol 88, Num 6, pp 649-652, issn 0340-6717Article

A mutation (IVS8+0.6kbdeITC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human β-glucuronidase geneVERVOORT, R; GITZELMANN, R; LISSENS, W et al.Human genetics. 1998, Vol 103, Num 6, pp 686-693, issn 0340-6717Article

Polyclonal antibodies against iduronate 2-sulphate sulphatase from human urineLISSENS, W; ZENATI, A; LIEBAERS, I et al.Biochimica et biophysica acta. 1984, Vol 801, Num 3, pp 365-371, issn 0006-3002Article

Free ionised calcium: a critical surveyVANSTAPEL, F. J; LISSENS, W. D.Annals of clinical biochemistry. 1984, Vol 21, Num 5, pp 339-351, issn 0004-5632Article

Pyruvate dehydrogenase E1α deficiency in a family : Different clinical presentation in two siblingsDE MEIRLEIR, L; SPECOLA, N; SENECA, S et al.Journal of inherited metabolic disease. 1998, Vol 21, Num 3, pp 224-226, issn 0141-8955Article

Importance of sequence analysis in NARP syndromeSENECA, S; DE MEIRLEIR, L; LIEBAERS, I et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 1, issn 0141-8955, p. 97Article

Pyruvate dehydrogenase deficiency due to a mutation of the E1 α subunitDE MEIRLEIR, L. J; LISSENS, W; VAMOS, E et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 3, pp 301-304, issn 0141-8955Article

Effect of calcium antagonism on intracellular concentrations and transmembrane fluxes of cations in erythrocytes of men at rest and during exerciseHESPEL, P; LIJNEN, P; FIOCCHI, R et al.Journal of hypertension. 1986, Vol 4, Num 6, pp 767-772, issn 0263-6352Article

Mild cystic fibrosis in child homozygous for G542 non-sense mutation in CF geneBONDUELLE, M; LISSENS, W; LIEBAERS, I et al.Lancet (British edition). 1991, Vol 338, Num 8760, issn 0140-6736, p. 189Article

A case of term mors in utero in a chromosme 11P linked long QT syndrome familyDESMYTTERE, S; BONDUELLE, M; DE WOLF, D et al.Genetic counseling. 1994, Vol 5, Num 3, pp 289-295, issn 1015-8146Article

Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndromeVANLANDER, A. V; JORENS, P. G; LISSENS, W et al.Acta anaesthesiologica scandinavica. 2012, Vol 56, Num 4, pp 520-525, issn 0001-5172, 6 p.Article

Krabbe leukodystrophy in a selected population with high rate of late onset forms: longer survival linked to c.121G>A (p.Gly41Ser) mutationFIUMARA, A; BARONE, R; ARENA, A et al.Clinical genetics. 2011, Vol 80, Num 5, pp 452-458, issn 0009-9163, 7 p.Article

The role of the testis-specific gene hTAF7L in the aetiology of male infertilitySTOUFFS, K; WILLEMS, A; LISSENS, W et al.Molecular human reproduction. 2006, Vol 12, Num 3-4, pp 263-267, issn 1360-9947, 5 p.Article

Preimplantation genetic diagnosis for medium-chain acyl-CoA dehydrogenase (MCAD) deficiencySERMON, K; HENDERIX, P; LISSENS, W et al.Molecular human reproduction. 2000, Vol 6, Num 12, pp 1165-1168, issn 1360-9947Article

Molecular analysis of the cystic fibrosis gene reveals a high frequency of the intron 8 splice variant 5T in Egyptian males with congenital bilateral absence of the vas deferensLISSENS, W; KAMAL ZAKI MAHMOUD; EL-GINDI, E et al.Molecular human reproduction. 1999, Vol 5, Num 1, pp 10-13, issn 1360-9947Article

Fluorescent PCR and automated fragment analysis for the clinical application of preimplantation genetic diagnosis of myotonic dystrophy (Steinert's disease)SERMON, K; DE VOS, A; VAN DE VELDE, H et al.Molecular human reproduction. 1998, Vol 4, Num 8, pp 791-796, issn 1360-9947Article

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