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ENZYMATIC SYNTHESIS OF NEOLACTOTETRAOSYLCERAMIDE BY THE N-ACETYLLACTOSAMINE SYNTHASE OF HUMAN SERUMZIELENSKI J; KOSCIELAK J.1982; EUR. J. BIOCHEM.; ISSN 0014-2956; DEU; DA. 1982; VOL. 125; NO 2; PP. 323-329; BIBL. 43 REF.Article

Genotype and phenotype in cystic fibrosisZIELENSKI, J.Respiration (Basel). 2000, Vol 67, Num 2, pp 117-133, issn 0025-7931Article

Sera of i subjects have the capacity to synthesize the branched GlcNAcβ(1→6)[GlcNAc(β1→3)]Gal... structureZIELENSKI, J; KOSCIELAK, J.FEBS letters. 1983, Vol 163, Num 1, pp 114-118, issn 0014-5793Article

Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermiaMAK, V; ZIELENSKI, J; TSUI, L.-C et al.JAMA, the journal of the American Medical Association. 1999, Vol 281, Num 23, pp 2217-2224, issn 0098-7484Article

Identification of mutations in exons 1 through 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneZIELENSKI, J; BOZON, D; BAT-SHEVA KEREM et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 1, pp 229-235, issn 0888-7543, 7 p.Article

Weak A phenotypes possibly caused by mutationKOSCIELAK, J; LENKIEWICZ, B; ZIELENSKI, J et al.Vox sanguinis (Basel. 1956). 1986, Vol 50, Num 3, pp 187-190, issn 0042-9007Article

Dinucleotide (CA/GT) repeat polymorphism in intron 17B of the cystic fibrosis transmembrane conductance regulator (CFTR) geneMORRAL, N; GIRBAU, E; ZIELENSKI, J et al.Human genetics. 1992, Vol 88, Num 3, issn 0340-6717, p. 356Article

A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator proteinCUTTING, G. R; KASCH, L. M; ROSENSTEIN, B. J et al.Nature (London). 1990, Vol 346, Num 6282, pp 366-369, issn 0028-0836, 4 p.Article

Section on metabolism and enzyme actionCOHEN, B; PATEL, H; LIAU, Y. H et al.Annals of the New York Academy of Sciences. 1987, Vol 494, pp 329-358, issn 0077-8923Conference Paper

Do common in silico tools predict the clinical consequences of amino-acid substitutions in the CFTR gene?DORFMAN, R; NALPATHAMKALAM, T; TAYLOR, C et al.Clinical genetics. 2010, Vol 77, Num 5, pp 464-473, issn 0009-9163, 10 p.Article

Complete screening of the CFTR gene in Argentine cystic fibrosis patientsVISICH, A; ZIELENSKI, J; CASTANOS, C et al.Clinical genetics. 2002, Vol 61, Num 3, pp 207-213, issn 0009-9163Article

Cystic fibrosis gene mutations and infertile men with primary testicular failureMAK, V; ZIELENSKI, J; TSUI, L.-C et al.Human reproduction (Oxford. Print). 2000, Vol 15, Num 2, pp 436-439, issn 0268-1161Article

Analysis of CFTR transcripts in nasal epithelial cells and lymphoblasts of a cystic fibrosis patient with 621+1G→T and 711+1G→T mutationsZIELENSKI, J; BOZON, D; MARKIEWICZ, D et al.Human molecular genetics (Print). 1993, Vol 2, Num 6, pp 683-687, issn 0964-6906Article

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis familiesDÖRK, T; NEUMANN, T; KLINGER, K et al.Human genetics. 1992, Vol 88, Num 4, pp 417-425, issn 0340-6717Article

Campylobacter pyloridis degrades mucin and undermines gastric mucosal integritySLOMIANY, B. L; BILSKI, J; SAROSIEK, J et al.Biochemical and biophysical research communications (Print). 1987, Vol 144, Num 1, pp 307-314, issn 0006-291XArticle

Molecular consequences of cystic fibrosis transmembrane regulator (CFTR) gene mutations in the exocrine pancreasAHMED, N; COREY, M; FORSTNER, G et al.Gut. 2003, Vol 52, Num 8, pp 1159-1164, issn 0017-5749, 6 p.Article

Analysis of the CFTR gene in Turkish cystic fibrosis patients : identification of three novel mutations (3172delAC, P1013L and M1028I)ONAY, T; TOPALOGLU, O; KIRDAR, B et al.Human genetics. 1998, Vol 102, Num 2, pp 224-230, issn 0340-6717Article

Higher proportion of intact exon 9 CFTR mRNA in nasal epithelium compared with vas deferensMAK, V; JARVI, K. A; ZIELENSKI, J et al.Human molecular genetics (Print). 1997, Vol 6, Num 12, pp 2099-2107, issn 0964-6906Article

Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutationsWILSCHANSKI, M; ZIELENSKI, J; MARKIEWICZ, D et al.The Journal of pediatrics. 1995, Vol 127, Num 5, pp 705-710, issn 0022-3476Article

Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis geneKEREM, B.-S; ZIELENSKI, J; LAP-CHEE TSUI et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 21, pp 8447-8451, issn 0027-8424, 5 p.Article

Prostaglandin protection against ethanol-induced gastric injury: regulatory effect on the mucus glucoprotein metabolismTSUKADA, H; ZIELENSKI, J; MIZUTA, K et al.Digestion. 1987, Vol 36, Num 4, pp 201-212, issn 0012-2823Article

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