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Human evolutionBIRKENMEIER, E. H.Birth defects original article series. 1987, Vol 23, Num 3, pp 209-219, issn 0547-6844Article

A single-base-pair deletion in the β-glucuronidase gene accounts for the phenotype of murine mucopolysaccharidosis type VIISANDS, M. S; BIRKENMEIER, E. H.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 14, pp 6567-6571, issn 0027-8424Article

Developmental regulation of a gene that encodes a cysteine-rich intestinal protein and maps near the murine immunoglobulin heavy chain locusBIRKENMEIER, E. H; GORDON, J. I.Proceedings of the National Academy of Sciences of the United States of America. 1986, Vol 83, Num 8, pp 2516-2520, issn 0027-8424Article

The fatty liver dystrophy (fld) mutation: a new mutant mouse with a developmental abnormality in triglyceride metabolism and associated tissue-specific defects in lipoprotein lipase and hepatic lipase activitiesLANGNER, C. A; BIRKENMEIER, E. H; BEN-ZEEV, O et al.The Journal of biological chemistry (Print). 1989, Vol 264, Num 14, pp 7994-8003, issn 0021-9258Article

Evolution of the apolipoproteins: structure of the rat APO-A-IV gene and its relationship to the human genes for APO-A-I, C-III, and EBOGUSKI, M. S; BIRKENMEIER, E. H; ELSHOURBAGY, N. A et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 14, pp 6398-6407, issn 0021-9258Article

Enzyme replacement with recombinant β-glucuronidase in the newborn mucopolysaccharidosis type VII mouseVOGLER, C; SANDS, M; HIGGINS, A et al.Pediatric research. 1993, Vol 34, Num 6, pp 837-840, issn 0031-3998Article

The human sucrase-isomaltase gene directs complex patterns of gene expression in transgenic miceMARKOWITZ, A. J; WU, G. D; BIRKENMEIER, E. H et al.American journal of physiology. Gastrointestinal and liver physiology. 1993, Vol 28, Num 3, pp G526-G539, issn 0193-1857Article

Expression of liver fatty acid-binding protein/human growth hormone fusion genes within the enterocyte and enteroendocrine cell populations of fetal transgenic miceROTH, K. A; RUBIN, D. C; BIRKENMEIER, E. H et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 9, pp 5949-5954, issn 0021-9258, 6 p.Article

Correction of murine mucopolysaccharidosis VII by a human β-glucuronidase transgeneKYLE, J. W; BIRKENMEIER, E. H; GWYNN, B et al.Proceedings of the National Academy of Sciences of the United States of America. 1990, Vol 87, Num 10, pp 3914-3918, issn 0027-8424, 5 p.Article

Clinical and pathologic findings in two new allelic murine models of polycystic kidney diseaseVOGLER, C; HOMAN, S; PUNG, A et al.Journal of the American Society of Nephrology. 1999, Vol 10, Num 12, pp 2534-2539, issn 1046-6673Article

Identification and genetic mapping of a new polycystic kidney disease on mouse chromosome 8JANASWAMI, P. M; BIRKENMEIER, E. H; COOK, S. A et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 101-107, issn 0888-7543Article

Syngeneic bone marrow transplantation reduces the hearing loss associated with murine mucopolysaccharidosis type VIISANDS, M. S; ERWAY, L. C; VOGLER, C et al.Blood. 1995, Vol 86, Num 5, pp 2033-2040, issn 0006-4971Article

Genomic organization and chromosome localization of the murine homeobox gene PmxKERN, M. J; ARGAO, E. A; BIRKENMEIER, E. H et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 2, pp 334-340, issn 0888-7543Article

Characterization of the peripheral neuropathy in neonatal and adult mice that are homozygous for the fatty liver dystrophy (fld) mutationLANGNER, C. A; BIRKENMEIER, E. H; ROTH, K. A et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 18, pp 11955-11964, issn 0021-9258Article

The human and rodent intestinal fatty acid binding protein genes: a comparative analysis of their structure, expression, and linkage relationshipsSWEETSER, D. A; BIRKENMEIER, E. H; KLISAK, I. J et al.The Journal of biological chemistry (Print). 1987, Vol 262, Num 33, pp 16060-16071, issn 0021-9258Article

Enzyme replacement with recombinant β-glucuronidase in murine mucopolysaccharidosis type VII : Impact of therapy during the first six weeks of life on subsequent lysosomal storage, growth, and survivalVOGLER, C; SANDS, M. S; LEVY, B et al.Pediatric research. 1996, Vol 39, Num 6, pp 1050-1054, issn 0031-3998Article

Neuropathology of murine mucopolysaccharidosis type VIILEVY, B; GALVIN, N; VOGLER, C et al.Acta neuropathologica. 1996, Vol 92, Num 6, pp 562-568, issn 0001-6322Article

Localization of the tight junction protein gene TJP1 to human chromosome 15q13 distal to the Prader-Willi/Angelman region, and the mouse chromosome 7MOHANDAS, T. K; CHEN, X.-N; ROWE, L. B et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 3, pp 594-597, issn 0888-7543Article

Epithelial cell differentiation in normal and transgenic mouse intestinal isograftsRUBIN, D. C; ROTH, K. A; BIRKENMEIER, E. H et al.The Journal of cell biology. 1991, Vol 113, Num 5, pp 1183-1192, issn 0021-9525Article

Temporal and spatial patterns of transgene expression in aging adult mice provide insights about the origins, organization, and differentiation of the intestinal epitheliumCOHN, S. M; ROTH, K. A; BIRKENMEIER, E. H et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 3, pp 1034-1038, issn 0027-8424, 5 p.Article

Transgenic mice containing intestinal fatty acid-binding protein: human growth hormone fusion genes exhibit correct regional and cell-specific expression of the reporter gene in their small intestineSWEETSER, D. A; HAUFT, S. M; HOPPE, P. C et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 24, pp 9611-9615, issn 0027-8424Article

Enzyme replacement in murine mucopolysaccharidosis type VII : Neuronal and glial response to β-glucuronidase requires early initiation of enzyme replacement therapyVOGLER, C; LEVY, B; GALVIN, N. J et al.Pediatric research. 1999, Vol 45, Num 6, pp 838-844, issn 0031-3998Conference Paper

Differential susceptibility of inbred mouse strains to dextran sulfate sodium-induced colitisMÄHLER, M; BRISTOL, I. J; LEITER, E. H et al.American journal of physiology. Gastrointestinal and liver physiology. 1998, Vol 37, Num 3, pp G544-G551, issn 0193-1857Article

Reversal of pathology in murine mucopolysaccharidosis type VII by somatic cell gene transferWOLFE, J. H; SANDS, M. S; BARKER, J. E et al.Nature (London). 1992, Vol 360, Num 6406, pp 749-753, issn 0028-0836Article

A murine model of mucopolysaccharidosis VII : gross and microscopic findings in beta-glucuronidase-deficient miceVOGLER, C; BIRKENMEIER, E. H; SLY, W. S et al.The American journal of pathology. 1990, Vol 136, Num 1, pp 207-217, issn 0002-9440Article

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