COMPUTER SIMULATION OF SINTERING PROCESSESBROSS P; EXNER HE.1979; ACTA METALLURG.; USA; DA. 1979; VOL. 27; NO 6; PP. 1013-1020; ABS. FRE/GER; BIBL. 19 REF.Article

MATERIAL TRANSPORT RATE AND STRESS DISTRIBUTION DURING GRAIN BOUNDARY DIFFUSION DRIVEN BY SURFACE TENSIONEXNER HE; BROSS P.1979; ACTA METALLURG.; USA; DA. 1979; VOL. 27; NO 6; PP. 1007-1012; ABS. FRE/GER; BIBL. 8 REF.Article

Anti-Inflammatory Heat Shock Protein 70 Genes are Positively Associated with Human SurvivalSINGH, R; KØLVRAA, S; BROSS, P et al.Current pharmaceutical design (Print). 2010, Vol 16, Num 7, pp 796-801, issn 1381-6128, 6 p.Article

The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiencyANDRESEN, B. S; VIANEY-SABAN, C; BROSS, P et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 2, pp 169-172, issn 0141-8955Article

Co-overexpression of bacterial GroESL chaperonins partly overcomes non-productive folding and tetramer assembly of E. coli-expressed human medium-chain acyl-CoA dehydrogenase (MCAD) carrying the prevalent disease-causing K304E mutationsBROSS, P; ANDRESEN, B. S; WINTER, V et al.Biochimica et biophysica acta. Molecular basis of disease. 1993, Vol 1182, Num 3, pp 264-274, issn 0925-4439Article

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: the prevalent mutation G985 (K304E) is subject to a strong founder effect from Northwestern EuropeGREGERSEN, N; WINTER, V; JIA-HUAN DING et al.Human heredity. 1993, Vol 43, Num 6, pp 342-350, issn 0001-5652Article

The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients : is there correlation between genotype and phenotype?ANDRESEN, B. S; BROSS, P; YOKOTA, I et al.Human molecular genetics (Print). 1997, Vol 6, Num 5, pp 695-707, issn 0964-6906Article

Amino adic polymorphism (Gly209Ser) in the ACADS geneKRISTENSEN, M. J; KMOCH, S; BROSS, P et al.Human molecular genetics (Print). 1994, Vol 3, Num 9, issn 0964-6906, p. 1711Article

A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)ANDRESEN, B. S; BROSS, P; CURTIS, D et al.American journal of human genetics. 1993, Vol 53, Num 3, pp 730-739, issn 0002-9297Article

Functional analysis of the adsorption protein of two filamentous phages with different host specificitiesBROSS, P; BUSSMANN, K; KEPPNER, W et al.Journal of general microbiology. 1988, Vol 134, pp 461-471, issn 0022-1287, 2Article

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in a family with a previous fatal case of sudden unexpected death in childhoodGREGERSEN, N; WINTER, V; JENSEN, P. K. A et al.Prenatal diagnosis. 1995, Vol 15, Num 1, pp 82-86, issn 0197-3851Article

Characterization of wild-type human medium-chain acyl-CoA dehydrogenase (MCAD) and mutant enzymes present in MCAD-deficient patients by two-dimensional gel electrophoresis : evidence for post-translational modification of the enzymeBROSS, P; JENSEN, T. G; ANDRESEN, B. S et al.Biochemical medicine and metabolic biology. 1994, Vol 52, Num 1, pp 36-44, issn 0885-4505Article

A silent A to G mutation in exon 11 of the medium-chain acyl-CoA dehydrogenase (MCAD) geneANDRESEN, B. S; KøLVRAA, S; BROSS, P et al.Human molecular genetics (Print). 1993, Vol 2, Num 4, issn 0964-6906, p. 488Article

Molecular characterization of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency : identification of a lys³²⁹ to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein in E. coliGREGERSEN, N; ANDRESEN, B. S; BOLUND, L et al.Human genetics. 1991, Vol 86, Num 6, pp 545-551, issn 0340-6717Article

Characterization of wild-type and an active site mutant of human medium chair acyl-CoA dehydrogenase after expression in Escherichia coliBROSS, P; ENGST, S; STRAUSS, A. W et al.The Journal of biological chemistry (Print). 1990, Vol 265, Num 13, pp 7116-7119, issn 0021-9258, 4 p.Article

Carbohydrate-modified conducting polymers : synthesis and electrochemistry of sugar-linked azulenes and polyazulenesBROSS, P. A; SCHöBER, U; DAUB, J et al.Advanced materials (Weinheim). 1991, Vol 3, Num 4, pp 198-200, issn 0935-9648Article

DECREASED EXPRESSION OF THE MITOCHONDRIAL MATRIX PROTEASES Lon AND CIpP IN CELLS FROM A PATIENT WITH HEREDITARY SPASTIC PARAPLEGIA (SPG13)HANSEN, J; CORYDON, T. J; PALMFELDT, J et al.Neuroscience. 2008, Vol 153, Num 2, pp 474-482, issn 0306-4522, 9 p.Article

The role of chaperone-assisted folding and quality control in inborn errors of metabolism : Protein folding disordersGREGERSEN, N; BROSS, P; ANDRESEN, B. S et al.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 189-212, issn 0141-8955Conference Paper

Defective folding and rapid degradation of mutant proteins is a common disease mechanism in genetic disordersGREGERSEN, N; BROSS, P; JØRGENSEN, M. M et al.Journal of inherited metabolic disease. 2000, Vol 23, Num 5, pp 441-447, issn 0141-8955Article

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiencyANDRESEN, B. S; OLPIN, S; BAUMGARTNER, E. R et al.American journal of human genetics. 1999, Vol 64, Num 2, pp 479-494, issn 0002-9297Article

Empiric antimicrobial therapy of febrile neutropenic patients undergoing haematopoietic stem cell transplantationANTABLI, B. A; BROSS, P; SIEGEL, R. S et al.International journal of antimicrobial agents. 1999, Vol 13, Num 2, pp 127-130, issn 0924-8579Article

Expression of transforming growth factor alpha and epidermal growth factor receptor in human bladder cancerTHØGERSEN, V. B; JØRGENSEN, P. E; SØRENSEN, B. S et al.Scandinavian journal of clinical & laboratory investigation. 1999, Vol 59, Num 4, pp 267-277, issn 0036-5513Article

Quantitative analysis of the human epidermal growth factor receptor messenger RNA using reverse transcription-PCR : A methodological study of imprecisionTHOGERSEN, V. B; BROSS, P; GREGERSEN, N et al.Clinical chemistry (Baltimore, Md.). 1998, Vol 44, Num 6, pp 1344-1346, issn 0009-9147, 1Article

Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiencyANDRESEN, B. S; BROSS, P; JENSEN, T. G et al.Scandinavian journal of clinical & laboratory investigation. Supplement. 1995, Vol 55, Num 220, pp 9-25, issn 0085-591XConference Paper

Disease-causing mutations in exon II of the medium-chain acyl-CoA dehydrogenase geneANDRESEN, B. S; JENSEN, T. G; CURTIS, D et al.American journal of human genetics. 1994, Vol 54, Num 6, pp 975-988, issn 0002-9297Article