STOCHASTIC THEORY OF COMPARTMENTS: AN OPEN, TWO COMPARTMENT, REVERSIBLE SYSTEM WITH INDEPENDENT POISSON ARRIVALS.PURDUE P.1975; BULL. MATH. BIOL.; G.B.; DA. 1975; VOL. 37; NO 3; PP. 269-275; BIBL. 4 REF.Article

AN URN MODEL FOR SOME EVOLUTIONARY PROCESSES.PURDUE P.1976; MATH. BIOSCI.; U.S.A.; DA. 1976; VOL. 32; NO 1-2; PP. 125-130; BIBL. 7 REF.Article

THE M/M/1 QUEUE IN A MARKOVIAN ENVIRONMENT.PURDUE P.1974; OPER. RES.; U.S.A.; DA. 1974; VOL. 22; NO 3; PP. 562-569; BIBL. 11 REF.Article

AN INVENTORY SYSTEM WITH BOTH DELAYED AND IMMEDIATE DELIVERYHOVEY PW; PURDUE P.1983; ADVANCES IN APPLIED PROBABILITY; ISSN 0001-8678; GBR; DA. 1983; VOL. 15; NO 3; PP. 691-694; BIBL. 4 REF.Article

THE STOCHASTIC THEORY OF COMPARTMENTS: A MAMMILARY SYSTEM.WEINER DL; PURDUE P.1977; BULL. MATH. BIOL.; G.B.; DA. 1977; VOL. 39; NO 5; PP. 533-542; BIBL. 5 REF.Article

A SEMI-MARKOV APPROACH TO STOCHASTIC COMPARTMENTAL MODELS.WEINER D; PURDUE P.1977; COMMUNIC. STATIST., THEORY METHODS; U.S.A.; DA. 1977; VOL. 6; NO 12; PP. 1231-1243; BIBL. 1 P. 1/2Article

AN INFINITE-SERVER QUEUE SUBJECT TO AN EXTRANEOUS PHASE PROCESS AND RELATED MODELSPURDUE P; LINTON D.1981; J. APPL. PROBAB.; ISSN 0021-9002; GBR; DA. 1981; VOL. 18; NO 1; PP. 236-244; BIBL. 11 REF.Article

Compartmental models with transfer delays: a semi-Markov approachLEITNAKER, M. G; PURDUE, P.Journal of applied probability. 1985, Vol 22, Num 3, pp 570-582, issn 0021-9002Article

Metabolic models for methyl and inorganic mercuryBERNARD, S. R; PURDUE, P.Health physics (1958). 1984, Vol 46, Num 3, pp 695-699, issn 0017-9078Article

Non-linear compartmental systems: extensions of S.R. Bernard's urn modelLEITNAKER, M. G; PURDUE, P.Bulletin of mathematical biology. 1985, Vol 47, Num 2, pp 193-204, issn 0092-8240Article

Identification of mutations associated with peroxisome-to-mitochondrion mistargeting of alanine/glyoxylate aminotransferase in primary hyperoxaluria type 1PURDUE, P. E; TAKADA, Y; DANPURE, C. J et al.The Journal of cell biology. 1990, Vol 111, Num 6, pp 2341-2351, issn 0021-9525, 11 p., p.1Article

A stochastic model of particle shatteringGRIFFITH, W. S; KRYSCIO, R. J; PURDUE, P et al.Advances in applied probability. 1984, Vol 16, Num 1, pp 70-87, issn 0001-8678Article

Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting : analysis of the marmoset and rabbit genesPURDUE, P. E; LUMB, M. J; DANPURE, C. J et al.European journal of biochemistry (Print). 1992, Vol 207, Num 2, pp 757-766, issn 0014-2956Article

Molecular evolution of alanine/glyoxylate aminotransferase 1 intracellular targeting : analysis of the feline geneLUMB, M. J; PURDUE, P. E; DANPURE, C. J et al.European journal of biochemistry (Print). 1994, Vol 221, Num 1, pp 53-62, issn 0014-2956Article

A glycine-to-glutamate substitution abolishes alanine : glyoxylate aminotransferase catalytic activity in a subset of patients with primary hyperoxaluria type 1PURDUE, P. E; LUMB, M. J; ALLSOP, J et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 1, pp 215-218, issn 0888-7543Article

Rhizomelic chondrodysplasia punctata, a peroxisomal biogenesis disorder caused by defects in Pex7p, a peroxisomal protein import receptor : A minireviewPURDUE, P. E; SKONECZNY, M; XUDONG YANG et al.Neurochemical research. 1999, Vol 24, Num 4, pp 581-586, issn 0364-3190Article

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptorPURDUE, P. E; JING WEI ZHANG; SKONECZNY, M et al.Nature genetics. 1997, Vol 15, Num 4, pp 381-384, issn 1061-4036Article

An intronic duplication in the alanine : glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1EDWARD PURDUE, P; LUMB, M. J; ALLSOP, J et al.Human genetics. 1991, Vol 87, Num 4, pp 394-396, issn 0340-6717Article

The cellular and molecular biology of periprosthetic osteolysisPURDUE, P. Edward; KOULOUVARIS, Panagiotis; POTTER, Hollis G et al.Clinical orthopaedics and related research. 2007, Num 454, pp 251-261, issn 0009-921X, 11 p.Article

Nucleotide sequence of a cDNA encoding the beta subunit of the mitochondrial ATP synthase from Zea maysWINNING, B. M; BATHGATE, B; PURDUE, P. E et al.Nucleic acids research. 1990, Vol 18, Num 19, issn 0305-1048, p. 5885Article

Mistargeting of peroxisomal L-alanine : glycoxylate aminotransferase to mitochondria in primary hyperoxaluria patients depends upon activation of a cryptic mitochondrial targeting sequence by a point mutationPURDUE, P. E; ALLSOP, J; ISAYA, G et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 23, pp 10900-10904, issn 0027-8424Article

Human peroxisomal L-alanine : glyoxylate aminotransferase : evolutionary loss of a mitochondrial targeting signal by point mutation of the initiation codonTAKADA, Y; KANEKO, N; ESUMI, H et al.Biochemical journal (London. 1906). 1990, Vol 268, Num 2, pp 517-520, issn 0006-2936, 4 p.Article

Characterization and chromosomal mapping of a genomic clone encoding human alanine : glyoxylate aminotransferasePURDUE, P. E; LUMB, M. J; FOX, M et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 1, pp 34-42, issn 0888-7543, 9 p.Article

A serine-to-phenylalanine substitution leads to loss of alanine:glyoxylate aminotransferase catalytic activity and immunoreactivity in a patient with primary hyperoxaluria type 1MINATOGAWA, Y; TONE, S; ALLSOP, J et al.Human molecular genetics (Print). 1992, Vol 1, Num 8, pp 643-644, issn 0964-6906Article

Subcellular distribution of hepatic alanine:glyoxylate aminotransferase in various mammalian speciesDANPURE, C. J; GUTTRIDGE, K. M; FRYER, P et al.Journal of Cell Science. 1990, Vol 97, pp 669-678, issn 0021-9533, 10 p., p.4Article