Autosomal dominant polycystic kidney disease : clues to pathogenesisHARRIS, P. C.Human molecular genetics (Print). 1999, Vol 8, Num 10, pp 1861-1866, issn 0964-6906Article

Dynamic fluid-loss characteristics of nitrogen foam fracturing fluidsHARRIS, P. C.Journal of petroleum technology. 1985, Vol 37, Num 11, pp 1847-1852, issn 0022-3522Article

Effects of texture on rheology of foam fracturing fluidsHARRIS, P. C.Annual SPE technical conference. 60. 1985, 12 p.Conference Paper

Idenfitication of a gene for autosomal dominant polycystic kidney disease : implications for understanding the pathogenesis and treatment of the diseaseHARRIS, P. C.Nephrology, dialysis, transplantation (Print). 1996, Vol 11, Num 2, pp 258-262, issn 0931-0509Article

Effects of texture on rheology of foam fracturing fluidsHARRIS, P. C.SPE production engineering. 1989, Vol 4, Num 3, pp 249-257, issn 0885-9221Conference Paper

Fracturing-fluid additivesHARRIS, P. C.Journal of petroleum technology. 1988, Vol 40, Num 10, pp 1277-1279, issn 0149-2136Article

Rhys-Davies exsanguinator : Pressure characteristics and technique for improving performanceHARRIS, P. C; ATKINSON, D; EVANS, R. A et al.Journal of hand surgery. British and european volume. 2000, Vol 25, Num 6, pp 578-581Article

Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissueONG, A. C. M; WARD, C. J; BUTLER, R. J et al.The American journal of pathology. 1999, Vol 154, Num 6, pp 1721-1729, issn 0002-9440Article

Haplotype analysis in autosomal dominant polycystic kidney diseasePOUND, S. E; THOMAS, S; SNAREY, A et al.Journal of medical genetics. 1995, Vol 32, Num 3, pp 208-212, issn 0022-2593Article

Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variabilityARMOUR, J. A. L; HARRIS, P. C; JEFFREYS, A. J et al.Human molecular genetics (Print). 1993, Vol 2, Num 8, pp 1137-1145, issn 0964-6906Article

A refined physical map of the long arm of human chromosome 16CHEN, L. Z; HARRIS, P. C; RICHARDS, R. I et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 2, pp 308-312, issn 0888-7543, 5 p.Article

Molecular and hematologic characterization of Scottish-Irish type (εγδβ)^° thalassemiaTRENT, R. J; WILLIAMS, B. G; KEARNEY, A et al.Blood. 1990, Vol 76, Num 10, pp 2132-2138, issn 0006-4971Article

Edema of cardiac origin: studies of body water and sodium, renal function, hemodynamic indexes, and plasma hormones in untreated congestive cardiac failureANAND, I. S; FERRARI, R; KALRA, G. S et al.Circulation (New York, N.Y.). 1989, Vol 80, Num 2, pp 299-305, issn 0009-7322Article

Stimulation results in the low-permeability Wasatch formation: an evolution to foam fracturingHARRIS, P. C; BAILEY, D. E; EVERTZ, G et al.Journal of petroleum technology. 1984, Vol 36, Num 10, pp 1545-1551, issn 0022-3522Article

A mouse model of autosomal recessive polycystic kidney disease with biliary duct and proximal tubule dilatationWOOLLARD, J. R; PUNYASHTITI, R; LARUSSO, N. F et al.Kidney international. 2007, Vol 72, Num 3, pp 328-336, issn 0085-2538, 9 p.Article

Caroli's disease: prenatal diagnosis, postnatal outcome and genetic analysisSGRO, M; ROSSETTI, S; BAROZZINO, T et al.Ultrasound in obstetrics & gynecology. 2004, Vol 23, Num 1, pp 73-76, issn 0960-7692, 4 p.Article

Genome duplications and other features in 12 Mb of DNA sequence from human chromosome 16p and 16qLOFTUS, B. J; KIM, U.-J; MAYS, A. D et al.Genomics (San Diego, Calif.). 1999, Vol 60, Num 3, pp 295-308, issn 0888-7543Article

Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease: a contiguous gene syndromeBROOK-CARTER, P. T; PERAL, B; WARD, C. J et al.Nature genetics. 1994, Vol 8, Num 4, pp 328-332, issn 1061-4036Article

Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomereVICKERS, M. A; PARESH VYAS; HARRIS, P. C et al.Proceedings of the National Academy of Sciences of the United States of America. 1993, Vol 90, Num 8, pp 3437-3441, issn 0027-8424Article

Clinical features and molecular analysis of the α thalassemia/mental retardation syndromes. I, Cases due to deletions involving chromosome band 16p13.3WILKIE, A. O. M; BUCKLE, V. J; TOLMIE, J. L et al.American journal of human genetics. 1990, Vol 46, Num 6, pp 1112-1116, issn 0002-9297, 5 p.Article

Enalapril as initial and sole treatment in severe chronic heart failure with sodium retentionANAND, I. S; KALRA, G. S; FERRARI, R et al.International journal of cardiology. 1990, Vol 28, Num 3, pp 341-346, issn 0167-5273, 6 p.Article

Hight-temperature rheological study of foam fracturing fluidsHARRIS, P. C; REIDENBACH, V. G.Journal of petroleum technology. 1987, Vol 39, Num 5, pp 613-619, issn 0149-2136Article

Influence of temperature and shear history on fracturing fluid efficiencyHARRIS, P. C; PENNY, G. S.Annual SPE technical conference. 60. 1985, 9 p.Conference Paper

The use of CO₂-based fracturing fluids in the Red Fork formation in the Anadarko Basin, OklahomaHARRIS, P. C; HAYNES, R. J; EGGER, J. P et al.Journal of petroleum technology. 1984, Vol 36, Num 7, pp 1003-1008, issn 0022-3522Article

Identification of a human homologue of the sea urchin receptor for egg jelly : a polycystic kidney disease-like proteinHUGHES, J; WARD, C. J; ASPINWALL, R et al.Human molecular genetics (Print). 1999, Vol 8, Num 3, pp 543-549, issn 0964-6906Article