Published Papers 1997 - 98

These publications were organised chronologically by O. M. Wrong. The catalogue reflects this organisation and here details the contents of each annual file. NOTE the physical file contains more than one set of published papers:

Journal article: 'The association between familial distal renal tubular acidosis and mutations in the red cell anion exchanger (band 3, AE1) gene', with Lesley J. Bruce, Robert J. Unwin, and Michael J. A. Tanner, Biochem. Cellular Biology (1998).

Journal article: 'Amelogenesis imperfecta, nephrocalcinosis, and hypocalciuria syndrome in two siblings from a large family with sonsanguineous parents', with Emma L. Dellow, Kathryn E. Harley, Robert J. Unwin, Gerald B. Winter and Brian J. Parkins, Nephrology Dialysis Transplantation (1998).

Abstract: 'Mutuations of the Renal Chloride Channel Gene (CLCN5) in Dent's Disease', with J. P. D. Cox, K. Yamamoto, C. Wooding, P. T. Christie, T. Feest, F. Flinter, P. Goodyer, E. Leumann, C. Reid, P. Williams, and R. V. Thakker, Journal of Endocrinology (1998).

Abstract: 'Mutational Analysis of the Calcium Sensing Receptor Gene in Familial Hypomagnesemic Hypercalciuria', with A. J. Curley, P. T. Christie, and R. V. Thakker, Journal of Endocrinology (1998).

Abstract: 'Quantitative Definition of Tubular Proteinuria Based on Studies of Patients with Mutations of the CLCN5 Chloride Channel Gene (Dents Disease and X-Linked Recessive Nephrolithiasis', with A. C. W. Norden, J. Asplin, M. M. Deschodt-Lanckman, M. Lapsley, J. L. Nortier, S. J. Scheinman, R. V. Thakker, and R. J. Unwin, Journal of the American Society of Nephrology (1998).

Abstract: 'Mutational Analysis of the Thiazide Sensitive Sodium Chloride Co-Transporter (NCCT) in Familial Hypomagnesemic Hypercalciuia', with K. Yamamoto, J. P. D. Cox, and R. V. Thakker, Pediatric Nephrology (1998).

Abstract: 'Renal Chloride Channel (CLCN5) Mutations in Dent's Disease', with K. Yamamoto, J. P. D. Cox, C. Wooding, P. T. Christie, T. Feest, F. Flinter, P. Goodyer, E. Leumann, C. Reid, P. Williams, and R. V. Thakker, Pediatric Nephrology (1998).

Journal article: 'Mutations in the chloride-bicarbonate exchanger gene AE1 cause autosomal dominant but not autosomal recessive distal renal tubular acidosis', with F. E. Karet, F. J. Gainza, A. Z. Gyory, R. J. Unwin, M. J. A. Tanner, A. Nayir, H. Alpay, F. Santos, S. A. Hulton, A. Bakkaloglu, Z. Ozen, M. J. Cunningham, A. Di Pietro, W. G. Walker, and R. P. Lifton, Proceedings of the National Academy of Sciences (May 1998).

Textbook entry: 'Nephrocalcinosis', Oxford Textbook of Clinical Nephrology (1998).

Unlabelled paper: 'Familial Distal renal Tubular Acidosis is Associated with Mutations in the Red Cell Anion Exchanger (Band 3, AE1) Gene', with Lesley J. Bruce, Diane L. Cope, Graham K. Jones, Ann E. Schofield, Mariwyn Burley, Susan Povey, Robert J. Unwin, and Michael J. A. Tanner (1997).

Abstract: 'Dominantly inherited distal renal tubular acidosis (dRTA) is associated with mutations in the red cell anion exchanger (BAND 3, AE1) gene', with Lesley Bruce, Diane Cope, Graham Jones, Ann Schofield, Mari-Wyn Burley, Susan Povey, Robert Unwin and Michael Tanner, Journal of the American Society of Nephrologists (September 1997).

Journal article: 'Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders', with Sarah E. Lloyd, Willy Gunther, Simon H. S. Pearce, Amelia Thomson, Maria L. Bianchi, Maurizio Bosio, Ian W. Craig, Simon E. Fisher, Steven J. Scheinman, Thomas J. Jentsch, and Rajesh V. Thakker, Human Molecular Genetics (1997).

Letter to the Editor: 'Live E. coli cells to treat uremia', Nature Medicine (January 1997).

January 1997 - 1998

1 File