Publications by authors named "Martin Barratt"

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Incompletely penetrant PKD1 alleles suggest a role for gene dosage in cyst initiation in polycystic kidney disease.
Sandro Rossetti, Vickie J Kubly, Mark B Consugar, Katharina Hopp, Sushmita Roy, T Martin Barratt

Kidney Int· April 2009

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Familial membranous nephropathy: an X-linked genetic susceptibility?
Detlef Bockenhauer, Hanna Debiec, Neil Sebire, Martin Barratt, Paul Warwicker

Nephron Clin Pract· April 2008

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An overall strategy for the testing of chemicals for human hazard and risk assessment under the EU REACH system.
Robert Combes, Martin Barratt, Michael Balls

Altern Lab Anim· March 2006

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An overall strategy for the testing of chemicals for human hazard and risk assessment under the EU REACH system.
Robert Combes, Martin Barratt, Michael Balls

Altern Lab Anim· October 2005

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Blood pressure in the long-term follow-up of children with haemolytic uremic syndrome.
T Martin Barratt, Margaret M Fitzpatrick

Pediatr Nephrol· May 2005

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Development and prevalidation of a list of structure-activity relationship rules to be used in expert systems for prediction of the skin-sensitising properties of chemicals.
Ingrid Gerner, Martin D Barratt, Stephan Zinke, Kerstin Schlegel, Eva Schlede

Altern Lab Anim· November 2004

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Structure-activity relationships and prediction of the phototoxicity and phototoxic potential of new drugs.
Martin D Barratt

Altern Lab Anim· November 2004

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The Third FRAME Toxicity Committee: working toward greater implementation of alternatives in toxicity testing.
Robert D Combes, Michael Balls, Lee Bansil, Martin Barratt, David Bell

Altern Lab Anim· June 2004

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QSAR, Read-across and REACH.
Martin D Barratt

Altern Lab Anim· November 2003

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An assessment of progress in the use of alternatives in toxicity testing since the publication of the report of the second FRAME Toxicity Committee (1991).
Robert Combes, Michael Balls, Lee Bansil, Martin Barratt, David Bell

Altern Lab Anim· November 2002

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The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease.
Sandro Rossetti, Sarah Burton, Lana Strmecki, Gregory R Pond, Jośe L San Millán, T Martin Barratt

J Am Soc Nephrol· May 2002

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