Blood Pressure in Genetically Hypertensive Rats: Influence of the Y Chromosome
Davidson, Anne O, Schork, Nicholas, Jaques, Bryon C, Kelman, Andrew W, Sutcliffe, Roger G, Reid, John L
Published in Hypertension (Dallas, Tex. 1979) (01.09.1995)
Published in Hypertension (Dallas, Tex. 1979) (01.09.1995)
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Conference Proceeding
A candidate gene for human neurodegenerative disorders: a rat PKCγ mutation causes a Parkinsonian syndrome
Davies, R. Wayne, Craig, Nicola J, Durán Alonso, María B, Hawker, Kim L, Shiels, Paul, Glencorse, Thora A, Campbell, Jacqueline M, Bennett, Neil K, Canham, Maurice, Donald, Denise, Gardiner, Mary, Gilmore, Desmond P, MacDonald, Raymond J, Maitland, Kirsty, McCallion, Andrew S, Russell, David, Payne, Anthony P, Sutcliffe, Roger G
Published in Nature neuroscience (01.11.2001)
Published in Nature neuroscience (01.11.2001)
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Journal Article
The impact of a landfill fire on ambient air quality in the north: A case study in Iqaluit, Canada
Weichenthal, Scott, Van Rijswijk, David, Kulka, Ryan, You, Hongyu, Van Ryswyk, Keith, Willey, Jeff, Dugandzic, Rose, Sutcliffe, Roger, Moulton, Jamessee, Baike, Maureen, White, Luc, Charland, Jean-Pierre, Jessiman, Barry
Published in Environmental research (01.10.2015)
Published in Environmental research (01.10.2015)
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MUTATIONS FLANKING THE POLYGLUTAMINE REPEAT IN THE MODULATORY DOMAIN OF RAT GLUCOCORTICOID RECEPTOR LEAD TO AN INCREASE IN AFFINITY FOR HORMONE
Heeley, Robert P., Rusconi, Sandro G., Sutcliffe, Roger G., Kenyon, Christopher J.
Published in Endocrine research (01.01.2002)
Published in Endocrine research (01.01.2002)
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Journal Article
Disordered locomotion in the AS/AGU mutant rat and the effects of L-dopa or fetal midbrain grafts
Payne, A P, Sutcliffe, R G, Campbell, J M, Favor, G, Russell, D, Bennett, N K, Clarke, D J, Branton, R, Davies, R W, Simpson, E, Tsang, C, Baxendale, R H
Published in Movement disorders (01.09.1998)
Published in Movement disorders (01.09.1998)
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P4C in Personal, Social and Health Education (PSHE)
Published in Philosophy for Children Through the Secondary Curriculum
(2012)
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Book Chapter
An Ecological Risk Assessment of Nonylphenol and Its Ethoxylates in the Aquatic Environment
Servos, Mark R., Maguire, R. James, Bennie, Donald T., Lee, Hing-Biu, Cureton, Philippa M., Davidson, Nicole, Sutcliffe, Roger, Rawn, Dorothea F.K.
Published in Human and ecological risk assessment (01.03.2003)
Published in Human and ecological risk assessment (01.03.2003)
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Journal Article
Cloning, Expression, and Physical Mapping of the 3β-Hydroxysteroid Dehydrogenase Gene Cluster (HSD3BP1–HSD3BP5) in Human
McBride, Martin W., McVie, Alison J., Burridge, Sandra M., Brintnell, Bill, Craig, Nicola, Wallace, A.Michael, Wilson, Richard H., Varley, Jenny, Sutcliffe, Roger G.
Published in Genomics (San Diego, Calif.) (01.11.1999)
Published in Genomics (San Diego, Calif.) (01.11.1999)
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A candidate gene for human neurodegenerative disorders: a rat PKCg mutation causes a Parkinsonian syndrome
Craig, Nicola J, Duran Alonso, Maria B, Hawker, Kim L, Shiels, Paul, Glencorse, Thora A, Campbell, Jacqueline M, Bennett, Neil K, Canham, Maurice, Donald, Denise, Gardiner, Mary, Gilmore, Desmond P, MacDonald, Raymond J, Maitland, Kirsty, McCallion, Andrew S, Russell, David, Payne, Anthony P, Sutcliffe, Roger G, Davies, RWayne
Published in Nature neuroscience (01.11.2001)
Published in Nature neuroscience (01.11.2001)
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Journal Article
A novel homozygous nonsense mutation E135 in the type II 3[beta]-hydroxysteroid dehydrogenase gene in a girl with salt-losing congenital adrenal hyperplasia
Marui, Suemi, Torrealba, Isabel M, Russell, Alan J, Latronico, Ana C, Sutcliffe, Roger G, Mendonca, Berenice B
Published in Human mutation (01.01.1998)
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Published in Human mutation (01.01.1998)
Journal Article
A Novel Homozygous Nonsense Mutation E135X in the Type II 3β-Hydroxysteroid Dehydrogenase Gene (3β-Hsd) of A Female Child With Salt-Losing Congenital Adrenal Hyperplasia (Cah). 32
Marui, Suemi, Torrealba, Isabel M, Russell, Alan J, Latronico, Ana C, Sutcliffe, Roger G, Mendonça, Berenice B
Published in Pediatric research (01.02.1998)
Published in Pediatric research (01.02.1998)
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