Publications

Export 76 results:
Sort by: Author [ Title (Asc)] Type Year
Filters: First Letter Of Title is G  [Clear All Filters]
A B C D E F [G] H I J K L M N O P Q R S T U V W X Y Z   [Show ALL]
G
Henderson NC, Mackinnon AC, Farnworth SL, Kipari T, Haslett C, Iredale JP, et al. Galectin-3 expression and secretion links macrophages to the promotion of renal fibrosis. Am J Pathol. 2008;172(2):288-98. Abstract
Farnworth SL, Henderson NC, Mackinnon AC, Atkinson KM, Wilkinson T, Dhaliwal K, et al. Galectin-3 reduces the severity of pneumococcal pneumonia by augmenting neutrophil function. Am J Pathol. 2008;172(2):395-405. Abstract
Henderson NC, Mackinnon AC, Farnworth SL, Poirier F, Russo FP, Iredale JP, et al. Galectin-3 regulates myofibroblast activation and hepatic fibrosis. Proc Natl Acad Sci USA. 2006;103(13):5060-5. Abstract
Labastie MC, Catala M, Gregoire JM, Peault B. The GATA-3 gene is expressed during human kidney embryogenesis. Kidney Int. 1995;47(6):1597-603. Abstract
Miranda-Carboni GA, Guemes M, Bailey S, Anaya E, Corselli M, Peault B, et al. GATA4 regulates estrogen receptor-alpha-mediated osteoblast transcription. Mol Endocrinol. 2011;25(7):1126-36. Abstract
Henriksen PA, Devitt A, Kotelevtsev Y, Sallenave J-. Gene delivery of the elastase inhibitor elafin protects macrophages from neutrophil elastase-mediated impairment of apoptotic cell recognition. FEBS Lett. 2004;574(1-3):80-4. Abstract
Clark AF, Sharp MG, Mullins JJ. Gene targeting and its application to basic hypertension research. Clinical science (London, England : 1979). 1996;90:435-46.
Péault B, Charbord P. Gene transfer into human haematopoietic stem cells. Transfus Sci. 1997;18(2):291-311. Abstract
Péault B, Tirouvanziam R, Sombardier MN, Chen S, Perricaudet M, Gaillard D. Gene transfer to human fetal pulmonary tissue developed in immunodeficient SCID mice. Hum Gene Ther. 1994;5(9):1131-7. Abstract
Tirouvanziam R, Péault B. Gene transfer to human respiratory airways developed in SCID mice. Biologicals. 1995;23(1):17-9.
McClive P, Pall G, Newton K, Lee M, Mullins J, Forrester L. Gene trap integrations expressed in the developing heart: insertion site affects splicing of the PT1-ATG vector. Dev Dyn. 1998;212(2):267-76. Abstract
O'Dushlaine C, McQuillan R, Weale ME, Crouch DJ, Johansson A, Aulchenko Y, et al. Genes predict village of origin in rural Europe. Eur J Hum Genet. 2010;18(11):1269-70. Abstract
Ganten D, Takahashi S, Lindpaintner K, Mullins J. Genetic basis of hypertension. The renin-angiotensin paradigm. Hypertension. 1991;18:III109-14.
Ganten D, Takahashi S, Lindpaintner K, Mullins J. Genetic basis of hypertension. The renin-angiotensin paradigm. Hypertension. 1991;18(5 Suppl):III109-14.
Mitchell KD, Bagatell SJ, Miller CS, Mouton CR, Seth DM, Mullins JJ. Genetic clamping of renin gene expression induces hypertension and elevation of intrarenal Ang II levels of graded severity in Cyp1a1-Ren2 transgenic rats. J Renin Angiotensin Aldosterone Syst. 2006;7(2):74-86. Abstract
Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, et al. Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 2009;5(10):e1000672. Abstract
Hicks AA, Pramstaller PP, Johansson A, Vitart V, Rudan I, Ugocsai P, et al. Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 2009;5(10):e1000672. Abstract
Paterson JM, Seckl JR, Mullins JJ. Genetic manipulation of 11beta-hydroxysteroid dehydrogenases in mice. American journal of physiology. Regulatory, integrative and comparative physiology. 2005;289:R642-52. Abstract
Kantachuvesiri S, Haley CS, Fleming S, Kurian K, Whitworth CE, Wenham P, et al. Genetic mapping of modifier loci affecting malignant hypertension in TGRmRen2 rats. Kidney international. 1999;56:414-20. Abstract
Whitworth CE, Fleming S, Kotelevtsev Y, Manson L, Brooker GA, Cumming AD, et al. A genetic model of malignant phase hypertension in rats. Kidney international. 1995;47:529-35. Abstract
Gambineri A, Vicennati V, Genghini S, Tomassoni F, Pagotto U, Pasquali R, et al. Genetic variation in 11beta-hydroxysteroid dehydrogenase type 1 predicts adrenal hyperandrogenism among lean women with polycystic ovary syndrome. The Journal of clinical endocrinology and metabolism. 2006;91:2295-302. Abstract
Saxena R, Hivert M-, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat Genet. 2010;42(2):142-8. Abstract
Velders FP, Kuningas M, Kumari M, Dekker MJ, Uitterlinden AG, Kirschbaum C, et al. Genetics of cortisol secretion and depressive symptoms: A candidate gene and genome wide association approach. Psychoneuroendocrinology. 2011. Abstract
Nasir J, Cohen W, Cowie H, Maclean A, Watson J, Seckl J, et al. Genetics of specific language impairment. Prostaglandins, leukotrienes, and essential fatty acids. 2000;63:101-7.
Repapi E, Sayers I, Wain LV, Burton PR, Johnson T, Obeidat M', et al. Genome-wide association study identifies five loci associated with lung function. Nat Genet. 2010;42(1):36-44. Abstract