Pemberton S - Search Results

1

Mannose receptor interacts with Fc receptors and is critical for the development of crescentic glomerulonephritis in mice.

Chavele KM, Martinez-Pomares L, Domin J, Pemberton S, Haslam SM, Dell A, Cook HT, Pusey CD, Gordon S, Salama AD. Chavele KM, et al. Among authors: pemberton s. J Clin Invest. 2010 May;120(5):1469-78. doi: 10.1172/JCI41560. Epub 2010 Apr 19. J Clin Invest. 2010. PMID: 20407205 Free PMC article.

2

Identification of novel contributions to high-affinity glycoprotein-receptor interactions using engineered ligands.

Coombs PJ, Harrison R, Pemberton S, Quintero-Martinez A, Parry S, Haslam SM, Dell A, Taylor ME, Drickamer K. Coombs PJ, et al. Among authors: pemberton s. J Mol Biol. 2010 Feb 26;396(3):685-96. doi: 10.1016/j.jmb.2009.11.073. Epub 2009 Dec 7. J Mol Biol. 2010. PMID: 20004209 Free PMC article.

3

Anti-neutrophil cytoplasmic antibodies (ANCA) from patients with systemic vasculitis recognize restricted epitopes of proteinase 3 involving the catalytic site.

Griffith ME, Coulthart A, Pemberton S, George AJ, Pusey CD. Griffith ME, et al. Among authors: pemberton s. Clin Exp Immunol. 2001 Jan;123(1):170-7. doi: 10.1046/j.1365-2249.2001.01420.x. Clin Exp Immunol. 2001. PMID: 11168015 Free PMC article.

4

A molecular model of the serine protease domain of activated protein C: application to the study of missense mutations causing protein C deficiency.

Wacey AI, Pemberton S, Cooper DN, Kakkar VV, Tuddenham EG. Wacey AI, et al. Among authors: pemberton s. Br J Haematol. 1993 Jun;84(2):290-300. doi: 10.1111/j.1365-2141.1993.tb03067.x. Br J Haematol. 1993. PMID: 8398833

5

A molecular model for the triplicated A domains of human factor VIII based on the crystal structure of human ceruloplasmin.

Pemberton S, Lindley P, Zaitsev V, Card G, Tuddenham EG, Kemball-Cook G. Pemberton S, et al. Blood. 1997 Apr 1;89(7):2413-21. Blood. 1997. PMID: 9116285 Free article.

6

Inherited factor VII deficiency: genetics and molecular pathology.

Tuddenham EG, Pemberton S, Cooper DN. Tuddenham EG, et al. Among authors: pemberton s. Thromb Haemost. 1995 Jul;74(1):313-21. Thromb Haemost. 1995. PMID: 8578478 Review. No abstract available.

7

Inherited factor X deficiency: molecular genetics and pathophysiology.

Cooper DN, Millar DS, Wacey A, Pemberton S, Tuddenham EG. Cooper DN, et al. Among authors: pemberton s. Thromb Haemost. 1997 Jul;78(1):161-72. Thromb Haemost. 1997. PMID: 9198147 Review. No abstract available.

8

Increase of activated factor VIIA and haemostatic molecular markers in juvenile chronic arthritis.

Inamo Y, Pemberton S, Tuddenham EG, Woo P. Inamo Y, et al. Among authors: pemberton s. Br J Rheumatol. 1995 May;34(5):466-9. doi: 10.1093/rheumatology/34.5.466. Br J Rheumatol. 1995. PMID: 7788178

9

Factor VIII gene analysis in Japanese CRM-positive and CRM-reduced haemophilia A patients by single-strand conformation polymorphism.

Morichika S, Shima M, Kamisue S, Tanaka I, Imanaka Y, Suzuki H, Shibata H, Pemberton S, Gale K, McVey J, Tuddenham EG, Yoshioka A. Morichika S, et al. Among authors: pemberton s. Br J Haematol. 1997 Sep;98(4):901-6. doi: 10.1046/j.1365-2141.1997.2963113.x. Br J Haematol. 1997. PMID: 9326186 Free article.

10

Factor VIII S373L: mutation at P1' site confers thrombin cleavage resistance, causing mild haemophilia A.

Johnson DJ, Pemberton S, Acquila M, Mori PG, Tuddenham EG, O'Brien DP. Johnson DJ, et al. Among authors: pemberton s. Thromb Haemost. 1994 Apr;71(4):428-33. Thromb Haemost. 1994. PMID: 8052958

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