Yazar Araması Sonucu :: UTM Library Massive Scholar Tracking

1

Complement C1q is hydroxylated by collagen prolyl 4 hydroxylase, and is sensitive to off target inhibition by prolyl hydroxylase domain inhibitors that stabilise Hypoxia Inducible... Yazar: Kiriakidis, S, Hoer, S, Burrows, N, Biddlecome, G, Khan, M, Thinnes, C, Schofield, C, Rogers, N, Botto, M, Paleolog, E, Maxwell, P

Baskı/Yayın Bilgisi 2017

Journal article
2

Humanized anti-CD4 monoclonal antibody therapy of autoimmune and inflammatory disease. Yazar: Isaacs, J, Burrows, N, Wing, M, Keogan, M, Rebello, P, Watts, R, Pye, R, Norris, P, Hazelman, B, Hale, G, Waldmann, H

Baskı/Yayın Bilgisi 1997

Journal article
3

The HIF complex recruits the histone methyltransferase SET1B to activate specific hypoxia-inducible genes Yazar: Ortmann, BM, Burrows, N, Lobb, IT, Arnaiz, E, Wit, N, Bailey, PSJ, Jordon, LH, Lombardi, O, Peñalver, A, McCaffrey, J, Seear, R, Mole, DR, Ratcliffe, PJ, Maxwell, PH, Nathan, JA

Baskı/Yayın Bilgisi 2021

Journal article
4

Dynamic regulation of hypoxia-inducible factor-1α activity is essential for normal B cell development Yazar: Burrows, N, Bashford-Rogers, RJM, Bhute, VJ, Peñalver, A, Ferdinand, JR, Stewart, BJ, Smith, JEG, Deobagkar-Lele, M, Giudice, G, Connor, TM, Inaba, A, Bergamaschi, L, Smith, S, Tran, MGB, Petsalaki, E, Lyons, PA, Espeli, M, Huntly, BJP, Smith, KGC, Cornall, RJ, Clatworthy, MR, Maxwell, PH

Baskı/Yayın Bilgisi 2020

Journal article
5

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. Yazar: Alam, N, Rowan, A, Wortham, N, Pollard, P, Mitchell, M, Tyrer, J, Barclay, E, Calonje, E, Manek, S, Adams, S, Bowers, P, Burrows, N, Charles-Holmes, R, Cook, L, Daly, B, Ford, G, Fuller, L, Hadfield-Jones, SE, Hardwick, N, Highet, A, Keefe, M, MacDonald-Hull, S, Potts, E, Crone, M, Wilkinson, S

Baskı/Yayın Bilgisi 2003

Journal article
6

Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency Yazar: Alam, N, Rowan, A, Wortham, N, Pollard, P, Mitchell, M, Tyrer, J, Barclay, E, Calonje, E, Manek, S, Adams, S, Bowers, P, Burrows, N, Charles-Holmes, R, Cook, L, Daly, B, Ford, G, Fuller, L, Hadfield-Jones, SE, Hardwick, N, Highet, A, Keefe, M, MacDonald-Hull, S, Potts, E, Crone, M, Wilkinson, S

Baskı/Yayın Bilgisi 2003

Journal article
7

Early loss of Crebbp confers malignant stem cell properties on lymphoid progenitors Yazar: Horton, S, Giotopoulos, G, Yun, H, Vohra, S, Sheppard, O, Bashford-Rogers, R, Rashid, M, Clipson, A, Chan, W, Sasca, D, Yiangou, L, Osaki, H, Basheer, F, Gallipoli, P, Burrows, N, Erdem, A, Sybirna, A, Foerster, S, Zhao, W, Sustic, T, Petrunkina Harrison, A, Laurenti, E, Okosun, J, Hodson, D, Wright, P, Smith, K, Maxwell, P, Fitzgibbon, J, Du, M, Adams, D, Huntly, B

Baskı/Yayın Bilgisi 2017

Journal article