Suchergebnisse - "Howarth, Rachel"

PubPharm (33)

21

The NF-κB1 is a key regulator of acute but not chronic renal injury

enthalten in: Cell death & disease | 2017

von Fearn, A. | Situmorang, G. | Fox, C. | +8

22

Lysosomal protease cathepsin D; a new driver of apoptosis during acute kidney injury

enthalten in: Scientific reports | 2016

von Cocchiaro, P. | Fox, C. | Tregidgo, N. | +6

23

Inhibition of lysosomal protease cathepsin D reduces renal fibrosis in murine chronic kidney disease

enthalten in: Scientific reports | 2016

von Fox, C. | Cocchiaro, P. | Oakley, F. | +8

24

Alcohol directly stimulates epigenetic modifications in hepatic stellate cells

enthalten in: Journal of hepatology | 2015

von Page, A. | Paoli, P. | Hill, S. | +8

25

Alcohol directly stimulates epigenetic modifications in hepatic stellate cells

enthalten in: Journal of hepatology | 2015

von Page, A. | Paoli, P. | Hill, S. | +8

26

A TLR2/S100A9/CXCL-2 signaling network is necessary for neutrophil recruitment in acute and chronic liver injury in the mouse

enthalten in: Journal of hepatology | 2014

von Moles, A. | Murphy, L. | Wilson, C. | +11

27

A TLR2/S100A9/CXCL-2 signaling network is necessary for neutrophil recruitment in acute and chronic liver injury in the mouse

enthalten in: Journal of hepatology | 2014

von Moles, A. | Murphy, L. | Wilson, C. | +11

28

Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia

enthalten in: American journal of medical genetics. Part A | 2008

von Robinson, D. | Howarth, R. | Williamson, K. | +3

29

Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridiaFNR HREF="fn1">FN ID="fn1">How to cite this article: Robinson DO, Howarth RJ, Williamson KA, van Heyningen V, Beal SJ, Crolla JA. 2008. Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia. Am J Med Genet Part A 146A:558-569.

enthalten in: American journal of medical genetics / C | 2008

von Robinson, D. | Howarth, R. | Williamson, K. | +3

30

Application of dHPLC for mutation detection of the fibrillin-1 gene for the diagnosis of Marfan syndrome in a National Health Service Laboratory

enthalten in: Genetic testing | 2007

von Howarth, R. | Yearwood, C. | Harvey, J.