Suchergebnisse - "O'Kelly, Ita"

PubPharm (43)

1

A 5’ UTR G-quadruplex controls localisation and translation of a potassium leak channel mRNA

enthalten in: bioRxiv.org | 2023

von Maltby, C. | Schofield, J. | Houghton, S. | +4

2

Defining cardiac cell populations and relative cellular composition of the early fetal human heart

enthalten in: PloS one | 2022

von Dewing, J. | Saunders, V. | O'Kelly, I. | +1

3

Defining Cardiac Cell Populations and Relative Cellular Composition of the Early Fetal Human Heart

enthalten in: bioRxiv.org | 2021

von Dewing, J. | Saunders, V. | O’Kelly, I. | +1

4

N-acetylcysteine, xCT and suppression of Maxi-chloride channel activity in human placenta

enthalten in: Placenta | 2021

von Lofthouse, E. | Manousopoulou, A. | Cleal, J. | +4

5

Tebentafusp, A TCR/Anti-CD3 Bispecific Fusion Protein Targeting gp100, Potently Activated Antitumor Immune Responses in Patients with Metastatic Melanoma

enthalten in: Clinical cancer research : an official journal of the American Association for Cancer Research | 2020

von Middleton, M. | McAlpine, C. | Woodcock, V. | +16

6

A 5' UTR GGN repeat controls localisation and translation of a potassium leak channel mRNA through G-quadruplex formation

enthalten in: Nucleic acids research | 2020

von Maltby, C. | Schofield, J. | Houghton, S. | +4

7

Ursodeoxycholic acid inhibits uptake and vasoconstrictor effects of taurocholate in human placenta

enthalten in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 2019

von Lofthouse, E. | Torrens, C. | Manousopoulou, A. | +6

8

Novel TCR-based biologics : mobilising T cells to warm 'cold' tumours

enthalten in: Cancer treatment reviews | 2019

von Lowe, K. | Cole, D. | Kenefeck, R. | +3

9

Estrone sulphate uptake by the microvillous membrane of placental syncytiotrophoblast is coupled to glutamate efflux

enthalten in: Biochemical and biophysical research communications | 2018

von Lofthouse, E. | Cleal, J. | O'Kelly, I. | +2

10

AMMECR1 : a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis

enthalten in: Journal of medical genetics | 2017

von Andreoletti, G. | Seaby, E. | Dewing, J. | +4

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