Suchergebnisse - "Wheeler, Lawrie"

PubPharm (27)

11

Compound heterozygous mutations in FBN1 in a large family with Marfan syndrome

enthalten in: Molecular Genetics & Genomic Medicine | 2020

von McInerney‐Leo, A. | West, J. | Wheeler, L. | +6

12

A rare SMAD9 mutation identifies the BMP signalling pathway as a potential osteoanabolic target

enthalten in: bioRxiv.org | 2019

von Gregson, C. | Bergen, D. | Leo, P. | +18

13

Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis

enthalten in: PLoS genetics | 2019

von Li, Z. | Akar, S. | Yarkan, H. | +27

14

Imputation-based analysis of MICA alleles in the susceptibility to ankylosing spondylitis

enthalten in: Annals of the rheumatic diseases | 2018

von Cortes, A. | Gladman, D. | Raychaudhuri, S. | +32

CommentIn: Ann Rheum Dis. 2020 Jan;79(1):e1. - PMID 30659049

15

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis

enthalten in: BMC medical genomics | 2018

von De Smit, E. | Lukowski, S. | Anderson, L. | +17

16

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis

enthalten in: BMC medical genomics | 2018

von De Smit, E. | Lukowski, S. | Anderson, L. | +17

17

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent giant cell arteritis

enthalten in: BMC medical genomics | 2018

von De Smit, E. | Lukowski, S. | Anderson, L. | +17

18

Non-classical human leucocyte antigens in ankylosing spondylitis: possible association with HLA-E and HLA-F

enthalten in: RMD open | 2018

von Santos, M. | Couto, A. | Foroni, I. | +12

19

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

enthalten in: Genome medicine | 2017

von Gratten, J. | Zhao, Q. | Benyamin, B. | +35

20

Whole-exome sequencing in amyotrophic lateral sclerosis suggests NEK1 is a risk gene in Chinese

enthalten in: Genome medicine | 2017

von Gratten, J. | Zhao, Q. | Benyamin, B. | +35