Suchergebnisse - "Wheeler, Lawrie"

PubPharm (24)

1

Interleukin-1 is overexpressed in injured muscles following spinal cord injury and promotes neurogenic heterotopic ossification

enthalten in: bioRxiv.org | 2022

von Tseng, H. | Kulina, I. | Girard, D. | +14

2

Interleukin-1 Is Overexpressed in Injured Muscles Following Spinal Cord Injury and Promotes Neurogenic Heterotopic Ossification

enthalten in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2022

von Tseng, H. | Kulina, I. | Girard, D. | +14

3

Germline ERBB3 mutation in familial non-small cell lung carcinoma: expanding ErbB’s role in oncogenesis

enthalten in: bioRxiv.org | 2021

von McInerney-Leo, A. | Chew, H. | Inglis, P. | +17

4

Germline ERBB3 mutation in familial non-small-cell lung carcinoma : expanding ErbB's role in oncogenesis

enthalten in: Human molecular genetics | 2021

von McInerney-Leo, A. | Chew, H. | Inglis, P. | +17

5

Polygenic Risk Scores have high diagnostic capacity in ankylosing spondylitis

enthalten in: Annals of the rheumatic diseases | 2021

von Li, Z. | Wu, X. | Leo, P. | +100

ErratumIn: Ann Rheum Dis. 2021 Nov;80(11):e187. - PMID 34642186

6

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

7

Longitudinal expression profiling of CD4+ and CD8+ cells in patients with active to quiescent Giant Cell Arteritis

enthalten in: bioRxiv.org | 2020

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

8

A Rare Mutation in SMAD9 Associated With High Bone Mass Identifies the SMAD-Dependent BMP Signaling Pathway as a Potential Anabolic Target for Osteoporosis

enthalten in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 2020

von Gregson, C. | Bergen, D. | Leo, P. | +19

9

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

10

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