Suchergebnisse - "Myers, Richard"

PubPharm (26)

1

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

enthalten in: Acta neuropathologica | 2019

von Geier, E. | Bourdenx, M. | Storm, N. | +22

2

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

enthalten in: Acta neuropathologica | 2018

von Geier, E. | Bourdenx, M. | Storm, N. | +22

3

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

enthalten in: Acta neuropathologica | 2018

von Geier, E. | Bourdenx, M. | Storm, N. | +22

4

Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia

enthalten in: Acta neuropathologica | 2018

von Geier, E. | Bourdenx, M. | Storm, N. | +22

5

Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus

enthalten in: Arthritis research & therapy | 2017

von Aterido, A. | Julià, A. | Carreira, P. | +22

6

Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus

enthalten in: Arthritis Research & Therapy | 2017

von Aterido, A. | Julià, A. | Carreira, P. | +22

7

Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus

enthalten in: Arthritis Research & Therapy | 2017

von Aterido, A. | Julià, A. | Carreira, P. | +22

8

IκB kinase ε (IKKε) regulates the balance between type I and type II interferon responses

Erschienen: 2011

von Ng, S. | Friedman, B. | Schmid, S. | +4

9

Retraction: Genetic Signatures of Exceptional Longevity in Humans

Erschienen: 2011

von SEBASTIANI, P. | SOLOVIEFF, N. | PUCA, A. | +10

10

Genomewide association study for onset age in Parkinson disease

in: BMC Medical Genetics | 2009

von Halter Cheryl | DeStefano Anita L | Mariani Claudio B | +10