[HTML][HTML] R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido, J Ruiz-Martínez… - Acta …, 2021 - Springer
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido, J Ruiz-Martínez… - Acta …, 2021 - cir.nii.ac.jp
抄録< jats: title> Abstract</jats: title>< jats: p> Heterozygous gain-of-kinase function variants
in< jats: italic> LRRK2</jats: italic>(leucine-rich repeat kinase 2) cause 1–2% of all cases of …
in< jats: italic> LRRK2</jats: italic>(leucine-rich repeat kinase 2) cause 1–2% of all cases of …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido… - Acta …, 2021 - pubmed.ncbi.nlm.nih.gov
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1-2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1-2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
[HTML][HTML] R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido… - Acta …, 2021 - ncbi.nlm.nih.gov
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
[PDF][PDF] R1441G but not G201S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils Ying Fan, Raja S. Nirujogi, Alicia …
P Markinez, R Alcalay, RA Hickman, J Duering… - scholar.archive.org
Gain-of kinase function variants in LRRK2 (leucine-rich repeat kinase 2) cause Parkinson's
disease (PD), albeit with incomplete and age-dependent penetrance, offering the prospect …
disease (PD), albeit with incomplete and age-dependent penetrance, offering the prospect …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils.
Y Fan, RS Nirujogi, A Garrido, J Ruiz-Martínez… - Acta …, 2021 - go.gale.com
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1-2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1-2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
[PDF][PDF] R1441G but not G201S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido, JR Martínez… - academia.edu
Gain-of kinase function variants in LRRK2 (leucine-rich repeat kinase 2) cause Parkinson's
disease (PD), albeit with incomplete and age-dependent penetrance, offering the prospect …
disease (PD), albeit with incomplete and age-dependent penetrance, offering the prospect …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido… - Acta …, 2021 - search.proquest.com
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils
Y Fan, RS Nirujogi, A Garrido… - Acta …, 2021 - discovery.dundee.ac.uk
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
R1441G but not G2019S mutation enhances LRRK2 mediated Rab10 phosphorylation in human peripheral blood neutrophils.
Y Fan, RS Nirujogi, A Garrido, J Ruiz-Martínez… - Acta …, 2021 - europepmc.org
Heterozygous gain-of-kinase function variants in LRRK2 (leucine-rich repeat kinase 2)
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …
cause 1–2% of all cases of Parkinson's disease (PD) albeit with incomplete and age …