The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson’s disease
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson’s disease ; volume:10 ; number:1 ; day:6 ; month:11 ; year:2024 ; pages:1-9 ; date:12.2024
npj Parkinson's Disease ; 10, Heft 1 (6.11.2024), 1-9, 12.2024
- Creator
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William, Martina B.
Hamed, Sharifa
Shalash, Ali
Khedr, Eman M.
Yousef, Mohamed H.
El-Jaafary, Shaimaa
Fawi, Gharib
Helmy, Asmaa
Hamid, Eman
Essam, Mohamed
Lee, Hamin
Jama, Alina
Koraym, Mohamed
Mahmoud, Doaa M.
Elfarrash, Sara
Elsaid, Yasmin
Gabr, Asmaa S.
Shebl, Nourhan
Abdelwahhab, Nesreen
Belal, Tamer M.
Elsayed, Nehal A. B.
El-Gamal, Mohamed
Elgamal, Shimaa
Ragab, Salma
Mekky, Jaidaa
Aly, Lobna
Nabhan, Samir
Ragab, Gaafar
Hussein, Mohamed A.
Hegazy, Mohamed Tharwat
Houlden, Henry
Salama, Mohamed
Rizig, Mie
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41531-024-00826-8
- URN
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urn:nbn:de:101:1-2501242110246.653439750903
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:26 AM CEST
Data provider
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Associated
- William, Martina B.
- Hamed, Sharifa
- Shalash, Ali
- Khedr, Eman M.
- Yousef, Mohamed H.
- El-Jaafary, Shaimaa
- Fawi, Gharib
- Helmy, Asmaa
- Hamid, Eman
- Essam, Mohamed
- Lee, Hamin
- Jama, Alina
- Koraym, Mohamed
- Mahmoud, Doaa M.
- Elfarrash, Sara
- Elsaid, Yasmin
- Gabr, Asmaa S.
- Shebl, Nourhan
- Abdelwahhab, Nesreen
- Belal, Tamer M.
- Elsayed, Nehal A. B.
- El-Gamal, Mohamed
- Elgamal, Shimaa
- Ragab, Salma
- Mekky, Jaidaa
- Aly, Lobna
- Nabhan, Samir
- Ragab, Gaafar
- Hussein, Mohamed A.
- Hegazy, Mohamed Tharwat
- Houlden, Henry
- Salama, Mohamed
- Rizig, Mie
- SpringerLink (Online service)
Other Objects (12)
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Fibroblast Biomarkers of Sporadic Parkinson’s Disease and LRRK2 Kinase Inhibition
Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease
LRRK2 contributes to monocyte dysregulation in Parkinson’s disease
LRRK2 and neuroinflammation: partners in crime in Parkinson’s disease?
Crystallizing the Parkinson’s disease protein LRRK2 under microgravity conditions
Parkinson’s Disease–Associated LRRK2 Interferes with Astrocyte-Mediated Alpha-Synuclein Clearance
Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease
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Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
Pathogenic Mutation of Lrrk2 : A Mouse Model for pre-motor Parkinson’s disease
LRRK2 Low-penetrance Mutations (Gly2019Ser) and Risk Alleles (Gly2385Arg)—Linking Familial and Sporadic Parkinson’s Disease
Fibroblast Biomarkers of Sporadic Parkinson’s Disease and LRRK2 Kinase Inhibition
Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease
LRRK2 contributes to monocyte dysregulation in Parkinson’s disease
LRRK2 and neuroinflammation: partners in crime in Parkinson’s disease?
Crystallizing the Parkinson’s disease protein LRRK2 under microgravity conditions
Parkinson’s Disease–Associated LRRK2 Interferes with Astrocyte-Mediated Alpha-Synuclein Clearance
Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease
A designed ankyrin-repeat protein that targets Parkinson’s disease-associated LRRK2
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
Pathogenic Mutation of Lrrk2 : A Mouse Model for pre-motor Parkinson’s disease
LRRK2 Low-penetrance Mutations (Gly2019Ser) and Risk Alleles (Gly2385Arg)—Linking Familial and Sporadic Parkinson’s Disease
Fibroblast Biomarkers of Sporadic Parkinson’s Disease and LRRK2 Kinase Inhibition
Transcriptomics and weighted protein network analyses of the LRRK2 protein interactome reveal distinct molecular signatures for sporadic and LRRK2 Parkinson’s Disease
LRRK2 contributes to monocyte dysregulation in Parkinson’s disease
LRRK2 and neuroinflammation: partners in crime in Parkinson’s disease?
Crystallizing the Parkinson’s disease protein LRRK2 under microgravity conditions
Parkinson’s Disease–Associated LRRK2 Interferes with Astrocyte-Mediated Alpha-Synuclein Clearance
Structural basis for Parkinson’s disease-linked LRRK2’s binding to microtubules
Pathophysiological evaluation of the LRRK2 G2385R risk variant for Parkinson’s disease
A designed ankyrin-repeat protein that targets Parkinson’s disease-associated LRRK2
Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)