Pathogenic LRRK2 variants are gain-of-function mutations that enhance LRRK2-mediated repression of β-catenin signaling. (Record no. 26800275)

MARC details
000 -LEADER
fixed length control field 01448 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250517134128.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201802s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1750-1326
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1186/s13024-017-0153-4
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Berwick, Daniel C
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20180222
245 00 - TITLE STATEMENT
Title Pathogenic LRRK2 variants are gain-of-function mutations that enhance LRRK2-mediated repression of β-catenin signaling.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Molecular neurodegeneration
Date of publication, distribution, etc. 01 2017
300 ## - PHYSICAL DESCRIPTION
Extent 9 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Animals
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Dopaminergic Neurons
General subdivision metabolism
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Immunoprecipitation
General subdivision methods
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mice, Knockout
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Parkinson Disease
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Protein Serine-Threonine Kinases
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Wnt Signaling Pathway
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element beta Catenin
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Javaheri, Behzad
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Wetzel, Andrea
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Hopkinson, Mark
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nixon-Abell, Jonathon
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Grannò, Simone
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pitsillides, Andrew A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Harvey, Kirsten
773 0# - HOST ITEM ENTRY
Title Molecular neurodegeneration
Related parts vol. 12
-- no. 1
-- p. 9
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1186/s13024-017-0153-4">https://doi.org/10.1186/s13024-017-0153-4</a>
Public note Available from publisher's website

No items available.