Protocol for Reconstituting Adaptor‐Mediated Activation of Full‐Length Kinesin‐1
Cytoskeleton, EarlyView.ABSTRACT Kinesin‐1 is a member of the kinesin superfamily that plays an essential role in intracellular cargo transport. In the absence of cargo, Kinesin‐1 exhibits low motor activity due to autoinhibition. Multiple studies have demonstrated that adaptor proteins, which link cargos to Kinesin‐1, can activate Kinesin‐1 by releasing the autoinhibition ...
Haruka Masumoto, Kyoko Chiba
wiley +1 more source
Inference of Cross-Species Gene Flow Using Genomic Data Depends on the Methods: Case Study of Gene Flow in Drosophila. [PDF]
Syst BiolJi J, Roberts T, Flouri T, Yang Z.
europepmc +1 more source
Survey on Drosophila suzukii Natural Short-Term Dispersal Capacities Using the Mark−Release−Recapture Technique [PDF]
, 2019 Sandra Vacas +4 more
openalex +1 more source
Cytoskeleton, EarlyView.ABSTRACT Cooperativity between cytoskeletal proteins is crucial for spatiotemporal coordination in biological processes, like oogenesis. In mammalian and Drosophila oogenesis, proper assembly and function of actin networks require coordination between actin assembly factors Spire and formins, as well as actin‐associated proteins like myosins and Rab ...
Joseph Y. Ong +7 more
wiley +1 more source
Chromatin assembly extracts from Drosophila embryos. [PDF]
, 1994 Becker, Peter B. +2 more
core +1 more source
Developmental Dynamics, EarlyView.Abstract Background Mutations in cohesins cause cohesinopathies such as Cornelia de Lange Syndrome (CdLS) and Roberts Syndrome (RBS). Prior findings demonstrate that Esco2 (a cohesin activator) and Smc3 (a core cohesin subunit) regulate the CRL4 E3 ubiquitin ligase. SMC3 mutations, however, account for a small percentage of CdLS.
Annie C. Sanchez +4 more
wiley +1 more source
The Gene Encoding the RCC1 (Regulator of Chromosome Condensation 1) Protein in <i>Drosophila melanogaster</i> and <i>Homo sapiens</i>. [PDF]
Int J Mol SciTurtapkina VA +10 more
europepmc +1 more source
Pss knockdown in the midgut causes growth retardation in Drosophila similar to that in human LMHD
Developmental Dynamics, EarlyView.Abstract Background Phosphatidylserine synthase (PSS), localized in the mitochondrial membrane, synthesizes phosphatidylserine. In humans, mutations in Pss lead to Lenz–Majewski hyperostotic dwarfism, a disorder affecting growth and development. The effects of Pss mutations on the growth of Drosophila melanogaster are not fully known. Hence, this study
Kwan‐Young Kim +4 more
wiley +1 more source
Human <i>RAP2A</i> homolog of the <i>Drosophila</i> asymmetric cell division regulator <i>Rap2l</i> targets the stemness of glioblastoma stem cells. [PDF]
ElifeFranco M +5 more
europepmc +1 more source
A GAL4-driver line resource for Drosophila neurobiology.
Cell Reports, 2012 Arnim Jenett +35 more
semanticscholar +1 more source