相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。The structural switch of nucleotide-free kinesin
Luyan Cao et al.
SCIENTIFIC REPORTS (2017)
Identification of two novel KIF5A mutations in hereditary spastic paraplegia associated with mild peripheral neuropathy
Eva Lopez et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2015)
Clinical and genetic heterogeneity in hereditary spastic paraplegias: From SPG1 to SPG72 and still counting
S. Klebe et al.
REVUE NEUROLOGIQUE (2015)
Hereditary spastic paraplegia: a novel mutation and expansion of the phenotype variability in SPG10
Laura Carosi et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2015)
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness
M. Muglia et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2014)
Extended phenotypic spectrum of KIF5A mutations
Yo-Tsen Liu et al.
NEUROLOGY (2014)
The structure of apo-kinesin bound to tubulin links the nucleotide cycle to movement
Luyan Cao et al.
NATURE COMMUNICATIONS (2014)
Structure of a kinesin-tubulin complex and implications for kinesin motility
Benoit Gigant et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2013)
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2
C. Crimella et al.
CLINICAL GENETICS (2012)
Three Routes to Suppression of the Neurodegenerative Phenotypes Caused by Kinesin Heavy Chain Mutations
Inna Djagaeva et al.
GENETICS (2012)
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Josef Finsterer et al.
JOURNAL OF THE NEUROLOGICAL SCIENCES (2012)
A metal switch for controlling the activity of molecular motor proteins
Jared C. Cochran et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2012)
Spastic Paraplegia Mutation N256S in the Neuronal Microtubule Motor KIF5A Disrupts Axonal Transport in a Drosophila HSP Model
Petra Fueger et al.
PLOS GENETICS (2012)
Kinesin-73 Is a Processive Motor That Localizes to Rab5-containing Organelles
Thomas M. Huckaba et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
A novel mutation in KIF5A gene causing hereditary spastic paraplegia with axonal neuropathy
Olimpia Musumeci et al.
NEUROLOGICAL SCIENCES (2011)
ATP Hydrolysis in Eg5 Kinesin Involves a Catalytic Two-water Mechanism
Courtney L. Parke et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Walking the walk: how kinesin and dynein coordinate their steps
Arne Gennerich et al.
CURRENT OPINION IN CELL BIOLOGY (2009)
Complicated Forms of Autosomal Dominant Hereditary Spastic Paraplegia Are Frequent in SPG10
Cyril Goizet et al.
HUMAN MUTATION (2009)
Identification of catalytic metal ion ligands in ribozymes
John K. Frederiksen et al.
METHODS (2009)
Effect of spastic paraplegia mutations in KIF5A kinesin on transport activity
Bettina Ebbing et al.
HUMAN MOLECULAR GENETICS (2008)
A novel KIF5A/SPG10 mutation in spastic paraplegia associated with axonal neuropathy
Alessandra Tessa et al.
JOURNAL OF NEUROLOGY (2008)
SPG10 is a rare cause of spastic paraplegia in European families
R. Schuele et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2008)
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia
MA Blair et al.
NEUROGENETICS (2006)
A missense mutation in the coiled-coil domain of the KIF5A gene and late-onset hereditary spastic paraplegia
M Lo Giudice et al.
ARCHIVES OF NEUROLOGY (2006)
Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia
M Fichera et al.
NEUROLOGY (2004)
Purification of brain tubulin through two cycles of polymerization-depolymerization in a high-molarity buffer
M Castoldi et al.
PROTEIN EXPRESSION AND PURIFICATION (2003)
A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)
E Reid et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
A structural pathway for activation of the kinesin motor ATPase
MY Yun et al.
EMBO JOURNAL (2001)
Hereditary spastic paraparesis: a review of new developments
CJ McDermott et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2000)