Spastic Paraplegia Type 7 Latest Advances

Beyond Binding Affinity: How a Conformation-Specific Salt Bridge Tunes KIF1A Mechanochemistry.

Journal: Cytoskeleton (Hoboken, N.J.)

Published: May 28, 2026

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

Journal: JCI insight

Published: May 19, 2026

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Journal: Journal of neurogenetics

Published: May 18, 2026

Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with Spastic paraplegia type 56 due to variants of CYP2U1 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 06, 2026

Analysis of PI4KA gene variants in a patient with Hereditary spastic paraplegia type 84

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: May 06, 2026

Proteomic analysis reveals early pathological defects in corticospinal motor neurons of a spastin model of hereditary spastic paraplegia, which are improved by NU-9 treatment.

Journal: Neurobiology of disease

Published: April 28, 2026

The Long Haul: Microtubule Motors as the Essential Supply Line for Neuronal Longevity.

Journal: Journal of neurochemistry

Published: April 20, 2026

Homozygous PNPLA6 Mutation (p.Arg1183Trp) Associated With Isolated Cerebellar Ataxia: A Familial Case Report.

Journal: Cureus

Published: April 14, 2026

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 13, 2026

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

Reply to: Mathematical Comments on Linking Neurofilament Light Chain Levels to Disease Severity in Hereditary Spastic Paraplegia Subtypes SPG11 and SPG15.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: April 04, 2026

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results

Journal: Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko

Published: April 03, 2026

Spastic Paraplegia Type 7 Latest Advances

Find the Latest Research About Spastic Paraplegia Type 7

Beyond Binding Affinity: How a Conformation-Specific Salt Bridge Tunes KIF1A Mechanochemistry.

Beyond Binding Affinity: How a Conformation-Specific Salt Bridge Tunes KIF1A Mechanochemistry.

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

CRISPR/Cas9 loss-of-function screen in a neuronal model of AP-4 deficiency identifies ATG9A trafficking modulators.

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models.

Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with Spastic paraplegia type 56 due to variants of CYP2U1 gene

Genetic analysis and prenatal diagnosis for a Chinese pedigree affected with Spastic paraplegia type 56 due to variants of CYP2U1 gene

Analysis of PI4KA gene variants in a patient with Hereditary spastic paraplegia type 84

Analysis of PI4KA gene variants in a patient with Hereditary spastic paraplegia type 84

Proteomic analysis reveals early pathological defects in corticospinal motor neurons of a spastin model of hereditary spastic paraplegia, which are improved by NU-9 treatment.

Proteomic analysis reveals early pathological defects in corticospinal motor neurons of a spastin model of hereditary spastic paraplegia, which are improved by NU-9 treatment.

The Long Haul: Microtubule Motors as the Essential Supply Line for Neuronal Longevity.

The Long Haul: Microtubule Motors as the Essential Supply Line for Neuronal Longevity.

Homozygous PNPLA6 Mutation (p.Arg1183Trp) Associated With Isolated Cerebellar Ataxia: A Familial Case Report.

Homozygous PNPLA6 Mutation (p.Arg1183Trp) Associated With Isolated Cerebellar Ataxia: A Familial Case Report.

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

Correction to "Loss-of-Function Variants in CPT1C: No Support for a Causal Role in Hereditary Spastic Paraplegia".

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

ER discontinuities are common in C. elegans neurons, revealing a genetically tractable model for ER network maintenance.

Reply to: Mathematical Comments on Linking Neurofilament Light Chain Levels to Disease Severity in Hereditary Spastic Paraplegia Subtypes SPG11 and SPG15.

Reply to: Mathematical Comments on Linking Neurofilament Light Chain Levels to Disease Severity in Hereditary Spastic Paraplegia Subtypes SPG11 and SPG15.

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results

Epidural spinal cord stimulation in hereditary spastic paraplegia: preliminary results