Embryonic mouse spinal cord motor neuron hybrid cells.

chemical circuit in the spinal cord generates a transient embryonic motor behavior.

Plastic changes in the spinal cord in motor neuron disease.

In vitro generation of motor neuron precursors from mouse embryonic stem cells using mesoporous nanoparticles.

Surface specializations of neurites in embryonic mouse spinal cord.

Glycoconjugates distribution during developing mouse spinal cord motor organizers.

Transcriptome profiling of spinal muscular atrophy motor neurons derived from mouse embryonic stem cells.

Ventral motor neuron alterations in rat spinal cord after chronic exercise.

Metals in spinal cord tissue of patients dying of motor neuron disease.

Motor neurons and the generation of spinal motor neuron diversity.

Acute lower motor neuron syndrome and spinal cord gray matter hyperintensities in HIV infection.

Oligodendroglial response in the spinal cord in TDP-43 proteinopathy with motor neuron involvement.

Blood-spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice.

Excitotoxicity in the embryonic chick spinal cord.

Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons.

Notch signaling regulates motor neuron differentiation of human embryonic stem cells.

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives.

Skeletal muscle DNA damage precedes spinal motor neuron DNA damage in a mouse model of Spinal Muscular Atrophy (SMA).

Functional effect of mouse embryonic stem cell implantation after spinal cord injury.

Expression of peroxiredoxins and thioredoxins in the mouse spinal cord during embryonic development.

Axonal growth cones and developing axonal collaterals form synaptic junctions in embryonic mouse spinal cord.

Spinal inhibitory circuits and their role in motor neuron degeneration.

Hereditary canine spinal muscular atrophy: canine motor neuron disease.

Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy.

Gestational Age-Dependent Increase of Survival Motor Neuron Protein in Umbilical Cord-Derived Mesenchymal Stem Cells.

Suggest Documents

chemical circuit in the spinal cord generates a transient embryonic motor behavior.

Plastic changes in the spinal cord in motor neuron disease.

In vitro generation of motor neuron precursors from mouse embryonic stem cells using mesoporous nanoparticles.

Surface specializations of neurites in embryonic mouse spinal cord.

Glycoconjugates distribution during developing mouse spinal cord motor organizers.

Transcriptome profiling of spinal muscular atrophy motor neurons derived from mouse embryonic stem cells.

Ventral motor neuron alterations in rat spinal cord after chronic exercise.

Metals in spinal cord tissue of patients dying of motor neuron disease.

Motor neurons and the generation of spinal motor neuron diversity.

Acute lower motor neuron syndrome and spinal cord gray matter hyperintensities in HIV infection.

Oligodendroglial response in the spinal cord in TDP-43 proteinopathy with motor neuron involvement.

Blood-spinal cord barrier disruption contributes to early motor-neuron degeneration in ALS-model mice.

Excitotoxicity in the embryonic chick spinal cord.

Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons.

Notch signaling regulates motor neuron differentiation of human embryonic stem cells.

Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives.

Skeletal muscle DNA damage precedes spinal motor neuron DNA damage in a mouse model of Spinal Muscular Atrophy (SMA).

Functional effect of mouse embryonic stem cell implantation after spinal cord injury.

Expression of peroxiredoxins and thioredoxins in the mouse spinal cord during embryonic development.

Axonal growth cones and developing axonal collaterals form synaptic junctions in embryonic mouse spinal cord.

Spinal inhibitory circuits and their role in motor neuron degeneration.

Hereditary canine spinal muscular atrophy: canine motor neuron disease.

Inherited Paediatric Motor Neuron Disorders: Beyond Spinal Muscular Atrophy.

Gestational Age-Dependent Increase of Survival Motor Neuron Protein in Umbilical Cord-Derived Mesenchymal Stem Cells.

Embryonic mouse spinal cord motor neuron hybrid cells.

Recommend Documents

Follow Us