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Associations between gender and health‐related quality of life in people with IgE‐mediated food allergy and their caregivers: A systematic review

Clinical and experimental allergy, 2024-02, Vol.54 (2), p.93-108

2024

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Activin A directs striatal projection neuron differentiation of human pluripotent stem cells

Development (Cambridge), 2015-04, Vol.142 (7), p.1375-1386

2015

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Mouse Models of Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.97

2018

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Translating Antisense Technology into a Treatment for Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.497

2018

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Large-Brained Animal Models of Huntington's Disease: Sheep

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.221

Morton, A J

2018

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Assessing Mitochondrial Function in In Vitro and Ex Vivo Models of Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.415

2018

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CRISPR/Cas9-Mediated Genome Editing for Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.463

2018

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Biofoundry-Scale DNA Assembly Validation Using Cost-Effective High-Throughput Long-Read Sequencing

ACS synthetic biology, 2024-02, Vol.13 (2), p.683-686

2024

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Motor Assessment in Huntington's Disease Mice

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.121

2018

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Dopaminergic Progenitors Derived From Epiblast Stem Cells Function Similarly to Primary VM-Derived Progenitors When Transplanted Into a Parkinson's Disease Model

Frontiers in neuroscience, 2020-04, Vol.14, p.312-312

2020

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Is there a place for human fetal-derived stem cells for cell replacement therapy in Huntington's disease?

Neurochemistry international, 2017-06, Vol.106, p.114-121

2017

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Dissection and Preparation of Human Primary Fetal Ganglionic Eminence Tissue for Research and Clinical Applications

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.573

2018

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Cellular Models: HD Patient-Derived Pluripotent Stem Cells

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.41

2018

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Murine Models of Huntington's Disease for Evaluating Therapeutics

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.179

2018

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Generating Excitotoxic Lesion Models of Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.209

2018

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Disease Modification Through Trophic Factor Delivery

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.525

2018

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Methods to Quantify Cell Signaling and GPCR Receptor Ligand Bias: Characterization of Drugs that Target the Endocannabinoid Receptors in Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.549

2018

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A Filter Retardation Assay Facilitates the Detection and Quantification of Heat-Stable, Amyloidogenic Mutant Huntingtin Aggregates in Complex Biosamples

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.31

2018

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Robust Induction of DARPP32-Expressing GABAergic Striatal Neurons from Human Pluripotent Stem Cells

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.585

2018

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Nonmammalian Models of Huntington's Disease

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.75

2018

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Stereological Methods to Quantify Cell Loss in the Huntington's Disease Human Brain

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.1

2018

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Neurophysiological Assessment of Huntington's Disease Model Mice

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.163

2018

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Induced pluripotent stem cells derived from the developing striatum as a potential donor source for cell replacement therapy for Huntington disease

Cytotherapy (Oxford, England), 2021-02, Vol.23 (2), p.111-118

2021

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Minipigs as a Large-Brained Animal Model for Huntington's Disease: From Behavior and Imaging to Gene Therapy

Methods in molecular biology (Clifton, N.J.), 2018-01, Vol.1780, p.241

2018

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Associations between gender and health‐related quality of life in people with IgE‐mediated food allergy and their caregivers: A systematic review

Activin A directs striatal projection neuron differentiation of human pluripotent stem cells

Mouse Models of Huntington's Disease

Translating Antisense Technology into a Treatment for Huntington's Disease

Large-Brained Animal Models of Huntington's Disease: Sheep

Assessing Mitochondrial Function in In Vitro and Ex Vivo Models of Huntington's Disease

CRISPR/Cas9-Mediated Genome Editing for Huntington's Disease

Biofoundry-Scale DNA Assembly Validation Using Cost-Effective High-Throughput Long-Read Sequencing

Motor Assessment in Huntington's Disease Mice

Dopaminergic Progenitors Derived From Epiblast Stem Cells Function Similarly to Primary VM-Derived Progenitors When Transplanted Into a Parkinson's Disease Model

Is there a place for human fetal-derived stem cells for cell replacement therapy in Huntington's disease?

Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Dissection and Preparation of Human Primary Fetal Ganglionic Eminence Tissue for Research and Clinical Applications

Cellular Models: HD Patient-Derived Pluripotent Stem Cells

Murine Models of Huntington's Disease for Evaluating Therapeutics

Generating Excitotoxic Lesion Models of Huntington's Disease

Disease Modification Through Trophic Factor Delivery

Methods to Quantify Cell Signaling and GPCR Receptor Ligand Bias: Characterization of Drugs that Target the Endocannabinoid Receptors in Huntington's Disease

A Filter Retardation Assay Facilitates the Detection and Quantification of Heat-Stable, Amyloidogenic Mutant Huntingtin Aggregates in Complex Biosamples

Robust Induction of DARPP32-Expressing GABAergic Striatal Neurons from Human Pluripotent Stem Cells

Nonmammalian Models of Huntington's Disease

Stereological Methods to Quantify Cell Loss in the Huntington's Disease Human Brain

Neurophysiological Assessment of Huntington's Disease Model Mice

Induced pluripotent stem cells derived from the developing striatum as a potential donor source for cell replacement therapy for Huntington disease

Minipigs as a Large-Brained Animal Model for Huntington's Disease: From Behavior and Imaging to Gene Therapy

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