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A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene ( HTT )

International journal of molecular sciences, 2021-02, Vol.22 (4), p.1689

2021

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Preclinical Safety of RNAi-Mediated HTT Suppression in the Rhesus Macaque as a Potential Therapy for Huntington's Disease

Molecular therapy, 2011-12, Vol.19 (12), p.2152-2162

2011

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Interaction of huntingtin with PRMTs and its subsequent arginine methylation affects HTT solubility, phase transition behavior and neuronal toxicity

Human molecular genetics, 2022-05, Vol.31 (10), p.1651-1672

2022

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Amyotrophic lateral sclerosis is over-represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion

Acta neuropathologica, 2022-01, Vol.143 (1), p.105-108

2022

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HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease

Neurobiology of aging, 2019-04, Vol.76, p.215.e9-215.e14

2019

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A Comprehensive Haplotype-Targeting Strategy for Allele-Specific HTT Suppression in Huntington Disease

American journal of human genetics, 2019-12, Vol.105 (6), p.1112-1125

2019

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Genetic Testing of HTT Modifiers for Huntington's Disease: Considerations for Clinical Guidelines

Movement disorders, 2023-12, Vol.38 (12), p.2151-2154

2023

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HTT (huntingtin) and RAB7 co-migrate retrogradely on a signaling LAMP1-containing late endosome during axonal injury

Autophagy, 2023-04, Vol.19 (4), p.1199-1220

2023

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High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study

Scientific reports, 2020-06, Vol.10 (1), p.9853-9853, Article 9853

2020

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Htt is a repressor of Abl activity required for APP-induced axonal growth

PLoS genetics, 2021-01, Vol.17 (1), p.e1009287-e1009287

2021

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Imaging and Assay of the Dynamics of Cytotoxic Huntingtin (HTT) Protein Aggregates Regulated by lncRNAs

Methods in molecular biology (Clifton, N.J.), 2024, Vol.2761, p.421

2024

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Translation of HTT mRNA with expanded CAG repeats is regulated by the MID1-PP2A protein complex

Nature communications, 2013, Vol.4 (1), p.1511, Article 1511

2013

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More than a co-incidence? Comment on: Amyotrophic lateral sclerosis is over‐represented in two Huntington’s disease brain bank cohorts: further evidence to support genetic pleiotropy of pathogenic HTT gene expansion

Acta neuropathologica, 2023-02, Vol.145 (2), p.257-258

2023

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Inherited HTT CAG repeat length does not have a major impact on Huntington disease duration

American journal of human genetics, 2022-07, Vol.109 (7), p.1338-1340

2022

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Aberrantly spliced HTT, a new player in Huntington's disease pathogenesis

RNA biology, 2013-11, Vol.10 (11), p.1647-1652

2013

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A series of cases with Huntington-like phenotype and intermediate repeats in HTT

Journal of the neurological sciences, 2021-06, Vol.425, p.117452-117452, Article 117452

2021

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Spanish HTT gene study reveals haplotype and allelic diversity with possible implications for germline expansion dynamics in Huntington disease

Human molecular genetics, 2023-03, Vol.32 (6), p.897-906

2023

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Analysis of HTT CAG repeat expansion among healthy individuals and patients with chorea in Korea

Parkinsonism & related disorders, 2024-01, Vol.118, p.105930-105930, Article 105930

2024

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Antisense oligonucleotide-mediated disruption of HTT caspase-6 cleavage site ameliorates the phenotype of YAC128 Huntington disease mice

Neurobiology of disease, 2024-01, Vol.190, p.106368-106368, Article 106368

2024

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Generation of an induced pluripotent stem cell line from a Huntington’s disease patient with a long HTT-PolyQ sequence

Stem cell research, 2023-04, Vol.68, p.103056-103056, Article 103056

2023

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Investigation of the Influence of TBP CAG/CAA Repeats in Conjunction with HTT CAG Repeats on Huntington’s Disease Age at Onset in a Brazilian Sample

Journal of molecular neuroscience, 2022-05, Vol.72 (5), p.1116-1124

2022

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Incidence and prevalence of Huntington disease (HD) in the Sultanate of Oman: the first Middle East post- HTT service-based study

Journal of neurology, neurosurgery and psychiatry, 2020-12, Vol.91 (12), p.1359

2020

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Excess Rab4 rescues synaptic and behavioral dysfunction caused by defective HTT-Rab4 axonal transport in Huntington's disease

Acta neuropathologica communications, 2020-07, Vol.8 (1), p.97-97, Article 97

2020

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Allele-specific quantitation of ATXN3 and HTT transcripts in polyQ disease models

BMC biology, 2023-02, Vol.21 (1), p.17-17, Article 17

2023

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HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia

European journal of human genetics : EJHG, 2011-05, Vol.19 (5), p.561-566

2011

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