Publications by authors named "Lis Hasholt"

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Upregulated Chaperone-Mediated Autophagy May Perform a Key Role in Reduced Cancer Incidence in Huntington's Disease.
Lis Frydenreich Hasholt

J Huntingtons Dis· December 2023

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Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.
Grigoris Effraimidis, Åse Krogh Rasmussen, Morten Dunoe, Lis F Hasholt, Flemming Wibrand

PLoS One· June 2023

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Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience.
Grigoris Effraimidis, Åse Krogh Rasmussen, Morten Dunoe, Lis F Hasholt, Flemming Wibrand

PLoS One· November 2022

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CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity.
Barbara A Perez, Hannah K Shorrock, Monica Banez-Coronel, Tao Zu, Lisa El Romano, Lis F Hasholt

EMBO Mol Med· November 2021

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Paroxysmal Cranial Dyskinesia and Nail-Patella Syndrome Caused by a Novel Variant in the LMX1B Gene.
Sara Bech, Annemette Løkkegaard, Troels T Nielsen, Anne Nørremølle, Sabine Grønborg, Lis Hasholt

Mov Disord· December 2020

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Ghrelin-mediated improvements in the metabolic phenotype in the R6/2 mouse model of Huntington's disease.
Olga Rudenko, Cecilie Springer, Louisa J Skov, Andreas N Madsen, Lis Hasholt

J Neuroendocrinol· July 2019

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Perturbations in the p53/miR-34a/SIRT1 pathway in the R6/2 Huntington's disease model.
Regina Hertfelder Reynolds, Maria Hvidberg Petersen, Cecilie Wennemoes Willert, Marie Heinrich, Nynne Nymann, Lis Hasholt

Mol Cell Neurosci· April 2018

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The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease.
Lis Hasholt, Martin Ballegaard, Henning Bundgaard, Michael Christiansen, Ian Law

Scand J Clin Lab Invest· December 2017

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Induced pluripotent stem cell - derived neurons for the study of spinocerebellar ataxia type 3.
Susanne K Hansen, Tina C Stummann, Helena Borland, Lis F Hasholt, Zeynep Tümer

Stem Cell Res· September 2016

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Seasonal difference in brain serotonin transporter binding predicts symptom severity in patients with seasonal affective disorder.
Brenda Mc Mahon, Sofie B Andersen, Martin K Madsen, Liv V Hjordt, Ida Hageman, Lis Hasholt

Brain· May 2016

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Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.A11.
Susanne K Hansen, Helena Borland, Lis F Hasholt, Zeynep Tümer, Jørgen E Nielsen

Stem Cell Res· May 2016

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Generation of spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cell line SCA3.B11.
Susanne K Hansen, Helena Borland, Lis F Hasholt, Zeynep Tümer, Jørgen E Nielsen

Stem Cell Res· May 2016

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Liver function in Huntington's disease assessed by blood biochemical analyses in a clinical setting.
Signe Marie Borch Nielsen, Tua Vinther-Jensen, Jørgen E Nielsen, Anne Nørremølle, Lis Hasholt

J Neurol Sci· March 2016

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Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a P301L mutation in microtubule-associated protein tau (MAPT).
Mikkel A Rasmussen, Lena E Hjermind, Lis F Hasholt, Gunhild Waldemar, Jørgen E Nielsen

Stem Cell Res· January 2016

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Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT).
Mikkel A Rasmussen, Lena E Hjermind, Lis F Hasholt, Gunhild Waldemar, Jørgen E Nielsen

Stem Cell Res· January 2016

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Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia.
Mikkel A Rasmussen, Lena E Hjermind, Lis F Hasholt, Gunhild Waldemar, Jørgen E Nielsen

Stem Cell Res· January 2016

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Progressive Impairment of Lactate-based Gluconeogenesis in the Huntington's Disease Mouse Model R6/2.
Signe Marie Borch Nielsen, Lis Hasholt, Anne Nørremølle, Knud Josefsen

PLoS Curr· April 2015

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Three-week bright-light intervention has dose-related effects on threat-related corticolimbic reactivity and functional coupling.
Patrick M Fisher, Martin K Madsen, Brenda Mc Mahon, Klaus K Holst, Sofie B Andersen, Lis F Hasholt

Biol Psychiatry· August 2014

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p53 increases caspase-6 expression and activation in muscle tissue expressing mutant huntingtin.
Dagmar E Ehrnhoefer, Niels H Skotte, Safia Ladha, Yen T N Nguyen, Xiaofan Qiu, Lis Hasholt

Hum Mol Genet· February 2014

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Reduced ceramide synthase 2 activity causes progressive myoclonic epilepsy.
Mai-Britt Mosbech, Anne S B Olsen, Ditte Neess, Oshrit Ben-David, Laura L Klitten, Lis Hasholt

Ann Clin Transl Neurol· February 2014

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Localization of A11-reactive oligomeric species in prion diseases.
Frederik H Aidt, Lis F Hasholt, Michael Christiansen, Henning Laursen

Histopathology· June 2013

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Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model.
Frederik Heurlin Aidt, Signe Marie Borch Nielsen, Jørgen Kanters, Dominik Pesta, Troels Tolstrup Nielsen, Lis Hasholt

PLoS Curr· April 2013

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ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia.
Troels Tolstrup Nielsen, Kirsten Svenstrup, Esben Budtz-Jørgensen, Hans Eiberg, Lis Hasholt

J Neurol Sci· October 2012

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Reversal of pathology in CHMP2B-mediated frontotemporal dementia patient cells using RNA interference.
Troels Tolstrup Nielsen, Sarah Mizielinska, Lis Hasholt, Adrian M Isaacs, Jørgen E Nielsen

J Gene Med· August 2012

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Diagnostic dilemma: a young woman with Fabry disease symptoms, no family history, and a "sequencing cryptic" α-galactosidase a large deletion.
Ulla Feldt-Rasmussen, Robert Dobrovolny, Irina Nazarenko, Martin Ballegaard, Lis Hasholt

Mol Genet Metab· November 2011

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