UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 52

Sortiert nach

HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism

Human molecular genetics, 2005-10, Vol.14 (19), p.2871-2880

2005

Volltextzugriff (PDF)

Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice

Human molecular genetics, 2003-03, Vol.12 (5), p.497-508

2003

Volltextzugriff (PDF)

Enhanced Akt Signaling Is an Early Pro-survival Response That Reflects N-Methyl-D-aspartate Receptor Activation in Huntington's Disease Knock-in Striatal Cells

The Journal of biological chemistry, 2003-12, Vol.278 (50), p.50514-50522

2003

Volltextzugriff (PDF)

Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

American journal of human genetics, 2008-01, Vol.82 (1), p.199-207

2008

Volltextzugriff (PDF)

Huntingtin facilitates polycomb repressive complex 2

Human molecular genetics, 2010-02, Vol.19 (4), p.573-583

2010

Volltextzugriff (PDF)

Hypomorphic mutation of the mouse Huntington's disease gene orthologue

PLoS genetics, 2019-03, Vol.15 (3), p.e1007765

2019

Volltextzugriff (PDF)

HD CAG-correlated gene expression changes support a simple dominant gain of function

Human molecular genetics, 2011-07, Vol.20 (14), p.2846-2860

2011

Volltextzugriff (PDF)

Full sequence of mutant huntingtin 3'-untranslated region and modulation of its gene regulatory activity by endogenous microRNA

Journal of human genetics, 2019-10, Vol.64 (10), p.995-1004

2019

Volltextzugriff (PDF)

Huntingtin's spherical solenoid structure enables polyglutamine tract-dependent modulation of its structure and function

eLife, 2016-03, Vol.5, p.e11184-e11184

2016

Volltextzugriff (PDF)

Allele-specific silencing of the gain-of-function mutation in Huntington’s disease using CRISPR/Cas9

JCI insight, 2022-10, Vol.7 (19)

2022

Volltextzugriff (PDF)

Purification of full-length recombinant human huntingtin proteins with allelic series of polyglutamine lengths

STAR protocols, 2021-12, Vol.2 (4), p.100886-100886, Article 100886

2021

Volltextzugriff (PDF)

Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity

Molecular therapy. Nucleic acids, 2018-06, Vol.11 (C), p.416-428

2018

Volltextzugriff (PDF)

Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis

Human molecular genetics, 2011-06, Vol.20 (12), p.2344-2355

2011

Volltextzugriff (PDF)

Differential effects of the Huntington's disease CAG mutation in striatum and cerebellum are quantitative not qualitative

Human molecular genetics, 2011-11, Vol.20 (21), p.4258-4267

2011

Volltextzugriff (PDF)

HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes

PloS one, 2014-04, Vol.9 (4), p.e95556

2014

Volltextzugriff (PDF)

Role of the GYVG Pore Motif of HslU ATPase in Protein Unfolding and Translocation for Degradation by HslV Peptidase

The Journal of biological chemistry, 2005-06, Vol.280 (24), p.22892-22898

2005

Volltextzugriff (PDF)

N-terminal Processing Is Essential for Release of Epithin, a Mouse Type II Membrane Serine Protease

The Journal of biological chemistry, 2001-11, Vol.276 (48), p.44581-44589

2001

Volltextzugriff (PDF)

Crystal structure of Bacillus subtilis CodW, a noncanonical HslV-like peptidase with an impaired catalytic apparatus

Proteins, structure, function, and bioinformatics, 2008-05, Vol.71 (2), p.1020-1026

2008

Volltextzugriff (PDF)

The C-terminal Tails of HslU ATPase Act as a Molecular Switch for Activation of HslV Peptidase

The Journal of biological chemistry, 2002-07, Vol.277 (29), p.25976-25982

2002

Volltextzugriff (PDF)

Mutant Huntingtin Is Cleared from the Brain via Active Mechanisms in Huntington Disease

The Journal of neuroscience, 2021-01, Vol.41 (4), p.780-796

2021

Volltextzugriff (PDF)

Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs

Human molecular genetics, 2021-04, Vol.30 (3-4), p.135-148

2021

Volltextzugriff (PDF)

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

American journal of human genetics, 2022-05, Vol.109 (5), p.885-899

2022

Volltextzugriff (PDF)

ATP-dependent degradation of SulA, a cell division inhibitor, by the HslVU protease in Escherichia coli

FEBS letters, 1999-07, Vol.456 (1), p.211-214

1999

Volltextzugriff (PDF)

The Polyglutamine Expansion at the N-Terminal of Huntingtin Protein Modulates the Dynamic Configuration and Phosphorylation of the C-Terminal HEAT Domain

Structure (London), 2020-09, Vol.28 (9), p.1035-1050.e8

2020

Volltextzugriff (PDF)

1 – 25 von 52

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(52)
Mit Volltextzugriff
(52)

Publikationsform

Artikel
(52)

Sprache

Englisch
(52)
Japanisch
(9)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

HD CAG repeat implicates a dominant property of huntingtin in mitochondrial energy metabolism

Specific progressive cAMP reduction implicates energy deficit in presymptomatic Huntington's disease knock-in mice

Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies

Enhanced Akt Signaling Is an Early Pro-survival Response That Reflects N-Methyl-D-aspartate Receptor Activation in Huntington's Disease Knock-in Striatal Cells

Disruption of Neurexin 1 Associated with Autism Spectrum Disorder

Huntingtin facilitates polycomb repressive complex 2

Hypomorphic mutation of the mouse Huntington's disease gene orthologue

HD CAG-correlated gene expression changes support a simple dominant gain of function

Full sequence of mutant huntingtin 3'-untranslated region and modulation of its gene regulatory activity by endogenous microRNA

Huntingtin's spherical solenoid structure enables polyglutamine tract-dependent modulation of its structure and function

Allele-specific silencing of the gain-of-function mutation in Huntington’s disease using CRISPR/Cas9

Purification of full-length recombinant human huntingtin proteins with allelic series of polyglutamine lengths

Novel DNA Aptamers that Bind to Mutant Huntingtin and Modify Its Activity

Striatal neurons expressing full-length mutant huntingtin exhibit decreased N-cadherin and altered neuritogenesis

Differential effects of the Huntington's disease CAG mutation in striatum and cerebellum are quantitative not qualitative

HD CAGnome: a search tool for huntingtin CAG repeat length-correlated genes

Role of the GYVG Pore Motif of HslU ATPase in Protein Unfolding and Translocation for Degradation by HslV Peptidase

N-terminal Processing Is Essential for Release of Epithin, a Mouse Type II Membrane Serine Protease

Crystal structure of Bacillus subtilis CodW, a noncanonical HslV-like peptidase with an impaired catalytic apparatus

The C-terminal Tails of HslU ATPase Act as a Molecular Switch for Activation of HslV Peptidase

Mutant Huntingtin Is Cleared from the Brain via Active Mechanisms in Huntington Disease

Mutations causing Lopes-Maciel-Rodan syndrome are huntingtin hypomorphs

Genetic modifiers of Huntington disease differentially influence motor and cognitive domains

ATP-dependent degradation of SulA, a cell division inhibitor, by the HslVU protease in Escherichia coli

The Polyglutamine Expansion at the N-Terminal of Huntingtin Protein Modulates the Dynamic Configuration and Phosphorylation of the C-Terminal HEAT Domain

Suchergebnisse filtern