Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease.

Stem cell research - 1 Mar 2018

Rosati Jessica, Bidollari Eris, Rotundo Giovannina, Ferrari Daniela, Torres Barbara, Bernardini Laura, Consoli Federica, De Luca Alessandro, Santimone Iolanda, Lamorte Giuseppe, Squitieri Ferdinando, Vescovi Angelo Luigi

Abstract excerpt

Huntington Disease (HD) is an autosomal dominant disorder characterized by motor, cognitive and behavioral features caused by a CAG expansion in the HTT gene beyond 35 repeats. The juvenile form (JHD) may begin before the age of 20years and is associated with expanded alleles as long as 60 or more CAG repeats. In this study, induced pluripotent stem cells were generated from skin fibroblasts of a 8-year-old child...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alleles
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to HTT gene

Share to Huntingtin Protein

Share to Huntington Disease

Share to Induced Pluripotent Stem Cells

Share to Mutation

Share to Trinucleotide Repeats

Source

Identifiers

PMID: 29342448
DOI: 10.1016/j.scr.2018.01.011

Genes

HTT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease.PMID 29342448Read ↗

Generation of induced pluripotent stem cells from three individuals with Huntington's disease.Semantic proximity Read ↗

Generation of a human induced pluripotent stem cell line (INEUi001-A) from an amyotrophic lateral sclerosis/frontotemporal dementia patient with a C9ORF72 G4C2 genotype of <2 (GGGGCCG) and 10 repeats.Semantic proximity Read ↗

Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H196.Semantic proximity Read ↗

Generation of an induced pluripotent stem cells line, CSSi014-A 9407, carrying the variant c.479C>T in the human iduronate 2-sulfatase (hIDS) gene.Semantic proximity Read ↗

Generation of an induced pluripotent stem cell line SDQLCHi026-A from a hereditary tyrosinemia type I patient carrying compound heterozygote mutations in FAH gene.Semantic proximity Read ↗

Generation of KCL013 research grade human embryonic stem cell line carrying a mutation in the HTT gene.Semantic proximity Read ↗

Generation of KCL012 research grade human embryonic stem cell line carrying a mutation in the HTT gene.Semantic proximity Read ↗

Generation of KCL028 research grade human embryonic stem cell line carrying a mutation in the HTT gene.Semantic proximity Read ↗

Generation of KCL027 research grade human embryonic stem cell line carrying a mutation in the HTT gene.Semantic proximity Read ↗

Generation of KCL036 research grade human embryonic stem cell line carrying a mutation in the HTT gene.Semantic proximity Read ↗

Three Huntington's Disease Specific Mutation-Carrying Human Embryonic Stem Cell Lines Have Stable Number of CAG Repeats upon In Vitro Differentiation into Cardiomyocytes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.