A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder
Published 2022 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
A (GCC) repeat in SBF1 reveals a novel biological phenomenon in human and links to late onset neurocognitive disorder
Authors
Keywords
-
Journal
Scientific Reports
Volume 12, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2022-09-15
DOI
10.1038/s41598-022-19878-y
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment
- (2022) S. Khamse et al. GENETICA
- Abundancy of polymorphic CGG repeats in the human genome suggest a broad involvement in neurological disease
- (2021) Dale J. Annear et al. Scientific Reports
- Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction
- (2021) Beatrice Berti et al. BMC Medical Genomics
- Microsatellites as Agents of Adaptive Change: An RNA-Seq-Based Comparative Study of Transcriptomes from Five Helianthus Species
- (2021) Chathurani Ranathunge et al. Symmetry-Basel
- Distinct roles for the Charcot–Marie–Tooth disease-causing endosomal regulators Mtmr5 and Mtmr13 in axon radial sorting and Schwann cell myelination
- (2021) Anna E Mammel et al. HUMAN MOLECULAR GENETICS
- Re-epithelialization and immune cell behaviour in an ex vivo human skin model
- (2020) Ana Rakita et al. Scientific Reports
- Hotspots of Human Mutation
- (2020) Alex V. Nesta et al. TRENDS IN GENETICS
- Substitutions Are Boring: Some Arguments about Parallel Mutations and High Mutation Rates
- (2019) Maximilian Oliver Press et al. TRENDS IN GENETICS
- Epigenetic dysregulation of enhancers in neurons is associated with Alzheimer’s disease pathology and cognitive symptoms
- (2019) Peipei Li et al. Nature Communications
- The impact of short tandem repeat variation on gene expression
- (2019) Stephanie Feupe Fotsing et al. NATURE GENETICS
- Null alleles and sequence variations at primer binding sites of STR loci within multiplex typing systems
- (2018) Yining Yao et al. Legal Medicine
- Tandem repeats mediating genetic plasticity in health and disease
- (2018) Anthony J. Hannan NATURE REVIEWS GENETICS
- Null alleles and sequence variations at primer binding sites of STR loci within multiplex typing systems
- (2018) Yining Yao et al. Legal Medicine
- Stabilizing selection on microsatellite allele length at arginine vasopressin 1a receptor and oxytocin receptor loci
- (2017) Phillip C. Watts et al. PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
- Validity and reliability of Abbreviated Mental Test Score (AMTS) among older Iranian
- (2017) Mahshid Foroughan et al. Psychogeriatrics
- Validity and reliability of Abbreviated Mental Test Score (AMTS) among older Iranian
- (2017) Mahshid Foroughan et al. Psychogeriatrics
- An exceptionally long CA-repeat in the core promoter of SCGB2B2 links with the evolution of apes and Old World monkeys
- (2016) M. Nikkhah et al. GENE
- Exceptionally long 5′ UTR short tandem repeats specifically linked to primates
- (2015) P. Namdar-Aligoodarzi et al. GENE
- Risk of Misdiagnosis Due to Allele Dropout and False-Positive PCR Artifacts in Molecular Diagnostics
- (2015) Jonatan Blais et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Exceptional expansion and conservation of a CT-repeat complex in the core promoter ofPAXBP1in primates
- (2014) Saeid Mohammadparast et al. AMERICAN JOURNAL OF PRIMATOLOGY
- The overdue promise of short tandem repeat variation for heritability
- (2014) Maximilian O. Press et al. TRENDS IN GENETICS
- Identification of new primer binding site mutations at TH01 and D13S317 loci and determination of their corresponding STR alleles by allele-specific PCR
- (2013) Fengrui Li et al. Forensic Science International-Genetics
- RNA Accessibility in cubic time
- (2011) Stephan H Bernhart et al. Algorithms for Molecular Biology
- ViennaRNA Package 2.0
- (2011) Ronny Lorenz et al. Algorithms for Molecular Biology
- Genomic Runs of Homozygosity Record Population History and Consanguinity
- (2010) Mirna Kirin et al. PLoS One
Find the ideal target journal for your manuscript
Explore over 38,000 international journals covering a vast array of academic fields.
SearchAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started