Found: 29
Select item for more details and to access through your institution.
Altering Presenilin Gene Activity in Zebrafish Embryos Causes Changes in Expression of Genes with Potential Involvement in Alzheimer's Disease Pathogenesis.
- Published in:
- Journal of Alzheimer's Disease, 2009, v. 16, n. 1, p. 133, doi. 10.3233/JAD-2009-0945
- By:
- Publication type:
- Article
Zebrafish Chromosome 14 Gene Differential Expression in the fmr1 <sup> h u 2787</sup> Model of Fragile X Syndrome.
- Published in:
- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.625466
- By:
- Publication type:
- Article
Dysregulation of Neuronal Iron Homeostasis as an Alternative Unifying Effect of Mutations Causing Familial Alzheimer’s Disease.
- Published in:
- Frontiers in Neuroscience, 2018, p. N.PAG, doi. 10.3389/fnins.2018.00533
- By:
- Publication type:
- Article
The impact of cholesterol intake on expression of Alzheimer's disease–related genes in the guinea pig brain
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Evaluation of color preference in zebrafish: A possible potential model for learning and memory disorders
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Transcriptome analyses of 7-day-old zebrafish larvae possessing a familial Alzheimer's disease-like mutation in psen1 indicate effects on oxidative phosphorylation, ECM and MCM functions, and iron homeostasis.
- Published in:
- BMC Genomics, 2021, v. 22, n. 1, p. 1, doi. 10.1186/s12864-021-07509-1
- By:
- Publication type:
- Article
The Guinea Pig as a Model for Sporadic Alzheimer’s Disease (AD): The Impact of Cholesterol Intake on Expression of AD-Related Genes.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066235
- By:
- Publication type:
- Article
Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.
- Published in:
- 2019
- By:
- Publication type:
- Correction Notice
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy.
- Published in:
- NPJ Genomic Medicine, 2018, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41525-018-0073-4
- By:
- Publication type:
- Article
Using the zebrafish model for Alzheimer's disease research.
- Published in:
- Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00189
- By:
- Publication type:
- Article
Brain transcriptome analysis reveals subtle effects on mitochondrial function and iron homeostasis of mutations in the SORL1 gene implicated in early onset familial Alzheimer's disease.
- Published in:
- Molecular Brain, 2020, v. 13, n. 1, p. 1, doi. 10.1186/s13041-020-00681-7
- By:
- Publication type:
- Article
Brain transcriptome analysis of a familial Alzheimer's disease-like mutation in the zebrafish presenilin 1 gene implies effects on energy production.
- Published in:
- Molecular Brain, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13041-019-0467-y
- By:
- Publication type:
- Article
An examination of the association between perceived stress and autistic traits in a rural predominately African American community sample.
- Published in:
- Current Psychology, 2024, v. 43, n. 7, p. 6672, doi. 10.1007/s12144-023-04851-3
- By:
- Publication type:
- Article
Hypoxia alters expression of Zebrafish Microtubule-associated protein Tau (mapta, maptb) gene transcripts.
- Published in:
- BMC Research Notes, 2014, v. 7, n. 1, p. 767, doi. 10.1186/1756-0500-7-767
- By:
- Publication type:
- Article
A hyperactive sleeping beauty transposase enhances transgenesis in zebrafish embryos.
- Published in:
- BMC Research Notes, 2010, v. 3, p. 282, doi. 10.1186/1756-0500-3-282
- By:
- Publication type:
- Article
Transcriptome analysis indicates dominant effects on ribosome and mitochondrial function of a premature termination codon mutation in the zebrafish gene psen2.
- Published in:
- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0232559
- By:
- Publication type:
- Article
Accelerated brain aging towards transcriptional inversion in a zebrafish model of the K115fs mutation of human PSEN2.
- Published in:
- PLoS ONE, 2020, v. 15, n. 1, p. 1, doi. 10.1371/journal.pone.0227258
- By:
- Publication type:
- Article
Alternative splicing in a presenilin 2 variant associated with Alzheimer disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 4, p. 762, doi. 10.1002/acn3.755
- By:
- Publication type:
- Article
Accelerated loss of hypoxia response in zebrafish with familial Alzheimer's disease-like mutation of presenilin 1.
- Published in:
- Human Molecular Genetics, 2020, v. 29, n. 14, p. 2379, doi. 10.1093/hmg/ddaa119
- By:
- Publication type:
- Article
Alzheimer's disease-related peptide PS2V plays ancient, conserved roles in suppression of the unfolded protein response under hypoxia and stimulation of γ-secretase activity.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 13, p. 3662, doi. 10.1093/hmg/ddv110
- By:
- Publication type:
- Article
Differential, dominant activation and inhibition of Notch signalling and APP cleavage by truncations of PSEN1 in human disease.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 602, doi. 10.1093/hmg/ddt448
- By:
- Publication type:
- Article
The evolved divergence of γ-secretase-susceptibility of homologous proteins Ngfrb and Nradd in zebrafish.
- Published in:
- BMC Research Notes, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13104-021-05876-2
- By:
- Publication type:
- Article
Interference with splicing of Presenilin transcripts has potent dominant negative effects on Presenilin activity.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 3, p. 402, doi. 10.1093/hmg/ddm317
- By:
- Publication type:
- Article
Aicardi Syndrome Is a Genetically Heterogeneous Disorder.
- Published in:
- Genes, 2023, v. 14, n. 8, p. 1565, doi. 10.3390/genes14081565
- By:
- Publication type:
- Article
Degenerate codon mixing for PCR‑based manipulation of highly repetitive sequences.
- Published in:
- BMC Research Notes, 2018, v. 11, p. 1, doi. 10.1186/s13104-018-3298-5
- By:
- Publication type:
- Article
The zebrafish orthologue of familial Alzheimer’s disease gene PRESENILIN 2 is required for normal adult melanotic skin pigmentation.
- Published in:
- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0206155
- By:
- Publication type:
- Article
No observed effect on brain vasculature of Alzheimer's disease-related mutations in the zebrafish presenilin 1 gene.
- Published in:
- Molecular Brain, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s13041-021-00734-5
- By:
- Publication type:
- Article
Mitochondrion to endoplasmic reticulum apposition length in zebrafish embryo spinal progenitors is unchanged in response to perturbations associated with Alzheimer’s disease.
- Published in:
- PLoS ONE, 2017, v. 12, n. 6, p. 1, doi. 10.1371/journal.pone.0179859
- By:
- Publication type:
- Article