Aller au contenu principal
Profil bibliographique

Devi Krishna Priya Karunakaran

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

23Publications signalées
96Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Single-cell and spatial transcriptomicsRetinal Development and DisordersRNA Research and SplicingGenomics and Chromatin DynamicsEpigenetics and DNA Methylation

Les publications récentes

Accès ouvert 2025 article OpenAlex

The UNC5C T835M mutation associated with Alzheimer’s disease leads to neurodegeneration involving oxidative stress and hippocampal atrophy in aged mice

Devi Krishna Priya Karunakaran, Makenna Ley, Ammaarah Khatri, Katherine R. Sadleir et autres

Abstract Alzheimer’s disease (AD) is characterized by amyloid plaques, neurofibrillary tangles, and synaptic and neuronal loss. Recently, a rare autosomal dominant coding mutation, T835M, in the Un-coordinated 5c (UNC5C) netrin receptor gene was segregated with late-onset AD (LOAD). Overexpression of T835M in …

us, it (code pays fourni par la source)

4 citations Molecular Neurodegeneration
Accès ouvert 2025 article OpenAlex

Annexin A6 membrane repair protein protects against amyloid-induced dystrophic neurites and tau phosphorylation in Alzheimer’s disease model mice

Katherine R. Sadleir, Karen Gómez, A. Edwards, Makenna Ley et autres

In Alzheimer's disease, accumulation of amyloid-β (Aβ) peptide is thought to cause formation of neurofibrillary tangles composed of hyperphosphorylated tau protein, which correlates with neuronal loss and cognitive impairment, but the mechanism linking Aβ and tau pathologies is unknown. Dystrophic neurites, which …

us (code pays fourni par la source)

14 citations Acta Neuropathologica
2018 article OpenAlex

P1‐163: MOLECULAR MECHANISMS OF THE ALZHEIMER'S RISK GENE UNC5C IN NEURONAL DEATH

Devi Krishna Priya Karunakaran, Katherine R. Sadleir, Shahrnaz Kemal, Leah K. Cuddy et autres

Alzheimer's disease (AD) is characterized by amyloid plaques, neurofibrillary tangles, and synaptic and neuronal loss. The mechanism of neuron death in AD, however, remains unexplored. Recently, a rare autosomal dominant coding mutation, T835M, was discovered in the Un-coordinated 5c (Unc5c) netrin receptor …

us (code pays fourni par la source)

0 citations Alzheimer s & Dementia
Accès ouvert 2016 article OpenAlex

Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

BACKGROUND: The retina as a model system with extensive information on genes involved in development/maintenance is of great value for investigations employing deep sequencing to capture transcriptome change over time. This in turn could enable us to find patterns in gene expression …

us, nl (code pays fourni par la source)

6 citations BMC Genomics
Accès ouvert 2016 dataset OpenAlex

Additional file 6: Table S5. of Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

DE based analysis results for static and temporal comparisons. DE based analyses for static (P21WT vs. P21KO) (S5.1) and temporal (P0 vs. P21WT and P0 vs. P21KO) comparisons (S5.2, S5.3). (XLSX 4196 kb)

0 citations Figshare
Accès ouvert 2016 dataset OpenAlex

Additional file 7: Table S6. of Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

DAVID analysis output of DE based analyses for static and temporal comparisons. Results of DAVID analysis based on DE genes for P0 vs. P21WT (S6.1), P0 vs. P21KO (S6.2), and P21WT vs. P21KO (S6.3) comparisons. (XLSX 41 kb)

0 citations Figshare
Accès ouvert 2016 dataset OpenAlex

Additional file 2: Table S1. of Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

Output of Binning in E16CE – P0CE and P0CE –P0NE comparisons. Custom bioinformatics pipeline and binning of E16CE - P0CE and P0CE-P0NE comparisons at the gene level (S1.1, S1.3) and isoform level (S1.2, S1.4) as discussed in the strategy in Fig. 1c. …

0 citations Figshare
Accès ouvert 2016 dataset OpenAlex

Additional file 5: Table S4. of Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

Binning results in P21-Nrl-WT vs. P21-Nrl-KO, P0 vs. P21-Nrl-WT and P0 vs. P21-Nrl-KO comparisons. Custom bioinformatics pipeline and binning of P21-Nrl-WT vs. P21-Nrl-KO (S4.1), P0 (P0CE + P0NE) vs. P21WTcomparison (S4.2) and P0 (P0CE + P0NE) vs. P21KO comparison (S4.3). (XLSX 4018 …

0 citations Figshare
Accès ouvert 2016 dataset OpenAlex

Additional file 3: Table S2. of Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development

Devi Krishna Priya Karunakaran, Sahar Al Seesi, Abdul Rouf Banday, Marybeth Baumgartner et autres

DAVID analysis output for static and temporal comparisons. DAVID output for genes belonging to bins in E16CE-P0CE comparison (S2.1), P0CE-P0NE comparison (S2.2), P0 vs. P21-Nrl-WT comparison (S2.3),P0 vs. P21-Nrl-KO comparison (S2.4) and P21-Nrl-WT vs. P21-Nrl-KO comparison (S2.5). (XLSX 140 kb)

0 citations Figshare

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.