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Paulina Carmona-Mora
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Paulina Carmona-Mora
Home
Research
Publications
Science Leadership Program LAC
Global engagement
Blog
Media
More
Home
Research
Publications
Science Leadership Program LAC
Global engagement
Blog
Media
New preprint:
A customizable secure DIY web application for accessing, sharing, and browsing aggregate experimental results and metadata.
Monocyte, neutrophil, and whole blood transcriptome dynamics following ischemic stroke - BMC Medicine
Early peripheral blood gene expression associated with good and poor 90-day ischemic stroke outcomes - Journal of Neuroinflammation
Distinct peripheral blood monocyte and neutrophil transcriptional programs following intracerebral hemorrhage and different etiologies of ischemic stroke - PubMed
Mitigating losses: how scientific organisations can help address the impact of the COVID-19 pandemic on early-career researchers - Humanities and Social Sciences Communications
Diverse Molecular Mechanisms Contribute to Differential Expression of Human Duplicated Genes
Call to Action: Supporting Latin American Early Career Researchers on the Quest for Sustainable Development in the Region
Creating New Opportunities for Genomics in Central Asia
Integrative Modeling and Novel Technologies in Human Genomics
The nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulation - Human Genetics
RAI1 Transcription Factor Activity Is Impaired in Mutants Associated with Smith-Magenis Syndrome
Functional and cellular characterization of human Retinoic Acid Induced 1 (RAI1) mutations associated with Smith-Magenis Syndrome - BMC Molecular Biology
Retinoic Acid Induced 1, RAI1: A Dosage Sensitive Gene Related to Neurobehavioral Alterations Including Autistic Behavior
Genetic variation contributes to gene expression response in ischemic stroke: an eQTL study
Gene expression changes implicate specific peripheral immune responses to Deep and Lobar Intracerebral Hemorrhages in humans
Syntaxins 6 and 8 facilitate tau into secretory pathways
RNA-Seq analysis of Gtf2ird1 knockout epidermal tissue provides potential insights into molecular mechanisms underpinning Williams-Beuren syndrome - BMC Genomics
Correct developmental expression level of Rai1 in forebrain neurons is required for control of body weight, activity levels and learning and memory
Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome - European Journal of Human Genetics
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Podocyte-Specific Overexpression of Wild Type or Mutant Trpc6 in Mice Is Sufficient to Cause Glomerular Disease
Mouse Models of Genomic Syndromes as Tools for Understanding the Basis of Complex Traits: An Example with the Smith-Magenis and the Potocki-Lupski Syndromes
Abnormal social behaviors and altered gene expression rates in a mouse model for Potocki-Lupski syndrome
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