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Items: 1 to 20 of 29

1.

Cytomegalovirus vaccine vector-induced effector memory CD4+ T cells protect cynomolgus macaques from lethal aerosolized heterologous avian influenza

(Submitter supplied) To investigate the transcriptional response in whole blood from administration of the Cytomegolovirus vaccine vector against heterologous avian flu
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
84 Samples
Download data: CSV
Series
Accession:
GSE268204
ID:
200268204
2.

Cynomolgus macaques as a translational model of human immune responses to yellow fever 17D vaccination

(Submitter supplied) The non-human primate (NHP) model (specifically rhesus and cynomolgus macaques) has facilitated our understanding of the pathogenic mechanisms of yellow fever (YF) disease and allowed evaluation of safety and efficacy of YF-17D vaccines. However, the accuracy of this model in mimicking vaccine-induced immunity in humans remains to be fully determined. We used a system biology approach to compare hematological, biochemical, transcriptomic, innate and antibody-mediated immune responses in cynomolgus macaques and human participants following YF-17D vaccination. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
81 Samples
Download data: TXT
Series
Accession:
GSE253538
ID:
200253538
3.

Cell-mediated Immune Response Signature to AAV Capsid in Cynomolgus Monkeys

(Submitter supplied) Cell-mediated immune (CMI) responses to adeno-associated virus (AAV) can lead to both tissue damage and loss of therapeutic transgene expression. Identifying robust biomarkers of CMI and understanding CMI mechanisms can be help to helpful in clinical practice and in advancement of AAV gene therapies. The present work evaluated PBMCs from non-human primates (NHP) before and 14 days following immunization with AAV9 capsid. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
102 Samples
Download data: TXT
Series
Accession:
GSE256418
ID:
200256418
4.

Characterization of early transcriptomic changes associated with hepatitis B virus exposure in human and macaque immune cell populations

(Submitter supplied) Chronic hepatitis B virus (HBV) infection affects close to 300 million individuals worldwide, representing one of the major etiological factors for the development of cirrhosis and hepatocellular carcinoma (HCC). At the molecular level, the mechanisms behind chronic HBV infection are based on the persistence of the viral genome as an episomal structure termed covalently closed circular DNA (cccDNA), and the evasion of both innate and adaptive immune responses. more...
Organism:
Homo sapiens; Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL18573 GPL22523
90 Samples
Download data: CSV
Series
Accession:
GSE223073
ID:
200223073
5.

Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca fascicularis; Homo sapiens
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
4 related Platforms
47 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE216206
ID:
200216206
6.

Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys (RNA-Seq II)

(Submitter supplied) Human in vitro oogenesis provides a framework for clarifying the mechanism of human oogenesis. To create its benchmark, it is vital to promote in vitro oogenesis using a model physiologically close to humans. Here, we establish a foundation for in vitro oogenesis in cynomolgus (cy) monkeys (Macaca fascicularis): cy female embryonic stem cells harboring one active and one inactive X chromosome (Xa and Xi, respectively) differentiate robustly into primordial germ cell-like cells, which in xenogeneic reconstituted ovaries develop efficiently into oogonia and, remarkably, further into meiotic oocytes at the zygotene stage. more...
Organism:
Macaca fascicularis; Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22523 GPL18573
23 Samples
Download data: TXT
Series
Accession:
GSE216205
ID:
200216205
7.

Induction of fetal meiotic oocytes from embryonic stem cells in cynomolgus monkeys ( RNA-Seq I )

(Submitter supplied) Human in vitro oogenesis provides a framework for clarifying the mechanism of human oogenesis. To create its benchmark, it is vital to promote in vitro oogenesis using a model physiologically close to humans. Here, we establish a foundation for in vitro oogenesis in cynomolgus (cy) monkeys (Macaca fascicularis): cy female embryonic stem cells harboring one active and one inactive X chromosome (Xa and Xi, respectively) differentiate robustly into primordial germ cell-like cells, which in xenogeneic reconstituted ovaries develop efficiently into oogonia and, remarkably, further into meiotic oocytes at the zygotene stage. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
8 Samples
Download data: TXT
Series
Accession:
GSE216204
ID:
200216204
8.

Rapid protection induced by a single-shot Lassa vaccine in cynomolgus monkeys

(Submitter supplied) Lassa fever outbreaks hit West African countries every year and there is still no licensed vaccine to limit the burden of this viral hemorrhagic fever. We previously developed MeV-NP, a single-shot vaccine that induces protective immunity in cynomolgus monkeys one month or more than a year before Lassa virus infection and that is able to protect against divergent viral strains. Given the limited dissemination area of Lassa virus during outbreaks and the high risk of nosocomial transmission, a vaccine that induces rapid protection could be useful to protect exposed people during outbreaks in the absence of preventive vaccination. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
51 Samples
Download data: CSV
Series
Accession:
GSE225258
ID:
200225258
9.

Evaluation of safety and immuno-efficacy of a next generation live attenuated yellow fever vaccine in cynomolgus macaques

(Submitter supplied) 36 male NHPs were randomized into groups of nine to receive subcutaneous injection in the deltoid muscle region of the upper arm with a single commercial dose of Stamaril (4 LogCCID50) or YF-VAX (6 LogCCID50), or 4 or 5 LogCCID50 vYF at WSL stage. Nine months after vaccination, NHPs along with six additional unvaccinated controls were challenged by a single sub-cutaneous injection of 3.0 LogCCID50 wild-type YFV Asibi strain in the scapula region. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
164 Samples
Download data: CSV
Series
Accession:
GSE222229
ID:
200222229
10.

Cytomegalovirus Vaccine-induced Unconventional T cell Priming and Protection against SIV Replication is Conserved Between Primate Species

(Submitter supplied) Bulk RNA Sequencing of Mauritian cynomolgus macaque (MCM) whole blood pre- and post-vaccination with CyCMV/SIV
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
80 Samples
Download data: CSV
Series
Accession:
GSE205080
ID:
200205080
11.

Meso-Seq for in-depth transcriptomics in ultra-low amounts of FACS-purified neuronal nuclei

(Submitter supplied) Profiling of gene expression in sparse populations of genetically defined neurons is essential for dissecting the molecular mechanisms that control the development and plasticity of neural circuits. However, current transcriptomic approaches are ill suited for detailed mechanistic studies in sparse neuronal populations, as they either are technically complex and relatively expensive (e.g., single-cell RNA sequencing [RNA-seq]) or require large amounts of input material (e.g., traditional bulk RNA-seq). more...
Organism:
Macaca fascicularis; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22523 GPL19057
80 Samples
Download data: CSV
Series
Accession:
GSE185221
ID:
200185221
12.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys [sc3seq_macfas]

(Submitter supplied) In vitro oogenesis is key to elucidating the mechanism of human female germ-cell development and its anomalies. Accordingly, pluripotent stem cells have been induced into primordial germ cell-like cells and into oogonia with epigenetic reprogramming, yet further reconstitutions remain a challenge. Here, we demonstrate ex vivo reconstitution of fetal oocyte development in both humans and cynomolgus monkeys (Macaca fascicularis). more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
153 Samples
Download data: TXT
Series
Accession:
GSE195989
ID:
200195989
13.

Ex vivo reconstitution of fetal oocyte development in humans and cynomolgus monkeys

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Mus musculus; Macaca fascicularis
Type:
Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing
5 related Platforms
320 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE194266
ID:
200194266
14.

The X-chromosome dosage compensation program during the development of cynomolgus monkeys

(Submitter supplied) X-chromosome dosage compensation ensures balanced gene dosage between the X chromosome and autosomes and between the sexes, involving divergent mechanisms among mammals. We elucidated a distinct mechanism for X-chromosome inactivation (XCI) in cynomolgus monkeys, a model for human development. The trophectoderm and cytotrophoblast acquire XCI around implantation through an active intermediate bearing repressive modifications and compacted structure, whereas the amnion, epiblast, and hypoblast maintain such an intermediate protractedly, attaining XCI by a week after implantation. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL27448 GPL22523 GPL19944
195 Samples
Download data: TXT
Series
Accession:
GSE151149
ID:
200151149
15.

The embryonic ontogeny of the gonadal somatic cells in mice and monkeys

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Mus musculus; Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22523 GPL19057
156 Samples
Download data: MTX, TSV, TXT
Series
Accession:
GSE160050
ID:
200160050
16.

The embryonic ontogeny of the gonadal somatic cells in mice and monkeys [sc3seq]

(Submitter supplied) In the early fetal stage, the gonads are bipotent and only later become the ovary or testis, depending on the genetic sex. Despite many studies examining how sex determination occurs from biopotential gonads, the spatial and temporal organization of bipotential gonads and their progenitors is poorly understood. Here, using lineage tracing in mice, we find that the gonads originate from a T+ primitive streak through WT1+ posterior intermediate mesoderm and appear to share origins anteriorly with the adrenal glands and posteriorly with the metanephric mesenchyme. more...
Organism:
Mus musculus; Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19057 GPL22523
152 Samples
Download data: TXT
Series
Accession:
GSE160049
ID:
200160049
17.

The embryonic ontogeny of the gonadal somatic cells in mice and monkeys [10x]

(Submitter supplied) In the early fetal stage, the gonads are bipotent and only later become the ovary or testis, depending on the genetic sex. Despite many studies examining how sex determination occurs from biopotential gonads, the spatial and temporal organization of bipotential gonads and their progenitors is poorly understood. Here, using lineage tracing in mice, we find that the gonads originate from a T+ primitive streak through WT1+ posterior intermediate mesoderm and appear to share origins anteriorly with the adrenal glands and posteriorly with the metanephric mesenchyme. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL22523
4 Samples
Download data: MTX, TSV
Series
Accession:
GSE160043
ID:
200160043
18.

RNA sequence of PBMCs of macaques infected with SARS-CoV-2

(Submitter supplied) The goals of this study are to analyze immune response of host against SARS-CoV-2 using PBMCs trascriptome
Organism:
Macaca fascicularis; Macaca mulatta
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL22523 GPL21120
16 Samples
Download data: TXT
Series
Accession:
GSE152439
ID:
200152439
19.

Induction of the Germ-Cell Fate from Pluripotent Stem Cells in Cynomolgus Monkeys

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Macaca fascicularis; Mus musculus
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19944 GPL15907 GPL22523
647 Samples
Download data
Series
Accession:
GSE134010
ID:
200134010
20.

Induction of the Germ-Cell Fate from Pluripotent Stem Cells in Cynomolgus Monkeys [scRNA-Seq]

(Submitter supplied) In vitro reconstitution of germ-cell development from pluripotent stem cells (PSCs) has created key opportunities to explore the fundamental mechanisms underlying germ-cell development, particularly in mice and humans. Importantly, such investigations have clarified critical species differences in the mechanisms regulating mouse and human germ-cell development, highlighting the necessity of establishing an in vitro germ-cell development system in other mammals, such as non-human primates. more...
Organism:
Macaca fascicularis
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL19944 GPL22523
605 Samples
Download data: TXT
Series
Accession:
GSE134009
ID:
200134009
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