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UnknownDelivery of seasonal malaria chemoprevention with enhanced infection prevention and control measures during the COVID-19 pandemic in Nigeria, Burkina Faso and Chad: a cross-sectional study.
Not available
S-EPMC8943494 | biostudies-literature
UnknownChad Genetic Diversity Reveals an African History Marked by Multiple Holocene Eurasian Migrations.
Not available
S-EPMC5142112 | biostudies-literature
UnknownAfrican 1, an epidemiologically important clonal complex of Mycobacterium bovis dominant in Mali, Nigeria, Cameroon, and Chad.
Not available
S-EPMC2648362 | biostudies-literature
TranscriptomicsA sumoylation-dependent transcriptional subprogram is required for Myc-driven tumorigenesis
Myc is an oncogenic transcription factor frequently dysregulated in human cancer. To identify pathways supporting the Myc oncogenic program, we employed a genome-wide RNAi screen for Myc-synthetic-lethal (MySL) genes and uncovered a role for the SUMO-activating-enzyme (SAE1/2). Loss of SAE1/2 enzyma...
ORGANISM(S): Homo sapiens 
2011-12-08 | E-GEOD-34055 | biostudies-arrayexpress
UnknownAfrican 2, a clonal complex of Mycobacterium bovis epidemiologically important in East Africa.
Not available
S-EPMC3021238 | biostudies-literature
TranscriptomicsTranscription profiling of DBA/1J mouse with collagen induced arthritis
Time course of collagen-induced arthritis in DBA/1J male mice, synchronized on day 28 with 10ug LPS
ORGANISM(S): Mus musculus 
2009-11-16 | E-TABM-661 | biostudies-arrayexpress
GenomicsGenetic Analysis of Limb Malformation Disorders: Miller Syndrome Sequencing Study (LMD-MS)

The overall goal of this project is to investigate the etiology and pathogenesis of malformations (i.e., birth defects) of the limb, concentrating on abnormalities of limb patterning such as limb deficiency/duplications and multiple congenital contractures.

The exome sequences of two s...

phs000244.v1.p1 | EGA
GenomicsChildren's Hospital of Philadelphia (CHOP) Control Copy Number Variation (CNV) Study

We present a database of copy number variations (CNVs) detected in 2,026 disease-free individuals, using high-density, SNP-based oligonucleotide microarrays. This large cohort analyzed for CNVs in a single study using a uniform array platform and computational tools, comprises mainly of Cau...

phs000199.v1.p1 | EGA
UnknownPrognostic value of CD103+ tumor-infiltrating lymphocytes and programmed death ligand-1 (PD-L1) combined positive score in recurrent laryngeal squamous cell carcinoma.
Not available
S-EPMC10099383 | biostudies-literature
UnknownGenetics Navigator: protocol for a mixed methods randomized controlled trial evaluating a digital platform to deliver genomic services in Canadian pediatric and adult populations.
Not available
S-EPMC11407190 | biostudies-literature
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