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NYU Dataset
Human Oral Microbiota Composition Data from UAE Healthy Future Study (UAEHFS) Pilot Participants
- Authors
- Yvonne VallèsClaire K. InmanBrandilyn A. PetersRaghib Ali24 more author(s)...
- Description
This dataset includes 330 Emirati adults participating in the UAE Healthy Future Study-Pilot (UAEHFS-pilot) who provided mouthwash samples. There were 225 non-smokers and 105 smokers who used cigarettes, dokha, shisha, or a combination of tobacco products. 101 of the 105 smokers were male. Tobacco use and frequency were assessed with a structured questionnaire and urine cotinine lab results. Gene...
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Health StatusRisk Factors
- Access Rights
- Free to AllApplication Required
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NYU Dataset
ORF2p Eludes Detection in Mass Spectrometry-Based Tumor Proteome Profiling
- Authors
- Daniel ArdeljanXuya WangMehrnoosh OghbaieMartin S. Taylor15 more author(s)...
- Description
This study showed that long interspersed element-1 (LINE-1) ORF2p expression is almost undetectable in human cancers. LINE-1 is the major driver of mobile DNA activity in humans. When expressed, LINE-1 loci produce bicistronic transcripts encoding two proteins essential for retrotransposition, ORF1p and ORF2p. ORF2p expression is not well characterized in human tissues and cell lines. For the study,...
- Subject
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GenomicsProteomics
- Access Rights
- Free to All
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NYU Dataset
Transposon Insertion Profiling by Sequencing (TIPseq) Utilized for LINE-1 Mapping in Single Cells
- Authors
- Wilson McKerrowZuojian TangJared P. SterankaLindsay M. Payer5 more author(s)...
- Description
This dataset was compiled to determine a genome-wide long interspersed element-1 (LINE-1) insertion site mapping method for bulk DNA. This study has shown that transposon insertion profiling by sequencing (TIPseq) is a method that can be used for LINE-1 mapping in single cells. For the study, live GM12878 lymphoblastoid cells were obtained from Coriell Institute for Medical Research. The dataset contains...
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Genomics
- Access Rights
- Free to All
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NYU Dataset
Genetic Sequencing Data Characterized Genetic Etiology of Craniofacial Microsomia
- Authors
- Andrew T. TimberlakeCasey GriffinCarrie L. HeikeAnne V. Hing25 more author(s)...
- Description
This dataset was collected to study the genetic cause of craniofacial microsomia (CFM), which is the second most common congenital facial anomaly. In this study, they performed whole exome or genome sequencing of 146 kindreds with sporadic or familial CFM. Blood or saliva samples were collected from the proband and DNA was extracted from blood and saliva using standard procedures. This resulted in...
- Subject
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Genomics
- Access Rights
- Free to All
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NYU Dataset
Whole Exome Sequencing Confirmed Progression of Smoldering Multiple Myeloma to Multiple Myeloma
- Authors
- Eileen M. BoyleShayu DeshpandeRuslana TytarenkoCody Ashby19 more author(s)...
- Description
Smoldering multiple myeloma (SMM) is an asymptomatic plasma cell disorder. It is associated with a high-risk of progression to multiple myeloma (MM). For this study, they performed targeted sequencing on 82 patients. The results showed fewer NRAS and FAM46C mutations with SMM, which is consistent with their role as drivers of the transition to MM. They also analyzed the change in clonal structure over...
- Subject
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CancerGenomics
- Access Rights
- Free to AllAuthor Approval Required
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Generation R
- Authors
- Vincent W. V. JaddoeGeneration R Study Group
- Description
Generation R is an ongoing prospective cohort study of child development from the prenatal period through young adulthood in a multi-ethnic population recruited from the Rotterdam, Netherlands metropolitan area. The study enrolled 9,778 mothers with a delivery date between April 2002 and January 2006; they had 9,749 live births. The primary objective of the study is to identify early environmental...
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- Author Approval Required
- Local Expert
- Akhgar Ghassabian
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NYU Dataset
NOGOB Receptor Deficiency Increases Cerebrovascular Permeability and Hemorrhage
- Authors
- Zhi FangXiaoran SunXiang WangJi Ma6 more author(s)...
- Description
Cerebral cavernous malformation (CCM) lesions are caused by loss of function of CCM genes. Previous study showed that NOGOB receptor (NGBR) knockout in endothelial cells (ECs) results in cerebrovascular lesions in the mouse embryo. However, the molecular mechanism by which NGBR regulates CCM1/2 expression has not been explained. This study revealed that genetic depletion of NGBR in ECs results in CCM1/2...
- Subject
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Genomics
- Access Rights
- Free to All