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TranscriptomicsIdentification of differentially expressed genes in Sfmbt1-knockdown C2C12 myoblasts
Gene expression profiling was performed to identify Sfmbt1-dependent regulation in myogenic programs. To establish the magnitude of the Sfmbt1 effect on muscle cells, we have compared gene expression profiles of C2C12 cells transduced with lentiviruses expressing scramble shRNA control or shSfmbt1. ...
ORGANISM(S): Mus musculus 
2013-01-28 | E-GEOD-24346 | biostudies-arrayexpress
MetabolomicsHyocholic acid species as novel biomarkers for metabolic disorders
Hyocholic acid (HCA) is a major bile acid (BA) species in the BA pool of pigs, a species known for its exceptional resistance to spontaneous development of diabetic phenotypes. HCA and its derivatives are also present in human blood and urine. We investigate whether human HCA profiles can predict th...
2021-10-06 | MTBLS2343 | MetaboLights
ModelsLiu1999_PulsatileSecretion
This a model from the article: A dynamical model for the pubsatile secretion of the hypothalamo-pituitary-adrenal axis. Yi-wei Liu, Zhi-Hong Hu, Jian-Hua Peng and Bing-Zheng Liu Mathematical and Computer Modelling Volume 29, Issue 4, February 1999, Pag...
2005-01-01 | MODEL1006230060 | BioModels
TranscriptomicsIdentification of CRTC1-MAML2 fusion oncogene-regulated transcriptional program in H3118 cells
Mucoepidermoid carcinomas (MEC) is the most common salivary gland malignancy. To date, advanced and nonresectable MEC have poor prognosis and no effective treatment. The CRTC1-MAML2 fusion oncogene, which is associated with more than 50% of MEC, consists of the N-terminal CREB-binding domain of the...
ORGANISM(S): Homo sapiens 
2014-04-21 | E-GEOD-46580 | biostudies-arrayexpress
UnknownClinical Characteristics of Coronavirus Disease 2019 in China.
Not available
S-EPMC7092819 | biostudies-literature
UnknownGenotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: a meta-analysis of genome-wide association studies.
Not available
S-EPMC3315211 | biostudies-literature
UnknownThe functional spectrum of low-frequency coding variation.
Not available
S-EPMC3308047 | biostudies-literature
UnknownDemographic history and rare allele sharing among human populations.
Not available
S-EPMC3142009 | biostudies-literature
UnknownDiversity of human copy number variation and multicopy genes.
Not available
S-EPMC3020103 | biostudies-literature
UnknownThe 1000 Genomes Project: data management and community access.
Not available
S-EPMC3340611 | biostudies-literature
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