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GenomicsGenome-wide binding profiles of an artificial zinc finger protein with or without a KLF3 functional domain
Transcription factors are often regarded as having two distinct components: a DNA binding domain (DBD) to allow binding to the regulatory region of a target gene and a trans-acting functional domain (FD) to modulate gene expression. Recently, it is becoming clear that the DBDs of transcription facto...
ORGANISM(S): Homo sapiens 
2016-01-05 | E-GEOD-69739 | biostudies-arrayexpress
UnknownActin filament assembly by bacterial factors VopL/F: Which end is up?
Not available
S-EPMC5412575 | biostudies-literature
UnknownSTRling: a k-mer counting approach that detects short tandem repeat expansions at known and novel loci.
Not available
S-EPMC9753380 | biostudies-literature
UnknownThe relationship between synaptic density marker SV2A, glutamate and N-acetyl aspartate levels in healthy volunteers and schizophrenia: a multimodal PET and magnetic resonance spectroscopy brain imaging study.
Not available
S-EPMC8290006 | biostudies-literature
MetabolomicsGNPS - greene_MauiCoralTissueMetabolomes
Coral tissue samples from the islands of Maui and Hawai'i collected by Dr. Austin Greene and Dr. Megan J. Donahue at the Hawai'i Institute of Marine Biology, University of Hawai'i at Manoa. Samples were collected from both Porites lobata and Montipora capitata.
ORGANISM(S): Montipora Capitata (ncbitaxon:46704) Porites Lobata (ncbitaxon:104759) 
2024-07-02 | MSV000095217 | GNPS
UnknownA role of glypican4 and wnt5b in chondrocyte stacking underlying craniofacial cartilage morphogenesis.
Not available
S-EPMC4679431 | biostudies-literature
UnknownThe genetic landscape of crystallins in congenital cataract.
Not available
S-EPMC7691105 | biostudies-literature
ProteomicsTwo siblings with strong NER inactivation due to inherited ERCC1 deficiency display mild clinical features of XP and CS with severe liver impairment
The ERCC1-XPF heterodimer is a multifunctional endonuclease involved in nucleotide excision repair (NER), inter-strand crosslink (ICL) repair, and DNA double-strand break (DSB) repair. Only two patients with inherited ERCC1 defects have been reported who both died at an early age. Here, we describe ...
ORGANISM(S): Homo sapiens (Human) 
2021-01-26 | PXD017940 | Pride
Nucleotide excission repair Ercc1 Cockayne syndrome Xeroderma pigmentosum 
TranscriptomicsATAC-seq of Mus musculus embryonic cell types in response to Pbx1 knockout
ATAC-seq was performed, mapped, and analyzed as previously described (PMID: 34446717: \\"ATAC-seq was performed on 50,000 cells per replicate as described in Buenrostro et al. (with modifications based on Corces et al.), on EpiSCs and PSM-differentiated cell populations at desired time-points. Libra...
ORGANISM(S): Mus musculus 
2023-12-01 | E-MTAB-13407 | biostudies-arrayexpress
UnknownExamination of the Interpersonal Model With Adolescent Military Dependents at High Risk for Adult Obesity.
Not available
S-EPMC7286799 | biostudies-literature
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