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The complete sequence of a human Y chromosome
Recombination between heterologous human acrocentric chromosomes
Myc promotes polyploidy in murine trophoblast cells and suppresses senescence
Semi-automated assembly of high-quality diploid human reference genomes
Mediator recruits the cohesin loader Scc2 to RNA Pol II transcribed genes and promotes sister chromatid cohesion
Complete genomic and epigenetic maps of human centromeres
The complete sequence of a human genome
From telomere to telomere: The transcriptional and epigenetic state of human repeat elements
Maternal Smc3 protects the integrity of the zygotic genome through DNA replication and mitosis
PCR amplicons to determine human centromeric array copy number reveal wide-spread size variation and instability in cancer
Immature Follicular Origins and Disrupted Oocyte Growth Pathways Contribute to Decreased Gamete Quality During Reproductive Juvenescence in Mice
The structure, function and evolution of a complete human chromosome 8
DNA replication, transcription, and H3K56 acetylation regulate copy number and stability at tandem repeats
Protocol for mouse trophoblast stem cell isolation, differentiation and cytokine detection
Origins and evolutionary patterns of the 1.688 satellite DNA family in Drosophila phylogeny
Telomere-to-telomere assembly of a complete human X chromosome
Persistent DNA damage and senescense in the placenta impacts developmental outcomes of embryos
Super-resolution microscopy reveals linkages between ribosomal DNA on heterologous chromosomes
The stoichiometry of the outer kinetochore is modulated by microtubule-proximal regulatory factors
Oocyte-specific deletion of Hdac8 in mice reveals stage-specific effects on fertility
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Nucleolar Organizer Regions as transcription-based scaffolds of nucleolar structure and function
Faulty ribosome biogenesis underlies the ANE syndrome ribosomopathy
Cornelia de Lange syndrome, related disorders, and the Cohesin complex: Abstracts from the 8th biennial scientific and educational symposium 2018
Ribosomal DNA and the nucleolus in the context of genome organization
Ribosomal DNA instability and genome adaptability
Ribosomal DNA-connecting ribosome biogenesis and chromosome biology
A transcription factor primes the condensin pump
Regulation of kinetochore configuration during mitosis
Mammalian oogenesis and female reproductive aging
Taking cohesin and condensin in context
Using fluorescent reporters in conjunction with cytometry and statistics to assess nuclear accumulation of ribosomal proteins
Cohesin and human disease: lessons from mouse models.
Etiology and pathogenesis of the cohesinopathies.
The SMC loader Scc2 regulates gene expression.
Roberts Syndrome: A deficit in acetylated cohesin leads to nucleolar dysfunction.
Translational mechanisms at work in the cohesinopathies.
The dynamics of the Cse4 chaperone Scm3.
Spc25 - How the kinetochore protein plays during oocyte meiosis.
Cse4 gets a kiss-of-death from Psh1.
Cohesinopathies, gene expression, and chromatin organization.
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