Publications by authors named "Mark D Robida"

Article Synopsis
  • - The study explores the role of CD8+ tissue-resident memory T cells, specifically those marked by CD103 expression, in suppressing cancer progression and their potential as predictors of immunotherapy response.
  • - Researchers analyzed data from 1,868 cancer patients undergoing treatment with atezolizumab and found evidence that CD103+ T cells are significantly upregulated in inflamed tumors, showcasing important characteristics related to their anti-cancer function.
  • - The results indicate that tracking the presence of CD103+ CD8+ T cells in tumors can help predict which patients are likely to benefit from PD-1/PD-L1 blockade treatments, implying ongoing anti-tumor immune responses are crucial for effective therapy outcomes.
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Background: Recent studies reported abnormal alpha-synuclein deposition in biopsy-accessible sites of the peripheral nervous system in Parkinson's disease (PD). This has considerable implications for clinical diagnosis. Moreover, if deposition occurs early, it may enable tissue diagnosis of prodromal PD.

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African swine fever virus (ASFV) causes an acute hemorrhagic fever in domestic pigs, with high socioeconomic impact. No vaccine is available, limiting options for control. Although live attenuated ASFV can induce up to 100% protection against lethal challenge, little is known of the antigens which induce this protective response.

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Background: Programmed Death Ligand 1 (PD-L1) is an immune modulating protein expressed on the surface of various inflammatory cells, including T Cells, B Cells, dendritic cells, and macrophages. PD-L1 represents an important diagnostic target; expression of PD-L1 on the surface of tumor cells, or within tumor-associated immune cells, is an important predictor of likely response to targeted therapies. In this study, we describe the optimization of immunohistochemistry (IHC) assays using two PD-L1 antibodies (SP263 and E1L3N) and compare the performance of the optimized assays.

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The Drosophila polypyrimidine tract-binding protein (dmPTB or hephaestus) plays an important role during spermatogenesis. The heph2 mutation in this gene results in a specific defect in spermatogenesis, causing aberrant spermatid individualization and male sterility. However, the array of molecular defects in the mutant remains uncharacterized.

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Article Synopsis
  • * A new method using genetic immunization in mice successfully created antibodies targeting 71% of tested membrane proteins, confirming the potential of this DNA-gold micronanoplex technique.
  • * Researchers also developed an easy in vitro method for expressing and capturing membrane proteins to assist in antibody characterization, paving the way for more research on important therapeutic membrane proteins.
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The PIK3CA gene at chromosome 3q26.32 was found to be amplified in up to 45% of patients with squamous cell carcinoma of the lung. The strong correlation between PIK3CA amplification and increased phosphatidylinositol 3-kinase (PI3K) pathway activities suggested that PIK3CA gene copy number is a potential predictive biomarker for PI3K inhibitors.

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The capA gene (FTT0807) from Francisella tularensis subsp. tularensis SCHU S4 encodes a 44.4 kDa integral membrane protein composed of 403 amino acid residues that is part of an apparent operon that encodes at least two other membrane proteins, CapB, and CapC, which together play a critical role in the virulence and pathogenesis of this bacterium.

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Burkholderia are highly evolved Gram-negative bacteria that primarily infect solipeds but are transmitted to humans by ingestion and cutaneous or aerosol exposures. Heightened concern over human infections of Burkholderia mallei and the very closely related species B. pseudomallei is due to the pathogens' proven effectiveness as bioweapons, and to the increased potential for natural opportunistic infections in the growing diabetic and immuno-compromised populations.

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Article Synopsis
  • There is a growing need for affordable and scalable gene assembly technologies to meet the demand for synthetic genes.
  • The authors present a new protocol that allows for high-quality gene assembly directly from low-cost, low-quality microarray-synthesized oligonucleotides, eliminating previous purification steps through hybridization.
  • Testing shows that genes assembled with this new method have comparable quality and performance to those made from more expensive, high-purity oligonucleotides, achieving a cost of about 5¢ per base.
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A new method for biolistic delivery of nucleic acids using a combination of cationic micro- and nanoparticles is reported. The new method is simpler to perform than the conventional calcium/spermidine-based formulations and shows 11-fold improved nucleic acid binding capacity and dose-dependent performance both for in vitro and in vivo applications relative to either the conventional preparation or our recently reported direct cationic microparticle method. These features may enable higher throughput gene delivery and genetic immunization programs and open new venues for the biolistic delivery method.

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Background: Alternative splicing plays an important role in generating molecular and functional diversity in multi-cellular organisms. RNA binding proteins play crucial roles in modulating splice site choice. The majority of known binding sites for regulatory proteins are short, degenerate consensus sequences that occur frequently throughout the genome.

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The Drosophila master sex-switch protein Sex-lethal (SXL) regulates the splicing and/or translation of three known targets to mediate somatic sexual differentiation. Genetic studies suggest that additional target(s) of SXL exist, particularly in the female germline. Surprisingly, our detailed molecular characterization of a new potential target of SXL, enhancer of rudimentary (e(r)), reveals that SXL regulates e(r) by a novel mechanism--polyadenylation switching--specifically in the female germline.

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Control of gene expression in chloroplasts is critically dependent upon post-transcriptional mechanisms, most of which require formation of RNA-protein complexes. The 5' untranslated regions (5'UTRs) of chloroplast mRNAs have been shown to affect stability and/or translation of the message. These effects are mediated by the binding of specific protein(s) to the 5'UTR.

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The mammalian polypyrimidine-tract binding protein (PTB), which is a heterogeneous ribonucleoprotein, is ubiquitously expressed. Unexpectedly, we found that, in Drosophila melanogaster, the abundant PTB transcript is present only in males (third instar larval, pupal and adult stages) and in adult flies is restricted to the germline. Most importantly, a signal from the somatic sex-determination pathway that is dependent on the male-specific isoform of the doublesex protein (DSX(M)) regulates PTB, providing evidence for the necessity of soma-germline communication in the differentiation of the male germline.

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Gene expression in chloroplasts is strongly regulated at the post-transcriptional level. Most post-transcriptional mechanisms require RNA-protein complexes. Here we report an analysis of RNA-protein complexes that form in the 5' untranslated regions (5'UTRs) of spinach chloroplast mRNAs.

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Synopsis of recent research by authors named "Mark D Robida"

  • - Mark D Robida's research primarily focuses on immunology, particularly the role of T cells and immune responses in cancer treatment, as demonstrated in his study on CD103+ CD8+ T cells which predicts responses to PD-L1 blockade in lung and bladder cancers.
  • - He also explores neurological aspects related to alpha-synuclein in skin biopsies for diagnosing Parkinson's disease, emphasizing the potential for early detection through peripheral nervous system analysis.
  • - Additionally, Robida investigates viral immunogenicity, notably in the context of African swine fever virus and the generation of antibodies against membrane proteins, showcasing applications in both animal health and biothreat mitigation.