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Full text 2026

Reduced immunogenicity of MYC amplified, metastatic prostate cancer

Kahlon S, Barker VR, Varkhedi M, et al.

<h4>Objectives</h4>Through a genomics-based approach analyzing gene expression levels and adaptive immune receptor recombinations, we sought to determine whether MYC amplification was associated with a worse outcome and reduced immunogenicity.<h4>Methods</h4>MYC copy numbers and the presence of …

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Structural Variants Transcriptomics
Full text 2026

Systematic Methods to Resolve Lineage-Specific Stress States in Early Mammalian Embryos and That May Enable Miscarriage Prediction

Ruden XL, Coddington C, Asplund L, et al.

Early mammalian embryos are highly sensitive to environmental, metabolic, hormonal, and genomic stress, yet embryo assessment during <b>I</b>n <b>V</b>itro <b>F</b>ertilization (<b>IVF)</b> relies largely on morphology and ploidy for embryo assessment, but these tests incompletely predict …

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Transcriptomics
Full text 2026

Chromatin-Remodeling Factor CHR5 Promotes Defense Gene Expression and SA Accumulation

Liu X, Cui N, Gong Z, et al.

Chromatin remodelers play essential roles in modulating nucleosome structure and enabling dynamic transcriptional control. Arabidopsis calmodulin-binding transcription activators CAMTA1/2/3 negatively regulate plant immunity by suppressing the expression of biosynthesis genes of major defence hormones salicylic …

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Epigenetics Transcriptomics
Full text 2025

Growth in biofilms prepares &lt;i&gt;Mycobacterium avium&lt;/i&gt; subsp. &lt;i&gt;hominissuis&lt;/i&gt; for the macrophage microenvironment

McManus WR, Mulvey K, Brooks EM, et al.

<h4>Introduction</h4><i>Mycobacterium avium</i> subs. <i>hominissuis</i> is an opportunistic pathogen, causing pulmonary infections in individuals who are immunocompromised or whose respiratory systems are damaged due to injuries or diseases such as cystic fibrosis, bronchiectasis, or chronic obstructive …

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Transcriptomics
Full text 2026

MECP2 mutations rewire human ESC fate and bias cortical lineage commitment

Guillon M, Brin M, Gabet E, et al.

Rett syndrome arises from loss-of-function mutations in the X-linked chromatin regulator MECP2, yet the earliest molecular derailments in development are poorly defined. Using isogenic human embryonic stem cell (hESC) models carrying three patient-derived MECP2 mutations, …

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Transcriptomics