Publications by authors named "Gervette M Penny"

Article Synopsis
  • Primary ciliary dyskinesia (PCD) is a genetic condition that affects tiny hair-like structures called cilia, making them not work properly.
  • Researchers studied cells from patients with PCD, their mothers, and healthy people to understand how these cells are different.
  • They found specific genes and proteins that were linked to problems in cilia movement, which could help develop new treatments for PCD in the future.
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Motile cilia assembly utilizes over 800 structural and cytoplasmic proteins. Variants in approximately 58 genes cause primary ciliary dyskinesia (PCD) in humans, including the dynein arm (pre)assembly factor (DNAAF) gene DNAAF4. In humans, outer dynein arms (ODAs) and inner dynein arms (IDAs) fail to assemble motile cilia when DNAAF4 function is disrupted.

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Genomic assemblies of the unicellular green alga Chlamydomonas reinhardtii have provided important resources for researchers. However, assembly errors, large gaps, and unplaced scaffolds as well as strain-specific variants currently impede many types of analysis. By combining PacBio HiFi and Oxford Nanopore long-read technologies, we generated a de novo genome assembly for strain CC-5816, derived from crosses of strains CC-125 and CC-124.

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Testicular Leydig cells produce androgens essential for proper male reproductive development and fertility. Here, we describe a new Leydig cell ablation model based on Cre/Lox recombination of mouse and , two genes implicated in the transcriptional regulation of steroidogenesis. The testicular interstitium of adult ; mice was injected with adenoviral vectors encoding Cre + GFP (Ad-Cre-IRES-GFP) or GFP alone (Ad-GFP).

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