Publications by authors named "J A Wambach"

We report three unrelated individuals with atypical clinical findings for cardio-facio-cutaneous (CFC) syndrome, all of whom have the same novel, heterozygous de novo p.H119Y (c.355 C>T) transition variant in MAP2K1, identified by exome sequencing.

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  • Children's interstitial and diffuse lung diseases (chILDs) are different types of lung problems that happen in kids and can cause breathing issues.
  • Kids with chILDs often show signs of lung trouble and have special images taken of their lungs that reveal abnormalities.
  • Improving care for these kids has come from teamwork between different doctors and hospitals, as well as research efforts to find better ways to diagnose and treat these lung diseases.
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  • * Through analysis of fibroblasts and a fruit fly model, we found that these variants resulted in decreased lipid droplet formation and impaired gene expression linked to SREBP, indicating disrupted pathway function.
  • * Our findings suggest that SREBF2 variants hinder the cleavage of S1P targets, causing disease symptoms by negatively affecting SREBP1 and SREBP2 activity.
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  • Tubulin is a key component of the cytoskeleton and has various isotypes in animals, but it's unclear how these isotypes influence microtubule structures in different cell types.
  • Research on 12 patients with primary ciliary dyskinesia and mouse models uncovered variants in the tubulin isotype that disrupted the formation of centrioles and cilia, impacting microtubule dynamics.
  • The study identified different variants causing distinct effects on tubulin interactions, allowing for the classification of patients into three types of ciliopathic diseases, highlighting the unique roles of specific tubulin isotypes in cellular functions.
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