Last Updated: 09/26/2026
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Found 91 publications
Development of a Cre-Inducible Rabl6a Transgenic Mouse Model That Enhances Sarcoma Growth In Vivo.
Journal: Cancers
Published: April 25, 2026
Intratumoral plasma cells mediate CD8+ T cell infiltration and successful immune checkpoint blockade therapy in de novo MPNSTs.
Journal: bioRxiv : the preprint server for biology
Published: February 27, 2026
Genome-wide machine learning analysis of anosmia and ageusia with COVID-19.
Journal: PloS one
Published: December 05, 2025
Intratumoural plasma cells mediate a pro-inflammatory response to kinase inhibition and successful immune checkpoint blockade therapy in malignant peripheral nerve sheath tumours.
Journal: EBioMedicine
Published: September 25, 2025
Heterozygous KRT32 variant is responsible for autosomal dominant loose anagen hair syndrome.
Journal: HGG advances
Published: June 13, 2025
A genetic variant in SMAD7 acts as a modifier of LMNA-associated muscular dystrophy, implicating SMAD signaling as a therapeutic target.
Journal: Science advances
Published: April 18, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance.
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant Inheritance.
Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association
Published: January 17, 2025
Genome-wide Machine Learning Analysis of Anosmia and Ageusia with COVID-19.
Journal: medRxiv : the preprint server for health sciences
Published: December 16, 2024
UDP-glucose dehydrogenase variants cause dystroglycanopathy.
Journal: Annals of clinical and translational neurology
Published: December 05, 2024
Multi-omic analyses of a twin pair with mirror image cleft lip identifies pathogenic variant in FGF20 modified by differential methylation upstream of ZFP57.
Journal: medRxiv : the preprint server for health sciences
Published: November 28, 2024
Finding buried genetic test results in the electronic health record is inefficient and variable across institutions.
Journal: Therapeutic advances in rare disease
Published: November 15, 2024
The Influence of X Chromosome Parent-of-Origin on Glycemia in Individuals with Turner Syndrome.
Journal: Hormone research in paediatrics
Published: September 30, 2024
Last Updated: 09/26/2026