Last Updated: 09/26/2026
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Found 198 publications
Myeloid sarcoma 'invading' a dedifferentiated liposarcoma: A rare collision tumour.
Journal: British journal of haematology
Published: August 28, 2026
RET fusion partners dictate oncogenic potential in undifferentiated spindle cell sarcomas.
Journal: Cancer biology & therapy
Published: June 04, 2026
Correction: Li et al. The Anthraquinone Derivative C2 Enhances Oxaliplatin-Induced Cell Death and Triggers Autophagy via the PI3K/AKT/mTOR Pathway. Int. J. Mol. Sci. 2024, 25, 6468.
Journal: International journal of molecular sciences
Published: May 25, 2026
NOTCH3 Internal Tandem Duplication Defines a Novel Oncogenic Activation Mechanism of NOTCH Signaling.
Journal: Genes, chromosomes & cancer
Published: May 14, 2026
Distinct cell-type contributions and network topography of theta-nested gamma oscillations in the medial entorhinal cortex.
Journal: bioRxiv : the preprint server for biology
Published: May 04, 2026
Distinct cell-type contributions and network topography of theta-nested gamma oscillations in the medial entorhinal cortex.
Journal: bioRxiv : the preprint server for biology
Published: May 04, 2026
An adaptive cellular source of IL-17A and IL-17F is critical for the induction of experimental autoimmune encephalomyelitis.
Journal: Science immunology
Published: April 24, 2026
FUS/EWSR1::TFCP2-rearranged bone and soft tissue tumors: evidence of gene promiscuity.
Journal: Virchows Archiv : an international journal of pathology
Published: March 18, 2026
Subthreshold membrane depolarization powerfully engages intracellular calcium dynamics in the brain.
Subthreshold membrane depolarization powerfully engages intracellular calcium dynamics in the brain.
Journal: bioRxiv : the preprint server for biology
Published: March 16, 2026
Novel SMARCA4::VEZF1 Rearrangement in Pediatric Sarcomas.
Journal: Genes, chromosomes & cancer
Published: March 05, 2026
Synovial Sarcoma With BRAF V600E Mutation: A Case Report and Literature Review.
Journal: Genes, chromosomes & cancer
Published: February 28, 2026
NRAS mutation in a central conducting lymphatic anomaly and PPFIBP1::ROS1 fusion in a Gorham-stout disease patient.
Journal: Human molecular genetics
Published: February 24, 2026
Last Updated: 09/26/2026