Perioperative Management of Hereditary Antithrombin Deficiency in a Patient Undergoing Minimally Invasive Thoracic Surgery: A Case Report. [PDF]
Domen H, Takakuwa Y, Yamada H.
europepmc +1 more source
Current Issues in Terminology and Classification of Hereditary Disorders at Endocrine Cancer
S. B. Pinsky +4 more
openalex +2 more sources
Hereditary epithelial dystrophy of the cornea: Meesmann type. [PDF]
P. P. H. Alkemade, A. T. van Balen
openalex +1 more source
Emerging role of ARHGAP29 in melanoma cell phenotype switching
This study gives first insights into the role of ARHGAP29 in malignant melanoma. ARHGAP29 was revealed to be connected to tumor cell plasticity, promoting a mesenchymal‐like, invasive phenotype and driving tumor progression. Further, it modulates cell spreading by influencing RhoA/ROCK signaling and affects SMAD2 activity. Rho GTPase‐activating protein
Beatrice Charlotte Tröster +3 more
wiley +1 more source
Genomic landscape of hereditary cancer syndromes in the largest cohort in Colombia: a retrospective study. [PDF]
López Rivera JJ +9 more
europepmc +1 more source
In this exploratory study, we investigated the relationship between the gut microbiota and outcome in patients with metastatic hormone receptor‐positive breast cancer, treated in a randomized clinical trial with chemotherapy alone or chemotherapy in combination with immune checkpoint blockade.
Andreas Ullern +7 more
wiley +1 more source
Precision Care for Hereditary Urologic Cancers: Genetic Testing, Counseling, Surveillance, and Therapeutic Implications. [PDF]
Somoto T +11 more
europepmc +1 more source
Modeling hepatic fibrosis in TP53 knockout iPSC‐derived human liver organoids
This study developed iPSC‐derived human liver organoids with TP53 gene knockout to model human liver fibrosis. These organoids showed elevated myofibroblast activation, early disease markers, and advanced fibrotic hallmarks. The use of profibrotic differentiation medium further amplified the fibrotic signature seen in the organoids.
Mustafa Karabicici +8 more
wiley +1 more source
Correction: Identification of a novel <i>ANK1</i> gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. [PDF]
Xiong T +6 more
europepmc +1 more source

