Results 141 to 150 of about 491,626 (323)

Clinical significance and immune microenvironment association of cuproptosis‐related genes in pan‐cancer

open access: yesExperimental Physiology, EarlyView.
Abstract Recent studies highlight the important roles of cuproptosis in cancer cells. However, the roles of the cuproptosis‐related genes (CRGs) in different cancers are still not fully understood. Comprehensive analysis was performed using open‐source bioinformatic platforms to disclose the expression profiles, prognostic significance, genomic and ...
Xinyu Ge   +10 more
wiley   +1 more source

RNA-Seq reveals the existence of a CDKN1C-E2F1-TP53 axis that is altered in human T-cell lymphoblastic lymphomas [PDF]

open access: gold, 2018
Pilar López‐Nieva   +13 more
openalex   +1 more source

Childhood acute leukemia and type 1 diabetes in children: A nationwide case–control study

open access: yesInternational Journal of Cancer, Volume 158, Issue 4, Page 924-930, 15 February 2026.
What's new? The etiology of childhood acute leukemia remains poorly understood. Accumulating evidence suggests a potential link between leukemia and autoimmune diseases. This nationwide, register‐based case–control study investigated the association between childhood acute leukemia and type 1 diabetes in Finland.
Julia Ventelä   +4 more
wiley   +1 more source

Hepatic Dysfunction during Induction Chemotherapy in Children with Acute Lymphoblastic Leukemia and Lymphoblastic Lymphoma and Its Effects on Subsequent Therapy and Outcome

open access: yesIndian Journal of Medical and Paediatric Oncology
Introduction The overall survival rate for childhood acute lymphoblastic leukemia (ALL) and lymphoblastic lymphoma (LBL) has shown tremendous growth in the recent years.
Nalla Anuraag Reddy   +2 more
doaj   +1 more source

Targeting the Menin–KMT2A interaction in leukemia: Lessons learned and future directions

open access: yesInternational Journal of Cancer, Volume 158, Issue 2, Page 342-356, 15 January 2026.
Abstract Chromosomal rearrangements involving the Mixed Lineage Leukemia gene (MLL1, KMT2A) are defining a genetically distinct subset in about 10% of human acute leukemias. Translocations involving the KMT2A‐locus at chromosome 11q23 are resulting in the formation of a chimeric oncogene, where the N‐terminal part of KMT2A is fused to a variety of ...
Florian Perner   +3 more
wiley   +1 more source

Dramatic increase in gene mutational burden after transformation of follicular lymphoma into TdT+ B-lymphoblastic leukemia/lymphoma [PDF]

open access: diamond, 2019
Jonathan P. Belman   +8 more
openalex   +1 more source

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