Results 121 to 130 of about 16,775 (201)
In animals, replication-independent incorporation of nucleosomes containing the histone variant H3.3 enables global reprogramming of histone modifications and transcriptional profiles.
Xin Nie +4 more
doaj +1 more source
Dynamic distribution of the replacement histone variant H3.3 in the mouse oocyte and preimplantation embryos [PDF]
Upon fertilization, the gametes undergo a drastic reprogramming that includes changes in DNA methylation and histone modifications. Currently, it is not known whether replacement of the major histones by histone variants is also involved in these ...
Bannister, Andrew J. +4 more
core
Histone H3.3 Mutations Are Cancer Type-Specific [PDF]
Abstract Most chondroblastomas have H3F3B mutations, but giant cell tumors only have mutations in H3F3A.
openaire +1 more source
Background: There can be a diagnostic challenge in differentiating giant cell tumor of bone (GCTB) from its mimics. Lately, histone H3F3A (Histone 3.3) G34W has been identified as a promising immunohistochemical marker.
Bharat Rekhi +7 more
doaj +1 more source
Genetically Engineered T-Cells for Malignant Glioma: Overcoming the Barriers to Effective Immunotherapy. [PDF]
Malignant gliomas carry a dismal prognosis. Conventional treatment using chemo- and radiotherapy has limited efficacy with adverse events. Therapy with genetically engineered T-cells, such as chimeric antigen receptor (CAR) T-cells, may represent a ...
Almeida, Neil D +4 more
core
Germ line mutations in H3F3A and H3F3B cause a previously unidentified neurodevelopmental syndrome. Although somatic mutations in Histone 3.3 (H3.3) are well-studied drivers of oncogenesis, the role of germline mutations remains unreported. We analyze 46 patients bearing de novo germline mutations in histone 3 family 3A (H3F3A) or H3F3B with ...
Bryant, Laura|| +131 more
openaire +1 more source
Introduction: Giant cell tumor of bone (GCTB) is a rare, typically benign neoplasm that primarily affects long bones in adults, with clival involvement being extremely rare, particularly in pediatric cases: a mini-review shows a total of 28 described ...
Gabriele Gaggero +8 more
doaj +1 more source
ARID1A governs the silencing of sex-linked transcription during male meiosis in the mouse
We present evidence implicating the BAF (BRG1/BRM Associated Factor) chromatin remodeler in meiotic sex chromosome inactivation (MSCI). By immunofluorescence (IF), the putative BAF DNA binding subunit, ARID1A (AT-rich Interaction Domain 1 a), appeared ...
Debashish U Menon +3 more
doaj +1 more source

