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Adam13 interacts with large protein complexes to regulate histone modification and gene expression. [PDF]
Pandey A +8 more
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Non-Isolated Dandy-Walker Malformation: Exome Sequencing Efficacy and Phenotypic Expansions. [PDF]
Araji S +4 more
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Abexinostat, a histone deacetylases inhibitor, for patients with relapsed or refractory follicular lymphoma: a multi-center, single-arm phase 2 study. [PDF]
Gui L +20 more
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Multiple system atrophy is associated with brain somatic mutations in clonal hematopoiesis genes
Thompson B +5 more
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KMT2D: A key emerging epigenetic regulator in head and neck diseases and tumors
Life SciencesHistone modifications are critical determinants of chromatin accessibility and gene expression, both of which are intrinsically linked to human development and disease. Lysine methyltransferase 2D (KMT2D), a prominent member of the H3K4 methyltransferase
Kexin Wang +8 more
exaly +2 more sources
PNAS Nexus
Hepatocellular carcinoma (HCC) has become a leading cause of cancer-related mortality worldwide. Conventional therapies tend to exacerbate comorbidities, liver dysfunction, and relapse, rendering an urgent demand for novel strategy for management of HCC.
Weiguang Yu +2 more
exaly +2 more sources
Hepatocellular carcinoma (HCC) has become a leading cause of cancer-related mortality worldwide. Conventional therapies tend to exacerbate comorbidities, liver dysfunction, and relapse, rendering an urgent demand for novel strategy for management of HCC.
Weiguang Yu +2 more
exaly +2 more sources
Small molecule inhibitors of the prostate cancer target KMT2D
Biochemical and Biophysical Research Communications, 2020Histone lysine N-methyltransferase 2D (KMT2D), an important methyltransferase that is involved in the methylation of lysine 4 in histone H3 (H3K4) and related to the development of prostate cancer. Hypermethylation of H3K4 is shown in prostate cancer (PCa). However, KMT2D inhibitors have not yet been developed.
Guochao Liao, Zhongqiu Liu, Yu Qi
exaly +3 more sources
Near complete deletion of
AbstractPathogenic variants in KMT2D are typically associated with Kabuki syndrome (KS), a rare multisystem disorder. KS is characterized by facial dysmorphisms, intellectual disability, skeletal and dermatoglyphic differences, and poor growth. Seventy percent of individuals with clinically diagnosed KS have a confirmed pathogenic variant in KMT2D or ...
Catherine Gooch +8 more
openaire +2 more sources
Nature Genetics
Members of the KMT2C/D–KDM6A complex are recurrently mutated in urothelial carcinoma and in histologically normal urothelium. Here, using genetically engineered mouse models, we demonstrate that Kmt2c/d knockout in the urothelium led to impaired ...
Naitao Wang +29 more
semanticscholar +1 more source
Members of the KMT2C/D–KDM6A complex are recurrently mutated in urothelial carcinoma and in histologically normal urothelium. Here, using genetically engineered mouse models, we demonstrate that Kmt2c/d knockout in the urothelium led to impaired ...
Naitao Wang +29 more
semanticscholar +1 more source

