Pages that link to "Q50098318"

The following pages link to De novo variants in SETD1B are associated with intellectual disability, epilepsy and autism (Q50098318):

Displaying 12 items.

• The H3K4 methyltransferase Setd1b is essential for hematopoietic stem and progenitor cell homeostasis in mice. (Q55437673) (← links)
• High‑level SETD1B gene expression is associated with unfavorable prognosis in hepatocellular carcinoma (Q64229246) (← links)
• EMT transcription factor ZEB1 alters the epigenetic landscape of colorectal cancer cells (Q89865753) (← links)
• Identification of de novo CSNK2A1 and CSNK2B variants in cases of global developmental delay with seizures (Q91100012) (← links)
• Roles and regulation of histone methylation in animal development (Q91565531) (← links)
• Comprehensive clinical and molecular studies in split-hand/foot malformation: identification of two plausible candidate genes (LRP6 and UBA2) (Q92093294) (← links)
• A novel de novo frameshift variant in SETD1B causes epilepsy (Q92172253) (← links)
• De novo variants in SETD1B cause intellectual disability, autism spectrum disorder, and epilepsy with myoclonic absences (Q92803739) (← links)
• A case of de novo splice site variant in SLC35A2 showing developmental delays, spastic paraplegia, and delayed myelination (Q92974712) (← links)
• SET domain containing 1B gene is mutated in primary hepatic neuroendocrine tumors (Q93048662) (← links)
• Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome (Q94452526) (← links)
• COMPASS and SWI/SNF complexes in development and disease (Q99594988) (← links)