GC−MS analysis of 786-O and isogenic SETD2-deficient 38E/38F cells. (A)

Integrated Genomic and Proteomic Analyses Reveal Novel Mechanisms

Fatty Acids Analysis Using Gas Chromatography-Mass Spectrometer

Phenotypic and molecular analyses of Prkdc gene editing in scid

SETD2 deficiency accelerates sphingomyelin accumulation and

GC−MS analysis of 786-O and isogenic SETD2-deficient 38E/38F

SETD2 deficiency accelerates sphingomyelin accumulation and

SETD2 mutation in renal clear cell carcinoma suppress autophagy

The stereo structures of protein-DNA complexes. A, The Zif268

PDF) Loss of SETD2 Induces a Metabolic Switch in Renal Cell

SETD2 mutation in renal clear cell carcinoma suppress autophagy

PDF) Loss of SETD2 Induces a Metabolic Switch in Renal Cell