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UnknownThe breast cancer oncogene IKK? coordinates mitochondrial function and serine metabolism
Not available
S-SCDT-EMBOR-2019-48260-T | biostudies-other
UnknownMacrophages induce malignant traits in mammary epithelium via IKK?/TBK1 kinases and the serine biosynthesis pathway
Not available
S-SCDT-EMM-2019-10491 | biostudies-other
UnknownHeterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects.
Not available
S-EPMC3928658 | biostudies-literature
UnknownBi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
Not available
S-EPMC6507039 | biostudies-literature
UnknownDistinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Not available
S-EPMC5988037 | biostudies-literature
UnknownTargeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability.
Not available
S-EPMC4833192 | biostudies-literature
UnknownMutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan.
Not available
S-EPMC3710768 | biostudies-literature
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