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Transcriptomics
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Proteomics
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All-ion fragmentation
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2010
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2023
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Transcription profiling by array
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(6)
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Proteomics, Leibniz-Institute for analytical sciences, Germany
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TCRA, P2RY11, and CPT1B/CHKB associations in Chinese narcolepsy.
Not available
S-EPMC3288279
|
biostudies-literature
Cite
Large heterozygous deletion and uniparental disomy masquerading as homozygosity in CHKB gene.
Not available
S-EPMC10337282
|
biostudies-literature
Cite
Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review.
Not available
S-EPMC9524117
|
biostudies-literature
Cite
CHKB-AS1 enhances proliferation and resistance to NVP-BEZ235 of renal cancer cells via regulating the phosphorylation of MAP4 and PI3K/AKT/mTOR signaling.
Not available
S-EPMC10720114
|
biostudies-literature
Cite
Identification of the variations in the CPT1B and CHKB genes along with the HLA-DQB1*06:02 allele in Turkish narcolepsy patients and healthy persons.
Not available
S-EPMC3976597
|
biostudies-literature
Cite
A mouse model of inherited choline kinase β-deficiency presents with specific cardiac abnormalities and a predisposition to arrhythmia.
Not available
S-EPMC8913350
|
biostudies-literature
Cite
Choline kinase beta is required for normal endochondral bone formation.
Not available
S-EPMC4143985
|
biostudies-literature
Cite
Mechanism of action and therapeutic route for a muscular dystrophy caused by a genetic defect in lipid metabolism.
Not available
S-EPMC8943011
|
biostudies-literature
Cite
Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.
Not available
S-EPMC6687948
|
biostudies-literature
Cite
Congenital megaconial myopathy due to a novel defect in the choline kinase Beta gene.
Not available
S-EPMC8276349
|
biostudies-literature
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