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Test-merged-2
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PubMed
28279980
GLUT4 Is Not Necessary for Overload-Induced Glucose Uptake or Hypertrophic Growth in Mouse Skeletal Muscle. GLUT4 is necessary for acute insulin- and contraction-induced skeletal muscle glucose uptake
1.62 KB
2017-08-30
8
46
2021-12-23
PubMed
28348168
FGFR2 is required for airway basal cell self-renewal and terminal differentiation. Airway stem cells slowly self-renew and produce differentiated progeny to maintain homeostasis throughout the lifespa
870 Bytes
2017-08-29
8
11
2021-12-23
PubMed
28481876
Oncogenic activity of amplified miniature chromosome maintenance 8 in human malignancies. Miniature chromosome maintenance (MCM) proteins play critical roles in DNA replication licensing, initiation a
1.26 KB
2017-08-29
8
34
2021-12-23
PubMed
28687665
Mutation of the α-tubulin Tuba1a leads to straighter microtubules and perturbs neuronal migration. Brain development involves extensive migration of neurons. Microtubules (MTs) are key cellular effect
1.33 KB
2017-08-29
8
22
2021-12-23
PubMed
29045486
Thiamine deficiency activates hypoxia inducible factor-1α to facilitate pro-apoptotic responses in mouse primary astrocytes. Thiamine is an essential enzyme cofactor required for proper metabolic func
1.74 KB
2021-12-23
8
45
2021-12-23
PubMed
30442153
Ca2+-dependent endoplasmic reticulum stress correlation with astrogliosis involves upregulation of KCa3.1 and inhibition of AKT/mTOR signaling. BACKGROUND: The intermediate-conductance Ca2+-activated
2.22 KB
2021-12-23
7
71
2021-12-23
PubMed
6086495
Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences. A linkage study in 30 Becker muscular dystrophy (BMD) kindreds using three c
765 Bytes
2015-11-28
33
8
2021-12-23
PubMed
7018927
Pituitary response to luteinizing hormone-releasing hormone during haloperidol-induced hyperprolactinemia. The effects of a 6-hour infusion with haloperidol on serum prolactin and luteinizing hormone
626 Bytes
2015-12-07
9
22
2021-12-23
PubMed
7811247
X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes. Fragments of the adrenoleukodystrophy (ALD) cDNA from a patient w
984 Bytes
2015-11-27
38
19
2021-12-23
PubMed
8944024
Detection of heterozygous mutations in BRCA1 using high density oligonucleotide arrays and two-colour fluorescence analysis. The ability to scan a large gene rapidly and accurately for all possible he
1.02 KB
2015-03-12
46
0
2021-12-23
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