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Activation of the p38 MAPK/Akt/ERK1/2 signal pathways is required for the protein stabilization of CDC6 and cyclin D1 in low-dose arsenite-induced cell proliferation.
- Published in:
- Journal of Cellular Biochemistry, 2010, v. 111, n. 6, p. 1546, doi. 10.1002/jcb.22886
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- Publication type:
- Article
In trans variant calling reveals enrichment for compound heterozygous variants in genes involved in neuronal development and growth.
- Published in:
- Genetics Research, 2019, v. 101, p. 1, doi. 10.1017/S0016672319000065
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- Publication type:
- Article
Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase.
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- PLoS Genetics, 2015, v. 11, n. 3, p. 1, doi. 10.1371/journal.pgen.1005022
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- Article
Correction: Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO).
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- 2017
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- Correction Notice
Recessive coding and regulatory mutations in FBLIM1 underlie the pathogenesis of chronic recurrent multifocal osteomyelitis (CRMO).
- Published in:
- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0169687
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- Article
A missense mutation in the MLKL brace region promotes lethal neonatal inflammation and hematopoietic dysfunction.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16819-z
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- Publication type:
- Article
D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 1, p. 357, doi. 10.1002/ajmg.a.62520
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- Publication type:
- Article