CHCHD2 accumulates in distressed mitochondria and facilitates oligomerization of CHCHD10.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3881, doi. 10.1093/hmg/ddy270
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2018 AND VI 27 AND IP 22
Results: 13
1
2
Rescue of biosynthesis of nicotinamide adenine dinucleotide protects the heart in cardiomyopathy caused by lamin A/C gene mutation.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3870, doi. 10.1093/hmg/ddy278
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- Publication type:
- Article
3
A putative human infertility allele of the meiotic recombinase DMC1 does not affect fertility in mice.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3911, doi. 10.1093/hmg/ddy286
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- Publication type:
- Article
4
Epigenetic changes of the thioredoxin system in the tx-j mouse model and in patients with Wilson disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3854, doi. 10.1093/hmg/ddy262
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- Publication type:
- Article
5
Tauopathy-associated PERK alleles are functional hypomorphs that increase neuronal vulnerability to ER stress.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3951, doi. 10.1093/hmg/ddy297
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- Publication type:
- Article
6
Amino acid position 37 of HLA-DRβ1 affects susceptibility to Crohn's disease in Asians.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3901, doi. 10.1093/hmg/ddy285
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- Publication type:
- Article
7
Carbamazepine reduces disease severity in a mouse model of metaphyseal chondrodysplasia type Schmid caused by a premature stop codon (Y632X) in the Col10a1 gene.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3840, doi. 10.1093/hmg/ddy253
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- Publication type:
- Article
8
A purely quantitative form of partial recessive IFN-γR2 deficiency caused by mutations of the initiation or second codon.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3919, doi. 10.1093/hmg/ddy275
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- Publication type:
- Article
9
PIN1 is a new therapeutic target of craniosynostosis.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3827, doi. 10.1093/hmg/ddy252
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- Publication type:
- Article
10
A non-coding genetic variant maximally associated with serum urate levels is functionally linked to HNF4A-dependent PDZK1 expression.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3964, doi. 10.1093/hmg/ddy295
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- Publication type:
- Article
11
In silico drug screening by using genome-wide association study data repurposed dabrafenib, an anti-melanoma drug, for Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3974, doi. 10.1093/hmg/ddy279
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- Publication type:
- Article
12
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3986, doi. 10.1093/hmg/ddy306
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- Publication type:
- Article
13
Fragile X mental retardation protein modulates the stability of its m6A-marked messenger RNA targets.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 22, p. 3936, doi. 10.1093/hmg/ddy292
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- Publication type:
- Article