Found: 9
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A Resilience Related Glial-Neurovascular Network Is Transcriptionally Activated after Chronic Social Defeat in Male Mice.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 21, p. 3405, doi. 10.3390/cells11213405
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- Publication type:
- Article
Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01959-1
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- Publication type:
- Article
The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis.
- Published in:
- Journal of Clinical Periodontology, 2018, v. 45, n. 12, p. 1498, doi. 10.1111/jcpe.13023
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- Publication type:
- Article
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase.
- Published in:
- 2006
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- Publication type:
- Letter
CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT).
- Published in:
- Nephrology Dialysis Transplantation, 2012, v. 27, n. 6, p. 2355, doi. 10.1093/ndt/gfr649
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- Publication type:
- Article
Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1).
- Published in:
- PLoS ONE, 2017, v. 12, n. 10, p. 1, doi. 10.1371/journal.pone.0186043
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- Publication type:
- Article
F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis.
- Published in:
- Frontiers in Genetics, 2019, p. N.PAG, doi. 10.3389/fgene.2019.00508
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- Publication type:
- Article
Pathogenic effects of novel mutations in the P-type ATPase ATP13A2 ( PARK9) causing Kufor-Rakeb syndrome, a form of early-onset parkinsonism.
- Published in:
- Human Mutation, 2011, v. 32, n. 8, p. 956, doi. 10.1002/humu.21527
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- Publication type:
- Article
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores.
- Published in:
- Molecular Genetics & Genomic Medicine, 2023, v. 11, n. 3, p. 1, doi. 10.1002/mgg3.2109
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- Publication type:
- Article