Found: 14
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Profound digital collagen atrophy: a new cutaneous presentation of adrenal-dependent Cushing's syndrome.
- Published in:
- British Journal of Dermatology, 1990, v. 123, n. 5, p. 667, doi. 10.1111/j.1365-2133.1990.tb01486.x
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- Publication type:
- Article
Microbial DNA profiling by multiplex terminal restriction fragment length polymorphism for forensic comparison of soil and the influence of sample condition.
- Published in:
- Journal of Applied Microbiology, 2008, v. 105, n. 3, p. 813, doi. 10.1111/j.1365-2672.2008.03819.x
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- Publication type:
- Article
Allele replacement: an application that permits rapid manipulation of herpes simplex virus type 1 genomes.
- Published in:
- Gene Therapy, 1999, v. 6, n. 5, p. 922, doi. 10.1038/sj.gt.3300887
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- Publication type:
- Article
Cell-type and subcellular compartment-specific APEX2 proximity labeling reveals activity-dependent nuclear proteome dynamics in the striatum.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25144-y
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- Publication type:
- Article
Ironing out neurodegeneration: mutations in a phospholipase A<sub>2</sub> cause neurodegenerative diseases with iron accumulation.
- Published in:
- Clinical Genetics, 2006, v. 70, n. 4, p. 306, doi. 10.1111/j.1399-0004.2006.00675_1.x
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- Publication type:
- Article
Pharmacogenetics of antidepressants: serotonin 2A receptor genotype strongly associated with treatment outcome.
- Published in:
- 2006
- By:
- Publication type:
- Other
Genetic variants of frizzled-4 gene in familial exudative vitreoretinopathy and advanced retinopathy of prematurity.
- Published in:
- 2005
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- Publication type:
- Letter
Mutations in TGF-β receptor type-2 cause Marfan's syndrome.
- Published in:
- 2005
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- Publication type:
- Other
Multiple rare alleles influence a complex trait: the case of HDL cholesterol.
- Published in:
- 2005
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- Publication type:
- Other
Hotspot Mutations in a G protein-coupled receptor cause hypogonadotropic hypogonadism in humans and mice.
- Published in:
- 2004
- By:
- Publication type:
- Other
Hotspot A putative E3 ubiquitin ligase is deficient in progressive myoclonus epilepsy.
- Published in:
- 2004
- By:
- Publication type:
- Other
Spleen sizing by ultrasound in polycythaemia and thrombocythaemia: comparison with SPECT.
- Published in:
- British Journal of Haematology, 1997, v. 98, n. 1, p. 103, doi. 10.1046/j.1365-2141.1997.1552969.x
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- Publication type:
- Article
Targeting the post-synaptic proteome has therapeutic potential for psychosis in Alzheimer Disease.
- Published in:
- Communications Biology, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42003-023-04961-5
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- Publication type:
- Article
Src kinase as a mediator of convergent molecular abnormalities leading to NMDAR hypoactivity in schizophrenia.
- Published in:
- Molecular Psychiatry, 2015, v. 20, n. 9, p. 1091, doi. 10.1038/mp.2014.115
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- Publication type:
- Article