Found: 13
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Structural basis for recruitment of RILP by small GTPase Rab7.
- Published in:
- EMBO Journal, 2005, v. 24, n. 8, p. 1491, doi. 10.1038/sj.emboj.7600643
- By:
- Publication type:
- Article
Concurrent paediatric medulloblastoma and Chiari I malformation with syringomyelia.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Post-operative diffusion weighted imaging as a predictor of posterior fossa syndrome permanence in paediatric medulloblastoma.
- Published in:
- Child's Nervous System, 2017, v. 33, n. 3, p. 457, doi. 10.1007/s00381-017-3356-7
- By:
- Publication type:
- Article
Platform Comparison for Evaluation of ALK Protein Immunohistochemical Expression, Genomic Copy Number and Hotspot Mutation Status in Neuroblastomas.
- Published in:
- PLoS ONE, 2014, v. 9, n. 9, p. 1, doi. 10.1371/journal.pone.0106575
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- Publication type:
- Article
Participation of Tom1L1 in EGF-stimulated endocytosis of EGF receptor.
- Published in:
- EMBO Journal, 2009, v. 28, n. 22, p. 3485, doi. 10.1038/emboj.2009.282
- By:
- Publication type:
- Article
Clear cell sarcomas of the kidney are characterised by BCOR gene abnormalities, including exon 15 internal tandem duplications and BCOR- CCNB3 gene fusion.
- Published in:
- Histopathology, 2018, v. 72, n. 1, p. 320, doi. 10.1111/his.13366
- By:
- Publication type:
- Article
The Development of Mounts and Mounting Techniques at the Albertina in Vienna from 1805 to 2018.
- Published in:
- Restaurator, 2019, v. 40, n. 3/4, p. 141, doi. 10.1515/res-2019-0026
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- Publication type:
- Article
Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma.
- Published in:
- BMC Cancer, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12885-022-09800-0
- By:
- Publication type:
- Article
Mutations of 1p genes do not consistently abrogate tumor suppressor functions in 1p-intact neuroblastoma.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Clinical insights.
- Published in:
- 2012
- By:
- Publication type:
- Journal Article
Clinical insights.
- Published in:
- Journal of Clinical Practice in Speech-Language Pathology, 2012, v. 14, n. 2, p. 79
- By:
- Publication type:
- Article
COG8 deficiency causes new congenital disorder of glycosylation type IIh.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 7, p. 731, doi. 10.1093/hmg/ddm028
- By:
- Publication type:
- Article
Hepatitis C virus mediated chronic inflammation and tumorigenesis in the humanised immune system and liver mouse model.
- Published in:
- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0184127
- By:
- Publication type:
- Article