Found: 38
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Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.
- Published in:
- Movement Disorders, 2010, v. 25, n. 13, p. 2052, doi. 10.1002/mds.23283
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- Article
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease.
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- Movement Disorders, 2010, v. 25, n. 13, p. 2156, doi. 10.1002/mds.23265
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- Article
LRRK2 variation and Parkinson's disease in African Americans.
- Published in:
- Movement Disorders, 2010, v. 25, n. 12, p. 1973, doi. 10.1002/mds.23163
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- Article
Expanding the clinical phenotype of SNCA duplication carriers.
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- Movement Disorders, 2009, v. 24, n. 12, p. 1811, doi. 10.1002/mds.22682
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- Article
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease.
- Published in:
- 2007
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- Publication type:
- journal article
Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.
- Published in:
- 2004
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- Publication type:
- journal article
Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations.
- Published in:
- Movement Disorders, 2004, v. 19, n. 6, p. 677, doi. 10.1002/mds.10703
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- Publication type:
- Article
Distinct spatial immune microlandscapes are independently associated with outcomes in triple-negative breast cancer.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37806-0
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- Article
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease.
- Published in:
- Neurogenetics, 2010, v. 11, n. 4, p. 401, doi. 10.1007/s10048-010-0241-x
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- Article
Discrete class I molecules on brain endothelium differentially regulate neuropathology in experimental cerebral malaria.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 2, p. 566, doi. 10.1093/brain/awad319
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- Article
Leucine-rich repeat kinase 1: a paralog of LRRK2 and a candidate gene for Parkinson’s disease.
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- Neurogenetics, 2007, v. 8, n. 2, p. 95, doi. 10.1007/s10048-006-0075-8
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- Publication type:
- Article
Lrrk2 pathogenic substitutions in Parkinson's disease.
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- Neurogenetics, 2005, v. 6, n. 4, p. 171, doi. 10.1007/s10048-005-0005-1
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- Publication type:
- Article
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.
- Published in:
- 2007
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- Publication type:
- Report
Fine-mapping and candidate gene investigation within the PARK10 locus.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 3, p. 336, doi. 10.1038/ejhg.2008.187
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- Article
DCTN1 mutations in Perry syndrome.
- Published in:
- Nature Genetics, 2009, v. 41, n. 2, p. 163, doi. 10.1038/ng.293
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- Article
Chromoanasynthesis is a common mechanism that leads to ERBB2 amplifications in a cohort of early stage HER2<sup>+</sup> breast cancer samples.
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- 2018
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- Publication type:
- journal article
Intrinsic Subtype and Therapeutic Response Among HER2-Positive Breast Tumors from the NCCTG (Alliance) N9831 Trial.
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- 2017
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- Publication type:
- journal article
The antineoplastic drug, trastuzumab, dysregulates metabolism in iPSC‐derived cardiomyocytes.
- Published in:
- Clinical & Translational Medicine, 2017, v. 6, n. 1, p. 1, doi. 10.1186/s40169-016-0133-2
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- Publication type:
- Article
The antineoplastic drug, trastuzumab, dysregulates metabolism in iPSC-derived cardiomyocytes.
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- Clinical & Translational Medicine, 2017, v. 6, n. 1, p. 1, doi. 10.1186/s40169-016-0133-2
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- Publication type:
- Article
Evidence of cerebellar TDP-43 loss of function in FTLD-TDP.
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- Acta Neuropathologica Communications, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40478-022-01408-6
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- Article
Towards defining morphologic parameters of normal parous and nulliparous breast tissues by artificial intelligence.
- Published in:
- 2022
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- Publication type:
- journal article
Gene Expression, Single Nucleotide Variant and Fusion Transcript Discovery in Archival Material from Breast Tumors.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081925
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- Publication type:
- Article
An Integrated Model of the Transcriptome of HER2-Positive Breast Cancer.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0079298
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- Publication type:
- Article
Rejuvenation of the aged brain immune cell landscape in mice through p16-positive senescent cell clearance.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-33226-8
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- Publication type:
- Article
MEN1 mutations in Hürthle cell (oncocytic) thyroid carcinoma.
- Published in:
- 2015
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- Publication type:
- journal article
Clinical and molecular features of hürthle cell carcinoma of the thyroid.
- Published in:
- 2015
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- Publication type:
- Journal Article
Truncated stathmin-2 is a marker of TDP-43 pathology in frontotemporal dementia.
- Published in:
- 2020
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- Publication type:
- journal article
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
- Published in:
- Nucleic Acids Research, 2014, v. 42, n. 22, p. 1, doi. 10.1093/nar/gku1005
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- Publication type:
- Article
Elevated methylation levels, reduced expression levels, and frequent contractions in a clinical cohort of C9orf72 expansion carriers.
- Published in:
- Molecular Neurodegeneration, 2020, v. 15, n. 1, p. 1, doi. 10.1186/s13024-020-0359-8
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- Publication type:
- Article
Multiplication of the α-synuclein gene is not a common disease mechanism in Lewy body disease.
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- Journal of Molecular Neuroscience, 2004, v. 24, n. 3, p. 337, doi. 10.1385/JMN:24:3:337
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- Publication type:
- Article
Genomic investigation of α-synuclein multiplication and parkinsonism.
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- Annals of Neurology, 2008, v. 63, n. 6, p. 743, doi. 10.1002/ana.21380
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- Article
Clinical features of LRRK2‐associated Parkinson's disease in central Norway.
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- Annals of Neurology, 2005, v. 57, n. 5, p. 762
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- Publication type:
- Article
Comparison of kindreds with parkinsonism and α-synuclein genomic multiplications.
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- Annals of Neurology, 2004, v. 55, n. 2, p. 174
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- Publication type:
- Article
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 11, p. 1223, doi. 10.1093/hmg/ddg134
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- Publication type:
- Article
Assessment of Tumor Heterogeneity, as Evidenced by Gene Expression Profiles, Pathway Activation, and Gene Copy Number, in Patients with Multifocal Invasive Lobular Breast Tumors.
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- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153411
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- Publication type:
- Article
Correction: Folate Receptor-α (FOLR1) Expression and Function in Triple Negative Tumors.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0127133
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- Publication type:
- Article
Folate Receptor-α (FOLR1) Expression and Function in Triple Negative Tumors.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0122209
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- Publication type:
- Article
Investigation of differentially expressed proteins through neurofibrillary tangle maturation in Alzheimer's disease using NanoString's GeoMx Digital Spatial Profiler.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 3, p. 1, doi. 10.1002/alz.066668
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- Publication type:
- Article