Found: 17
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Whole Blood Gene Expression Reveals Specific Transcriptome Changes in Neonatal Encephalopathy.
- Published in:
- Neonatology (16617800), 2019, v. 115, n. 1, p. 68, doi. 10.1159/000492420
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- Publication type:
- Article
miRNAs and Genes Involved in the Interplay between Ocular Hypertension and Primary Open-Angle Glaucoma. Oxidative Stress, Inflammation, and Apoptosis Networks.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 11, p. 2227, doi. 10.3390/jcm10112227
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- Publication type:
- Article
The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease.
- Published in:
- Nature Genetics, 2002, v. 30, n. 1, p. 22, doi. 10.1038/ng798
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- Publication type:
- Article
High-Throughput Sequencing of RNA Silencing- Associated Small RNAs in Olive (Olea europaea L.).
- Published in:
- PLoS ONE, 2011, v. 6, n. 11, p. 1, doi. 10.1371/journal.pone.0027916
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- Publication type:
- Article
Microbial Diversity in the Midguts of Field and Lab-Reared Populations of the European Corn Borer Ostrinia nubilalis.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0021751
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- Publication type:
- Article
Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease.
- Published in:
- Journal of Cellular & Molecular Medicine, 2008, v. 12, n. 2, p. 679, doi. 10.1111/j.1582-4934.2007.00158.x
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- Publication type:
- Article
Clinical, electrophysiological and morphological findings of Charcot–Marie–Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
- Published in:
- Brain: A Journal of Neurology, 2003, v. 126, n. 9, p. 2023, doi. 10.1093/brain/awg202
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- Publication type:
- Article
Expanding the phenotype of PIGP deficiency to multiple congenital anomalies‐hypotonia‐seizures syndrome.
- Published in:
- Clinical Genetics, 2023, v. 104, n. 2, p. 245, doi. 10.1111/cge.14340
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- Publication type:
- Article
Evolutionary and Structural Analyses of GDAP1, Involved in Charcot-Marie-Tooth Disease, Characterize a Novel Class of Glutathione Transferase-Related Genes.
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- Molecular Biology & Evolution, 2004, v. 21, n. 1, p. 176
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- Publication type:
- Article
The Transcriptome Analysis of Strongyloides stercoralis L3i Larvae Reveals Targets for Intervention in a Neglected Disease.
- Published in:
- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 2, p. 1, doi. 10.1371/journal.pntd.0001513
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- Publication type:
- Article
The Transcriptome Analysis of Strongyloides stercoralis L3i Larvae Reveals Targets for Intervention in a Neglected Disease.
- Published in:
- PLoS Neglected Tropical Diseases, 2012, v. 6, n. 2, p. 1, doi. 10.1371/journal.pntd.0001513
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- Publication type:
- Article
Evolutionary Trends in the Mitochondrial Genome of Archaeplastida: How Does the GC Bias Affect the Transition from Water to Land?
- Published in:
- Plants (2223-7747), 2020, v. 9, n. 3, p. 358, doi. 10.3390/plants9030358
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- Publication type:
- Article
GDAP1, the protein causing Charcot–Marie–Tooth disease type 4A, is expressed in neurons and is associated with mitochondria.
- Published in:
- Human Molecular Genetics, 2005, v. 14, n. 8, p. 1087, doi. 10.1093/hmg/ddi121
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- Article
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 Caused by a Novel PIGA Variant Not Associated with a Skewed X-Inactivation Pattern.
- Published in:
- 2024
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- Publication type:
- Case Study
Prenatal Genome-Wide Cell-Free DNA Screening: Three Years of Clinical Experience in a Hospital Prenatal Diagnostic Unit in Spain.
- Published in:
- Genes, 2024, v. 15, n. 5, p. 568, doi. 10.3390/genes15050568
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- Publication type:
- Article
New mutations found by Next-Generation Sequencing screening of Spanish patients with Nemaline Myopathy.
- Published in:
- PLoS ONE, 2018, v. 13, n. 12, p. 1, doi. 10.1371/journal.pone.0207296
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- Publication type:
- Article
De Novo Assembly and Functional Annotation of the Olive (Olea europaea) Transcriptome.
- Published in:
- DNA Research, 2013, v. 20, n. 1, p. 93, doi. 10.1093/dnares/dss036
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- Publication type:
- Article