Found: 22
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Study of Estrogen Receptor-α and Receptor-β Gene Polymorphisms on Alzheimer's Disease.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 26, n. 3, p. 431, doi. 10.3233/JAD-2011-110362
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- Article
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
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- Journal of Human Genetics, 2015, v. 60, n. 7, p. 399, doi. 10.1038/jhg.2015.37
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- Article
Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease.
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- BMC Pulmonary Medicine, 2016, v. 16, p. 1, doi. 10.1186/s12890-016-0309-y
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- Publication type:
- Article
Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy.
- Published in:
- Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1226766
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- Publication type:
- Article
Functional interaction of DYX1C1 with estrogen receptors suggests involvement of hormonal pathways in dyslexia.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2802, doi. 10.1093/hmg/ddp215
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- Publication type:
- Article
Alpha-cardiac actin mutations produce atrial septal defects.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 2, p. 256, doi. 10.1093/hmg/ddm302
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- Publication type:
- Article
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 6, p. 667, doi. 10.1093/hmg/ddm009
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- Publication type:
- Article
Mutations in the gene encoding fibroblast growth factor 10 are associated with aplasia of lacrimal and salivary glands.
- Published in:
- Nature Genetics, 2005, v. 37, n. 2, p. 125, doi. 10.1038/ng1507
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- Article
The molecular network of the dyslexia candidate gene DYX1C1 shows connection to neuronal migration genes and cytoskeletal proteins
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- 2012
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- Publication type:
- Abstract
DCDC2 Polymorphism Is Associated with Left Temporoparietal Gray and White Matter Structures during Development.
- Published in:
- Journal of Neuroscience, 2014, v. 34, n. 43, p. 14455, doi. 10.1523/JNEUROSCI.1216-14.2014
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- Publication type:
- Article
Familial transient erythroblastopenia of childhood is associated with the chromosome 19q13.2 region but not caused by mutations in coding sequences of the ribosomal protein S19 (RPS19) gene.
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- British Journal of Haematology, 2002, v. 119, n. 1, p. 261, doi. 10.1046/j.1365-2141.2002.03776.x
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- Article
Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report.
- Published in:
- BMC Medical Genetics, 2020, v. 21, n. 1, p. 1, doi. 10.1186/s12881-020-01020-2
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- Publication type:
- Article
The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure.
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- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050321
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- Publication type:
- Article
Increased Expression of the Dyslexia Candidate Gene DCDC2 Affects Length and Signaling of Primary Cilia in Neurons.
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- PLoS ONE, 2011, v. 6, n. 6, p. 1, doi. 10.1371/journal.pone.0020580
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- Publication type:
- Article
Human ROBO1 regulates white matter structure in corpus callosum.
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- Brain Structure & Function, 2017, v. 222, n. 2, p. 707, doi. 10.1007/s00429-016-1240-y
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- Publication type:
- Article
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia.
- Published in:
- Nature Genetics, 1999, v. 21, n. 2, p. 169, doi. 10.1038/5951
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- Publication type:
- Article
Mutation in CEP63 co-segregating with developmental dyslexia in a Swedish family.
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- Human Genetics, 2015, v. 134, n. 11/12, p. 1239, doi. 10.1007/s00439-015-1602-1
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- Publication type:
- Article
Multiple epiphyseal dysplasia.
- Published in:
- Acta Orthopaedica, 2009, v. 80, n. 6, p. 711, doi. 10.3109/17453670903473032
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- Publication type:
- Article
Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma.
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- Clinical Chemistry, 2015, v. 61, n. 11, p. 1408, doi. 10.1373/clinchem.2015.238543
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- Publication type:
- Article
Polymorphisms in the Dopamine Receptor 2 Gene Region Influence Improvements during Working Memory Training in Children and Adolescents.
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- Journal of Cognitive Neuroscience, 2014, v. 26, n. 1, p. 54, doi. 10.1162/jocn_a_00478
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- Publication type:
- Article
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
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- Human Molecular Genetics, 2019, v. 28, n. 2, p. 332, doi. 10.1093/hmg/ddy347
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- Publication type:
- Article
SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations.
- Published in:
- Behavior Genetics, 2011, v. 41, n. 1, p. 134, doi. 10.1007/s10519-010-9431-4
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- Publication type:
- Article