Found: 16
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Beckwith-Wiedemann syndrome and long QT syndrome due to familial-balanced translocation t(11;17)(p15.5;q21.3) involving the KCNQ1 gene.
- Published in:
- Clinical Genetics, 2013, v. 84, n. 1, p. 78, doi. 10.1111/cge.12038
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- Publication type:
- Article
Suppressing aberrant GluN3A expression rescues synaptic and behavioral impairments in Huntington's disease models.
- Published in:
- Nature Medicine, 2013, v. 19, n. 8, p. 1030, doi. 10.1038/nm.3246
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- Publication type:
- Article
Dual activities of the anti-cancer drug candidate PBI-05204 provide neuroprotection in brain slice models for neurodegenerative diseases and stroke.
- Published in:
- Scientific Reports, 2016, p. 25626, doi. 10.1038/srep25626
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- Publication type:
- Article
Perturbation with Intrabodies Reveals That Calpain Cleavage Is Required for Degradation of Huntingtin Exon 1.
- Published in:
- PLoS ONE, 2011, v. 6, n. 1, p. 1, doi. 10.1371/journal.pone.0016676
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- Publication type:
- Article
Inhibition of Jurkat-T-lymphocyte Na<sup>+</sup>/H<sup>+</sup>-exchanger by CD95(Fas/Apo-1)-receptor stimulation.
- Published in:
- Pflügers Archiv: European Journal of Physiology, 2000, v. 440, n. 6, p. 902, doi. 10.1007/s004240000358
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- Publication type:
- Article
Contribution of the amino and carboxyl termini for PHA‐4/FoxA function in Caenorhabditis elegans.
- Published in:
- Developmental Dynamics, 2005, v. 234, n. 2, p. 346
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- Publication type:
- Article
IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome.
- Published in:
- Journal of Cell Biology, 2009, v. 187, n. 7, p. 1083, doi. 10.1083/jcb.200909067
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- Publication type:
- Article
A G polymorphism in the CRBN gene acts as a biomarker of response to treatment with lenalidomide in low/int-1 risk MDS without del(5q).
- Published in:
- Leukemia (08876924), 2013, v. 27, n. 7, p. 1610, doi. 10.1038/leu.2013.59
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- Publication type:
- Article
NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951.
- Published in:
- 2010
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- Publication type:
- journal article
Activating mutation in the TSLPR gene in B-cell precursor lymphoblastic leukemia.
- Published in:
- Leukemia (08876924), 2010, v. 24, n. 3, p. 642, doi. 10.1038/leu.2009.231
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- Publication type:
- Article
Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies.
- Published in:
- 2010
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- Publication type:
- Letter
Brigatinib in patients with ALK‐positive anaplastic large cell lymphoma who have failed brentuximab vedotin.
- Published in:
- Hematological Oncology, 2023, v. 41, p. 505, doi. 10.1002/hon.3164_373
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- Publication type:
- Article
HIGH‐RISK MANTLE CELL LYMPHOMA IN THE LYMA TRIAL: A LYSA STUDY.
- Published in:
- Hematological Oncology, 2021, v. 39, p. 1, doi. 10.1002/hon.64_2880
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- Publication type:
- Article
Huntingtin Interacting Proteins Are Genetic Modifiers of Neurodegeneration.
- Published in:
- PLoS Genetics, 2007, v. 3, n. 5, p. e82, doi. 10.1371/journal.pgen.0030082
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- Publication type:
- Article
BIPHASIC OPTICAL SIGNAL OF AN OSCILLATING NONSTATIONARY BELOUSOV–ZHABOTINSKY BULK REACTION AND ITS SIMILARITY TO SOME NEUROPHYSIOLOGICAL EVENTS.
- Published in:
- International Journal of Bifurcation & Chaos in Applied Sciences & Engineering, 2007, v. 17, n. 4, p. 1329, doi. 10.1142/S0218127407017823
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- Publication type:
- Article
Adiponectin receptor gene expression in human skeletal muscle cells is not regulated by fibrates and thiazolidinediones.
- Published in:
- International Journal of Obesity, 2005, v. 29, n. 7, p. 760, doi. 10.1038/sj.ijo.0802957
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- Publication type:
- Article