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An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterning†.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 11, p. 2464, doi. 10.1093/hmg/dds060
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- Article
A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotype.
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- Human Molecular Genetics, 2009, v. 18, n. 5, p. 847
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- Publication type:
- Article
Genomic Analysis of Hematopoietic Stem Cell at the Single-Cell Level: Optimization of Cell Fixation and Whole Genome Amplification (WGA) Protocol.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 19, p. 7366, doi. 10.3390/ijms21197366
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- Article
Wnt/CTNNB1 Signal Transduction Pathway Inhibits the Expression of ZFP36 in Squamous Cell Carcinoma, by Inducing Transcriptional Repressors SNAI1, SLUG and TWIST.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 16, p. 5692, doi. 10.3390/ijms21165692
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- Article
Mutated clones driving leukemic transformation are already detectable at the single-cell level in CD34-positive cells in the chronic phase of primary myelofibrosis.
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- NPJ Precision Oncology, 2021, v. 5, n. 1, p. 1, doi. 10.1038/s41698-021-00144-9
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- Article
Increased Plasma Levels of lncRNAs LINC01268 , GAS5 and MALAT1 Correlate with Negative Prognostic Factors in Myelofibrosis.
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- Cancers, 2021, v. 13, n. 19, p. 4744, doi. 10.3390/cancers13194744
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- Article
Depletion of Trichoplein (TpMs) Causes Chromosome Mis-Segregation, DNA Damage and Chromosome Instability in Cancer Cells.
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- Cancers, 2020, v. 12, n. 4, p. 993, doi. 10.3390/cancers12040993
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- Article
Control of pelvic girdle development by genes of the Pbx family and Emx2.
- Published in:
- Developmental Dynamics, 2011, v. 240, n. 5, p. 1173, doi. 10.1002/dvdy.22617
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- Publication type:
- Article