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Epigenetic alterations in disseminated neuroblastoma tumour cells: influence of TMS1 gene hypermethylation in relapse risk in NB patients.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2010, v. 136, n. 9, p. 1415, doi. 10.1007/s00432-010-0796-9
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- Publication type:
- Article
Clinical findings and molecular characterization of six subtelomeric imbalances.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Mutation screening ofUSH3gene (clarin-1) in Spanish patients with Usher syndrome: low prevalence and phenotypic variability.
- Published in:
- Clinical Genetics, 2004, v. 66, n. 6, p. 525, doi. 10.1111/j.1399-0004.2004.00352.x
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- Publication type:
- Article
Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome.
- Published in:
- Clinical Genetics, 2003, v. 64, n. 6, p. 491
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- Publication type:
- Article
Li–Fraumeni syndrome heterogeneity.
- Published in:
- Clinical & Translational Oncology, 2020, v. 22, n. 7, p. 978, doi. 10.1007/s12094-019-02236-2
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- Publication type:
- Article
Isoform-specific function of calpains in cell adhesion disruption: studies in postlactational mammary gland and breast cancer.
- Published in:
- Biochemical Journal, 2016, v. 473, n. 18, p. 2893, doi. 10.1042/BCJ20160198
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- Publication type:
- Article
Genomic Profiling of Uterine Aspirates and cfDNA as an Integrative Liquid Biopsy Strategy in Endometrial Cancer.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 2, p. 585, doi. 10.3390/jcm9020585
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- Publication type:
- Article
Sun exposure and PDZK1 genotype modulate PDZK1 gene expression in normal skin.
- Published in:
- Photodermatology, Photoimmunology & Photomedicine, 2020, v. 36, n. 1, p. 70, doi. 10.1111/phpp.12508
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- Publication type:
- Article
Mutation screening of AURKB and SYCP3 in patients with reproductive problems.
- Published in:
- Molecular Human Reproduction, 2013, v. 19, n. 2, p. 102
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- Publication type:
- Article
Genome-wide DNA methylation profiling in anorexia nervosa discordant identical twins.
- Published in:
- Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-021-01776-y
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- Publication type:
- Article
RUNAT-BI: A Ruthenium(III) Complex as a Selective Anti-Tumor Drug Candidate against Highly Aggressive Cancer Cell Lines.
- Published in:
- Cancers, 2023, v. 15, n. 1, p. 69, doi. 10.3390/cancers15010069
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- Publication type:
- Article
Loxl3 Promotes Melanoma Progression and Dissemination Influencing Cell Plasticity and Survival.
- Published in:
- Cancers, 2022, v. 14, n. 5, p. 1200, doi. 10.3390/cancers14051200
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- Publication type:
- Article
Predictive Role of Leptin Receptor (Ob-R) Overexpression in Patients with Early Breast Cancer Receiving Neoadjuvant Systemic Treatment.
- Published in:
- Cancers, 2021, v. 13, n. 13, p. 3269, doi. 10.3390/cancers13133269
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- Publication type:
- Article
HDAC5 Inhibitors as a Potential Treatment in Breast Cancer Affecting Very Young Women.
- Published in:
- Cancers, 2020, v. 12, n. 2, p. 412, doi. 10.3390/cancers12020412
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- Publication type:
- Article
Genetic analysis of 2299delG and C759F mutations (USH2A) in patients with visual and/or auditory impairments.
- Published in:
- European Journal of Human Genetics, 2004, v. 12, n. 5, p. 407, doi. 10.1038/sj.ejhg.5201138
- By:
- Publication type:
- Article
Autosomal-dominant hypohidrotic ectodermal dysplasia caused by a novel mutation.
- Published in:
- 2008
- By:
- Publication type:
- Letter
miR302a and 122 are deregulated in small extracellular vesicles from ARPE-19 cells cultured with H<sub>2</sub>O<sub>2</sub>.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-54373-x
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- Publication type:
- Article
Acceleration in the DNA methylation age in breast cancer tumours from very young women.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51457-6
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- Publication type:
- Article
miRNA Expression Analysis: Cell Lines HCC1500 and HCC1937 as Models for Breast Cancer in Young Women and the miR-23a as a Poor Prognostic Biomarker.
- Published in:
- Breast Cancer: Basic & Clinical Research, 2020, p. 1, doi. 10.1177/1178223420977845
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- Publication type:
- Article
Breast Cancer in Very Young Patients in a Spanish Cohort: Age as an Independent Bad Prognostic Indicator.
- Published in:
- Breast Cancer: Basic & Clinical Research, 2019, v. 13, p. N.PAG, doi. 10.1177/1178223419828766
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- Publication type:
- Article
Rare chromosomal complement of trisomy 21 in a boy conceived by IVF and cryopreservation.
- Published in:
- 2009
- By:
- Publication type:
- Case Study
Sex-specific genetic effects associated with pigmentation, sensitivity to sunlight, and melanoma in a population of Spanish origin.
- Published in:
- Biology of Sex Differences, 2016, v. 7, p. 1, doi. 10.1186/s13293-016-0070-1
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- Publication type:
- Article
Role of cfDNA and ctDNA to improve the risk stratification and the disease follow-up in patients with endometrial cancer: towards the clinical application.
- Published in:
- Journal of Experimental & Clinical Cancer Research (17569966), 2024, v. 43, n. 1, p. 1, doi. 10.1186/s13046-024-03158-w
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- Publication type:
- Article
Mutation profile of the MYO7A gene in Spanish patients with Usher syndrome type I.
- Published in:
- Human Mutation, 2006, v. 27, n. 3, p. 290, doi. 10.1002/humu.9404
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- Publication type:
- Article
Methylation deregulation of miRNA promoters identifies miR124-2 as a survival biomarker in Breast Cancer in very young women.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-32393-3
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- Publication type:
- Article
MicroRNA profile in very young women with breast cancer.
- Published in:
- BMC Cancer, 2014, v. 14, p. 1, doi. 10.1186/1471-2407-14-529
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- Publication type:
- Article
MicroRNA profile in very young women with breast cancer
- Published in:
- BMC Cancer, 2014, v. 14, n. 1, p. 529, doi. 10.1186/1471-2407-14-529
- By:
- Publication type:
- Article
De novo Interstitial Triplication of MECP2 in a Girl with Neurodevelopmental Disorder and Random X Chromosome Inactivation.
- Published in:
- Cytogenetic & Genome Research, 2011, v. 135, n. 2, p. 93, doi. 10.1159/000330917
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- Publication type:
- Article
Corpus Callosum Abnormalities and the Controversy about the Candidate Genes Located in 1q44.
- Published in:
- Cytogenetic & Genome Research, 2010, v. 127, n. 1, p. 5, doi. 10.1159/000279261
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- Publication type:
- Article
Submicroscopic Duplication of the Wolf-Hirschhorn Critical Region with a 4p Terminal Deletion.
- Published in:
- Cytogenetic & Genome Research, 2009, v. 125, n. 2, p. 103, doi. 10.1159/000227833
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- Publication type:
- Article
Recombinant X chromosome in a prenatal diagnosis.
- Published in:
- Cytogenetic & Genome Research, 2006, v. 112, n. 3/4, p. 337, doi. 10.1159/000089890
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- Publication type:
- Article
MicroRNA profile in very young women with breast cancer.
- Published in:
- 2014
- By:
- Publication type:
- journal article